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The Journal of Neuroscience, November 15, 2000, 20(22):8614-8619

Key Role for the Epsilon Isoform of Protein Kinase C in Painful Alcoholic Neuropathy in the Rat

Olayinka A. Dina1, Justine Barletta1, Xiaojie Chen1, Annick Mutero1, Annick Martin2, Robert O. Messing2, and Jon D. Levine1

1 Departments of Medicine and Oral and Maxillofacial Surgery, Division of Neuroscience and Biomedical Sciences Program, National Institutes of Health Pain Center (UCSF), University of California at San Francisco, San Francisco, California 94143-0440, and 2 Department of Neurology, University of California at San Francisco and Ernest Gallo Clinic and Research Center, Emeryville, California 94608


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Chronic alcohol consumption produces a painful peripheral neuropathy for which there is no reliably successful therapy, attributable to, in great part, a lack of understanding of the underlying mechanisms. We tested the hypothesis that neuropathic pain associated with chronic alcohol consumption is a result of abnormal peripheral nociceptor function. In rats maintained on a diet to simulate chronic alcohol consumption in humans, mechanical hyperalgesia was present by the fourth week and maximal at 10 weeks. Thermal hyperalgesia and mechanical allodynia were also present. Mechanical threshold of C-fibers in ethanol fed rats was lowered, and the number of action potentials during sustained stimulation increased. The hyperalgesia was acutely attenuated by intradermal injection of nonselective protein kinase C (PKC) or selective PKCepsilon inhibitors injected at the site of nociceptive testing. Western immunoblot analysis indicated a higher level of PKCepsilon in dorsal root ganglia from alcohol-fed rats, supporting a role for enhanced PKCepsilon second-messenger signaling in nociceptors contributing to alcohol-induced hyperalgesia.

Key words: protein kinase C epsilon ; alcoholic peripheral neuropathy; pain; hyperalgesia; allodynia; primary afferent nociceptor


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Ethanol consumption is the most common cause of peripheral nervous system, as well as CNS, neurotoxicity. Ethanol is thought to exert a direct neurotoxic action on the peripheral nervous system, resulting in a neuropathy that mostly involves small-diameter fibers (Diamond and Messing, 1994; Monforte et al., 1995; Kielhorn, 1996; Ortiz-Plata et al., 1998; Tredici et al., 1999). The peripheral neuropathy is a potentially incapacitating complication of chronic consumption of ethanol, characterized by pain and dysesthesias, primarily in the lower extremities, and is poorly relieved by available therapies (Ratcliff, 1979; Monforte et al., 1995; Ortiz-Plata et al., 1998).

Whereas enhanced nociception and primary afferent nociceptor hypersensitivity have been demonstrated in animal models of other neuropathic pain states, such as those induced by diabetes (Ahlgren and Levine, 1994), chemotherapy (Tanner et al., 1998; Authier et al., 1999), or trauma (Bennett and Xie, 1988; Campbell et al., 1988; Seltzer et al., 1990; Xie and Xiao, 1990; Kim and Chung, 1992; Kim et al., 1993; Sheen and Chung, 1993; Yoon et al., 1996; Pedersen and Kehlet, 1998; Zahn and Brennan, 1999), an animal model for alcohol-induced neuropathy does not exist, nor has it even been demonstrated that primary afferent nociceptor function is altered by chronic exposure to alcohol.

In animal models of other painful peripheral neuropathies, enhanced nociception involves alterations in intracellular signaling. Specifically, protein kinase C (PKC) (Ahlgren and Levine, 1994) [particularly the epsilon (epsilon ) isoform (Gerstin et al., 1998; Khasar et al., 1999] and protein kinase A (PKA) (Ahlgren and Levine, 1994) signaling pathways have been implicated in enhancing nociceptor function. Because alcohol has been shown to activate PKC and PKA (Coe et al., 1996; Pandey, 1996; Gerstin et al., 1998; Constantinescu et al., 1999; Sisson et al., 1999; Yoshimura and Tabakoff, 1999), we hypothesized that, in a well established model for chronic ethanol consumption in the rat, both enhanced nociception and nociceptor function occur and that PKC and PKA pathways contribute to the enhanced nociception.


