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The mechanisms controlling pain in newborns during delivery are poorly understood. We explored the hypothesis that oxytocin, an essential hormone for labor and a powerful neuromodulator, exerts analgesic actions on newborns during delivery. Using a thermal tail-flick assay, we report that pain sensitivity is two-fold lower in rat pups immediately after birth than 2 days later. Oxytocin receptor antagonists strongly enhanced pain sensitivity in newborn, but not in 2-day-old rats, whereas oxytocin reduced pain at both ages suggesting an endogenous analgesia by oxytocin during delivery. Similar analgesic effects of oxytocin, measured as attenuation of pain-vocalization induced by electrical whisker pad stimulation, were also observed in decerebrated newborns. Oxytocin reduced GABA-evoked calcium responses and depolarizing GABA driving force in isolated neonatal trigeminal neurons suggesting that oxytocin effects are mediated by alterations of intracellular chloride. Unlike GABA signaling, oxytocin did not affect responses mediated by P2X3 and TRPV1 receptors. In keeping with a GABAergic mechanism, reduction of intracellular chloride by the diuretic NKCC1 chloride co-transporter antagonist bumetanide mimicked the analgesic actions of oxytocin and its effects on GABA responses in nociceptive neurons. Therefore, endogenous oxytocin exerts an analgesic action in newborn pups that involves a reduction of the depolarizing action of GABA on nociceptive neurons. Therefore, the same hormone that triggers delivery also acts as a natural pain killer revealing a novel facet of the protective actions of oxytocin in the fetus at birth.
Delivery is stressful and potentially painful event for the newborn (Lagercrantz and Bistoletti, 1977; Bistoletti et al., 1983; Hagnevik et al., 1984; Lagercrantz and Slotkin, 1986; Fitzgerald, 2005). Sources of pain during delivery can be natural, such as mechanical compression of the fetus (Derek, 1999), and iatrogenic, such as forceps extraction, blood samples – including fetal scalp blood samples – and injections. Clinical studies indicate that painful experiences in neonates may disrupt the adaptation of newborn infants to their postnatal environment and in the long term, lead to psychological sequelae (Anand and Hickey, 1987). In mice, early exposure to noxious or stressful stimuli alters pain sensitivity and behavior in adult life, possibly by altering the stress-axis and antinociceptive circuitry (Sternberg et al., 2005; Laprairie and Murphy, 2009). Therefore, the problem of pain and its treatment in the newborn is of clinical importance (Anand, 2001; Slater et al., 2010); however, the mechanisms involved in pain regulation at birth are poorly understood.
Recently, comparison of the pain responses in human neonates born with vaginal delivery or elective cesarean section revealed diminished physiological, behavioral and vocalization responses to painful stimuli following vaginal delivery when compared to C-sections, suggesting that antinociceptive mechanisms are activated and last for few hours during and after normal delivery (Bergqvist et al., 2008). The mechanisms underlying this transient newborn analgesia at present remain unknown. Here, we explored an involvement of oxytocin in newborn analgesia. Oxytocin, who's levels sharply increase during vaginal delivery, is not only involved in labor but also exerts multiple actions in the nervous system (Argiolas and Gessa, 1991; Gimpl and Fahrenholz, 2001; Raggenbass, 2001; Russell et al., 2003; Tomizawa et al., 2003; Huber et al., 2005; Kosfeld et al., 2005; Theodosis et al., 2006). In adult rats, oxytocin exerts an analgesic action (Arletti et al., 1993; Lundeberg et al., 1993, 1994; Agren et al., 1995; Petersson et al., 2001; Yu et al., 2003; Condés-Lara et al., 2006; Miranda-Cardenas et al., 2006). The analgesic effects of oxytocin in adults is mediated by GABAergic inhibition of the nociceptive inputs to the dorsal horn of the spinal cord (Condés-Lara et al., 2009). Nociception is strongly regulated not only by amount of the GABA(A) receptor mediated anionic conductance, but also by its reversal potential (EGABA), as depolarizing shifts in EGABA in the nociceptive and dorsal horn neurons are associated with elevated pain (De Koninck, 2007; Price et al., 2009). Pain is alleviated by pharmacological blockade or genetic knock out of NKCC1 chloride co-transporter, which is the primary cause for elevated chloride and depolarizing action of GABA in the nociceptive neurons (Delpire and Mount, 2002; Granados-Soto et al., 2005; Pieraut et al., 2007; Rocha-González et al., 2008). In the immature cortical neurons, oxytocin and NKCC1 blockers produce similar negative shift in EGABA (Tyzio et al., 2006; Khazipov et al., 2008). We now report that oxytocin causes pain relief in the newborn at birth, via reduction in depolarizing action of GABA on the nociceptive neurons.
