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Spinal glial reaction and proinflammatory cytokine induction play an important role in the development of chronic pain states after tissue and nerve injury. The present study investigated the cellular and molecular mechanisms underlying descending facilitation of neuropathic pain with an emphasis on supraspinal glial-neuronal relationships. An early and transient reaction of microglia and prolonged reaction of astrocytes were found after chronic constriction injury (CCI) of the rat infraorbital nerve in the rostral ventromedial medulla (RVM), a major component of brain stem descending pain modulatory circuitry. There were prolonged elevations of cytokines tumor necrosis factor (TNF)-α and interleukin (IL)-1β after CCI and they were expressed in RVM astrocytes at 14 d after injury. Intra-RVM injection of microglial and astrocytic inhibitors attenuated mechanical hyperalgesia and allodynia at 3 d and 14d after CCI, respectively. Moreover, TNFR1 and IL-1R, receptors for TNF-α and IL-1β, respectively, were expressed primarily in RVM neurons exhibiting immunoreactivity to the NMDA receptor (NMDAR) subunit NR1. CCI increased TNFR1 and IL-1R levels and NR1 phosphorylation in the RVM. Neutralization of endogenous TNF-α and IL-1β in the RVM significantly reduced CCI-induced behavioral hypersensitivity and attenuated NR1 phosphorylation. Finally, intra-RVM administration of recombinant TNF-α or IL-1β upregulated NR1 phosphorylation and caused a reversible and NMDAR-dependent allodynia in normal rats, further suggesting that TNF-α and IL-1β couple glial hyperactivation with NMDAR function. These studies have addressed a novel contribution of supraspinal astrocytes and associated cytokines as well as central glial-neuronal interactions to the enhancement of descending facilitation of neuropathic pain.
The rostral ventromedial medulla (RVM) is an important component of the descending nociceptive system that projects to the spinal cord and trigeminal brain stem nuclei and constitutes a major mechanism in the control of pain transmission (Millan 2002; Ren and Dubner 2002; Fields et al., 2006). Recent studies indicate that hyperalgesia and allodynia in animal models of persistent pain are closely linked to long lasting activation of descending modulatory circuits involving descending facilitation (Porreca et al., 2002; Dubner and Ren, 2004; Gebhart 2004; Vanegas and Schaible, 2004), which significantly contributes to the development of persistent pain after peripheral inflammation (Wei et al., 1999; Urban and Gebhart, 1999; Guo et al., 06) and nerve injury (Pertovaara et al., 1996; Kovelowski et al., 2000). Despite extensive studies on the role of RVM in descending pain modulation, the cellular mechanisms of its involvement in descending pain facilitation are poorly understood.
A considerable amount of evidence has demonstrated the existence of dynamic and bidirectional communication between glia and neurons at the synapse, suggesting that glia play an active role in regulation of synaptic transmission in the CNS (Fields and Stevens-Graham 2002; Newman 2003; Perea and Araque 2006). Glial cells, primarily microglia and astrocytes, exhibit dynamic plasticity by converting from a relatively resting or quiescent state to a reactive or hyperactive state and appear to modulate neuronal activity. Interestingly, after hyperactivation, glia subsequently release cytokines at the spinal cord (DeLeo et al., 2004; Salter, 2004; Sommer & Kress 2004; Marchand et al., 2005, Watkins et al., 2007) and spinal trigeminal nucleus (Piao et al., 2006; Guo et al., 2007) which may be implicated in central mechanisms of persistent pain (Ren and Dubner, 2008). Whether supraspinal glial hyperactivity and their interactions with neurons in the RVM circuitry constitute a mechanism underlying descending facilitation during the development of persistent pain has not been studied.
Here, we have developed a quantitative behavioral measure of mechanical hyperalgesia and allodynia associated with a rat model of orofacial painful neuropathy, chronic constriction injury of the infraorbital nerve (CCI-ION), to investigate the mechanisms of neuropathic pain with an emphasis on glial-neuronal interactions in the pain modulatory circuitry. We found a prolonged astrocytic reaction and increased expression of cytokines TNF-α and IL1β in astrocytes and their receptors in RVM neurons after nerve injury. Intra-RVM microinjection of glial inhibitors and neutralization of endogenous TNF-α and IL1β significantly attenuated CCI-induced mechanical hyperalgesia and allodynia. We further found that CCI-induced enhancement of NMDA receptor (NMDAR) subunit NR1 phosphorylation in the RVM was significantly reversed by glial inhibitors or cytokine receptor antagonists. An elevated NMDAR subunit NR1 phosphorylation in the RVM and moderate behavioral hypersensitivity were also observed after microinjection of recombinant TNF-α and IL1β in the RVM of normal rats, and were reversed by pretreatment with NMDAR antagonists. This is the first study showing that glial-neuronal interactions coupling proinflammatory cytokines to NMDAR function at the supraspinal level contribute to descending pain facilitation.
Adult male Sprague Dawley rats weighing 175-350 g (Harlan, Indianapolis, IN) were used in all experiments. Rats were on a 12 h light/dark cycle and received food and water ad libitum. The experiments were approved by the Institutional Animal Care and Use Committee of the University of Maryland Dental School.
A model of trigeminal neuropathic pain was made by chronic constriction injury to the unilateral infraorbital nerve (CCI-ION), which was performed based on the original description (Bennett and Xie, 1988) and via an intraoral approach described by Imamura et al (1997). Animals were anesthetized with pentobarbital sodium (50 mg/kg i.p.). Surgery was performed under an operation microscope. The head of the rat was supine and fixed on a table. A one-cm long incision was made along the gingivobuccal margin in the buccal mucosa, beginning immediately next to the first molar. The ION was freed from surrounding connective tissue by a glass rod and clearly visualized using a surgical microscope. At 3-4 mm from the nerve where its branches emerge from the infraorbital foramen, the ION was loosely tied with two chromic gut (4.0) ligatures, 2 mm apart. This caused minor constriction of the ION such that the superficial vasculature was minimally retarded. The wound was checked for hemostasis and the incision was closed using three 4.0 silk sutures. The sham-operated rats received only a unilateral nerve exposure without ligature. All surgical procedures were performed aseptically. In some cases, a long lasting anesthetic agent 0.25% bupivacaine was injected at the incision sites before and after surgery to block local nociceptive inputs induced by acute tissue injury and then twice per day for another 2 days. Changes in gross behavior and body weight gain in CCI and sham rats were monitored throughout the study and were not significantly different when compared with that in naïve rats.
