脊髓p38絲裂原活化蛋白激酶激活參與坐骨神經(jīng)壓迫性損傷所致神經(jīng)病理性痛

1、545Acta Physiologica Sinica, October 25, 2005, 57 (5: 545-551Research PaperReceived 2005-03-17 Accepted 2005-05-20This work was supported by the Natural Science Foundation of Jiangsu Province (No. BK2004028 and the National Natural ScienceFoundation of China (No. 30200267.*Corresponding author. Tel:

2、 +86-516-5748426; Fax: +86-516-5748431; E-mail: lczhangActivation of p38 mitogen-activated protein kinase in spinal cord contributesto chronic constriction injury-induced neuropathic painZHANG Fei-E, CAO Jun-Li, ZHANG Li-Cai *, ZENG Yin-MingJiangsu Institute of Anesthesiology, Jiangsu Province Key L

3、aboratory of Anesthesiology, Xuzhou 221002, ChinaAbstract: The present study aimed to investigate the role of spinal p38 mitogen-activated protein kinase (p38 MAPK activation inchronic constriction injury (CCI of the sciatic nerve induced neuropathic pain. CCI model was produced by loosely ligating

4、the leftsciatic nerve proximal to the sciaticas trifurcation with 4-0 silk thread in male Sprague-Dawley rat. SB203580, a specific inhibitor ofthe p38 MAPK, was intrathecally administered on day 5 post-CCI. Thermal and mechanical nociceptive thresholds were assessed withthe paw withdrawal lantency (

5、PWL to radiant heat and the paw withdrawal threshold (PWT to von Frey filaments respectively. Theprotein levels of the phosphorylated p38 MAPK (p-p38 MAPK and phosphorylated cAMP response element binding protein(pCREB were assessed by Western blot analysis. The results showed that CCI significantly

6、increased the expressions of cytosolic andnuclear p-p38 MAPK in the spinal cord. Intrathecal administration of SB203580 dose-dependently reversed the established mechanicalallodynia and thermal hyperalgesia induced by CCI. Correlated with behavior results, SB203580 dose-dependently inhibited the CCI

7、-induced increase of the expressions of cytosolic and nuclear p-p38 MAPK and nuclear pCREB in the spinal cord. Taken together, thesefindings suggest that the activation of p38 MAPK pathway contributes to the development of neuropathic pain induced by CCI, andthat the function of p-p38 MAPK may partl

8、y be accomplished via the CREB-dependent gene expression.Key words: p38 mitogen-activated protein kinase; cAMP response element binding protein; neuropathic pain; spinal cord脊 髓 p 38絲 裂 原 活 化 蛋 白 激 酶 激 活 參 與 坐 骨 神 經(jīng) 壓 迫 性 損 傷 所 致 神 經(jīng) 病理性痛張飛娥,曹君利,張勵(lì)才 *,曾因明江蘇省麻醉醫(yī)學(xué)研究所,江蘇省麻醉學(xué)重點(diǎn)實(shí)驗(yàn)室,徐州 221002摘 要:本研究旨在觀察脊髓

9、 p38 絲裂原活化蛋白激酶 (p38 mitogen-activated protein kinase, p38 MAPK在坐骨神經(jīng)壓迫性損傷 所致神經(jīng)病理性痛中的作用。雄性 Sprague-Dawley 大鼠鞘內(nèi)置管后, 4-0絲線松結(jié)扎左側(cè)坐骨神經(jīng)制作慢性壓迫性損傷 (chronicconstriction injury, CCI 模型。 CCI 后第 5天,鞘內(nèi)注射不同劑量的 p38 MAPK特異性抑制劑 SB203580,并在給藥前及給藥 后不同時(shí)間點(diǎn),分別用 von Frey機(jī)械痛敏監(jiān)測(cè)儀和熱輻射刺激儀監(jiān)測(cè)大鼠損傷側(cè)后爪機(jī)械和熱刺激反應(yīng)閾值,用免疫印跡技 術(shù) (Western bl

10、ot觀察給藥前后脊髓磷酸化 p38 MAPK (p-p38 MAPK和磷酸化環(huán)磷酸腺苷反應(yīng)元件結(jié)合蛋白 (phosphorylated cAMPresponse element binding protein, pCREB表達(dá)變化。結(jié)果發(fā)現(xiàn):坐骨神經(jīng)壓迫性損傷引起脊髓 p-p38 MAPK蛋白表達(dá)明顯增 加;鞘內(nèi)注射 SB203580能劑量依賴性逆轉(zhuǎn) CCI 引起的機(jī)械性痛覺異常和熱痛覺過敏及脊髓水平 p-p38 MAPK表達(dá)的增加,也 明顯抑制 CCI 引起的脊髓 pCREB 表達(dá)的增加。結(jié)果提示,脊髓水平 p38 MAPK激活參與坐骨神經(jīng)壓迫性損傷所致神經(jīng)病理 性痛的發(fā)展,其作用可能通過