All animal use protocols conformed to the INSERM guidelines and the Italian act Decreto Legislativo 27/1/92 n. 116 implementing the European Community directives n. 86/609 and 93/88 on the use of laboratory animals. Pregnant and maternal Wistar rats were housed with a 12-h light–dark cycle, at 24±1°C, and food and water ad libitum. Pregnant rats were monitored hourly on the day of expected delivery. During delivery, which lasts in the rat from a 30min to 1h, newborn pups were numbered, weighted and stored in a warmed box prior to the pain assays. Delay from delivery to the onset of pain assays varied from 30min to 1h. Pups born first were assayed first. Together with the time for the pain tests and drug injections (tests for each drug were performed 30min after injection) all the measurements were obtained within 2h after birth.
The pup was held in a box with a hole allowing the tail to protrude from it. The inner surface of the box was covered with an aluminum sheet forming an electrical contact with the rat body. The electrical circuit via the sheet, body, tail, and water bath was powered by a 1.5-V battery and its connection and disconnection could be easily detected upon the tail immersion and withdrawal from the water, respectively. Electrical signals were digitized at 1kHz using a Digidata 1200 and recorded to a computer. The distal tip of the tail was lowered into the water bath (50°C). Latency to withdrawal was recorded as the “pain” parameter, with a 15-s maximum allowable threshold. After three habituation tests, the latency to withdrawal was determined from the average of three consecutive measurements.
Under isoflurane (1.5%) anesthesia, rat pups were implanted with bipolar electrodes into the whisker pad and decerebrated at the upper pons level. After 10min (P0) or 1h (P1–2 pups) of recovery, the pups were wrapped by cotton and placed on a thermal blanket (38°C). The whisker pad was stimulated by electrical pulse trains (1ms pulse duration, 5–25V amplitude, 50Hz, 1min inter-train interval). It has been shown that pain vocalization includes A-delta and C-fibers – triggered audible “peeps” (with the most prominent peak at 4–5kHz) and “chatters” (peak at 2.5kHz) followed by ultrasonic vocalizations patterned by respiration cycles (Jourdan et al., 1995, 1997). In the present study, audible component of the vocalization response was recorded by microphone, digitized at 10kHz using Digidata 1440 interface (Axon Instruments) and analyzed offline using Matlab (MathWorks, Natick, MA, USA). To quantify the vocalization response, we calculated scalar integral (Σ) as following: (i) raw sonogram was converted to scalar sonogram by inverting all negative values to positive values; (ii) scalar sonogram was corrected for the baseline activity level by subtraction of the mean scalar sonogram value calculated during 1min before stimulation; (iii) scalar sonogram integral was calculated as cumulative, corrected for the baseline, scalar sonogram during 5s after stimulation.