    MATERIALS AND METHODS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Chronic alcohol consumption. Male Sprague Dawley rats (200-450 gm; Bantin and Kingman, Fremont, CA), individually caged and maintained under a 12 hr light/dark cycle, were used in these experiments. The experimental rats were fed Lieber-DeCarli liquid diet (Dyets Inc., Bethlehem, PA) (Lieber and DeCarli, 1982, 1989; Lieber et al., 1989) with ethanol (ED) (6.5% ethanol) for 12 weeks. The control diet (CD) rats were pair-fed (i.e., calorically matched to the ethanol-exposed rats) by giving a diet in which equal calories of maltose-dextrin or alcohol (Gold Shield Chem Co., Hayward, CA) was consumed (Lieber et al., 1989). Using a subset of a group of rats that had been maintained for 12 weeks on ethanol diet, an alcohol withdrawal study was performed by switching the rats to CD for a period of 5 weeks.

The Institutional Animal Care Committee of the University of California, San Francisco, approved the experimental protocol.

Blood ethanol determination. Blood ethanol concentration was measured by drawing 100 µl blood samples from the tail vein of ED rats into heparinized Eppendorf tubes. The blood samples, collected 3 hr after commencement of feeding, were centrifuged to separate plasma. The samples were analyzed for alcohol by gas chromatography (Eriksson, 1973; Tabakoff et al., 1976). The blood samples were taken on the last day of the eighth week of ED to a separate group of rats, at which time behavioral testing had demonstrated a significant hyperalgesia.

Mechanical nociceptive threshold. The nociceptive flexion reflex was quantified using the Randall-Selitto paw pressure device (Stoelting, Chicago, IL), which applies a linearly increasing mechanical force to the dorsum of the rat's hindpaw (Taiwo et al., 1989b). The mechanical nociceptive threshold was defined as the force in grams at which the rat withdrew its paw. Rats were familiarized in the test apparatus at 5 min intervals for a period of 1 hr per day for 3 d in the week preceding the experiment to decrease nociceptive thresholds (Taiwo et al., 1989b). The rat was allowed to crawl into a cotton sock, which is then placed on a Perspex block and covered with an elastic blanket that is attached to the block, on two sides, by Velcro strips. The rat was allowed to acclimatize in the restrainer as described for a period of 15-20 min, after which it was exposed to the test stimulus (Taiwo et al., 1989b). Briefly, the training procedure consisted of repeated paw-withdrawal tests at 5 min intervals for 1 hr per day. The stimulus was applied using a Basile analgesy meter, an instrument that applied a linearly increasing mechanical force onto the dorsum of the rat's paw at the same site at which test agents were to be injected. Baseline paw-withdrawal threshold was defined as the mean of the last six readings before test agents were injected. Behavioral testing was done on both ED and CD rats once per week, and the two groups were tested the same day. After 8 weeks of ethanol diet feeding, the decrease in paw-withdrawal threshold had plateaued, and test agents were injected intradermally into the dorsum of the hindpaws.

Stimulation with von Frey hair. Mechanical allodynia was assessed with von Frey hairs (VFH) using the up-down method, as described previously (Chaplan et al., 1994; Kinnman and Levine, 1995; Aley et al., 1996). Calibrated VFH (1.32, 3.63, 10.0, and 27.5 mN; Ainsworth, London, UK) were applied to the plantar skin of each hindpaw in these studies.

Thermal stimulation. The thermal nociceptive threshold was measured as described by Hargreaves et al. (Hargreaves et al., 1988), in both hindpaws, only once to avoid tissue injury (Aley et al., 1996).

