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Logo of jcinvestThe Journal of Clinical InvestigationCurrent IssueArchiveSubscriptionAbout the Journal
J Clin Invest. 2010 November 1; 120(11): 3760–3772.
Published online 2010 November 1. doi:  10.1172/JCI42843
PMCID: PMC2964977

Nociceptors: the sensors of the pain pathway


Specialized peripheral sensory neurons known as nociceptors alert us to potentially damaging stimuli at the skin by detecting extremes in temperature and pressure and injury-related chemicals, and transducing these stimuli into long-ranging electrical signals that are relayed to higher brain centers. The activation of functionally distinct cutaneous nociceptor populations and the processing of information they convey provide a rich diversity of pain qualities. Current work in this field is providing researchers with a more thorough understanding of nociceptor cell biology at molecular and systems levels and insight that will allow the targeted design of novel pain therapeutics.


Pain, as a submodality of somatic sensation, has been defined as a “complex constellation of unpleasant sensory, emotional and cognitive experiences provoked by real or perceived tissue damage and manifested by certain autonomic, psychological, and behavioral reactions” (1). The benefit of these unpleasant sensations, however, is underscored by extreme cases: patients lacking the ability to perceive pain due to hereditary neuropathies often maintain unrealized infections, self mutilate, and have curtailed life spans (2). Normally, nociception (see Glossary, Sidebar 1) and the perception of pain are evoked only at pressures and temperatures extreme enough to potentially injure tissues and by toxic molecules and inflammatory mediators. These high threshold physical and noxious chemical stimuli are detected by specialized peripheral sensory neurons (nociceptors). This is in contrast to the high sensitivity of visual, auditory, olfactory, taste, and somatosensory organs to their adequate stimuli. Pain is described as having different qualities and temporal features depending on the modality and locality of the stimulus, respectively: first pain is described as lancinating, stabbing, or pricking; second pain is more pervasive and includes burning, throbbing, cramping, and aching and recruits sustained affective components with descriptors such as “sickening” (3). The intensity of these global reactions underscores the importance of avoiding damaging situations for survival and maintaining homeostasis. As opposed to the relatively more objective nature of other senses, pain is highly individual and subjective (4, 5) and the translation of nociception into pain perception can be curtailed by stress or exacerbated by anticipation (6).

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Here, we review the nociceptive aspect of pain perception, focusing on nociceptors innervating the skin and subserving exteroception of noxious stimuli. Discussion of the similarities and differences among cutaneous, visceral, muscle, and joint nociception can be found elsewhere (79). We provide an overview of how noxious stimuli are detected, encoded, and conveyed to the CNS. Since recent reviews have described in detail the molecules involved in detecting noxious stimuli (1013) and contributing to protective mechanisms mediating enhanced pain at the site of injury (14), we take an integrative approach that highlights recently discovered cellular transduction/conduction mechanisms in the context of different nociceptor fiber types identified in vivo and ex vivo. We further discuss innovations using genetic and pharmacological tools that begin to address how particular nociceptor populations contribute to the perception of specific pain qualities. Since maladaptive changes in normal physiological mechanisms underlie a variety of pathologies leading to chronic pain, a thorough understanding of nociception is required to identify the interventions most likely to provide therapeutic benefit.

Anatomy and physiology of cutaneous nociception

Significant insights into the cellular and molecular basis of cutaneous nociception have been realized from studies on conscious humans and surrogate animal models (15, 16), although we are far from understanding the cell biology of pain perception. Advances are hampered by the difficulties inherent in studying neuronal processes in humans, cellular changes in nociceptors induced by invasive methods, the inability to record directly from the tiny structures where transduction of noxious stimuli occurs, and the uncertainty in model systems that an animal’s behavior is due to its perception of pain (15, 17). Although the morphology of sensory nociceptive nerve endings is highly conserved in animals from rodents to humans (5, 9, 1719), cutaneous nociceptors are an extremely heterogeneous group of neurons housed in peripheral sensory ganglia located just outside the CNS that transduce external noxious stimuli in the skin, up to meters away from their cell bodies.

Minimally invasive extracellular single unit recordings from nerve fibers in peripheral nerves (microneurography) and skin-nerve preparations in mammals (20) and microneurography combined with psychophysical measurements in human subjects (15, 16, 21) have revealed the existence of distinct classes of nociceptor activated by noxious stimuli. Adequate stimuli include temperature extremes (> ~40°C–45°C or < ~15°C), intense pressure, and chemicals signaling potential or actual tissue damage. Nociceptors are generally electrically silent (12) and transmit all-or-none action potentials only when stimulated. However, nociceptor activity does not per se lead to the perception of pain. The latter requires peripheral information to reach higher centers and normally depends on the frequency of action potentials in primary afferents, temporal summation of pre- and postsynaptic signals, and central influences (7).

The speed of transmission is directly correlated to the diameter of axons of sensory neurons and whether or not they are myelinated. Most nociceptors have small diameter unmyelinated axons (C-fibers) (12) bundled in fascicles surrounded by Schwann cells and support conduction velocities of 0.4–1.4 m/s (22) (Figure (Figure1).1). Initial fast-onset pain is mediated by A-fiber nociceptors whose axons are myelinated and support conduction velocities of approximately 5–30 m/s (most in the slower Aδ range) (22). Nociceptive fibers have been classified (23) on the basis of their conduction velocity and sensitivity and threshold to noxious mechanical (M), heat (H), and cold (C) (Tables (Tables11 and and2)2) (9, 23). Units responding to thermal, mechanical, and chemical stimuli (polymodal) are the most common C-fiber type observed in fiber recordings (C-MH, C-MC, C-MHC) (7, 9, 24) (Table (Table1).1). The expression of differential repertoires of transduction molecules (particularly chemical sensors) confers a rich functional heterogeneity upon this class. The use of electrical stimulation to search for receptive fields, rather than mechanical stimulation, identified nociceptors normally insensitive to mechanical and heat stimulation (silent; C-MiHi) that become sensitive to noxious mechanical or temperature only after being sensitized by inflammatory mediators (25, 26). C-fibers responsive to noxious heat (C-H; ~10% of C-nociceptors) play a major role in heat sensation (see below). A-fiber nociceptors are predominately heat- and or mechanosensitive (A-MH, A-H, A-M) (19, 27) (Table (Table2);2); however, sensitivity to noxious cold is also observed (2729). Determining the contribution of each of these fiber types to pain perception requires an understanding of the molecular mechanisms underlying the detection of particular stimulus modalities and nociceptor connectivity in central circuits.

Figure 1
Anatomy of nociceptors.
Table 1
Major heat and/or mechanosensitive nociceptor C-fiber classes
Table 2
Major heat and/or mechanosensitive nociceptor A-fiber classes

Noxious stimuli are transduced into electrical signals in free “unencapsulated” nerve endings that have branched from the main axon and terminate in the wall of arterioles and surrounding connective tissue, and may innervate distinct regions in the dermis and epidermis (17, 30). The endings are ensheathed by Schwann cells except at the end bulb and at mitochondria- and vesicle-rich varicosities (17). A–fibers lose their myelin sheath and the unmyelinated A-fiber branches cluster in separated small spots within a small area, the anatomical substrate for their receptive field (17). C-fiber branches are generally more broadly distributed, precluding precise localization of the stimulus (17). In contrast, specialized nonneuronal structures conferring high sensitivity to light touch, stretch, vibration, and hair movement are innervated by low threshold A-fibers (11). Nociceptive endings are in the vicinity of keratinocytes, mast cells, and Langerhans cells, indicating the capacity of peripheral sensory endings to monitor the status of the skin (31). Nociceptors, like other primary somatosensory neurons, are pseudounipolar (Figure (Figure1):1): a single process emanates from the cell body in the dorsal root ganglion (DRG) or trigeminal ganglion (TG) and bifurcates, sending a peripheral axon to innervate the skin and a central axon to synapse on second-order neurons in the dorsal horn of the spinal cord or the trigeminal subnucleus caudalis (Vc) (13), respectively (Figure (Figure1A).1A). In this way, propagating electrical signals between periphery and spinal cord (or brainstem) follow a direct axonal pathway, thus reducing the risk of conduction failure (32). Nociceptors are excitatory neurons and release glutamate as their primary neurotransmitter as well as other components including peptides (e.g., substance P, calcitonin gene-related peptide [CGRP], somatostatin) important in both central synaptic signaling and efferent signaling in the skin (13). Invasion of action potentials into the nociceptor soma via the short stem axon (32) can lead to biochemical changes (e.g., phosphorylation and activation of MAPK superfamily of signaling pathways) that ultimately alter gene expression and functional phenotype (33, 34). Although it is thought that direct communication between the soma of primary sensory neurons does not occur, vesicle exocytosis is observed in dissociated soma and may influence associated Schwann cells and possibly nearby neurons (35, 36). The central axon of DRG neurons enters the spinal cord via the dorsal root and sprouts branches that innervate multiple spinal segments in the rostral and caudal direction as well as the segment associated with the particular DRG and dorsal column nuclei of the caudal medulla (7). They terminate predominantly in laminae I, II, and V of the dorsal horn on relay neurons and local interneurons important for signal modification (13, 37, 38) (Figure (Figure1,1, B and C). The relay neurons project to the medulla, mesencephalon, and thalamus, which in turn project to somatosensory and anterior cingulate cortices to drive sensory-discriminative and affective-cognitive aspects of pain, respectively (38). Local inhibitory and excitatory interneurons in the dorsal horn as well as descending inhibitory and facilitatory pathways originating in the brain modulate the transmission of nociceptive signals, thus contributing to the prioritization of pain perception relative to other competing behavioral needs and homeostatic demands (39).