All behavioral tests were conducted under blind conditions as previously described (Ren, 1999). The rat was not restrained but habituated to stand on its hind paws and lean against the experimenter’s hand who was wearing a regular leather work glove. The habituation required no more than normal petting of the rat, and it was achieved within half an hour. A series of calibrated von Frey filaments with bending forces ranging from 9 mg to 118 g were slightly applied to the skin within the infraorbital territory, near the center of the vibrissal pad on hairy skin surrounding the mystacial vibrissae. These areas were stimulated on both sides: ipsilateral and contralateral to the side where surgery was performed. An active withdrawal of the head from the probing filament was defined as a response. Each von Frey filament was applied 5 times at intervals of a few sec. The response frequencies [(number of responses/number of stimuli) X100%] to a range of von Frey filament forces were determined and an S-R curve was plotted. After a non-linear regression analysis, an EF50 value, defined as the von Frey filament force (g) that produces a 50% response frequency, was derived from the S-R curve. We used EF50 value as a measure of mechanical sensitivity.
As previously described (Guo et al., 2006), animals were anaesthetized with 2-3% isoflurane in a gas mixture of 30% O2 balanced with nitrogen, and placed in a Kopf stereotaxic instrument. A midline incision was made after infiltration of lidocaine (2%) into the skin. A midline opening was made in the skull with a dental drill to insert a microinjection needle into the target site. The coordinates for the nucleus raphe magnus (NRM), the major structure of RVM, were: 10.5 mm caudal to the bregma, midline and 9.0 mm ventral to the surface of the cerebellum (Paxinos and Watson, 2005). To avoid penetration of the transverse sinus, the incisor bar was set at 4.7 mm below the horizontal plane passing through the interaural line. Animals were subsequently maintained at around 1% halothane. Microinjections were performed by delivering drug solutions slowly over a 10-min period using a 0.5 μl Hamilton syringe with a 32 gauge needle. The needle was withdrawn 5 min after the completion of the injection and the incision sutured. All wound margins were covered with a local anesthetic ointment (Nupercainal, Rugby Laboratories, Inc., Norcross, GA, USA). Different groups of animals were subjected to intra-RVM microinjection with a 0.5 μl volume solution of 1) glial metabolic inhibitors propentofylline (1 fmol, 100 fmol and 10 pmol, Sigma, St. Louis, MO), fluorocitrate (1 fmol and 100 fmol, Sigma) and minocycline (10 fmol and 1 pmol, Sigma); 2) cytokine receptor antagonists TNFRI/Fc (TNFRI antagonist, 50 fmol, R & D Systems, Minneapolis, MN) and IL-ra (Kineret, IL-1R antagonist, 3 pmol, Amgen, Thousand Oaks, CA); 3) recombinant rat TNF-α (rTNF-α, TNFR agonist, 120 fmol, R & D systems) or IL-1β (rIL-1β, IL-1R agonist, 120 fmol, Peprotech, Rocky Hill, NJ); and 4) glutamate receptor antagonists MK801 (noncompetitive NMDAR antagonist, 10 pmol, Sigma). All drugs except for fluorocitrate were dissolved or reconstituted in endotoxin-free sterile distilled water, aliquoted and stored at -70 °C. At the time of testing, the stored aliquot was thawed on ice and diluted in sterile 0.9% saline to a final concentration. The doses of these agents were carefully chosen by referring to the literature and adjusted by our pilot experiments. For example, in the RVM, we have found that a dose ≤ 0.1 pmol is necessary to avoid an apparent effect of fluorocitrate on neurons (Fig. S1) (Sweitzer et al., 2001b; Raghavendra et al., 2003 a and b; Ledeboer et al., 2005; Guo et al., 2006, 2007). The control rats underwent identical procedures with injection of the same volume (0.5 μl) of sterile 0.9% saline as vehicle treatment. The fluorocitrate solution was prepared as described by Paulsen et al. (1987). The vehicle solution was prepared in the same manner for separate control experiments, except that fluorocitrate was omitted.
At different time points after nerve injury, rats were behaviorally tested to identify CCI-ION induced mechanical allodynia, and then deeply anesthetized with pentobarbital and perfused transcardially with 200 ml of saline followed by 500 ml of cold (4°C) 0.1 M phosphate buffer(PB) containing 4% paraformaldehyde. The brainstem was removed, immersed in the same fixative overnight at 4°C, and transferred to 30% sucrose (w/v) in phosphate buffer for several days for cryoprotection. Thirty micrometer-thick coronal sections of the brainstem were cut with a cryostat at -20°C. Free-floating tissue sections including RVM were incubated with relevant antibodies overnight. After washes, the sections were incubated with AffiniPure biotinylated secondary IgG (1:800, Jackson ImmunoResearch Lab, West Grove, PA) for 1 h. For fluorescence staining, the sections were incubated with Streptavidin-Alexa Fluor 568 or 488 (1:600, Molecular Probes, Eugene, OR) for 1 h. For peroxidase identification, the sections were reacted with avidin and biotinylated HRP complex (1:200, Vector Laboratories, Burlingame, CA) for 1 h, and reacted with 0.025% diaminobenzidine (DAB, Sigma) and 0.003% hydrogen peroxide for 5-20 min. Immunostaining control studies were performed by omission of the primary or secondary antibodies, and by preabsorption with an excess (10 μg/ml) of the respective antigens. Double labeling was performed simultaneously with two primary antibodies obtained from different species. After overnight, the sections were incubated for 2 h in solutions containing species-specific secondary antibodies coupled to Alexa 568 or 488, respectively. After washes, all sections were mounted on gelatin-coated slides and coverslipped with Vectashield (Vector Laboratories). Images were collected sequentially using a Zeiss fluorescence microscope and a charge-coupled device camera controlled by SPOT software. If necessary, a Zeiss 510 MATA laser-scanning confocal microscope was further used. Adobe Photoshop (version CS) was used for image cropping and adjustment.
Naive and treated rats were anesthetized with 2% halothane and decapitated. The RVM tissues were removed as previously described (Guo et al., 2006) and homogenized in solubilization buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1 mM EDTA, 1% TritonX-100, 0.5% deoxycholic acid, 0.1% SDS, 1 mM Na3VO4, 1 U/ml aprotinin, 2 μg/ml leupetin, 2 μg/ml pepstatin A). The homogenate was centrifuged at 20,200 x g for 10 min at 4°C, and the supernatant was removed. The protein concentration was determined. Each sample contained proteins from one animal. The proteins (50 μg) were separated on a 7.5% SDS-PAGE gel and blotted to nitrocellulose membrane (GE Healthcare). The blot was incubated with the respective antibody overnight at 4°C. The membrane was washed with TBS and incubated for 1 h with anti-goat IgG horseradish peroxidase (HRP) (1:3000; Santa Cruz Biotechnology, Santa Cruz, CA) in 5% milk/TBS. The immunoreactivity was detected using enhanced chemiluminescence (ECL) (GE Healthcare). The loading and blotting of equal amount of proteins were verified by reprobing the membrane with anti β-actin antiserum (Sigma). The ECL-exposed films were digitized, and densitometric quantification of immunoreactive bands was performed using U-SCAN-IT gel (ver. 4.3, Silk Scientific Corp.).