Trigeminal sensory neurons were obtained from P0 rats. Animals were anesthetized and decapitated. Trigeminal ganglia were excised and enzymatically dissociated in F12 medium containing 0.25mg/ml trypsin, 1mg/ml collagenase, and 0.2mg/ml DNase (Sigma) at 37°C. Cells were plated on poly-l-lysine-coated Petri dishes in F12 medium with 10% fetal bovine serum and examined 5h after plating. For Ca2+ imaging experiments cells were incubated for 40min at 20–22°C in physiological solution containing fluo-3 (AM ester cell-permeable compound; 1μM; Invitrogen), followed by a 30-min washout period. Fluorescence in neurons was imaged using Cell-R imaging system (Olympus Europe, Hamburg, Germany). The imaging system consisted of the Olympus IX-70 inverted microscope equipped with a 175-W xenon burner light source. Fluorescence of fluo-3 was excited at 490±5nm and collected at 520±15nm. Images were collected in a time-lapse mode (2Hz; 100ms exposure time) with a CCD camera (Orca, Hamamatsu, Japan). To prevent photobleaching, illumination was used only during agonist application (with 10min intervals). Fluorescent signals from single cells were quantified as the ΔF/F0, where F0 is the background subtracted baseline fluorescence and ΔF is the increment over the baseline). All drugs were applied via fast perfusion system (solution exchange time ~30ms, RDS-200, Bio-Logic - Science Instruments, Grenoble, France). P2X3 receptors were activated with the selective agonist α,β-methylenATP (α,β-meATP, 10μM) while TRPV1 receptors were activated with capsaicin (200nM). Plots and figures were constructed using Origin software (OriginLab, version 8.0).
Single GABA channel recordings were performed from the trigeminal sensory neurons prepared as described above. Cell-attached patch-clamp recordings were performed using EPC-9 amplifier (HEKA Elektronik Dr. Schulze GmbH, Lambrecht/Pfalz, Germany). Patch electrodes were made from borosilicate glass capillaries (GC150F-15, Clark Electromedical Instruments). For recordings of single GABA(A) channels, patch pipette solution contained (in mM): NaCl 120, TEA-Cl 20, KCl 5, 4-aminopyridine 5, CaCl2 0.1, MgCl2 10, glucose 10, HEPES–NaOH 10 buffered to pH 7.2–7.3 and GABA (1–5μM) was added at the day of experiment from 1mM frozen stock solution. Driving force for GABA(A) receptor mediated currents was determined from the current–voltage relationships of the currents through single GABA(A) channels single as described earlier (Tyzio et al., 2006) and corrected for an error of 2mV (Tyzio et al., 2008).
In the experiments in vivo, oxytocin (Sigma-Aldrich, St. Louis, MO, USA) 50μM was injected at 0.1ml/5g (diluted in saline) i.p., 30min before testing. Bumetanide (Burinex, LEO pharmaceutical Products, Denmark) solution 25μg/ml was injected i.p. at the dose of 5μmol/kg, 30min before testing. Atosiban (Sigma) (diluted in saline) was injected at 2μg/kg, i.p., 30min before testing. SSR126768A (gift from Sanofi-Synthelabo) diluted in saline injected at 1μg/kg i.p, 30min before testing. Sham injections in the control group were performed with equal volumes of saline.
Results are expressed as mean±SEM. Data were analyzed by a two-way analysis of variance (ANOVA) followed, when the F value was significant, by a Fischer t-test, when the time-course of the effect was compared. Significance of changes in experiments with vocalization in vivo was tested by the Kruskal–Wallis test (H-test). In calcium imaging experiments significance was analyzed by non-parametric Mann–Whitney test. The level of statistical significance (*) was set at P<0.05.
In the present study, we used a combination of behavioral tests including thermal tail-flick and electrical stimulation evoked vocalizations, as well as electrophysiological and imaging approaches in isolated trigeminal neurons to study pain control by oxytocin in the newborn rats.