11、pCREB 介導(dǎo)。關(guān)鍵詞:p 38絲裂原活化蛋白激酶; cAMP 反應(yīng)元件結(jié)合蛋白;神經(jīng)病理性痛;脊髓 中圖分類號(hào):R363Acta Physiologica Sinica, October 25, 2005, 57 (5: 545-551 546V arying etiologies-induced peripheral nerve injury may pro-duce chronic neuropathic pain states characterized by hyperalgesia, allodynia and spontaneous pain 1. To date, there

12、 is no effective treatment for releasing neuropathic pain and its mechanisms are unclear. Recently, synaptic plasticity of the spinal cord neurons induced by long-last-ing nociceptive stimuli (also called central sensitization is under intensive investigation 2-4. It is believed that the cen-tral se

13、nsitization is mediated by a complex biochemical cascade initiated by the activation of primary afferent fibers. A large number of studies have shown that several protein kinases, for example, protein kinase A (PKA, protein ki-nase C (PKC, and calcium/calmodulin-dependent protein kinase (CaMK , play

14、 a role in the induction, devel-opment and maintenance of central sensitization 5-7. Recently, some studies have reported that p38 mitogen-activated protein kinase(p38 MAPK, a member of MAPK family, contributes to pain hypersensitivity and central sensitization. Acute noxious stimuli, such as formal

15、in, capsaicin, and spinal nerve ligation (SNL, induced p38 MAPK phosphorylation in the spinal dorsal horn neurons and p38 MAPK inhibitor reduced the acute pain behavior after subcutaneous formalin, capsaicin injection, or SNL 8-10. However, the roles of p38 MAPK in the devel-opment of chronic neurop

16、athic pain are unknown. The transcription factor cAMP response element bind-ing protein (CREB, one of the important downstream sub-strates of p38 MAPK, is critical for activity-dependent gene expression. CREB has been proposed to contribute to cen-tral sensitization associated with persistent pain s

17、tates 11-13. In a generally accepted view, NMDA activation-induced Ca 2+ influx triggers an early phase of CREB phosphoryla-tion and a persistent phase of CREB phosphorylation me-diated by a delayed MAPK signal cascade 14. The latter is more important during the development and maintenance of chroni

18、c pain. Therefore, we hypothesize that peripheral nerve injury can activate the p38 MAPK in the spinal cord, and then the p38 MAPK translates to nuclear and phos-phorylates CREB. The latter mediates the roles of p38 MAPK in the development of chronic neuropathic pain. In the present study, we used t

19、he chronic constriction injury (CCI of the sciatic nerve model to investigate (1 whether activation of p38 MAPK in the spinal cord is involved in the maintenance of chronic neuropathic pain; (2 the ef-fect of activation of p38 MAPK on phospho-CREB (pCREB expression.1 MATERIALS AND METHODS 1.1 Animal

20、sSprague-Dawley rats (200250 g provided by the Ex-perimental Animal Center of Xuzhou Medical College, were kept under a 12 h/12 h light-dark cycle regime, with free access to food and water. All experiments were approved by the Animal Care and Use Committee at the Xuzhou Medical College and were in

21、accordance with the colleges guidelines for the care and use of laboratory animals. 1.2 Implantation of intrathecal catheterFor intrathecal drug administration, rats were implanted with catheters as described by Yaksh and Rudy 15. In brief, under anesthesia with pentobarbital sodium (40 mg/kg, i.p.,

22、 rats were fixed, the occipital muscles were bluntly separated, and then the cisternal membrane was exposed. Polyethylene catheters (PE-10 were inserted via an inci-sion in the cisterna magna, and advanced 7.07.5 cm cau-dally to the level of the lumbar enlargement. Correct in-trathecal placement was

23、 confirmed by injection of 10 l 2% lidocaine through the catheter. The catheter was judged to be intrathecal if paralysis and dragging of bilateral hind limbs occurred within 30 s of this injection. Animals with signs of motor dysfunction were excluded from the experiment. The rats were housed indiv

24、idually after sur-gery and allowed to recover 57 d before the CCI test. 1.3 Chronic constriction injuryChronic constriction injury of the sciatic nerve was per-formed as previously described by Bennett and Xie 16. Briefly, under anesthesia with isoflurane, the left sciatic nerves of rats were expose

25、d at the level of the middle of the thigh, and then four ligatures (4-0, silk thread were tied loosely around proximal to the sciaticas trifurcation at 1.0-mm intervals. Sham surgery was done by exposing the left sciatic nerve without ligation.1.4 Drug administrationIntrathecal drug administration w