The cell body (soma) has served as an extremely useful model to study molecules and modulatory mechanisms mediating transduction of noxious stimuli, transmission of electrical signals to the CNS, and release of neurotransmitters and neuropeptides at central and peripheral terminals (40, 41). The soma expresses many molecular entities that are expressed in free nerve endings, central terminals, and axon (13). However, data from whole-cell soma recordings have been shown in a few cases to be at odds with behavioral or peripheral physiological data (e.g., heat transduction, refs. 4244; and proton responsiveness, ref. 45). Although the underlying differences in these cases may be due to differential distribution of transduction molecules, it is also possible that nonneuronal peripheral components are required in vivo and lacking in dissociated neuronal cultures. This underscores the importance of corroborating results from cultured neurons with behavior and/or acute preparations retaining intact terminal fields. Labeling with retrograde dyes injected into the target tissue has enabled characterization of functional attributes of the soma of nociceptors innervating those tissues. The heterogeneity of functional phenotypes observed in isolated sensory cell bodies (46, 47) appears to reflect the variability observed in cutaneous nociceptor fiber types observed in studies in which recordings from fiber or soma during receptive field stimulation are combined with subsequent nociceptor labeling to identify terminal morphology (48, 49) and the expression of nocisensors (50), markers, and peptides (48) (Table (Table1).1). Nociceptors differentially express a variety of anatomical and biochemical markers (e.g., the expression of versican, the binding partner for the isolectin B4 [IB4]; ref. 51), however the functional significance of these markers, especially given striking species differences (49, 52), are unknown. Here, we will address how the functional heterogeneity of the nociceptor has an impact on the perception of pain.

The response of nociceptors to noxious stimuli

Close proximity of distal extremities to a hot or cold surface, intense pressure or squeezing, and irritating chemicals can result in a subsecond somatopic withdrawal response. Activation of nociceptors requires that adequate stimuli depolarize peripheral terminals (producing a receptor potential) with sufficient amplitude and duration. This ensures that despite any attenuation and slowing of the receptor potential by passive propagation between the sites of transduction and action potential generation, information such as stimulus intensity will be encoded in the resulting train of impulses. Although the distance to action potential initiation is not known for fibers innervating the skin, action potential generation has been proposed to be at or near the site of transduction in Aδ cold fibers innervating the guinea pig cornea (53). In this model, action potentials can be generated at differing distances from the terminal ending depending on the extent of depolarization of the fiber and resulting inactivation of voltage-gated channels involved in conduction (53). Theoretically, the depolarizing receptor potential can be accomplished by multiple membrane conductance changes and electrogenic pump activity. Since the electrochemical gradients for sodium (Na+), calcium (Ca+2), and chloride (Cl) (37) are more positive than the resting membrane potential in sensory neurons, the opening of ion channels permeable to these ions will cause the membrane potential to shift in the positive direction (depolarize). Since the electrochemical gradient for potassium (K+) is more negative than resting potential, closure of active potassium channels not only depolarizes the membrane potential but amplifies current-induced voltage fluctuations due to the resulting increase in membrane resistance (54).

The identification of the molecules that mediate or contribute to heat-, cold-, mechanical-, and chemical-induced generator potentials has been achieved by careful characterization of currents in native cells, the use of novel approaches to identify genes encoding channels and receptors, genome sequencing and bioinformatics, chemical tools (e.g., calcium dyes, pharmacological agents), and innovative genetic approaches. Although significant progress has been made in the study of heat and chemical transduction, many pieces of the puzzle are still missing (Table (Table33 and Figure Figure2). 2).

Figure 2
Known or proposed transduction mechanisms in uninjured mammalian nociceptor peripheral terminals.
Table 3
Proposed ion channel sensors of cutaneous noxious stimuli

Transduction of noxious heat

At least 5 classes of nociceptor reveal an increase in activity dependent on the intensity of the heat stimulus beyond the threshold for pain perception (~40°C–45°C) into the noxious range (9, 24). Microneurography studies on conscious human subjects have addressed whether activity in a particular fiber correlates with the psychological rating of pain. Under normal conditions, the activity in only a subset of heat-responsive fibers correlates to the degree of pain perceived (C-MH, A-MH type I, A-MH type II; Tables Tables11 and and2).2). A-fibers (A-MH Type II innervating hairy skin) responding to temperatures slightly cooler than the perceptual pain threshold for heat are proposed to mediate first pain in humans (55). These fibers rapidly activate, adapt during prolonged heat stimulation, fatigue between heat stimuli, and are sensitive to capsaicin (5557), a selective agonist of the mammalian heat-activated nonselective cation (NSC) channel transient receptor potential VI (TRPV1) (58) (Table (Table3).3). In humans and monkeys, slowly developing second pain is evoked by activation of C-fibers and A-MH type I–fibers (9, 24), the latter requiring longer exposures to noxious temperatures to achieve maximal firing rates (Tables (Tables11 and and2).2). Heat-induced C-MH fiber activity in primates correlates with human pain perception in the absence of injury (9). In human glabrous skin, however, neither first pain (56) nor A-MH type II–fiber innervation is observed (59). Investigation of noxious heat transduction in animal models is complicated because the conservation of these pathways is unknown.

Although human C-MH polymodal nociceptors are activated in a temperature range (39°C–51°C) similar to recombinant TRPV1 (58) and have been reported to be transiently activated by capsaicin (60), genetic deletion of TRPV1 in mice only partially reduces noxious heat sensitivity in behavioral assays (42, 43) and has no effect on heat responsiveness of the C-fibers tested (42, 44, 49). This suggests that, at least in mice, heat sensors other than TRPV1 are the major contributors to acute heat-induced pain. Cultures of rodent sensory ganglia indicate expression of TRPV1 in approximately 50% of neurons (61) and 75% of small-medium diameter neurons (43), similar to the proportion of C-MH fibers in a skin-nerve-sensory ganglion–spinal cord preparation (49). Although functionally characterized mouse C-MH neurons were not immunoreactive for TRPV1 (50), neurons with low expression levels may have been missed. Importantly, every identified mouse C-H neuron (~10% of the population) revealed TRPV1-like immunoreactivity (50) and no functionally identified C-H nociceptors were observed in TRPV1-deficient animals. This result cannot be explained by a phenotypic switch to C-MH fibers in these mice since mechanical sensitivity of the C-fiber population was unchanged (50). Furthermore, noxious acute heat responses evoked in rat C-MH saphenous fibers were not decreased by ruthenium red at concentrations that block the capsaicin response (45). In humans, the prolonged time course of the strong C-H response to capsaicin applied to the receptive field matched the duration of the perceived pain (60) and is consistent with the results of rodent studies (50). Disparities regarding the contribution of TRPV1 to fiber subtype functionality (especially C-MH fibers) may depend on species, stimulation techniques, tissue preparation, and sensitivity of the assay. However, it is clear that acute heat responses are mediated by mechanisms in addition to TRPV1 activation, at least in mouse. In the context of tissue injury, however, polymodal C-MH fibers are certainly important in TRPV1-mediated thermal hyperalgesia, indicating that inflammation upregulates the contribution of TRPV1 to heat-evoked nocifensive behaviors in mouse (see below). TRPV2 (Table (Table3)3) has been suggested to mediate, at least in part, the receptor potential in A-MH type I–fibers, since it is activated by temperatures greater than 52°C in recombinant expression studies (62); however, the lack of selective pharmacological tools for manipulation of TRPV2 activity has hindered rigorous evaluation of this hypothesis. Transducers of heat stimuli into the noxious range other than TRPV1 and TRPV2 (45, 49) include other TRPV channels (TRPV3 and TRPV4) that have been reported to exist on sensory neurons (10) as well as constitutively active K+ channels (KCNK2) inhibited by heat (63) (Table (Table3).3). Although TRPV3 undergoes dramatic sensitization to repeated heat stimuli, TRPV3 does not appear to be involved in agonist sensitization of C-fiber heat responses (44). Nocisensors directly activated by heat are also expressed on resident skin cells (e.g., TRPV3 and TRPV4 on keratinocytes; refs. 10 and 31) and cause the release of allogenic substances that indirectly influence nociceptor firing (64) (Table (Table3). 3).