The following antibodies were used for immunostaining and Western blot: Rabbit or mouse anti-GFAP (astrocytic marker, 1: 1000, Dako, Carpinteria, CA), rabbit anti-S100β (for labeling astrocytic calcium-binding protein, 1:800, Fitzgerald, Concord, MA), mouse anti-OX-42 (for labeling CD11b as microglial marker, 1:800, Serotec, Oxford, UK), rabbit anti-Iba-1 (for labeling microglial calcium-binding protein, 1:1000, Wako, Japan), mouse anti-NeuN (neuronal marker, 1:1000, Chemicon, Temecula, CA), goat anti-TNF-α (1:1000, R & D Systems), rabbit anti-IL1β (1:2000, Chemicon), goat anti-TNFR1 (1:500, Santa Cruz, CA), rabbit anti-IL1R (1:500, Santa Cruz Biotech., Santa Cruz, CA), mouse anti-NR1 (1:5000, Upstate, Lake Placid, NY), rabbit anti-P-ser896 NR1 (Sigma) and mouse anti-β-actin (Sigma).
The locations of microinjection sites in the RVM were determined by visualization of serial Nissl-stained tissue sections under a microscope. Rats with misplaced microinjection sties were excluded from the data analysis or considered as controls in some cases.
Results were expressed as mean ± SEM. Statistical comparisons included Student’s t test or one- or two-way ANOVA with the post hoc Scheffe F test in Western blot analysis or the Student-Newman-Keuls test in behavioral experiments (ANOVA with repeated measures). In all cases, p < 0.05 was considered to be statistically significant.
To probe a role of central glial-neuronal interaction in the development of persistent pain, we adapted and improved the chronic constriction injury of the infraorbital nerve (CCI-ION) model in the rat (Vos et al. 1994; Imamura et al. 1997). The ION is a pure sensory nerve, the largest branch of the maxillary division of the trigeminal nerve, and innervates the mystacial vibrissae, the hairy vibrissal pad, the upper lip, lateral nose and teeth, and mucosa of the upper jaw (Waite & Tracey 1995). To reduce injury related to the surgical procedure and keep the facial skin intact, we performed the CCI-ION operation through an intraoral approach (Imamura et al. 1997). While the testing of behavioral hyperalgesia and allodynia in spinal models of pain is straightforward, assessing nocifensive behavior of the trigeminal region is difficult. Moreover, in the CCI-ION model, only responses to noxious thermal stimulation (Imamura et al. 1997) or mechanical stimulation (Kitagawa et al. 2006) have been examined in restrained rats. To reduce the stress of rats in an experimental environment, we have developed an appropriate handling approach without restraint to assess the mechanical hyperalgesia and allodynia of the orofacial region in rats (Ren 1999; Sugiyo et al. 2005). The response frequencies to a range of von Frey filament forces applied to the ION territory were determined and a stimulus-response frequency (S-R) curve was plotted (Fig. 1A). An EF50 value was defined as the von Frey filament force (g) that produces a 50% response frequency. Compared to the baseline, the left ward shift of the S-R curve, resulting in a reduction of EF50, represents mechanical hyperalgesia and allodynia at 1 and 14 d after CCI-ION (Fig. 1A), since there was an increased response to suprathreshold stimuli and a decreased response threshold for nocifensive behavior. Compared to naive and sham-operated rats, there was a significant reduction of the EF50s in the ipsilateral ION territory from 1 to 28 d after unilateral CCI-ION in rats (p < 0.001 vs. sham group) (Fig. 1B). There were no changes in the contralateral EF50s. A moderate and transient (for 1-3 d) reduction of the EF50s was also seen in sham rats (p < 0.05 vs. naïve group), and was completely blocked by local anesthesia of the surrounding tissues with 0.25% bupivacaine (Moore 1984) (Fig. 1B), suggesting that the response to the surgical procedure alone at 1-3 d is caused by input from local tissue after incision and inflammation. Thus, we have shown a long lasting and stable hyperalgesia/allodynia in the CCI-ION rats and used this model to study the involvement of supraspinal glia/cytokines in neuropathic pain of the orofacial origin.
To examine whether nerve injury induced glial reaction in the RVM, we first observed changes in the expression of glial fibrillary acidic protein (GFAP), a marker of reactive gliosis and proliferation of astrocytes, in RVM sections from naïve rats and after CCI-ION (Fig. 1C). As shown in sample sections at 3 d (Fig. 1C c) and at 14 d (Fig. 1C d) after CCI-ION, increased GFAP immunoreactivity (IR) was seen in small cell bodies and their processes, compared with naive animals (Fig. 1C a and b), suggesting prolonged hyperactivation of astrocytes in RVM after nerve injury. It is known that S100β is a Ca2+ binding protein that is produced primarily in astrocytes in the CNS. Thus enhanced S100β expression was also used as a specific functional marker of astrocytes in the brain (Tanga et al., 2006). The pattern of enhanced expression of S100β was compared to GFAP expression by immunohistochemistry in the RVM of the CCI-ION (Fig. 1D b-d) and naive rats (Fig. 1D a), beginning from 1 d to 28 d, further confirming the long lasting hyperactivation of astrocytes in the RVM after nerve injury. We then used Western blot to quantify the time course of changes of GFAP levels in the RVM tissue (Fig. 1E). Although increased GFAP expression was found in both sham and CCI rats at 1d and 3d after surgery, the level of GFAP expression was consistently increased in the RVM at 7 d (by 234.3 ± 12.1%, p < 0.001, n=4 rats), 14 d (by 231.70 ± 6.64%, p< 0.001, n=4), 21 d (by 176.70 ± 18.70%, p< 0.05, n=3) and 28 d (by 194.54 ± 8.30%, p< 0.001, n=3) after CCI but not sham treatment (by 123.10 ± 7.38% at 7 d and 121.70 ± 5.64% at 14 d, p > 0.05, n=4 per group) compared to the naïve group (n = 3, Fig. 1E). Consistent with a small and short-lasting behavioral hyperalgesia and allodynia at 1 and 3 d in the sham-operated rats (Fig. 1B), the transiently increased GFAP expression in the RVM of the sham-operated rats was found at the same time points (Fig. 1E). To distinguish whether these early effects in the CCI rats were partically attributable to the tissue incision during the oral surgery, we utilized local anesthesia of the surgical site to block the increased neural activity associated with tissue injury during the first 3 days in sham animals. Long-lasting anesthesia with 0.25% bupivacaine totally eliminated the increased GFAP expression at 3 d after sham operation (n=3 per group, Fig. 1F), suggesting that the earlier increase in GFAP expression observed in the RVM at 1 and 3 d after CCI-ION is partially caused by tissue injury. This observation is also consistent with a recent study (Obata et al., 2006) that hindpaw incision results in glial hyperactivation in the spinal dorsal horn, beginning within 1d and reaching a maximum hyperactivation at 3d after tissue injury.