In vivo electrophysiology. Single-fiber electrophysiological techniques were similar to those used in our previous studies of painful peripheral neuropathy (Tanner et al., 1998; Chen and Levine, 1999). Briefly, the rats were anesthetized with sodium pentobarbital (initially 50 mg/kg, i.p., with additional doses given throughout the experiments to maintain areflexia). Single cutaneous C-fibers from the saphenous nerve were recorded. A total of 10 C-fibers (one fiber per rat) were evaluated in this study. The action potential corresponding to the C-fiber whose receptive field had been identified was determined by the latency delay technique, in which a mechanically induced orthodromic spike produced a delay in the electrically induced orthodromic spike (Iggo, 1958; Handwerker, 1991). The conduction velocity of a fiber was determined by dividing the distance between the stimulating and recording electrodes by the action potential latency. Fibers with conduction velocities <2 m/sec were classified as C-fibers (Willis, 1985).

Mechanical threshold of C-fibers was determined with calibrated (VFH) (Ainsworth, London, UK) and defined as the lowest force that elicited two or more spikes within 1 sec, in at least 6 of 10 trials. Sustained threshold stimulation was performed using a calibrated VFH that was placed, by hand, on the receptive field for 60 sec. Sustained (60 sec) suprathreshold stimulation was performed with an apparatus consisting of a 10 gm monofilament VFH connected in series with a mechanical force transducer (Entran, Fairfield, NJ). Three separate applications of the sustained stimulus were performed for each fiber; the average of the values for the three applications was taken as the response of that fiber.

Western blot analysis for PKCepsilon . Eight lumbar dorsal root ganglia (DRGs) (L2-L5 bilaterally) were harvested from both ethanol-treated and control rats. The DRGs were desheathed, frozen in a dry ice ethanol bath, and stored at -80°C. The samples were homogenized in 5 vol of 20 mM Tris-HCl, pH 7.5, 2 mM EDTA, 10 mM EGTA, 1 mM phenylmethylsulphonyl fluoride, and 20 µg/ml each of leupeptin, aprotinin, and pepstatin using a pestle (Pellet Pestle Motor; Kontes, Vineland, NJ). After homogenization, the samples were spun at 13,000 rpm for 15 min (4°C). The supernatants were collected, and a portion of each was used for protein quantification (Micro BCA Protein Assay Reagent kit; Pierce, Rockford, IL). Concentrated sample buffer was added to each sample so that the final solutions contained 56 mM Tris-HCl, 5% glycerol, 1.67% SDS, and 0.02 mg/ml bromophenol blue. The samples were then boiled for 10 min, cooled on ice, and stored at 4°C. Protein samples (8.3 µg/lane) were separated by SDS-PAGE on 8% minigels and thereafter transferred to polyvinylidene difluoride (PVDF) transfer membranes (Immobilon-P; Millipore, Bedford, MA) for 1 hr at 100 V. The membranes were washed briefly with TBS (20 mM Tris-HCl, pH 7.6, and 150 mm NaCl) and then blocked for 1 hr in Blotto [5% nonfat dry milk in TBS containing 0.05% Tween 20 (TBS-T)]. After blocking, the blots were incubated at room temperature for 45 min in Blotto with 1 µg/ml rabbit polyclonal antibody to PKCepsilon (Santa Cruz Biotechnology, Santa Cruz, CA) and 0.05% sodium azide. Blots were washed three times for 10 min with TBS-T, incubated at room temperature for 30 min in Blotto with HRP-conjugated goat anti-rabbit IgG antibody at 1:4000 dilution (Vector Laboratories, Burlingame, CA), and then washed again three times for 12 min in TBS-T and once in TBS alone. PKCepsilon bands were visualized using the ECLplus kit (Amersham Pharmacia Biotech, Little Charlton, Buckinghamshire, UK). Autoradiograms of the blots were then digitized, and the density of the immunoreactive bands was quantified, in arbitrary units, using NIH Image software.