Transduction of noxious cold

Identifying the mechanisms used by nociceptors to transduce noxious cold has lagged behind progress in understanding heat transduction mechanisms (65). The intensity of cold pain in humans increases linearly with stimulus intensity between about 20°C and 0°C. The threshold for pain perception to cold is much less precise than that for heat, but is about 15°C (66). There is tremendous variability in threshold for cutaneous cold-evoked fiber activity observed in mammals in part due to the rate of cooling (approximately +30°C to –18°C; refs. 27, 66–68). Homeostatic processes engaged during in vivo studies (e.g., vasculature changes) and potential tissue damage occurring at subfreezing temperatures are likely to indirectly influence nociceptor responsiveness. Furthermore, measuring cold nocifensive behavior in animals has proven to be challenging, perhaps due to the prolonged exposure time in most assays (68).

Cooling the skin to 4°C activates A- and C-fibers sensitive to innocuous cooling and cold-sensitive nociceptors (2729, 67, 69), consistent with the presence of two populations of cold-sensitive neurons observed in culture (7072). Cool-sensitive nonnociceptive afferents are spontaneously active at normal skin temperature and their excitability increases with decreasing temperature (53, 67). The menthol-activated NSC channel TRPM8 (10) is responsible for the detection of innocuous cooling (69, 73, 74) and contributes to spontaneous firing (69) in mice. The effective range for TRPM8-mediated cold coding extends from just below skin temperature into the noxious range (10°C–15°C and below; ref. 10). Although mouse studies have yielded conflicting results regarding the requirement of TRPM8 in behavioral responses to noxious stimuli, more recent work using a novel cold-plate assay convincingly demonstrates a role for mouse TRPM8 in sensing noxious cold (75). Furthermore, the analgesic effects of cold temperature (17°C) were lost in mice lacking TRPM8 in the context of formalin-induced inflammation (74). Whether TRPM8-mediated analgesia is dependent on peripheral and/or central sites of action is unknown but may be addressed now that TRPM8-expressing neurons and their peripheral and central fibers can be visualized by GFP expression driven by the TRPM8 promoter (76, 77). Importantly, studies in humans and mice reveal species differences in pathways sensing innocuous cold: A-fiber block completely suppresses the cold response in humans (78), yet the majority of TRPM8-expressing fibers responsible for innocuous cold transduction in mice have small diameters (76, 77)

Noxious cold stimuli activate NSC currents and calcium influx (10, 79) and decrease K+ channel activity (80) and Na+/K+-ATPase function (65) (Table (Table3).3). The temporal dissociation of the qualities of pain/ache vs. prickle/heat to noxious cold (3°C) suggest underlying differences in transduction mechanisms or information processing (66). The cation channel TRPA1 (10) has been proposed to play a role in this process because it has a threshold near 17°C, is expressed in nociceptors together with TRPV1 (10), and is required for cold sensation in mice (81, 82). Human genetic studies have suggested TRPA1 contributes to variation in cold-pain sensitivity (5). Although TRPA1 may respond to cold indirectly through cold-induced intracellular calcium release (10), slow temperature ramps can activate TRPA1 in excised patches in the absence of calcium (82, 83). However, the contribution of TRPA1 to cold sensation is debated since TRPA1 activation was not observed in a heterologous expression system or cultured TG neurons to which relatively short cold stimuli to 5°C were applied (84), and not all mouse lines constitutively lacking TRPA1 reveal a cold phenotype in behavioral and neural assays (85). However, two independent studies recently demonstrated a role of TRPA1 in noxious cold sensitivity (75, 82). TRPA1 is established as a general sensor for noxious irritating electrophilic compounds (including allyl isothiocyanate [mustard oil] [AITC] and cinnamaldehyde, the active pungent ingredients in hot mustard and cinnamon, respectively; refs. 84 and 86) and is sensitized by inflammatory mediators (87). These electrophilic agonists open an integral channel pore by covalent binding to the intracellular N terminus of the channel protein (88, 89). Importantly, endogenous reactive chemicals are also effective agonists of TRPA1 (90). How TRPA1-expressing neurons might mediate the burning sensation of hot mustard (AITC) may be explained by anatomical and psychophysical results: AITC is a strong chemical activator of a subset of TRPV1-expressing neurons, and activity in peripheral fibers transmitting information about cold stimuli in the presence of an A-fiber block (presumably C-fibers) evoke burning, aching, and pricking qualities (67). Interestingly, the activation of some cold fibers by noxious heat may be the basis for the paradoxical cold sensation felt by stimulating cold spots with noxious heat stimuli (67).

Transduction of noxious mechanical stimuli

Whereas heat- and chemical-induced nociceptor responses correlate with pain perception in humans (9, 24), mechanical stimulation of C-MH (24) and rapidly adapting A-HTM (18) fibers may not (24) (Tables (Tables11 and and2).2). The perception of pinprick pain intensity, however, is related to activity in capsaicin-insensitive A-fiber nociceptors (e.g., A-M and A-MH type I) (78). Transduction channels mediating mammalian noxious (and innocuous) mechanical stimuli have been elusive (5, 91, 92). Transduction in soma membranes on a submillisecond time scale suggests direct gating by pressure of ion channels with NSC and possibly Na+ permeability (91). No orthologs for the well-studied prokaryotic mechanosensitive channels MscL and MscS are present in mammalian genomes (93). In addition, there is no strong evidence that mammalian orthologs of invertebrate components of structures involved in mechanosensation (92) are the transduction channel in cutaneous sensory neurons, although acid-sensitive ion channels (ASICs) appear to play a role (11). Some progress has been made in the identification of proteins (e.g., stomatin-like protein 3; ref. 94) involved in sensing innocuous touch, but their genetic deletion in mouse does not compromise behavioral responses to noxious pressure. TRP channels are candidates based on expression and functional similarities to evolutionary counterparts, but whether these contribute to the molecular sensor/transducer or function in a sensitizing role is still unclear (11) (Table (Table3).3). The challenges encountered in assigning a role for transducers of noxious mechanical stimuli include the efficacy of stimulation protocols applied in behavioral and ex vivo tissue assays (e.g., phenotypes can differ when challenged with thin calibrated von Frey nylon filaments vs. distributed pinch that may also induce local ischemia; ref. 95), the suppressive influence of innocuous A-fiber mechanosensitive inputs at a systems level (18), and the extrapolation of cellular assays to nociception (e.g., poking, ref. 96; stretching, ref. 97; hypo-osmotic–induced swelling, ref. 98). This topic is reviewed in more detail elsewhere (12, 19, 9193).


Nociceptors express a wide variety of voltage-gated channels (e.g., Nav, Cav, Kv) that transduce the receptor potential into an action potential or, more commonly, a set of action potentials that encode the intensity of a noxious stimulus applied within their receptive fields. There are 9 known Nav, 10 Cav, and 40 Kv genes in mammals (, many of which have multiple splice variants with different functional characteristics (99). Cell excitability and firing behavior (e.g., threshold for action potential generation, action potential and undershoot amplitude and duration, and maximal firing frequency) depend on the complement of these channels as well as those contributing to frequency modulation (e.g., hyperpolarization-activated cyclic nucleotide-gated cation channel [HCN] and A-type Kv4.3 and Kv3.4 channels) (54). For instance, nociceptors responsive to noxious cold require the expression of the tetrodotoxin-resistant (TTX-resistant) Nav1.8 channel at the peripheral terminal (100), and mice lacking Nav1.8 and Nav1.7 display deficits in mechanosensation (95, 101). Peripheral CGRP release by inflammatory mediators is unaffected by TTX, suggesting an important role of TTX-resistant Nav in regulated pain thresholds, consistent with their robust modulation by bradykinin (BK) and PGE2 (102) (see below). Since enhanced excitability of primary sensory neurons in inflammatory and pathologic pain states is a major contributor to the perception of pain, specific pharmacological agents that specifically dampen aberrant activity are desirable in the design of pain therapeutics. To this end, an understanding of species-specific differences is critical, as exemplified by the dramatically different phenotypes in mice and humans lacking Nav1.7: although mice lacking Nav1.7 show a mechanosensory (pinch) and formalin-induced (5%) pain phenotype (103), humans lacking Nav1.7 are insensitive to pain altogether (104).

Central modulation

Nociceptors release a variety of substances from their central terminals that have the potential of exciting second-order neurons through multiple mechanisms. Fast and slow synaptic transmission are mediated in large part by glutamate and peptides (e.g., substance P, CGRP), respectively (7, 38). Of particular importance to pain perception is the plasticity in synaptic strength (i.e., the ability to enhance homosynaptic as well as heterosynaptic connections) between primary afferents and the relay and interneurons they drive, presynaptic and postsynaptic modulation by descending facilitatory and inhibitory pathways in the spinal cord, and the efferent aspects of nociceptor function activated by strong GABAergic/glycinergic depolarization of presynaptic terminals leading to the dorsal root reflex (37, 105). Anterograde transmission of action potentials from the spinal cord to the periphery results in release of peptides and other inflammatory mediators in the skin and exacerbates nociceptor excitability and pain (see below). It is at the spinal level that nonnociceptive neurons are recruited by strong nociceptor activation through functional modulation of local circuits (105).