In a parallel experiment, we extended our analysis to determine whether microglial reaction occurs by examining expression of microglial markers in the RVM (Fig. 2). Different from GFAP expression, CD11b expression in the RVM was primarily increased at 1 d (not shown) and 3 d, but not 14 d and later, after CCI-ION compared to the naive condition (Fig. 2A). This early hyperactivation of microglia was also confirmed by immunostaining with a functional microglia marker, ionized calcium-binding adaptor molecule 1 (Iba1) (Fig. 2B). With Western blot analysis, an increase in CD11b expression in RVM tissues was only detected at early time points (1-3 d) in both CCI and sham-operated rats (p < 0.05, n=3 per group), compared to naïve animals (Fig. 2C). Local tissue anesthesia also completely blocked CD11b increase in the RVM from sham-operated rats at 3 d (n=3 per group, Fig. 2D), suggesting that tissue injury also caused microglial hyperactivation. These results indicate that nerve and tissue injury activate acutely (1-3 d) both astrocytes and microglia in the RVM, both of which are likely involved in supraspinal mechanisms underlying the generation of trigeminal neuropathic pain, consistent with previous studies on glial function in the spinal cord (DeLeo & Yezierski 2001; Raghavendra et al., 2004; Ledeboer et al., 2006; Obata et al., 2006). In addition, nerve injury also induced a prolonged hyperactivation (at least for 28 d) of astrocytes in the RVM. The role of the long-term astrocytic reaction in the RVM during development of neuropathic pain was the focus of our subsequent studies below.
Consistent with previous studies (Piao et al., 2006; Guo et al., 2007), the time course-dependent upregulation of GFAP and CD-11b expression was also observed after CCI-ION in the spinal trigeminal nucleus ipsilateral to the nerve injury (data not shown), a trigeminal site known to receive direct peripheral nociceptive input. Importantly, glial reaction in the RVM is specifically related to CCI-ION. The facial nucleus lateral to the RVM did not exhibit changes in GFAP and CD-11b expression after CCI-ION (data not shown).
By its inhibition on aconitase, fluorocitrate interrupts the tricarboxylic acid (TCA) cycle and can be used as a mitochondrial inhibitor (Voloboueva et al., 2007). Fluorocitrate-induced glial inhibition results in a variety of metabolic effects including reduced ATP production and increased glucose metabolism (Fonnum et al., 1997; Hirose et al., 2007). Although not selectively affecting aconitase of different cellular origin per se, fluorocitrate primarily inhibits TCA cycle of astrocytes due to more avid uptake by astrocytes and has been used to assess the importance of glial cells for brain function in vivo (Fonnum et al., 1997; Zielke et al., 2007). However, fluorocitrate may also produce neuronal damage (Hornfeldt and Larson, 1990; Largo et al., 1996). Intrastriatal injection of 1 nmol fluorocitrate produces ultrastructural alterations of astrocytes without affecting neurons while a larger dose at 2 nmol also affects neuronal structures and metabolism (Paulsen et al., 1987).
To search for a safe range of doses for the selective effect of fluorocitrate on glial cells, we performed double staining for the neuronal marker, NeuN, with TUNEL, a label for cell apoptosis, or Fluoro-Jade, a marker of cell necrosis, in RVM sections after microinjection of the drug [supplementary Fig. 1 (Fig. S1)]. When doses of fluorocitrate in the range between 1 fmol (2.2 ± 0.41 double-labeled cells/ section, n=4, p > 0.05) and 100 fmol (2.1 ± 0.27, n=4, P > 0.05, Fig. S1A c and C) were used, there was no apparent cellular damage shown by Nissl (see Fig. S1A a) and TUNEL staining (Fig. S1A b and c) except within the track of the microinjection needle and its nearby area compared to that seen in naïve (0.25 ±0.16 labeled cells/ section, n=4, Fig. S1C) and vehicle treatment (1.38 ±0.18, n=4, Fig. S1A b and C). This finding suggests that a few damaged cells may be induced by placement of the injection needle during the microinjection procedure but not by fluorocitrate. However, when a higher dose of fluorocitrate (10 pmol) was injected, TUNEL labeled cells were significantly increased in the RVM (11.88 ± 1.26, n=4, p <0.001 vs. vehicle group n=4, Fig. S1A d and C), with labeled cells in areas far away from the tissue track of the injection needle. Double immunostaining identified that all TUNEL labeled cells were also positive to NeuN (Fig. S1B). These results suggest that a dose-dependent neuronal apoptosis occurred after microinjection of fluorocitrate into the RVM. Fluoro-Jade B staining was performed to examine whether fluorocitrate induces neuronal necrosis in the RVM. Many Fluoro-Jade positive cells were located in the microinjection sites from rats injected with high (10 pmol, n=4) but not low (100 fmol) dose of fluorocitrate (n=4 per group, Fig. S1D). No double labeled cells for both Fluoro-Jade B and NeuN were found in the RVM, although Fluoro-Jade positive cells and NeuN-IR neurons was also seen in the same RVM region after microinjection of fluorocitrate (Fig. S1D). This finding suggests that no significant necrosis of RVM neurons was apparent after microinjection of fluorocitrate. The Fluoro-Jade B positive population may represent selective degeneration of RVM glial cells resulting from toxic effects of a high dose of fluorocitrate.