Drugs. Bisindolylmaleimide (BIMM) (nonspecific PKC inhibitor), PKCepsilon -specific translocation inhibitor peptide (PKCepsilon -I) (Johnson et al., 1996; Khasar et al., 1999) (Calbiochem, La Jolla, CA), and Walsh inhibitor peptide (WIPTIDE) (PKA inhibitor; Peninsula Laboratories, Belmont, CA) were used. Stock solutions (1 µg/µl) of BIMM (in 10% dimethylsulfoxide) and PKCepsilon -I and WIPTIDE (in 0.9% saline) were stored at -20°C. All inhibitors were diluted with distilled water before intradermal injections into the paw. The effects of the various antagonists, BIMM, PKCepsilon -I, and WIPTIDE, were assessed to determine second-messenger system(s) contributing to alcohol-induced hyperalgesia. Injections of PKCepsilon -I and WIPTIDE (1 µg/2.5 µl), using a 10 µl microsyringe (Hamilton, Reno, NV), were always preceded by injection of distilled water (2.5 µl) to produce hypo-osmotic shock, thereby enhancing cell membrane permeability to these cell membrane-impermeable agents (Tsapis and Kepes, 1977; West and Huang, 1980; Taiwo and Levine, 1989; Khasar et al., 1995; Widdicombe et al., 1996). The dose of each protein kinase inhibitor was separated from the distilled water by an air bubble (<1 µl). Paw-withdrawal threshold was remeasured 10, 15, and 20 min after injecting the test agent. The mean of the paw-withdrawal thresholds obtained at these three points was then taken as the mechanical nociceptive threshold at the dose of the test agent used. The effect of each dose of a test agent was calculated as the percentage change from baseline.

Statistical analysis. The data are presented as mean ± SEM and were compared using the Student's t test, ANOVA [one-way or repeated measures followed by Fisher's protected least significant difference (PLSD) post hoc analysis] or Mann-Whitney U test, as appropriate. p <=  0.05 was considered statistically significant.


    RESULTS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Effect on weight of chronic exposure to ethanol compared with an isocaloric diet

Just before initiation of the Lieber-DeCarli liquid diets, rats assigned to the CD group weighed 211.0 ± 1.0 gm compared with 223.8 ± 1.7 gm in rats assigned to the ED group (Fig. 1A). Animals in the two groups gained weight comparably throughout the period of study. After 12 weeks of feeding with the Lieber-DeCarli diets, CD and ED rats weighed 409.3 ± 4.7 and 405.0 ± 9.3 gm, respectively (p > 0.05) (Fig. 1A). Blood ethanol concentration was determined as 66.8 ± 7.0 mmol/l (mean ± SEM; range, 46.4-92.6 mmol/l; n = 6 ethanol-treated rats).



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  		Figure 1.   A, Effect of long-term ethanol feeding on body weight using the Lieber-DeCarli liquid diet pair-feeding technique. The average weight of ethanol-fed (filled squares; n = 17) and isocalorically fed control (open triangles; n = 12) rats is plotted against the duration of administration of the liquid diet. Each point represents mean ± SEM weight (in grams) (error bars). B, Decrease in paw-withdrawal threshold to mechanical stimulation of the dorsum of the rat hindpaw induced by chronic administration of ethanol (alcohol-induced mechanical hyperalgesia). The paw-withdrawal threshold (in grams) of ethanol-fed (filled squares; n = 34 paws) and control diet-fed (open triangles; n = 24 paws) rats plotted against the duration (in weeks) of chronic exposure to ethanol administered by the Lieber-DeCarli liquid diet technique and pair-fed isocaloric diet controls. From the fourth week of ethanol diet feeding, *p < 0.0001 (repeated measures ANOVA).

Effect of ethanol on mechanical nociceptive threshold (mechanical hyperalgesia)

Before the administration of the liquid diets, the mean baseline paw-withdrawal threshold of ED rats (104.9 ± 1.1 gm; n = 34) (Fig. 1B) was not significantly different (p > 0.05) from that in CD rats (109.3 ± 2.8 gm; n = 24). A significant decrease in mechanical nociceptive threshold (i.e., hyperalgesia) was produced in the ED rats after 4 weeks (p < 0.0001; F = 234.1) (Fig. 1B). Further reduction (p < 0.05) in the paw-withdrawal threshold of ED rats to 81.6 ± 1.3 gm occurred at 10 weeks, after which hyperalgesia was maintained in the range of 81.6-84.1 gm until the conclusion of the study, at 12 weeks. There was no significant change (p > 0.05) in the mean paw-withdrawal threshold of CD rats over the same time period.