We first tested pain sensitivity in the newborn rats using a thermal tail-flick response. In this test, pain sensitivity is reciprocal to the delay in tail withdrawal from the hot water. Previous developmental studies using this test indicated that nociceptive withdrawal thresholds are low in rat pups during the first postnatal week and only increase to adult values by the second or third postnatal week (Fitzgerald and Gibson, 1984; Falcon et al., 1996; Jiang and Gebhart, 1998; Teng and Abbott, 1998; Marsh et al., 1999). We studied thermal tail-flick responses in two age groups: (i) newborn animals within an hour after birth (P0) and (ii) 2-day-old rat pups (P2). Oxytocin levels are maximal during and immediately after birth, and wane during the first postnatal day, as deduced from the dynamic changes in GABA signaling in the cortical neurons (Tyzio et al., 2006). Under control conditions, P0 rats withdrew their tails within 4.7±0.19s (n=15; Figure Figure1A).1A). In P2 rats, delay in the tail withdrawal was of 2.4±0.16s (n=15; Figure Figure1B),1B), that is nearly two times shorter than P0 control rats (P<0.0001). Thus, pain sensitivity in the newborn rats is significantly lower than in 2-day-old rats. To determine the contribution of endogenous oxytocin to this difference, we used selective blockers of oxytocin receptors atosiban (2μg/kg, i.p.) and SSR126768A (1μg/kg, i.p.). Both competitive antagonists caused a nearly three-fold acceleration of tail withdrawal in P0 pups; rendering them similar to that seen in P2 rats under control conditions (Figures (Figures1A,B).1A,B). In contrast, oxytocin receptor blockers did not significantly modify the tail-flick delays in P2 animals (Figure (Figure1B).1B). These findings suggest a strong analgesic effect of endogenous oxytocin in the newborn rats, and that this effect wanes with a postnatal reduction in oxytocin levels. Systemic administration of exogenous oxytocin (1μg/kg) resulted in a dramatic analgesic effect both in newborn and P2 rats (Figures (Figures1A,B).1A,B). In the newborn rats, exogenous oxytocin could also partially reverse the effects of the competitive oxytocin receptor blockers, indicating that endogenous oxytocin levels are not saturated, and that therapeutic elevation of oxytocin levels could result in more powerful analgesia in the newborn.
As a second approach, we studied oxytocin-dependent modulation of trigeminal pain responses by measuring vocalization induced by electrical stimulation of the whisker pad. Animals were decerebrated at caudal midbrain levels (Figure (Figure2A)2A) to cut the descending oxytocin projections from the VPN and to prevent noxious input to the forebrain. Electrical stimulation of the whisker pad evoked vocalization in the neonatal rats despite this decerebration (Figure (Figure2).2). Vocalizing responses were composed of several bursts with a dominant frequency in the range from 2.7 to 5kHz (mean frequency 3.9±0.1kHz, n=24, rat P0–2). To quantify vocalization response, we calculated a scalar sonogram integral. In agreement with the results of the thermal tail-flick assay, the oxytocin receptor blocker atosiban (2μg/kg) increased vocalization responses in P0 rats (to 155±28% of control values, n=8, P=0.0003; Figure Figure3A).3A). In P1–2 rats, injections of saline did not change the vocalization response (105±21% of control values; n=6; P>0.05). However, exogenous oxytocin strongly reduced vocal responses from 15.2±6.4 to 8.2±5.6 a.u., that is to 42±12% (n=6; P=0.00004), and this effect was partially reversed by atosiban to 84±38% from the control values (n=6; P=0.0017, Figures Figures22 and and3).3). Taken together, the results of both behavioral tests indicate that endogenous oxytocin reduces pain in newborn rats.
Oxytocin induces a transient excitatory-to-inhibitory switch in the action of GABA on immature neurons at birth (Tyzio et al., 2006), and GABAergic mechanisms are implicated in the analgesic actions of oxytocin in adult animals (Condés-Lara et al., 2009). To examine the role of oxytocin-mediated regulation of GABA current polarity in neonatal analgesia, we used bumetanide – a selective blocker of NKCC1 co-transporter that, like oxytocin, lowers intracellular chloride and shifts the depolarizing/excitatory actions of GABA on immature neurons (Tyzio et al., 2006). Bumetanide (5μmol/kg) strongly delayed the tail-flick responses in both age groups, and, importantly, prevented effects of oxytocin receptor blockers in newborn rats (Figure (Figure1).1). Vocalizations induced in decerebrated pups were also reduced in P1–2 rats by bumetanide to 72±16% of control (n=6; P=0.004, Figure Figure3).3). Taken together, these results suggest that endogenous oxytocin reduces pain in newborn rats by shifting the level of intracellular chloride that in turn changes the action of GABA in the pain circuits.