Neuronal damage has been found in the rat spinal dorsal horn after sciatic nerve injury (Polgar et al., 2005; Scholz et al., 2005). To test whether CCI-ION alone affected the extent of neuronal damage in the RVM, we also examined TUNEL and Fluoro-Jade staining in RVM sections from rats with the CCI or sham treatment at 7 and 14 d after surgery. In comparison with the naïve animal, there were no significant differences in the number of TUNEL or Fluoro-Jade labeled cells in the RVM in the CCI- or sham-operated rats (p > 0.05, n= 4 per group, data not shown), suggesting that there was no apparent neuronal damage in the RVM produced by the CCI-ION alone.
We then examined the effects of low dose of fluorocitrate on the glia cells in the RVM of CCI rats (Fig. S1E). We confirmed the lack of any neuronal apoptosis in the RVM sections from 3 d (n=4 rat, data not shown) and 14 d (n=4, Fig. S1E d) CCI-treated rats after microinjection of low dose fluorocitrate (100 fmol) compared to vehicle (n=3, Fig. S1E a). With regard to long GFAP turnover time, we examined changes in GFAP protein expression in RVM tissue at 6 h after astrocytic inhibition. Upregulation of GFAP expression in the RVM at 14 d after CCI (n=4, Fig. S1E b) was decreased after microinjection of fluorocitrate (100 fmol) (n=4, Fig. S1E e). In contrast, there was no effect of this dose of fluorocitrate on the elevated CD11b expression in the RVM sections at 3 d after CCI-treated rats (n=4, Fig. S1E f) compared to vehicle injection (n=3, Fig. S1E c). Western blot further confirmed that fluorocitrate (100 fmol) induced the selective inhibition of enhanced GFAP expression (91 ± 21.5 % (FC, n=3) vs. 238 ± 45.9% (vehicle, n=3), p < 0.05, Fig. 3A) and S100β expression (83.3 ± 9.5% (FC, n=3) vs. 159.7 ± 17% (vehicle, n=3), p < 0.001, Fig. 3B) at 14 d after CCI in the RVM compared to vehicle treatment.
To order to determine whether astrocytic inhibition by fluorocitrate functionally reduces cytokine production in the RVM after CCI, we measured changes in TNF-α and IL-1β protein levels in the RVM. Fluorocitrate (100 fmol) totally prevented CCI-induced enhancement of TNF-α expression (86.3 ± 27.5% (FC, n=3) vs. 241.3 ± 30.1% (vehicle, n=3), p < 0.001, Fig. 3C) and IL-1β expression (109.7 ± 16.2 % (FC, n=3) vs. 199 ± 25.4% (vehicle, n=3), p < 0.01, Fig. 3D) at 14 d in the RVM compared to vehicle treatment. However, this dose of fluorocitrate did not affect the basal GFAP (Fig. 3A) and S100β (Fig. 3B) and TNF-α and IL-1β protein levels in the RVM tissue at 14 d after a sham operation (Fig. 3C and D).
It was shown that intrathecal injection of fluorocitrate (0.1 to 1 nmol) reduced injury-induced elevation of CD11b expression in the spinal cord (Clark et al., 2006; Sun et al., 2008), questioning its preferential inhibition of astrocytic function. We examined the effect of fluorocitrate on microglial function in the RVM in our model and with the low dose used to study astrocytic function. The results showed that fluorocitrate (100 fmol) did not block tissue injury-induced enhancement of CD11b expression (159 ± 5% (FC, n=3) vs. 153 ± 3.93% (vehicle, n=3), p > 0.05, Fig. 3E) at 3 d in the RVM tissues of sham operated rats, and also did not prevent nerve injury-induced elevation of CD 11b expression (171.3 ± 22.1% (FC, n=3) vs. 168.3 ± 16.3% (vehicle, n=3) p > 0.05, Fig. 3E) in the RVM at 3 d after CCI. In contrast, the enhanced expression of CD11b in the RVM at 3 d after sham operation or CCI was attenuated or abolished by minocycline (MC, 1 pmol) at 4 hr after the microinjection (n=3 per group, p < 0.05, Fig. 3E) compared to vehicle. Thus, our results suggest that low doses of fluorocitrate could be used to locally and effectively inhibit hyperactive astrocytes and their function without apparent neuronal degeneration and microglial disruption in the RVM.
To identify participation of supraspinal glial hyperactivation in the cellular mechanisms underlying the initiation and maintenance of neuropathic pain, we tested the effects of selective disruption of glial metabolism by microinjection of single doses of glial inhibitors into the RVM on mechanical hyperalgesia and allodynia at early (3 d) and later time points (14 d) after CCI. Propentofylline has been known to depress both microglial and astrocytic activation, reduce proinflammatory cytokine release, and attenuate allodynia and hyperalgesia induced by nerve injury and inflammation when systemically or intrathecally injected (Sweitzer et al, 2001a; Raghavendra et al., 2003a, b; Dorazil-Dudzk et al., 2004; Tawfik et al., 2008). The antiallodynic effect of propentofylline is associated with a reduction of reactive gliosis involving astroglia and microglia (Sweitzer et al., 2001b, 2006; Raghavendra et al., 2003b), which is consistent with a role of propentofylline as a non-selective glial modulator. Minocycline is a semisynthetic tetracycline antibiotic with a number of other properties distinct from its antimicrobial action including neuroprotection and anti-inflammatory action (Elewa et al., 2006). It has been used to evaluate the involvement of microglia in the development of neuropathic pain, and has no direct action on astrocytes or neurons (Tikka et al. 2001; Raghavendra et al. 2003a; Ledeboer et al. 2005). Recent studies indicate that minocycline reduces microglial migration to cellular debris and decreases microglial Kv1.3 expression (Nutile-McMenemy et al., 2007).