Adaptive and maladaptive shifts in pain threshold

Injury to the skin induces protective physiological responses aimed at decreasing the likelihood of exacerbating the injury. After an injury induced by pungent chemicals (e.g., capsaicin, mustard oil) and burn, stimulation of the injured area produces enhanced pain to noxious stimuli (primary mechanical and thermal hyperalgesia) dependent on C-fiber activity that manifests as a decrease in threshold to activate C-MH fibers and to perceive pain (9, 19, 106). Immediately surrounding the injured area, a zone of flare (reddening) develops and stimulation of even a larger secondary zone produces pain in response to normally innocuous stimuli (e.g., brush stroke) (secondary mechanical allodynia) as well as enhanced responsiveness to noxious mechanical (secondary mechanical hyperalgesia) and thermal (heat) hyperalgesia if spatial summation is invoked (secondary thermal hyperalgesia) (21, 105, 107). Here, noxious punctate stimulation of C-nociceptors induces secondary mechanical hyperalgesia mediated by A-nociceptors (7) and innocuous dynamic mechanical stimuli (gentle stroking) provokes nonnociceptor A-fiber–mediated pain (108). Cellular mechanisms underlying this complicated response involve both peripheral and central processes (14, 38, 105, 107) and require nociceptor input, particularly A-MH and C-MH fibers (19, 91, 105). After a burn, A-MH fibers (most likely type I) mediate primary heat hyperalgesia in glabrous skin (9).

What are the cellular mechanisms mediating hyperalgesia? Electrical stimulation of the majority of C-polymodal fibers produced plasma extravasation in their peripheral receptor field (109). Centrally propagating impulses can antidromically invade peripheral arborizations innervating other areas in the afferent’s receptive field (axon reflex), causing the release of peptides (e.g., substance P, CGRP, somatostatin) and/or other bioactive substances from the terminal (e.g., cytokines) into the interstitial tissue (17). The released substances produce a myriad of autocrine or paracrine effects on endothelial, epithelial, and resident immune cells (Langerhans), which lead to arteriolar vasodilatation (“flare,” via CGRP) and/or increased vascular permeability and plasma extravasation from venules (edema, via substance P). Liberated enzymes (e.g., kallikreins) and blood cells (e.g., platelets, mast cells) further contribute to the accumulation of inflammatory mediators and neurogenic inflammation (110, 111). A large variety of substances feed back onto nociceptors innervating the injured region and sensitize peripheral terminals by direct and indirect actions at ion channels, receptors, and second messenger cascades (87, 102, 111, 112). The mechanisms by which inflammatory mediators recruit “silent” C-MiHi fibers by endowing these fibers with prolonged mechanical and heat sensitivity (25, 60) is unknown but may involve long-lasting alterations in second messenger signaling cascades and sensitization of nocisensors. Decreased thermal and chemical thresholds in the primary area are due in part to sensitization of TRPV1 and TRPA1 by numerous components of the “inflammatory soup” including BK (36, 8587, 112). Although TRPV1 is not the only transducer of acute noxious heat, it is the major contributor to the development of heat hyperalgesia, perhaps due to its expression in polymodal neurons capable of inducing neurogenic inflammation and modifying central connections (42, 43). As a polymodal nocisensor, TRPV1 is the target for acute acid responsiveness in the skin of mice, although species differences are apparent (113). A recently described phenomenon (“hyperalgesic priming”) evoked by cytokine- and neurotrophin-induced recruitment of Gi/o-PKCε signaling in nociceptors can produce prolonged sensitization and mechanical hyperalgesia and may contribute to chronic pain (114). Prolonged pain perception observed in inflammatory pain models is generally believed to be produced by ongoing nociceptor activity (15); formalin, for instance, produces nocifensive behaviors through its activation of TRPA1 (115, 116). Secondary hyperalgesia to punctate pinprick stimuli is mediated at least in part by capsaicin-insensitive A-fiber nociceptors (e.g., A-MH type I and A-M; Table Table2)2) by central sensitization processes (78, 108).

Do labeled lines transmit noxious stimulus information?

Determining the extent to which pain qualities are dependent on the activation of subpopulations of neurons and intensity coding poses a considerable challenge and is an active area of research (13). Psychophysical studies on spinal cord injury patients suffering from partial or complete loss of thermal sensitivity support a model in which both pain-specific pathways and nonnociceptive pathways are integrated (117). Significant crosstalk between these pathways exists at multiple levels including stimulus transduction (118), peripheral terminals during neurogenic inflammation, and central connections during central sensitization and may underlie paradoxical temperature sensation. To address the extent by which particular nociceptive signaling pathways encode particular modalities, a number of approaches have been taken. Genetically encoded tracers have enabled visualization of specific subpopulations of sensory neurons (e.g., Mrgpr family, ref. 30; TRPM8, refs. 76 and 77) and determination of their innervation patterns as well as cellular function. Pharmacologic and hereditary genetic ablations have defined the role of nociceptors in pain but until recently have included multiple or entire nociceptor populations (e.g., capsaicin-induced ablation of TRPV1-expressing neurons; refs. 42 and 119) or sensory and autonomic populations (2). Genetically mediated ablation using toxins (e.g., diphtheria A) transcribed by promoters of genes expressed in specific neuronal subtypes (e.g., Nav1.8-expressing neurons, ref. 120) provides a means to address the contributions of particular cells to acute nociception and hyperalgesia and allodynia after injury.

Mice expressing diphtheria toxin under the Nav1.8 promoter reveal significant loss of sensory neurons (85% and 13% of unmyelinated and myelinated neurons, respectively, consistent with Nav1.8 expression in most nociceptors as well as some myelinated sensory neurons). These mice are unresponsive to acute noxious mechanical (pressure-induced, not punctate) and cold stimuli and defective in the development of inflammatory pain, but are normal with regard to acute responsiveness to heat stimuli and the ability to develop neuropathic pain (120). These data are remarkably consistent with gene-deletion studies (103). The sensitivity of C-MH fibers innervating hairy skin to cold, heat, and mechanical stimuli is reduced in mice constitutively lacking MrgprD-expressing cells reported to be TRPV1 and peptide negative (121). However, when genetic ablation of this population of cells is done in adulthood, behavioral deficits were observed to mechanical but not thermal stimuli (122). An additive loss of both mechanical- and heat-induced nocifensive behaviors was achieved after further pharmacologic ablation of central TRPV1+ terminals, suggesting a separation of mechanical and thermal modalities at all levels of sensory processing in the pain pathways subserved by MrgprD- and TRPV1-expressing cells (122). The extent to which this separation is maintained for other murine nociceptor populations is a subject of active research.

Future challenges

Despite significant progress in understanding the complexities of mammalian nociception and pain perception in the last half century, our knowledge is far from complete with regard to the identity of the full complement of sensors of noxious stimuli (particularly with regard to mechanotransduction), the role of nociceptor heterogeneity in physiological and pathological pain, the coding of the quality of the stimulus, and the modulation of pain pathways by peripheral and central mechanisms. A focus on mechanisms underlying thermal nociception and hyperalgesia is in large part due to the identification of the TRP family of channels. The future identification of elusive mechanotransducers in somatosensory neurons will likewise thrust the direction of research toward a cellular/molecular understanding of mechanical hyperalgesia and allodynia. The application of genetic technologies and pharmacological approaches to understanding the contributions of molecules, signaling pathways, and cell populations to nocifensive behaviors to particular stimulus modalities in normal and pathophysiological states in rodents will inspire hypotheses that ultimately must be tested in humans.


We gratefully acknowledge Jorg Grandl, Daniel Dubin, Takashi Miyamoto, and Arturo Galvez for helpful discussion. The work was supported by NIH grants R01 DE016927 and R01 NS046303 (to A. Patapoutian).


Conflict of interest: The authors have declared that no conflict of interest exists.

Citation for this article: J Clin Invest. 2010;120(11):3760–3772. doi:10.1172/JCI42843.