As the actions of oxytocin in adult rats involve modulation of GABAergic control of the primary nociceptive afferents (Condés-Lara et al., 2009), we studied the effect of oxytocin on GABA responses in trigeminal sensory neurons, which detect noxious stimuli from the head and facial tissues and conduct them to the brainstem. Experiments were performed in primary cultures of trigeminal neurons dissociated from newborn rats and kept for 5h in vitro. In keeping with previous observations (Reichling et al.,1994; Wang et al., 1994), activation of GABA receptors induced robust transient increases of intracellular calcium in trigeminal neurons, indicating a depolarizing action of GABA and calcium entry into the cells via voltage-gated calcium channels (Figure (Figure4).4). Application of 1μM oxytocin induced slow transient responses lasting ~60–80s (not shown) and significantly reduced GABA-evoked calcium transients. It is known that the depolarizing action of GABA in sensory neurons results from elevated intracellular chloride concentration, set by the highly expressed NKCC1 membrane chloride co-transporter (Delpire and Mount, 2002). In keeping with this observation, bumetanide suppressed GABA-evoked calcium transients like oxytocin confirming the importance of chloride and GABA in mediating these analgesic responses (Figures (Figures44A,B).
To determine the specificity of oxytocin/GABA interactions in pain modulation, we tested the effects of the hormone on P2X3 receptors and TRPV1 receptors which represent two major types of pain transducers in trigeminal neurons (Simonetti et al., 2006). Figure Figure55 shows that repetitive (at 10min intervals) 2s long applications of the selective P2X3 receptor agonist α,β-meATP (n=276 cells) and the TRPV1 agonist capsaicin (n=223 cells) evoked transient, and essentially reproducible Ca2+ transients in neonatal trigeminal neurons. Application of 1μM oxytocin for 20–30min did not change the amplitude of these responses (n=283 and 248 cells for α β-meATP and capsaicin, respectively). Thus, oxytocin does not modify P2X3 and TRPV1 receptor mediated responses in trigeminal neurons, further supporting our hypothesis that antinociceptive effects of oxytocin involve modulation of GABA signaling in the nociceptive neurons.
Because the results of calcium imaging suggest that oxytocin reduces the depolarizing action of GABA, we studied the effect of oxytocin on the GABA driving force (DFGABA) using cell-attached recordings of single GABA(A) channels (Figure (Figure6).6). DFGABA was deduced from reversal potential of the currents via GABA(A) channels (Serafini et al., 1995; Tyzio et al., 2006, 2008). In control conditions, GABA exerted strongly depolarizing action on the immature trigeminal neurons with DFGABA of 38.7±2.4mV (n=6). In the presence of oxytocin (1μM), DFGABA was reduced to 17.7±6.7mV (n=5; P<0.05), indicating that oxytocin strongly diminishes the depolarizing action of GABA on neonatal trigeminal neurons via a reduction of intracellular chloride as described in neonatal cortical neurons (Tyzio et al., 2006).
Our results indicate that like human neonates (Bergqvist et al., 2008), newborn rats are born with a natural analgesia. Firstly, pain sensitivity in the thermal tail-flick assay was significantly lower in the newborn rats compared to P2 rats. This difference is unlikely due to a rapid developmental increase in the pain sensitivity during this short period because developmental studies indicate that pain sensitivity only reduces with age (Fitzgerald and Gibson, 1984; Falcon et al., 1996; Jiang and Gebhart, 1998; Teng and Abbott, 1998; Marsh et al., 1999), but rather reflects a birth-related phenomenon. Secondly, blockade of oxytocin receptors that did not significantly modify the response in P2 rats, when birth-derived oxytocin levels have waned, but did strongly increase pain sensitivity in the rats immediately after birth. The present results are in agreement with clinical findings of newborn analgesia in vaginal delivery when compared to elective cesarean sections without labor (Bergqvist et al., 2008). Relying on this observation, it has been proposed that the fetus exhibits a high pain threshold during delivery, and that this threshold decreases significantly within hours after spontaneous vaginal birth. Thus, newborn analgesia exists both in human and rodent suggesting that it is a fundamental mechanism developed and conserved through the mammalian evolution. The physiological role for the newborn analgesia is likely to prevent newborns from experiencing the pain inherent in the mechanical compression in the delivery channel. Indeed, during delivery the human newborn's head is squeezed with an intermittent pressure as high as 2kg/cm−2 for several hours (Derek, 1999). However, it should equally alleviate pain resulting from iatrogenic factors, including forceps and vacuum extraction, placement of electrodes, blood samples during labor, and injections of vitamins and immunization. In keeping with the time course of newborn analgesia, which wanes within few hours, it has been recommended that painful procedures such as vitamin K injection or blood sampling to be performed within 90min after birth in order to minimize neonatal pain and possible long-lasting changes in pain behavior (Bergqvist et al., 2008).