We injected fluorocitrate, propentofylline and minocycline into the RVM of the CCI and sham-operated rats at 3 d and 14d after surgery. As shown in Fig. 4, all vehicle-treated CCI rats exhibited stable and strong hypersensitivity in behavioral tests (Fig. 4 A-C). A single dose of propentofylline (PPF, 10 pmol) had no effect on EF50s in the sham animals at 14 d after surgery (Fig. 4A left). However, propentofylline (1 fmol, 100 fmol and 10 pmol) significantly attenuated mechanical hyperalgesia and allodynia at 14 d after CCI in a dose-dependent manner, lasting for 4 h or longer (Fig. 4A left). Similarly, at 3 d after nerve injury, a high dose of propentofylline (10 pmol) completely reversed hyperalgesia and allodynia at least for 6 hr, and also transiently blocked moderate behavioral hypersensitivity in sham-treated animals at 3 d (Fig. 4A right). Although it had no effect on EF50s in the sham rats at 14 d, fluorocitrate (1 and 100 fmol) significantly attenuated mechanical hyperalgesia and allodynia to an extent similar to the high dose of propentofylline at 14 d after CCI, when compared to the vehicle-treated CCI rats (Fig. 4B left). Interestingly, fluorocitrate at these doses did not reverse hyperalgesia and allodynia observed at 3 d after CCI (Fig. 4B right). Fluorocitrate did produce a trend towards inhibition of behavioral hypersensitivity at 3 d in sham animals when compared to the vehicle-treated sham rats (Fig. 4B right). In contrast, minocycline (1 pmol) produced inhibition of behavioral hyperalgesia and allodynia, which persisted over the 6 hr observation period, at 3 d (Fig. 4C right)) but not 14 d (Fig. 4C left) after CCI-ION. This dose of minocycline also transiently and significantly attenuated the moderate hyperalgesia and allodynia induced by sham operation at 3d (Fig. 4C right). These results support our hypothesis that the development of neuropathic pain behavior in CCI-ION rats involves glial hyperactivation in the RVM. In combination with the immunohistochemistry and Western blot results, our behavioral analysis further suggests that persistent astrocytic hyperactivation in the RVM contributes to mechanisms underlying the maintenance of neuropathic pain after nerve injury. These results also suggest that the initiation of behavioral hyperalgesia and allodynia in the CCI-ION rats primarily depends on cellular mechanisms relevant to microglial reaction in the RVM after nerve injury and tissue injury. It is known that minocycline interferes with the activity of matrix metalloproteinases 2 and 9 (MMP-2 and MMP9) (Machado et al., 2006) which are a family of zinc dependent proteases responsible for extracellular matrix turnover and degradation of bioactive proteins. MMP-2 and MMP-9 have been found in dorsal root ganglion neurons and satellite cells and are involved in induction and maintenance of neuropathic pain through IL-1β cleavage and glial hyperactivation at the spinal cord (Kawasaki et al., 2008). Although the distribution of MMPs in the RVM and their regulation after nerve injury are not known, we cannot exclude the possible effect of minocycline on glial function via MMPs and other factors in the RVM.
Upon hyperactivation, astrocytes and microglia increase expression and secretion of proinflammatory cytokines, such as TNF-α and IL-1β. These cytokines have been shown to increase synaptic efficacy in the hippocampus (Woolf and Salter, 2000; Beattie et al., 2002; Viviani et al., 2003; Perea and Araque 2006, 2007) and contribute to neuronal hypersensitivity in spinal dorsal horn (DeLeo and Yezierski 2001; Sommer & Kress 2004; Marchand et al. 2005, Watkins et al., 2007). Hence, we next examined whether astrocytic hyperactivation during the development of neuropathic pain is accompanied by an increase in cytokine levels in the RVM. Western blots showed that the expression of TNF-α and IL-1β in the RVM tissues was significantly upregulated by 58% and 62%, respectively, at 14d after CCI compared to sham-operated animals (p < 0.05, n=3 per group, Fig. 5A). An increase of TNF-α- and IL-1β immunostaining in the RVM cells was found after CCI-ION (n= 6, Fig. 5B). To verify the source of cells expressing these cytokines, double labeling was performed and showed that both TNF-α- and IL-1β-IR were colocalized with GFAP-IR but not NeuN-IR in RVM cells at 14d after CCI-ION (Figs. 5C and D). We did not find coexpression of the cytokines with CD11b (data not shown), possibly because of the very few hyperactivated microglia seen at 14 d. These results suggest that hyperactivated astrocytes are a primary source of the increased TNF-α and IL-1β in the RVM in the maintenance of neuropathic pain at 14 d after nerve injury.
As a possible mechanism of glial-neuronal interaction, we wanted to know whether cytokine receptors were distributed in RVM neurons as a link between astrocytes and neurons and if these receptors were upregulated in the RVM after trigeminal nerve injury. Immunostaining showed stronger expression of TNFR1, receptor for TNF-α, and IL-1RI, receptor for IL-1β, in the RVM at 14d after CCI (Fig. 6A a and b, and 6 C a and b, respectively) compared to naïve and sham-operated animals (data not shown). Double labeling indicated that TNFR1-IR and IL-1RI-IR were primarily localized in RVM neurons (Fig. 6A and 6C). Western blot showed that the levels of TNFR1 and IL-1RI were significantly increased at 14d after CCI when compared to naive and sham-operated rats (p < 0.05, n=3 per group, Fig. 6B and 6D). These data demonstrate enhanced expression of cytokine receptors for TNF-α for IL-1β in the RVM neurons during maintenance of neuropathic pain.
We have shown that glutamate receptor subunit NMDARs are widely expressed in rat RVM neurons and are upregulated and phosphorylated in the RVM after tissue injury, contributing to thermal hyperalgesia and mechanical allodynia after peripheral inflammation (Guan et al., 2002; Guo et al, 2006). To provide morphological evidence that supports the interactions between glia/cytokines and neuronal glutamate receptors, we performed double immunostaining. The results showed that cytokine receptors TNFR1 and IL-1RI co-localized with NR1 expression, a principle component of NMDARs in RVM neurons at 14d after CCI-ION (n=4, Fig. 7A and B), similar to the distribution pattern from untreated rats (data not shown). To examine whether CCI-ION also induces NMDAR activation, the phosphorylation levels of the NMDAR subunit NR1 were measured in RVM tissues. As shown in Fig. 7C, the immunostaining against pNR1ser896 was clearly increased by 2-fold (P < 0.001, n=3) at 14d after CCI-ION compare to the sham-operated (data not shown) and naive rats (n=3).
To further explore whether astrocytic hyperactivation and consequent secretion of cytokines contributes to NMDAR activation, we examined the effect of local application of fluorocitrate on increased expression of pNR1 produced by nerve injury. Western blot showed that the increased pNR1ser896 was blocked by fluorocitrate (100 fmol) at 2 h after microinjection into the RVM at 14d after CCI-ION (p < 0.01, n=3) compared to vehicle treatment (n=3) (Fig. 7D), whereas the same dose of fluorocitrate had no effect on pNR1 expression in sham rats (n=3, Fig. 7D). Moreover, the CCI-induced enhancement of pNR1 was also completely eliminated by the soluble anti-TNFR1 IgG, a biological sequester for endogenous TNF-α (TNFR/Fc (T/Fc), 50 fmol, n=3, p< 0.05, Fig. 7E) and IL-1ra, an IL-1RI antagonist, (3 pmol, p < 0.05, n=3, Fig. 7F) at 2 hr after intra-RVM injections, compared to vehicle injections (n=3). We did not detect any effects of the immune agents on pNR1 expression in the RVM tissue in sham-operated rats (p > 0.05, n=3 each group, Fig. 7E-F), when compared to that in naïve animals (n=3). These results suggest that NMDAR activation in the RVM after CCI is facilitated by the activation of RVM astrocytes and the cytokine receptors for TNF-α and IL-1β during the maintenance of neuropathic pain.