Role of PKC/PKCepsilon and PKA in ethanol-induced mechanical hyperalgesia

After 8 weeks of ethanol administration, the intradermal injection of BIMM or PKCepsilon -I (each administered at 1 µg) resulted in a significant reduction in mechanical hyperalgesia in ED rats (each p < 0.0001; F = 14.8) (Fig. 2A,B). There was no significant difference (p > 0.05) in the effect of these two inhibitors on paw-withdrawal threshold in the hyperalgesic ED rats. WIPTIDE did not significantly (p = 0.07) affect nociceptive threshold in hyperalgesic ED or nonhyperalgesic CD rats, although there was a trend toward an effect.



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  		Figure 2.   A, Effect of WIPTIDE (WIP; 1 µg; n = 12 paws), BIMM (1 µg; n = 12 paws), and PKCepsilon -I (1 µg; n = 12 paws) on the baseline (BL) paw threshold (grams ± SEM) of ethanol-fed (filled bars; n = 12 paws) and isocalorically fed control (hatched bars; n = 12 paws) rats. *p < 0.0001 (ANOVA, followed by Fisher's PLSD post hoc test). NS, Not statistically significant. B, Reduction in lowered paw-withdrawal threshold (hyperalgesia) produced by WIPTIDE (WIP; 1 µg; n = 12 paws), BIMM (1 µg; n = 12 paws), and PKCepsilon -I (1 µg; n = 12 paws) plotted as percentage change in nociceptive threshold in ethanol-fed (filled bars; n = 12 paws) and isocalorically fed control (hatched bars; n = 12 paws) rats. *p < 0.0001 (one-way ANOVA and Fisher's PLSD post hoc test). NS, Not statistically significant.

von Frey hair stimulation (mechanical allodynia)

To determine whether the mechanical hyperalgesia induced by alcohol was associated with mechanical allodynia, we examined responses to von Frey hair stimulation in ED and CD rats. ED rats demonstrated a significantly (p < 0.05) increased response frequency to 27.5 mN VFH stimulation (Fig. 3A) when compared with the response in CD rats.



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  		Figure 3.   A, Effect of chronic alcohol consumption on response to stimulation by calibrated 1.32, 3.63, 10.0, and 27.5 mN (represented on the abscissa by 1, 2, 3, and 4) VFH measured in ethanol-fed (filled squares; n = 24 paws) and control-diet fed (open triangles; n = 12 paws) rats. *p < 0.05 (repeated measures ANOVA). NS, Not statistically significant. B, Effect on sensitivity, as measured by the paw-withdrawal latency, to thermal stimulation from a 50 W radiant heat stimulus, in ethanol-fed (filled bar; n = 12 paws) and control (hatched bar; n = 12 paws) rats. *p < 0.03 (Student's unpaired t test).

Thermal hyperalgesia

Because thermal hyperalgesia also occurs in patients with neuropathic pain, we compared thermal responses in ED and CD rats using the method of Hargreaves et al. (1988). ED rats demonstrated a significantly (p < 0.05) lower (6.8 ± 0.4 sec) paw-withdrawal latency in response to thermal stimulation when compared with CD rats (8.6 ± 0.5 sec) (Fig. 3B). Thus, ethanol treatment evoked thermal hyperalgesia.

Effect of ethanol withdrawal on ethanol-induced hyperalgesia

After 12 weeks of ethanol diet, a subset, comprised of three rats, from the ED rats were placed on the control diet to determine whether ethanol-induced hyperalgesia was reversible. In ED rats placed on a CD for 2 weeks, the paw-withdrawal threshold was not significantly different (p > 0.05) than it had been after 12 weeks on the ethanol diet (Fig. 4). Interestingly, 5 weeks after being placed on the CD, the nociceptive threshold in this group was even more reduced than during the last week of ethanol treatment (p < 0.0002), indicating that hyperalgesia had increased during the 5 week period on CD (Fig. 4).