What are the mechanisms of newborn analgesia? Because delivery is associated with stress, and because stress induces analgesia, it likely stress-induced noradrenalin and opioids releases mediate newborn analgesia (Bistoletti et al., 1983; Hagnevik et al., 1984; Lagercrantz and Slotkin, 1986; Lagercrantz, 1996; Mogil et al., 1996). The results of the present study also indicate an involvement of oxytocin, who's analgesic actions have been well documented in adult animals (Arletti et al., 1993; Lundeberg et al., 1993, 1994; Agren et al., 1995; Petersson et al., 2001; Yu et al., 2003; Condés-Lara et al., 2006; Miranda-Cardenas et al., 2006). Indeed, blockade of oxytocin receptors significantly increased pain in both assays in the newborn animals, suggesting an involvement of endogenous oxytocin. Conversely, exogenous oxytocin exerted analgesic actions in the animals newborn and in 1- to 2-day-old rat pups, when endogenous oxytocin has waned. Thus, newborn analgesia is likely achieved by activation of several complementary antinociceptive stress-induced (catecholamines and opioids) and birth-related (oxytocin) mechanisms to optimally protect newborn from the pain. Although the relative contributions of these various mechanisms to newborn analgesia remain to be determined, the powerful proalgesic effects of the oxytocin receptor antagonists in the newborn rats indicate that endogenous oxytocin provides a significant contribution to newborn analgesia.
What is the source for oxytocin in the newborn? In the fetal brain, oxytocin may be provided both by the mother and the fetus, and the maternal and fetal contributions may differ in rodents and humans. In the newborn rat the principal source of oxytocin is maternal, with only a limited contribution of fetus. This is because the hypothalamo-neurohypophysial system develops mainly post partum (Choy and Watkins, 1979; Lipari et al., 2001) and the production of fully functional amidated oxytocin begins only after birth and increases rapidly during postnatal development (Alstein et al., 1988; Lipari et al., 2001). Thus, the onset of intrinsic oxytocin production does not match with the observed perinatal oxytocin-mediated changes in GABA signaling, which is already half-maximal by E20 (Tyzio et al., 2006), nor with the analgesic actions of endogenous oxytocin at birth. In addition, we found that blockade of oxytocin receptors exerted pro-nociceptive action in the decerebrated newborn rats in which the descending oxytocin fibers from PVN and the upstream pain pathways are cut. Taken together, these results indicate that oxytocin in the newborn rat brain is mainly provided by the mother.