To examine whether NMDARs and the cytokine receptors TNFR1 and IL-1RI contribute to CCI-induced mechanical hyperalgesia and allodynia, we injected the receptor antagonists into the RVM at 14 d after nerve injury. MK-801 (10 pmol), an NMDAR channel blocker that did not affect baseline EF50s in sham-treated rats (n=6, Fig. 7G), however, it significantly attenuated mechanical hyperalgesia and allodynia after CCI at least for 6 h (n=6, p < 0.05, Fig. 7G). The post-treatment with TNFR/Fc (50 fmol) or IL-1ra (3 pmol) in the RVM also temporally reversed behavioral hypersensitivity to a similar extent in the CCI rats but did not alter EF50s recorded in sham rats (Fig. 7H). The microinjection of these compounds into the facial nucleus near the RVM in CCI-ION rats did not disrupt the development of behavioral hypersensitivity (data not shown), suggesting that the inhibitory effects of the receptor antagonists on CCI-induced hypersensitivity indeed occurred in the RVM but not the surround regions. Thus, we have demonstrated the involvement of RVM NMDAR activation in CCI-induced hyperalgesia /allodynia and its dependence on local astrocytic hyperactivation and cytokine release.
To test whether the cytokines directly increase NMDAR function and are implicated in descending pain facilitation, we microinjected recombinant rat TNF-α (rTNF-α) and IL-1β (r IL-1β) into the RVM of normal rats and further evaluated their effects on local pNR1 expression and mechanical nociception (Fig. 8). In comparison with vehicle, both exogenous rTNF-α (120 fmol) and rIL-1β (120 fmol) produced a significant upregulation of NR1 ser896 phosphorylation (by 1.8-fold and 1.71-fold, respectively, p < 0.05, n=4 per group) at 2 h after microinjections (Fig. 8A). The cytokine-induced pNR1 increase was completely blocked by pretreatment with the NMDAR antagonist MK-801 (10 pmol, p < 0.05, n=4 per group) (Fig. 8A), suggesting that besides activating cytokine receptors at postsynaptic sites, these cytokines may enhance glutamate release from presynaptic terminals and glia. Finally, we examined the effects of exogenous cytokines on mechanical nociceptive thresholds (Fig. 8 B and C). A single dose of rTNF-α (120 fmol) in the RVM produced behavioral hyperalgesia and allodynia, as indicated by a significant reduction of EF50s (p < 0.05, n=8) compared to vehicle injection (n=5) (Fig. 8B). The rTNF-α-produced effect on EF50 began at 30 min and lasted for at least 4 h. Microinjection of rIL-1β (120 fmol) produced a similar descending facilitation to a lesser extent (Fig. 8 C). The hyperalgesic/allodynic effects of these cytokines were completely blocked by pretreatment with MK-801 (10 pmol, n=5-8). MK-801 alone did not affect EF50s in normal rats (n=5, Fig. 8 B). Thus, these results further confirm that the regulation of NMDAR activation by locally elevated cytokines TNF-α and IL-1β induces hyperexcitability in RVM neurons and contributes to NMDAR-dependent descending facilitation of hyperalgesia and allodynia.
In the present study, we observed early microglial hyperactivation at 1-3 d after CCI-ION, followed by a prolonged astrocytic hyperactivation in the RVM lasting at least for 28 d, with a peak expression at 14 d. As expected, inhibition of local glial hyperactivation in the RVM using propentofylline significantly attenuated mechanical hyperalgesia/allodynia at both 3 d and 14 d after nerve injury. Interestingly, microinjection of the microglial inhibitor minocycline in the RVM blocked CCI-induced hyperalgesia/allodynia at the early phase (3 d) but not the later phase (14 d). In contrast, fluorocitrate, when used at lower doses in the RVM, only attenuated behavioral hypersensitivity at the later phase. Consistent with our finding, studies with disruption of spinal microglial function by intrathecal injection or local application of minocycline suggest that spinal microglial hyperactivation is required for the initiation, but not the maintenance of nerve injury-induced hyperalgesia (Ledeboer et al., 2005) and evoked neuronal activity in the spinal dorsal horn (Owolabi and Saab 2006). Similar to CCI-ION-induced glial reaction in the RVM and behavioral hypersensitivity, microglial hyperactivation preceding astrocytic hyperactivation is also observed in the spinal cord after inflammation (Raghavendra et al., 2004) and nerve injury (Kawasaki et al., 2008). In addition, recent evidence suggests that the prolonged reaction of astrocytes in the spinal cord plays an important role in maintaining neuropathic pain (Tanga et al, 2006, Zhuang et al., 2006; Kawasaki et al., 2008). Our data further support an important role of RVM microglia in the initiation phase and astrocytes in maintaining mechanical hyperalgesia/allodynia after nerve injury. Although supraspinal glial hyperactivation and cytokine expression had been found after injury (Raghavendra et al., 2004; Apkarian et al., 2006), no studies have investigated the possibility that they are involved in mechanisms underlying descending modulation of persistent pain. Thus, we provide the first evidence that a signaling sequence from glial hyperactivation, cytokine release and glutamate receptor phosphorylation in the descending pain modulatory circuitry contributes to the cellular and molecular mechanisms of neuropathic pain.
Upon glial activation, cytokines including TNF-α and IL-1β are secreted from glial cells and modulate neuronal activity as chemical mediators between glia and neurons. Specifically, TNF-α and IL-1β signaling have been shown to facilitate central glutamate transmission and potentiate synaptic strength (Beattie et al., 2002; Viviani et al. 2003; Yang et al. 2005, Pickering et al. 2005). The current literature implicates an important role of TNF-α and IL-1β in the peripheral nerve (Zelenka et al., 2005), the spinal cord (Ferreira et al.,1988; Lindenlaub et al., 2000; Sweitzer et al., 2001a; Ohtori et al., 2004), or the trigeminal nucleus (Guo et al., 2007) in the genesis or maintenance of persistent pain depending on locally enhanced NMDAR functions (Bursztajn et al., 2004; Guo et al., 2007; Zhang et al 2007). Our study further shows that the sustained elevation of TNF-α and IL-1β in the RVM occurred at 14 d after CCI. More importantly, the use of antagonists for TNF-α receptor and IL-1β receptor neutralize the action of these endogenous cytokines in the RVM and greatly attenuate mechanical hyperalgesia and allodynia at 14 d after CCI. Therefore, these data suggest that secreted TNF-α and IL-1β upon astrocytic hyperactivation in the RVM are involved in supraspinal mechanisms related to the maintenance of neuropathic pain.