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  		Figure 4.   Effect of ethanol withdrawal (initiation of the CD in a group of rats fed ED in the preceding 12 weeks) on the paw threshold (in grams) of rats fed for 12 weeks on ED (12ED, filled bar; n = 34 paws) and at 2 (12ED+2CD, hatched bar; n = 6 paws) and 5 (12ED+5CD, cross-hatched bar; n = 6 paws) weeks after initiation of CD. *p < 0.0002. NS, Not significant (p > 0.05). Comparisons were by one-way ANOVA and Fisher's post hoc test.

Effect of ethanol on C-fiber threshold and responsivity

Study of C-fibers from ED and CD rats revealed no spontaneous activity in most fibers. In a few fibers, spontaneous activity, although present, was <0.01 Hz. The conduction velocities for C-fibers in ED and CD rats were 0.9 ± 0.1 and 0.8 ± 0.1 m/sec, respectively (p > 0.05) (Fig. 5A). The location of receptive fields of C-fibers on the dorsum of the hindpaw from CD and ED rats was also similar. However, the mean mechanical threshold for C-fibers from the ED rats was lower than that from CD rats (p < 0.05) (Fig. 5B). Also, the mean number of action potentials evoked by a sustained 60 sec threshold or suprathreshold (10 gm) stimulus was significantly higher for C-fibers from ED rats compared with those from CD rats (p < 0.05) (Fig. 5C,D).



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  		Figure 5.   Conduction velocity and mechanical threshold of C-fibers in CD and ED rats. A, There was no difference in conduction velocity between C-fibers from ED (filled bar; n = 10) and CD (hatched bar; n = 14) rats. Unpaired t test, p > 0.05. B, The mechanical threshold of C-fibers from ED rats (filled bar; n = 10) was significantly lower than that of C-fibers from control rats (hatched bar; n = 14) using nonparametric Mann-Whitney U test; * p < 0.05. C, The number of action potentials evoked by sustained (60 sec) threshold stimulation was significantly greater in C-fibers in ED rats (filled bar; n = 10) compared with controls (hatched bar; n = 14). D, The number of action potentials evoked by sustained suprathreshold (10 gm) stimulation was significantly greater in C-fibers in ethanol-fed rats (filled bar; n = 10) compared with controls (hatched bar; n = 14). Unpaired (one-tailed) t test; *p < 0.05 (Student's unpaired t test).

PKCepsilon  level

To determine whether the PKCepsilon -dependent decrease in nociceptive threshold observed in ED rats is associated with a higher level of expression of PKCepsilon in primary afferents, a Western analysis of DRG protein samples from CD and ED rats was performed. There was a higher level of PKCepsilon in dorsal root ganglia in ED rats (Fig. 6). When the PKCepsilon -immunoreactive bands observed were quantified, the average PKCepsilon level in alcohol-fed (n = 11) rats was found to be 50% higher (p < 0.001) (Fig. 6A,B) than that in the control rats (n = 10).



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  		Figure 6.   PKCepsilon levels in DRG from CD and ED rats. A, Representative blot of PKC immunoreactivity in DRG samples from CD and ED rats (after 10 weeks of ethanol administration). Proteins were separated by SDS-PAGE, transferred to a PVDF membrane, and immunoblotted with PKCepsilon -specific antibody. B, Mean ± SEM for data showed a statistically significant difference between control diet-fed (hatched bar; n = 10) and ethanol-fed (filled bar; n = 11) rats. *p < 0.01 (Student's t test).


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

We have developed the first animal model for alcohol-induced painful peripheral neuropathy and describe alterations in primary afferent nociceptor function and in specific second-messenger signaling that contributes to the enhanced nociception. Rats chronically fed ethanol exhibited mechanical and thermal hyperalgesia and tactile allodynia, all of which are symptoms frequently occurring in patients with painful peripheral neuropathy (Scadding, 1992). This model is highly relevant to painful alcoholic neuropathy in humans because the blood alcohol level that results in neuropathic changes is similar (Bosch et al., 1979; Lieber and DeCarli, 1989; Lieber et al., 1989). Also, the fact that hyperalgesia is stable for weeks renders this model very useful for study of underlying mechanism.