Whether our findings on the perinatal analgesic action of oxytocin can be translated to human newborn remains unknown. However such a hypothesis is supported by the findings of higher pain threshold in the vaginally born compared to cesarean-born newborns (Bergqvist et al., 2008), elevated oxytocin levels under normal delivery but not during C-sections (Russell et al., 2003; Wei et al., 2009), and by the analgesic effects of oxytocin in humans (Yang, 1976). On the other hand, the level of maturity of human brain at term is more advanced compared with altricial rats (Clancy et al., 2001) and nociceptive systems undergo significant changes during development (Fitzgerald and Gibson, 1984; Falcon et al., 1996; Jiang and Gebhart, 1998; Teng and Abbott, 1998; Marsh et al., 1999). In regards to the source of oxytocin, the contribution of fetal oxytocin to perinatal analgesia may be more significant in humans as their hypothalamo-neurohypophyseal system is more advanced at term and is capable of producing proper oxytocin. Thus, in humans, oxytocin levels at birth are higher in the umbilical artery than in the umbilical vein (Chard et al., 1971; Dawood et al., 1978; Otsuki et al., 1983; Patient et al., 1999). In addition, no oxytocin was detected in either arterial or venous cord blood of anencephalic newborns (Chard et al., 1971; Otsuki et al., 1983). This may suggest that oxytocin-mediated newborn analgesia in the rat is mainly provided by mother oxytocin whereas in human, it is mainly provided by fetal oxytocin.
How does oxytocin exert an analgesic action? In adult rats, electrical stimulation of the PVN, or topical application of oxytocin, selectively inhibits A-delta and C-fiber responses in superficial dorsal horn neurons, and this inhibition is reversed by a selective oxytocin antagonists (Robinson et al., 2002; Condés-Lara et al., 2006; Rojas-Piloni et al., 2007, 2008). These effects are blocked by the GABA(A) receptor antagonist bicuculline, suggesting that the analgesic actions of oxytocin involve enhancement of presynaptic GABAergic inhibition of the primary nociceptive inputs conveyed by A-delta and C-fibers to the spinal cord (Condés-Lara et al., 2009). This is in keeping with a preferential expression of oxytocin receptors in the superficial layers of the dorsal spinal cord, which is already high at birth (Uhl-Bronner et al., 2005).
An increase in GABAergic inhibition of the primary nociceptive afferents likely contributes to the analgesic actions of oxytocin observed in the present study in the newborn rats. However, in addition to the increase in the amount of GABA release caused by increased interneuron firing, a change in EGABA seems to contribute to the oxytocin-mediated increase in GABAergic inhibition. Indeed, we found that oxytocin reduces DFGABA and reduces GABA-evoked calcium transients in the trigeminal neurons. EGABA shifts toward more depolarizing values in different models of chronic pain in adult animals (for reviews De Koninck, 2007; Price et al., 2009). Blockade of NKCC1 co-transporter, which is the primary mediator of chloride accumulation in primary nociceptive neurons with bumetanide, causes a negative shift in EGABA and reduces pain (Alvarez-Leefmans et al., 1988; Sung et al., 2000; Laird et al., 2004; Granados-Soto et al., 2005; Valencia-de Ita et al., 2006). Our findings that bumetanide exerts an analgesic action in rat pups, and most notably, that its analgesic action persists after blockade of oxytocin receptors, provides additional support to our hypothesis that changes in EGABA in the nociceptive neurons are involved in the newborn analgesia and analgesic actions of oxytocin. Because depolarizing action of GABA on primary nociceptive neurons persists through the development (Alvarez-Leefmans et al., 1988; Sung et al., 2000; Gilbert et al., 2007; Rocha-González et al., 2008), it would be of interest to determine whether similar changes in EGABA contribute to oxytocin-mediated analgesia in adults, and notably in parturient women.
In conclusion, our results indicate that (i) like human neonates (Bergqvist et al., 2008), newborn rats are born with a natural analgesia, that (ii) this newborn analgesia involves the antinociceptive effects of endogenous oxytocin, and that (iii) the antinociceptive action of oxytocin involves modulation of GABA signaling in the nociceptive neurons. This reveals a novel facet of the protective actions of oxytocin for the newborn, which include previously described role in the transient switch in cortical actions of GABA from excitatory-to-inhibitory and an increase in brain resistance to hypoxia (Tyzio et al., 2006; Khazipov et al., 2008). In future clinical studies it would be of interest to verify the role for oxytocin in perinatal analgesia in the human newborn.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Financial support from INSERM, ANR, FRM, LFCE, Rothschild/INSERM “interface” programs to Rustem Khazipov and Yehezkel Ben-Ari. Anastasia Shakirzyanova and Rashid Giniatullin were supported by Finnish Academy.