1. Terman GW, Bonica JJ. Spinal mechanisms and their modulation. In: Loeser JD, Butler SH, Chapman CR, Turk DC, eds.Bonica’s Management of Pain . 3rd ed. Philadelphia, Pennsylvania, USA: Lippincott Williams and Wilkins; 2003:73.
2. Axelrod FB, Hilz MJ. Inherited Autonomic Neuropathies. Semin Neurol. 2003;23(4):381–390. doi: 10.1055/s-2004-817722. [PubMed] [Cross Ref]
3. Price D, Dubner R. Mechanisms of first and second pain in the peripheral and central nervous systems. J Invest Dermatol. 1977;69(1):167–171. doi: 10.1111/1523-1747.ep12497942. [PubMed] [Cross Ref]
4. LaCroix-Fralish ML, Mogil JS. Progress in genetic studies of pain and analgesia. Annu Rev Pharmacol Toxicol. 2009;49:97–121. doi: 10.1146/annurev-pharmtox-061008-103222. [PMC free article] [PubMed] [Cross Ref]
5. Foulkes T, Wood JN. Pain genes. PLoS Genet. 2008;4(7):e1000086. doi: 10.1371/journal.pgen.1000086. [PMC free article] [PubMed] [Cross Ref]
6. Eccleston C. Role of psychology in pain management. Br J Anaesth. 2001;87(1):144–152. doi: 10.1093/bja/87.1.144. [PubMed] [Cross Ref]
7. Willis WD, Coggeshall RE.Sensory Mechanisms of the Spinal Cord . 3rd ed. New York, New York, USA: Kluwer Academic/Plenum; 2004.
8. Robinson DR, Gebhart GF. Inside Information: The Unique Features of Visceral Sensation. Mol Interv. 2008;8(5):242–253. doi: 10.1124/mi.8.5.9. [PMC free article] [PubMed] [Cross Ref]
9. Raja SN, Meyer RA, Campbell JN. Peripheral mechanisms of somatic pain. Anesthesiology. 1988;68(4):571–590. doi: 10.1097/00000542-198804000-00016. [PubMed] [Cross Ref]
10. Patapoutian A, Tate S, Woolf CJ. Transient receptor potential channels: targeting pain at the source. Nat Rev Drug Discov. 2009;8(1):55–68. doi: 10.1038/nrd2757. [PMC free article] [PubMed] [Cross Ref]
11. Smith E, Lewin G. Nociceptors: a phylogenetic view. 2009. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2009;195(12):1089–1106. [PMC free article] [PubMed]
12. Woolf CJ, Ma Q. Nociceptors—noxious stimulus detectors. Neuron. 2007;55(3):353–364. doi: 10.1016/j.neuron.2007.07.016. [PubMed] [Cross Ref]
13. Basbaum AI, Bautista DM, Scherrer G, Julius D. Cellular and molecular mechanisms of pain. Cell. 2009;139(2):267–284. doi: 10.1016/j.cell.2009.09.028. [PMC free article] [PubMed] [Cross Ref]
14. Hucho T, Levine JD. Signaling pathways in sensitization: toward a nociceptor cell biology. Neuron. 2007;55(3):365–376. doi: 10.1016/j.neuron.2007.07.008. [PubMed] [Cross Ref]
15. Le Bars D, Gozariu M, Cadden SW. Animal models of nociception. Pharmacol Rev. 2001;53(4):597–652. [PubMed]
16. Namer B, Handwerker H. Translational nociceptor research as guide to human pain perceptions and pathophysiology. Exp Brain Res. 2009;196(1):163–172. doi: 10.1007/s00221-009-1777-6. [PubMed] [Cross Ref]
17. Mense S, et al. Anatomy of nociceptors. In: Bushnell MC, Smith DV, Beauchamp GK, Firestei SJ, eds.The Senses: A Comprehensive Reference . New York, New York, USA: Academic Press; 2008:11–41.
18. Andrew D, Greenspan JD. Peripheral coding of tonic mechanical cutaneous pain: comparison of nociceptor activity in rat and human psychophysics. . J Neurophysiol. 1999;82(5):2641–2648. [PubMed]
19. Lewin GR, Moshourab R. Mechanosensation and pain. J Neurobiol. 2004;61(1):30–44. doi: 10.1002/neu.20078. [PubMed] [Cross Ref]
20. Zimmermann K, et al. Phenotyping sensory nerve endings in vitro in the mouse. Nat Protoc. 2009;4(2):174–196. doi: 10.1038/nprot.2008.223. [PubMed] [Cross Ref]
21. Schmelz M. Translating nociceptive processing into human pain models. Exp Brain Res. 2009;196(1):173–178. [PubMed]
22. Djouhri L, Lawson SN. A[beta]-fiber nociceptive primary afferent neurons: a review of incidence and properties in relation to other afferent A-fiber neurons in mammals. Brain Res Brain Res Rev. 2004;46(2):131–145. doi: 10.1016/j.brainresrev.2004.07.015. [PubMed] [Cross Ref]
23. Kumazawa T, Mizumura K, Kruger L, eds.The Polymodal Receptor-- A Gateway to Pathological Pain .Progress in Brain Research . Vol. 113. New York, New York, USA: Elsevier; 1996.
24. Van Hees J, Gybels J. C nociceptor activity in human nerve during painful and non painful skin stimulation. J Neurol Neurosurg Psychiatry. 1981;44(7):600–607. doi: 10.1136/jnnp.44.7.600. [PMC free article] [PubMed] [Cross Ref]
25. Schmidt R, Schmelz M, Forster C, Ringkamp M, Torebjörk E, Handwerker H. Novel classes of responsive and unresponsive C nociceptors in human skin. J Neurosci. 1995;15(1 pt 1):333–341. [PubMed]
26. Meyer RA, Davis KD, Cohen RH, Treede RD, Campbell JN. Mechanically insensitive afferents (MIAs) in cutaneous nerves of monkey. Brain Res. 1991;561(2):252–261. doi: 10.1016/0006-8993(91)91601-V. [PubMed] [Cross Ref]
27. Cain DM, Khasabov SG, Simone DA. Response properties of mechanoreceptors and nociceptors in mouse glabrous skin: an in vivo study. J Neurophysiol. 2001;85(4):1561–1574. [PubMed]
28. Darian–Smith I, Johnson KO, Dykes R. “Cold” fiber population innervating palmar and digital skin of the monkey: responses to cooling pulses. . J Neurophysiol. 1973;36(2):325–346. [PubMed]
29. Koltzenburg M, Stucky CL, Lewin GR. Receptive properties of mouse sensory neurons innervating hairy skin. J Neurophysiol. 1997;78(4):1841–1850. [PubMed]
30. Zylka MJ, Rice FL, Anderson DJ. Topographically distinct epidermal nociceptive circuits revealed by axonal tracers targeted to mrgprd. Neuron. 2005;45(1):17–25. doi: 10.1016/j.neuron.2004.12.015. [PubMed] [Cross Ref]
31. Lumpkin EA, Caterina MJ. Mechanisms of sensory transduction in the skin. Nature. 2007;445(7130):858–865. [PubMed]
32. Amir R, Devor M. Electrical excitability of the soma of sensory neurons is required for spike invasion of the soma, but not for through-conduction. Biophys J. 2003;84(4):2181–2191. doi: 10.1016/S0006-3495(03)75024-3. [PubMed] [Cross Ref]
33. Woolf CJ, Costigan M. Transcriptional and posttranslational plasticity and the generation of inflammatory pain. Proc Natl Acad Sci U S A. 1999;96(14):7723–7730. [PubMed]
34. Neurochem Res. 2008;33(10):1970–1978. doi: 10.1007/s11064-008-9711-z. [PMC free article] [PubMed] [Cross Ref]
35. Huang L-YM, Neher E. Ca2+-dependent exocytosis in the somata of dorsal root ganglion neurons. Neuron. 1996;17(1):135–145. doi: 10.1016/S0896-6273(00)80287-1. [PubMed] [Cross Ref]
36. Schmidt M, Dubin AE, Petrus MJ, Earley TJ, Patapoutian A. Nociceptive signals induce trafficking of TRPA1 to the plasma membrane. Neuron. 2009;64(4):498–509. [PMC free article] [PubMed]
37. Alvarez-Leefmans FJ. Chloride transporters in presynaptic inhibition, pain and neurogenic inflammation. In: Alvarez-Leefmans FJ, Delpire E, eds.Physiology and Pathology of Chloride Transporters and Channels in the Nervous System . New York, New York, USA: Academic Press; 2009:439–470.
38. Millan MJ. The induction of pain: an integrative review. Prog Neurobiol. 1999;57(1):1–164. doi: 10.1016/S0301-0082(98)00048-3. [PubMed] [Cross Ref]
39. Heinricher MM, Tavares I, Leith JL, Lumb BM. Descending control of nociception: Specificity, recruitment and plasticity. Brain Res Rev. 2009;60(1):214–225. [PMC free article] [PubMed]
40. Cummins TR, Rush AM, Estacion M, Dib-Hajj SD, Waxman SG. Voltage-clamp and current-clamp recordings from mammalian DRG neurons. Nat Protoc. 2009;4(8):1103–1112. doi: 10.1038/nprot.2009.91. [PubMed] [Cross Ref]