Ethanol-induced hyperalgesia did not resolve and, in fact, continued to increase at 5 weeks after cessation of alcohol intake. This is consistent with reports of persisting or even worsening peripheral neuropathy in patients who have withdrawn from chronic ethanol use (Gadner, 1972; Weise et al., 1985; Yokoyama et al., 1991; Spahn et al., 1995).

We tested whether two intracellular second-messenger pathways contribute to ethanol-induced hyperalgesia. PKC and PKA are both known to be important in nociceptor function (Taiwo et al., 1989a; Ahlgren and Levine, 1994; Khasar et al., 1999) and in mediating other effects of alcohol (Diamond et al., 1987; Hoffman et al., 1987; Hoek et al., 1988, 1992; Messing et al., 1991; Lovinger and Zhou, 1994; Gordon et al., 1997). PKC was found to contribute to the enhanced nociception, whereas cAMP/PKA, if it does contribute, appears to be less important. This second-messenger dependence differs from that for the enhanced nociception produced by hyperalgesic inflammatory mediators, to which both PKA and PKC contribute (Taiwo et al., 1989a; Taiwo and Levine, 1991; Khasar et al., 1999). Because the PKCepsilon antagonist (PKCepsilon -I) alone was able to reverse the hyperalgesia to the same extent as the nonspecific PKC antagonist BIMM, the epsilon isoform of PKC accounts for the role of PKC in ethanol-induced enhanced nociception (Khasar et al., 1999). Because the PKCepsilon antagonist was able to attenuate established ethanol-induced hyperalgesia, ongoing PKCepsilon activity must be required to maintain the hyperalgesia. A role for the epsilon  isoform of PKC is consistent with previous demonstrations that chronic ethanol exposure increases levels of PKCepsilon in cultured cells (Messing et al., 1991; Coe et al., 1996) and that ethanol consumption causes sustained translocation (activation) of PKCepsilon , but not of PKCdelta or PKCalpha , in cardiac tissue (Miyamae et al., 1999). PKC activity also contributes to neuropathic pain induced by cancer chemotherapy (vincristine) (K. O. Aley and J. D. Levine, unpublished observation) and diabetes (Ahlgren and Levine, 1994). The fact that neither PKC antagonist had an effect on mechanical threshold in control animals strongly supports the suggestion that the contribution of PKCepsilon to enhanced nociception develops during chronic ethanol exposure.

It appears, for several reasons, that the PKCepsilon activity that maintains ethanol-induced hyperalgesia occurs in the peripheral nociceptor terminal. First, we observed hyper-responsiveness (i.e., decrease in threshold and enhanced responsivity to mechanical stimuli) in C-fiber nociceptors. Second, intradermal injections of extremely small amounts of inhibitors attenuated the enhanced nociception. Finally, at the site of study, the skin of the hindpaw, PKCepsilon is believed to be expressed only in primary afferent terminals (Khasar et al., 1999).

In summary, we have demonstrated that hyperalgesia is present in an established model in the rat for chronic alcohol consumption in humans and that PKCepsilon signaling plays a critical role in the enhanced nociception produced by chronic alcohol. The findings suggest that PKCepsilon might be an excellent therapeutic target for this common and, at present, primarily untreatable chronic pain syndrome.


    FOOTNOTES

Received June 29, 2000; revised Aug. 24, 2000; accepted Aug. 30, 2000.

This work was funded by National Institutes of Health Grant DE08973 and funds provided by the state of California for medical research on alcohol and substance abuse through UCSF (R.O.M.).

Correspondence should be addressed to Dr. Jon D. Levine, National Institutes of Health Pain Center (UCSF), Box 0440, University of California at San Francisco, San Francisco, CA 94143-0440. E-mail: levine{at}itsa.ucsf.edu.


    REFERENCES
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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