NMDAR-containing neurons are widely distributed in the RVM and NMDAR-dependent descending pain facilitation contributes to the development of hyperalgesia after injury (Guo et al., 2006). We have now shown colocalization of cytokine receptors TNFR1 and IL1RI with the NMDAR subunit NR1 in RVM neurons. Neutralizing these cytokines also completely blocked CCI-induced NR1 phosphorylation. Further, recombinant TNF-α and IL-1β induced robust increases in NR1 phosphorylation in the RVM. Thus, TNF-α and IL-1β associated with glial hyperactivation may affect NMDAR function, similar to other gliotransmitters including chemokines, ATP and nitric oxide (Pickering et al., 2005; Perea and Araque, 2006, 2007). Coupling of cytokine receptors to the NMDAR may involve several steps. Indeed, recent evidence indicates that intracellular signaling pathways related to Src family tyrosine kinase, PKC, extracellular signal-regulated kinase (ERKs), PSD-95, phospholipase C and phospholipase A2 contribute to IL-1β-induced NMDAR phosphorylation (Viviani et al., 2003, 2006; Guo et al., 2007). Activation of intracellular signaling pathways involving neuronal pERK and glial p38 MAP kinases in dorsal root ganglion, spinal dorsal horn and the RVM contribute importantly to synaptic plasticity in central sensitization and the development of persistent pain (Katsura et al., 2006; Wei et al., 2006; Imbe et al., 2007, 2008; Zhuang et al., 2005; Kawasaki et al., 2008). We hypothesize that the secreted TNF-α and IL-1β enhance phosphorylation of NMDARs by binding to their respective receptors expressed on NMDAR-containing neurons and trigger the intracellular signaling cascades. In addition, both TNF-α and IL-1β also potentiate presynaptic glutamate signaling (Beattie et al., 2002; Viviani et al., 2003; Pickering et al., 2005). Collectively, cytokine TNF-α and IL-1β signaling mediates communication from glial hyperactivation to neuronal hyperexcitability in the RVM by coincidently promoting NMDARs and amplifying glutamate signaling. Such supraspinal glial-cytokine-neuronal interactions may be critical for the development of descending pain facilitation of neuropathic pain. The role of the MAP kinase signaling cascades in RVM glial cells and neurons in the pathogenesis of neuropathic pain also requires further study.
The present study demonstrated that nerve injury induced upregulation of TNFR1 and IL1RI and enhanced phosphorylation of NR1 in RVM, and that microinjection of TNF-α and IL-1βin the RVM of normal rats evoked NMDAR-dependent descending pain facilitation, suggesting that descending facilitation may originate from hyperactivity of RVM neurons that express these cytokine receptors and NMDARs. However, the physiological properties of these RVM neurons are unknown. In the RVM, three populations of neurons have been identified based on the correlation of their action potential firing rates with nocifensive responses (Fields et al., 1991). On-cells are thought to promote nociception, whereas off-cells to inhibit nociception. While the role of neutral cells remains unknown, studies suggest that they might be involved in pain modulation after inflammation (Montagne-Clavel and Oliveras, 1994; Miki et al. 02). We now know that there are parallel descending facilitatory and inhibitory systems modulating spinal nociceptive transmission (Millan 2002; Gebhart 2004; Dubner 2006). After tissue and nerve injury, not only the enhanced descending facilitation parallels enhanced descending inhibition from the RVM, but also the net facilitatory may become dominant, resulting in behavioral hyperalgesia and allodynia (Porreca et al., 2002). Although lesions of cells expressing mu-opioid receptors with dermorphin-saporin conjugate in the RVM do reverse later maintenance of hyperalgesia (Porreca et al., 2001; Burgess et al., 2002), mu-opioid receptors are found not only on on-cells (Heinricher et al., 1992), but also are located on serotonergic cells (Kalyuzhny et al, 1996) that are considered as neutral cells in the RVM. Evidence also indicates that the majority of spinally projecting serotonergic neurons in the RVM respond to mu-receptor agonists (Marinelli et al., 2002; Zhang et al., 2006). At present, it is still difficult to attribute the net effect of descending modulation to a single class of RVM neuronal activity.
It is important to address the finding that fluorocitrate may lead to neuronal damage after application with large doses into cell cultures (Hassel et al.; 1995), brain slices (Stone et al., 1990) or in vivo brain tissue (Paulsen et al., 1987; Hornfeldt and Larson, 1990; Largo et al., 1996) and even induces animal seizures (Willoughby et al., 2003). One reason may be that astrocytic inhibition may lead to accumulation of extracellular glutamate in the CNS (Conti and Weinberg, 1999). We examined possible neuronal damage induced by microinjection of fluorocitrate, and observed that fluorocitrate caused neuronal apoptosis and glial necrosis in the RVM in a dose-dependent manner, which occurred only when high doses (10 pmol) were used. Consistent with the present study, Fonnum and colleagues (1997) have reported that low doses of fluorocitrate result in selective and reversible glial disruption in the striatum, without any ultrastructural evidence of neuronal damage at synaptic sites. In our experiment, the lower doses of fluorocitrate (100 fmol) did not cause cell damage and also had no effect on function of astrocytes in the RVM of normal animals; however, the lower doses completely abolished upregulation of GFAP, S100β, TNF-α and IL-1β levels in the RVM and mechanical hypersensitivity at 14 d after CCI. These findings verifie that fluorocitrate inhibits CCI-induced astrocytic hyperactivity at low doses after focal application in vivo. Interestingly, long lasting hyperactivation of astrocytes paralleled an initial upregulation of glutamate transporter-1 (GLT-1) that is expressed predominantly in astrocytes in the spinal cord at 1-3 d, and down-regulation of spinal GLT-1 at 7-14 d after nerve injury (Sung et al., 2003; Tawfik et al, 2008; Wang et al., 2008). Propentofylline prevented the decrease in astrocytic GLT-1 expression in the spinal cord at 14 d after nerve injury (Tawfik et al., 2008). Future studies are necessary to examine temporal changes in GLT-1 expression in the RVM after nerve injury and whether the glial inhibitors change astrocytic GLT-1 expression after CCI-ION.
This work was supported by NIH grants DE18573, 11964 and 15374.