41. Malin SA, Davis BM, Molliver DC. Production of dissociated sensory neuron cultures and considerations for their use in studying neuronal function and plasticity. Nat Protoc. 2007;2(1):152–160. doi: 10.1038/nprot.2006.461. [PubMed] [Cross Ref]
42. Caterina MJ, et al. Impaired nociception and pain sensation in mice lacking the capsaicin receptor. Science. 2000;288(5464):306–313. doi: 10.1126/science.288.5464.306. [PubMed] [Cross Ref]
43. Davis JB, et al. Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia. Nature. 2000;405(6783):183–187. doi: 10.1038/35012076. [PubMed] [Cross Ref]
44. Zimmermann K, Leffler A, Fischer MM, Messlinger K, Nau C, Reeh PW. The TRPV1/2/3 activator 2-aminoethoxydiphenyl borate sensitizes native nociceptive neurons to heat in wildtype but not TRPV1 deficient mice. Neuroscience. 2005;135(4):1277–1284. doi: 10.1016/j.neuroscience.2005.07.018. [PubMed] [Cross Ref]
45. St Pierre M, Reeh PW, Zimmermann K. Differential effects of TRPV channel block on polymodal activation of rat cutaneous nociceptors in vitro. Exp Brain Res. 2009;196(1):31–44. doi: 10.1007/s00221-009-1808-3. [PubMed] [Cross Ref]
46. Petruska JC, Napaporn J, Johnson RD, Cooper BY. Chemical responsiveness and histochemical phenotype of electrophysiologically classified cells of the adult rat dorsal root ganglion. Neuroscience. 2002;115(1):15–30. doi: 10.1016/S0306-4522(02)00409-8. [PubMed] [Cross Ref]
47. Hjerling-Leffler J, Alqatari M, Ernfors P, Koltzenburg M. Emergence of functional sensory subtypes as defined by transient receptor potential channel expression. J Neurosci. 2007;27(10):2435–2443. doi: 10.1523/JNEUROSCI.5614-06.2007. [PubMed] [Cross Ref]
48. Lawson SN. Phenotype and function of somatic primary afferent nociceptive neurones with C-, Adelta- or Aalpha/beta-fibres. Exp Physiol. 2002;87(2):239–244. [PubMed]
49. Woodbury CJ, et al. Nociceptors lacking TRPV1 and TRPV2 have normal heat responses. J Neurosci. 2004;24(28):6410–6415. doi: 10.1523/JNEUROSCI.1421-04.2004. [PubMed] [Cross Ref]
50. Lawson JJ, McIlwrath SL, Woodbury CJ, Davis BM, Koerber HR. TRPV1 unlike TRPV2 is restricted to a subset of mechanically insensitive cutaneous nociceptors responding to heat. J Pain. 2008;9(4):298–308. doi: 10.1016/j.jpain.2007.12.001. [PMC free article] [PubMed] [Cross Ref]
51. Bogen O, Dreger M, Gillen C, Schröder W, Hucho F. Identification of versican as an isolectin B4-binding glycoprotein from mammalian spinal cord tissue. FEBS J. 2005;272(5):1090–1102. doi: 10.1111/j.1742-4658.2005.04543.x. [PubMed] [Cross Ref]
52. Price TJ, Flores CM. Critical evaluation of the colocalization between calcitonin gene-related peptide, substance P, transient receptor potential vanilloid subfamily type 1 immunoreactivities and isolectin B4 binding in primary afferent neurons of the rat and mouse. J Pain. 2007;8(3):263–272. doi: 10.1016/j.jpain.2006.09.005. [PMC free article] [PubMed] [Cross Ref]
53. Carr RW, Pianova S, McKemy DD, Brock JA. Action potential initiation in the peripheral terminals of cold-sensitive neurones innervating the guinea-pig cornea. J Physiol. 2009;587(pt 6):1249–1264. doi: 10.1113/jphysiol.2008.167023. [PubMed] [Cross Ref]
54. Hille B.Ion Channels of Excitable Membranes . 3rd ed. Sunderland, Massachusetts, USA: Sinauer Associates, Inc.; 2001.
55. Treede RD, Meyer RA, Raja SN, Campbell JN. Evidence for two different heat transduction mechanisms in nociceptive primary afferents innervating monkey skin. J Physiol. 1995;483(pt 3):747–758. [PubMed]
56. Campbell JN, LaMotte RH. Latency to detection of first pain. Brain Res. 1983;266(2):203–208. doi: 10.1016/0006-8993(83)90650-9. [PubMed] [Cross Ref]
57. Ringkamp M, Peng YB, Wu G, Hartke TV, Campbell JN, Meyer RA. Capsaicin responses in heat-sensitive and heat-insensitive A-fiber nociceptors. J Neurosci. 2001;21(12):4460–4468. [PubMed]
58. Caterina MJ, Schumacher MA, Tominaga M, Rosen TA, Levine JD, Julius D. The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature. 1997;389(6653):816–824. doi: 10.1038/39807. [PubMed] [Cross Ref]
59. Treede R-D, Meyer RA, Campbell JN. Myelinated mechanically insensitive afferents from monkey hairy skin: heat-response properties. J Neurophysiol. 1998;80(3):1082–1093. [PubMed]
60. Schmelz M, Schmid R, Handwerker HO, Torebjörk HE. Encoding of burning pain from capsaicin-treated human skin in two categories of unmyelinated nerve fibres. Brain. 2000;123(pt 3):560–571. doi: 10.1093/brain/123.3.560. [PubMed] [Cross Ref]
61. Wood JN, Winter J, James IF, Rang HP, Yeats J, Bevan S. Capsaicin-induced ion fluxes in dorsal root ganglion cells in culture. J Neurosci. 1988;8(9):3208–3220. [PubMed]
62. Caterina MJ, Rosen TA, Tominaga M, Brake AJ, Julius D. A capsaicin-receptor homologue with a high threshold for noxious heat. Nature. 1999;398(6726):436–441. doi: 10.1038/18906. [PubMed] [Cross Ref]
63. Alloui A, et al. TREK–1, a K(+) channel involved in polymodal pain perception. EMBO J. 2006;25(11):2368–2376. [PubMed]
64. Mandadi S, et al. TRPV3 in keratinocytes transmits temperature information to sensory neurons via ATP. Pflugers Arch. 2009;458(6):1093–1102. doi: 10.1007/s00424-009-0703-x. [PMC free article] [PubMed] [Cross Ref]
65. Foulkes T, Wood J. Mechanisms of cold pain. Channels. 2007;1(3):154–16. [PubMed]
66. Davis KD, Pope GE. Noxious cold evokes multiple sensations with distinct time courses. Pain. 2002;98(1–2):179–185. doi: 10.1016/S0304-3959(02)00043-X. [PubMed] [Cross Ref]
67. Schepersm RJ, Ringkamp M. Thermoreceptors and thermosensitive afferents. Neurosci Biobehav Rev. 2010;34(2):177–184. [PubMed]
68. Allchorne A, Broom D, Woolf C. Detection of cold pain, cold allodynia and cold hyperalgesia in freely behaving rats. Mol Pain. 2005;1:36. doi: 10.1186/1744-8069-1-36. [PMC free article] [PubMed] [Cross Ref]
69. Bautista DM, et al. The menthol receptor TRPM8 is the principal detector of environmental cold. Nature. 2007;448(7150):204–208. doi: 10.1038/nature05910. [PubMed] [Cross Ref]
70. Babes A, Zorzon D, Reid G. Two populations of cold-sensitive neurons in rat dorsal root ganglia and their modulation by nerve growth factor. Eur J Neurosci. 2004;20(9):2276–2282. doi: 10.1111/j.1460-9568.2004.03695.x. [PubMed] [Cross Ref]
71. Thut PD, Wrigley D, Gold MS. Cold transduction in rat trigeminal ganglia neurons in vitro. Neuroscience. 2003;119(4):1071. doi: 10.1016/S0306-4522(03)00225-2. [PubMed] [Cross Ref]
72. Babes A. Ion channels involved in cold detection in mammals: TRP and non-TRP mechanisms. Biophysical Rev. 2009;1(4):193–200.
73. Colburn RW, et al. Attenuated cold sensitivity in TRPM8 null mice. Neuron. 2007;54(3):379–386. doi: 10.1016/j.neuron.2007.04.017. [PubMed] [Cross Ref]
74. Dhaka A, Murray AN, Mathur J, Earley TJ, Petrus MJ, Patapoutian A. TRPM8 is required for cold sensation in mice. Neuron. 2007;54(3):371–378. doi: 10.1016/j.neuron.2007.02.024. [PubMed] [Cross Ref]
75. Gentry C, Stoakley N, Andersson DA, Bevan S. The roles of iPLA2, TRPM8 and TRPA1 in chemically induced cold hypersensitivity. Mol Pain. 2010;6:4. doi: 10.1186/1744-8069-6-4. [PMC free article] [PubMed] [Cross Ref]
76. Dhaka A, Earley TJ, Watson J, Patapoutian A. Visualizing cold spots: TRPM8-expressing sensory neurons and their projections. J Neurosci. 2008;28(3):566–575. [PubMed]
77. Takashima Y, Daniels RL, Knowlton W, Teng J, Liman ER, McKemy DD. Diversity in the neural circuitry of cold sensing revealed by genetic axonal labeling of transient receptor potential melastatin 8 neurons. J Neurosci. 2007;27(51):14147–14157. doi: 10.1523/JNEUROSCI.4578-07.2007. [PMC free article] [PubMed] [Cross Ref]
78. Magerl W, Fuchs PN, Meyer RA, Treede RD. Roles of capsaicin-insensitive nociceptors in cutaneous pain and secondary hyperalgesia. Brain. 2001;124(pt 9):1754–1764. [PubMed]
79. Viana F. Understanding the mechanisms of cold–evoked pain in humans. Pain. 2009;147(1–3):7–8. doi: 10.1016/j.pain.2009.08.012. [PubMed] [Cross Ref]
80. Reid G, Flonta M-L. Cold transduction by inhibition of a background potassium conductance in rat primary sensory neurones. Neurosci Lett. 2001;297(3):171–174. doi: 10.1016/S0304-3940(00)01694-3. [PubMed] [Cross Ref]
81. Kwan KY, et al. TRPA1 contributes to cold, mechanical, and chemical nociception but is not essential for hair-cell transduction. Neuron. 2006;50(2):277–289. [PubMed]
82. Karashima Y, et al. TRPA1 acts as a cold sensor in vitro and in vivo. Proc Natl Acad Sci U S A. 2009;106(4):1273–127. [PubMed]
83. Sawada Y, Hosokawa H, Hori A, Matsumura K, Kobayashi S. Cold sensitivity of recombinant TRPA1 channels. Brain Res. 2007;1160:39–46. doi: 10.1016/j.brainres.2007.05.047. [PubMed] [Cross Ref]
84. Jordt S-E, et al. Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1. Nature. 2004;427(6971):260–265. doi: 10.1038/nature02282. [PubMed] [Cross Ref]
85. Bautista DM, Jordt S-E, Nikai T, et al. TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents. Cell. 2006;124(6):1269–1282. [PubMed]
86. Bandell M, et al. Noxious cold ion channel TRPA1 is activated by pungent compounds and bradykinin. . Neuron. 2004;41(6):849–857. doi: 10.1016/S0896-6273(04)00150-3. [PubMed] [Cross Ref]
87. Dai Y, et al. Sensitization of TRPA1 by PAR2 contributes to the sensation of inflammatory pain. . J Clin Invest. 2007;117(7):1979–1987. doi: 10.1172/JCI30951. [PMC free article] [PubMed] [Cross Ref]
88. Hinman A, Chuang HH, Bautista DM, Julius D. TRP channel activation by reversible covalent modification. Proc Natl Acad Sci U S A. 2006;103(51):19564–19568. [PubMed]
89. Macpherson LJ, et al. Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines. Nature. 2007;445(7127):541–545. doi: 10.1038/nature05544. [PubMed] [Cross Ref]
90. Bang S, Hwang SW. Polymodal ligand sensitivity of TRPA1 and its modes of interactions. J Gen Physiol. 2009;133(3):257–262. doi: 10.1085/jgp.200810138. [PMC free article] [PubMed] [Cross Ref]
91. Hu J, Milenkovic N, Lewin GR. The high threshold mechanotransducer: A status report. Pain. 2006;120(1–2):3–7. [PubMed]
92. Chalfie M. Neurosensory mechanotransduction. Nat Rev Mol Cell Biol. 2009;10(1):44–52. doi: 10.1038/nrm2595. [PubMed] [Cross Ref]
93. Garcia-Anoveros J, Corey DP. The molecules of mechanosensation. Annu Rev Neurosci. 1997;20:567–594. doi: 10.1146/annurev.neuro.20.1.567. [PubMed] [Cross Ref]
94. Wetzel C, et al. A stomatin-domain protein essential for touch sensation in the mouse. Nature. 2007;445(7124):206–209. [PubMed]
95. Nassar MA, et al. Nociceptor-specific gene deletion reveals a major role for Nav1.7 (PN1) in acute and inflammatory pain. Proc Natl Acad Sci U S A. 2004;101(34):12706–12711. [PubMed]
96. McCarter GC, Reichling DB, Levine JD. Mechanical transduction by rat dorsal root ganglion neurons in vitro. Neurosci Lett. 1999;273(3):179–182. doi: 10.1016/S0304-3940(99)00665-5. [PubMed] [Cross Ref]
97. Bhattacharya MR, Bautista DM, Wu K, Haeberle H, Lumpkin EA, Julius D. Radial stretch reveals distinct populations of mechanosensitive mammalian somatosensory neurons. Proc Natl Acad Sci U S A. 2008;105(50):20015–2002. [PubMed]
98. Alessandri-Haber N, et al. Hypotonicity induces TRPV4-mediated nociception in rat. Neuron. 2003;39(3):497–511. doi: 10.1016/S0896-6273(03)00462-8. [PubMed] [Cross Ref]
99. Schulz DJ, Temporal S, Barry DM, Garcia ML. Mechanisms of voltage-gated ion channel regulation: from gene expression to localization. Cell Mol Life Sci. 2008;65(14):2215–2231. doi: 10.1007/s00018-008-8060-z. [PubMed] [Cross Ref]
100. Zimmermann K, et al. Sensory neuron sodium channel Nav1.8 is essential for pain at low temperatures. Nature. 2007;447(7146):855–858. doi: 10.1038/nature05880. [PubMed] [Cross Ref]
101. Akopian AN, et al. The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways. Nat Neurosci. 1999;2(6):541–548. doi: 10.1038/9195. [PubMed] [Cross Ref]
102. Rush AM, Cummins TR, Waxman SG. Multiple sodium channels and their roles in electrogenesis within dorsal root ganglion neurons. J Physiol. 2007;579(pt 1):1–14. doi: 10.1113/jphysiol.2006.121483. [PubMed] [Cross Ref]
103. Nassar MA, Levato A, Stirling LC, Wood JN. Neuropathic pain develops normally in mice lacking both Nav1.7 and Nav1.8. Mol Pain. 2005;1:24. doi: 10.1186/1744-8069-1-24. [PMC free article] [PubMed] [Cross Ref]
104. Cox JJ, et al. An SCN9A channelopathy causes congenital inability to experience pain. Nature. 2006;444(7121):894–898. [PubMed]
105. Latremoliere A, Woolf CJ. Central sensitization: a generator of pain hypersensitivity by central neural plasticity. J Pain. 2009;10(9):895–926. [PMC free article] [PubMed]
106. Campbell JN, Meyer RA. Sensitization of unmyelinated nociceptive afferents in monkey varies with skin type. J Neurophysiol. 1983;49(1):98–110. [PubMed]
107. Sandkuhler J. Models and mechanisms of hyperalgesia and allodynia. Physiol Rev. 2009;89(2):707–758. doi: 10.1152/physrev.00025.2008. [PubMed] [Cross Ref]
108. Koltzenburg M, Lundberg LER, Torebjörk HE. Dynamic and static components of mechanical hyperalgesia in human hairy skin. Pain. 1992;51(2):207–219. [PubMed]
109. Bharali LAM, Lisney SJW. The relationship between unmyelinated afferent type and neurogenic plasma extravasation in normal and reinnervated rat skin. Neuroscience. 1992;47(3):703–712. doi: 10.1016/0306-4522(92)90178-5. [PubMed] [Cross Ref]
110. Lin Q, Li D, Xu X, Zou X, Fang L. Roles of TRPV1 and neuropeptidergic receptors in dorsal root reflex-mediated neurogenic inflammation induced by intradermal injection of capsaicin. Mol Pain. 2007;3:30. doi: 10.1186/1744-8069-3-30. [PMC free article] [PubMed] [Cross Ref]
111. Richardson JD, Vasko MR. Cellular mechanisms of neurogenic inflammation. J Pharmacol Exp Ther. 2002;302(3):839–845. [PubMed]
112. Mizumura K, Sugiura T, Katanosaka K, Banik RK, Kozaki Y. Excitation and sensitization of nociceptors by bradykinin: what do we know? Exp Brain Res. 2009;196(1):53–65. doi: 10.1007/s00221-009-1814-5. [PubMed] [Cross Ref]
113. Leffler A, Monter B, Koltzenburg M. The role of the capsaicin receptor TRPV1 and acid-sensing ion channels (ASICS) in proton sensitivity of subpopulations of primary nociceptive neurons in rats and mice. Neuroscience. 2006;139(2):699–709. doi: 10.1016/j.neuroscience.2005.12.020. [PubMed] [Cross Ref]
114. Reichling DB, Levine JD. Critical role of nociceptor plasticity in chronic pain. Trends Neurosci. 2009;32(12):611–618. [PMC free article] [PubMed]
115. Macpherson LJ, et al. An ion channel essential for sensing chemical damage. J Neurosci. 2007;27(42):11412–11415. [PubMed]
116. McNamara CR, et al. TRPA1 mediates formalin-induced pain. Proc Natl Acad Sci U S A. 2007;104(33):13525–13530. doi: 10.1073/pnas.0705924104. [PubMed] [Cross Ref]
117. Defrin R, Ohry A, Blumen N, Urca G. Sensory determinants of thermal pain. Brain. 2002;125(pt 3):501–510. doi: 10.1093/brain/awf055. [PubMed] [Cross Ref]
118. Belmonte C, Viana F. Molecular and cellular limits to somatosensory specificity. Mol Pain. 2008;4:14. doi: 10.1186/1744-8069-4-14. [PMC free article] [PubMed] [Cross Ref]
119. Nagy JI, van der Kooy D. Effects of neonatal capsaicin treatment on nociceptive thresholds in the rat. J Neurosci. 1983;3(6):1145–1150. [PubMed]
120. Abrahamsen B, et al. The cell and molecular basis of mechanical, cold, and inflammatory pain. Science. 2008;321(5889):702–705. doi: 10.1126/science.1156916. [PubMed] [Cross Ref]
121. Rau KK, et al. Mrgprd enhances excitability in specific populations of cutaneous murine polymodal nociceptors. J Neurosci. 2009;29(26):8612–8619. doi: 10.1523/JNEUROSCI.1057-09.2009. [PMC free article] [PubMed] [Cross Ref]
122. Cavanaugh DJ, et al. Distinct subsets of unmyelinated primary sensory fibers mediate behavioral responses to noxious thermal and mechanical stimuli. . Proc Natl Acad Sci U S A. 2009;106(22):9075–9080. doi: 10.1073/pnas.0901507106. [PubMed] [Cross Ref]
123. Torebjork HE, LaMotte RH, Robinson CJ. Peripheral neural correlates of magnitude of cutaneous pain and hyperalgesia: simultaneous recordings in humans of sensory judgments of pain and evoked responses in nociceptors with C-fibers. J Neurophysiol. 1984;51(2):325–339. [PubMed]
124. Weidner C, Schmelz M, Schmidt R, Hansson B, Handwerker HO, Torebjörk HE. Functional attributes discriminating mechano-insensitive and mechano-responsive C nociceptors in human skin. J Neurosci. 1999;19(22):10184–10190. [PubMed]
125. Koltzenburg M, Handwerker HO. Differential ability of human cutaneous nociceptors to signal mechanical pain and to produce vasodilatation. . J Neurosci. 1994;14(3 pt 2):1756–1765. [PubMed]
126. Schmidt R, Schmelz M, Torebjörk HE, Handwerker HO. Mechano-insensitive nociceptors encode pain evoked by tonic pressure to human skin. Neuroscience. 2000;98(4):793–800. doi: 10.1016/S0306-4522(00)00189-5. [PubMed] [Cross Ref]
127. Koppert W, Brueckl V, Weidner C, Schmelz M. Mechanically induced axon reflex and hyperalgesia in human UV-B burn are reduced by systemic lidocaine. Eur J Pain. 2004;8(3):237–244. doi: 10.1016/j.ejpain.2003.08.007. [PubMed] [Cross Ref]
128. Lynn B, Schütterle S, Pierau FK. The vasodilator component of neurogenic inflammation is caused by a special subclass of heat-sensitive nociceptors in the skin of the pig. J Physiol. 1996;494(pt 2):587–593. [PubMed]
129. Obreja O, et al. Patterns of activity-dependent conduction velocity changes differentiate classes of unmyelinated mechano-insensitive afferents including cold nociceptors, in pig and in human. Pain. 2010;148(1):59–69. doi: 10.1016/j.pain.2009.10.006. [PubMed] [Cross Ref]
130. Schmelz M, Michael K, Weidner C, Schmidt R, Torebjörk HE, Handwerker HO. Which nerve fibers mediate the axon reflex flare in human skin? Neuroreport. 2000;11(3):645–648. doi: 10.1097/00001756-200002280-00041. [PubMed] [Cross Ref]
131. Baumann TK, Simone DA, Shain CN, LaMotte RH. Neurogenic hyperalgesia: the search for the primary cutaneous afferent fibers that contribute to capsaicin-induced pain and hyperalgesia. J Neurophysiol. 1991;66(1):212–227. [PubMed]
132. Ziegler EA, Magerl W, Meyer RA, Treede RD. Secondary hyperalgesia to punctate mechanical stimuli: Central sensitization to A-fibre nociceptor input. Brain. 1999;122(pt 12):2245–2257. doi: 10.1093/brain/122.12.2245. [PubMed] [Cross Ref]
133. Meyer RA, Campbell JN. Evidence for two distinct classes of unmyelinated nociceptive afferents in monkey. Brain Res. 1981;224(1):149–152. doi: 10.1016/0006-8993(81)91124-0. [PubMed] [Cross Ref]
134. Bölcskei K, et al. Investigation of the role of TRPV1 receptors in acute and chronic nociceptive processes using gene-deficient mice. Pain. 2005;117(3):368–376. [PubMed]
135. Peier AM, et al. A heat-sensitive TRP channel expressed in keratinocytes. Science. 2002;296(5575):2046–2049. doi: 10.1126/science.1073140. [PubMed] [Cross Ref]
136. Xu H, et al. TRPV3 is a calcium-permeable temperature-sensitive cation channel. Nature. 2002;418(6894):181–186. [PubMed]
137. Huang SM, et al. Overexpressed transient receptor potential vanilloid 3 ion channels in skin keratinocytes modulate pain sensitivity via prostaglandin E2. . J Neurosci. 2008;28(51):13727–13737. doi: 10.1523/JNEUROSCI.5741-07.2008. [PMC free article] [PubMed] [Cross Ref]
138. Moqrich A, et al. Impaired thermosensation in mice lacking TRPV3, a heat and camphor sensor in the skin. Science. 2005;307(5714):1468–1472. doi: 10.1126/science.1108609. [PubMed] [Cross Ref]
139. Lee H, Iida T, Mizuno A, Suzuki M, Caterina MJ. Altered thermal selection behavior in mice lacking transient receptor potential vanilloid 4. J Neurosci. 2005;25(5):1304–1310. doi: 10.1523/JNEUROSCI.4745.04.2005. [PubMed] [Cross Ref]
140. Todaka H, Taniguchi J, Satoh J, Mizuno A, Suzuki M. Warm temperature-sensitive transient receptor potential vanilloid 4 (TRPV4) plays an essential role in thermal hyperalgesia. J Biol Chem. 2004;279(34):35133–35138. [PubMed]
141. Alessandri-Haber N, Dina OA, Joseph EK, Reichling D, Levine JD. A transient receptor potential vanilloid 4-dependent mechanism of hyperalgesia is engaged by concerted action of inflammatory mediators. J Neurosci. 2006;26(14):3864–3874. doi: 10.1523/JNEUROSCI.5385-05.2006. [PubMed] [Cross Ref]
142. Suzuki M, Mizuno A, Kodaira K, Imai M. Impaired pressure sensation in mice lacking TRPV4. J Biol Chem. 2003;278(25):22664–22668. doi: 10.1074/jbc.M302561200. [PubMed] [Cross Ref]
143. Cohen A, Sagron R, Somech E, Segal-Hayouna Y, Zilberberg N. Pain-associated signals, acidosis and lysophosphatidic acid, modulate the neuronal K2P2.1 channel. Mol Cell Neurosci. 2009;40(3):382–389. doi: 10.1016/j.mcn.2008.12.004. [PubMed] [Cross Ref]
144. Noel J, et al. The mechano-activated K+ channels TRAAK and TREK-1 control both warm and cold perception. EMBO J. 2009;28(9):1308–1318. doi: 10.1038/emboj.2009.57. [PubMed] [Cross Ref]
145. Proudfoot CJ, et al. Analgesia mediated by the TRPM8 cold receptor in chronic neuropathic pain. Curr Biol. 2006;16(16):1591–1605. doi: 10.1016/j.cub.2006.07.061. [PubMed] [Cross Ref]
146. Obata K, et al. TRPA1 induced in sensory neurons contributes to cold hyperalgesia after inflammation and nerve injury. J Clin Invest. 2005;115(9):2393–2401. doi: 10.1172/JCI25437. [PMC free article] [PubMed] [Cross Ref]
147. Petrus M, et al. A role of TRPA1 in mechanical hyperalgesia is revealed by pharmacological inhibition. . Mol Pain. 2007;3:40. doi: 10.1186/1744-8069-3-40. [PMC free article] [PubMed] [Cross Ref]
148. Kwan KY, Glazer JM, Corey DP, Rice FL, Stucky CL. TRPA1 modulates mechanotransduction in cutaneous sensory neurons. J Neurosci. 2009;29(15):4808–4819. [PMC free article] [PubMed]
149. Alessandri-Haber N, Joseph E, Dina OA, Liedtke W, Levine JD. TRPV4 mediates pain-related behavior induced by mild hypertonic stimuli in the presence of inflammatory mediator. Pain. 2005;118(1–2):70–79. [PubMed]
150. Chien LY, Cheng JK, Chu D, Cheng CF, Tsaur ML. Reduced expression of A-type potassium channels in primary sensory neurons induces mechanical hypersensitivity. J Neurosci. 2007;27(37):9855–9865. [PubMed]

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