26、as accomplished using a microinjection syringe connected to the intrathecal cath-eter in awake, briefly restrained rats. The injection was performed manually over a 30 s period in a single injection volume of 10 l followed by a flush with 10 l physiologi-cal saline.Different doses (0.1, 0.5, 2.5, 5

27、g of 4-(4-fluorophenyl-2- (4-methylsulfonylphenyl-5-(4-pyridyl-1H-imidazole (SB203580 (Biomol Research Laboratories Inc., USA dissolved in 2% dimethylsulfoxide (DMSO, a p38 MAPK inhibitor, were intrathecally injected on day 5 post-CCI. DMSO was injected as control. Behavioral tests were per-formed 1

28、 h pre-drug and 0.5, 3, 6, 12, and 24 h post-drug.547ZHANG Fei-E et al: Activation of p38 MAPK in Spinal Cord Contributes to CCI-induced-neuropathic Pain1.5 Behavioral studiesMechanical allodynia was assessed by using von Frey fila-ments (Stoelting, Wood Dale, IL. Animals were placed inindividual pl

29、astic boxes (20 cm 25 cm 15 cm on a metalmesh floor and allowed to acclimate for 30 min. The fila-ments were presented, in ascending order of strength, per-pendicular to the plantar surface with sufficient force tocause slight bending against the paw and held for 68 s.Brisk withdrawal or paw flinchi

30、ng were considered aspositive responses. The paw withdrawal threshold (PWTwas determined by sequentially increasing and decreasingthe stimulus strength (the “up-and-down” method, andthe data were analyzed using the nonparametric method ofDixon, as described by Chaplan et al 17.Thermal hyperalgesia w

31、as assessed with the paw with-drawal latency (PWL to radiant heat according to the pro-tocol of Hargreaves et al 18. Rats were placed in clearplastic cages on an elevated glass plate and allowed to ac-climate for 30 min before test. A high intensity light beamwas focused onto the plantar surface of

32、the hindpaw throughthe glass plate. The nociceptive endpoints in the radiantheat test were the characteristic lifting or licking of thehindpaw, and the time to the endpoint was considered thePWL. To avoid tissue damage, a cut-off time of 30 s wasused. There were 3 trials per rat and 5 min intervals

33、be-tween trials.To study the effect of SB203580 on the rats motorfunction, motor functions were evaluated by the observa-tion of placing/stepping reflexes and righting reflexes andthe rat was conducted 5 min before the assessment ofnociceptive responses. Eight animals per group were usedfor behavior

34、 tests.1.6 Western blotRats were deeply anesthetized with pentobarbital (100 mg/kg, i.p. The lumbosacral spinal cords of the rats wereextracted and stored in liquid nitrogen. Tissue samples werehomogenized in lysis buffer A (in mmol/L, pH 7.9: HEPES10, Na3VO 4 1, MgCl2 1.5, KCl 10, NaF 50, edetic ac

35、id(EDTA 0.1, egtazic acid (EGTA 0.1, phenylmethylsulfonylfluoride (PMSF 0.5, dithiothreitol (DTT 1 and 0.02%protease inhibitor cocktail. After the addition of 90 l NP-40 (10%, the homogenates were vortexed for 30 s andthen centrifuged at 800 g for 15 min at 4 C. The superna-tants were used for Weste

36、rn blot analysis as cytosolicproteins. The nuclear pellets were resuspended in buffer B(in mmol/L, pH 7.9: HEPES 20, NaCl 420, MgCl2 1.5,EDTA 1, EGTA 1, PMSF 0.5, DTT 1, 20 % glycerol, and0.02% protease inhibitor cocktail. The homogenates wereincubated for 30 min in ice-cold water with constant agit

37、a-tion and then centrifuged at 13 000 g for 15 min at 4 C toseparate the nuclear proteins. Protein concentrations weredetermined using the Bradford method 19 and the proteinsamples were stored at 80 C.Protein samples were dissolved in 4 sample buffer (inmmol/L: Tris-HCl 250, Sucrose 200, DTT 300, 0.

38、01%Coomassie brilliant blue-G, and 8% sodium dodecyl sulfate,pH 6.8, and denatured at 95 C for 5 min, then the equiva-lent amounts of proteins (40 g were separated by using10% SDS-polyacrylamide gel electrophoresis (PAGE andtransferred onto a nitrocellulose membrane. The membraneswere incubated over

39、night at 4 C with the following pri-mary antibodies: mouse monoclonal anti-p-p38 MAPKantibody (1:400, Santa Cruz, Biotechnology, USA or rab-bit polyclonal anti-Ser133-pCREB (1:400, Santa Cruz,Biotechnology, USA. The membranes were extensivelywashed with Tris-Buffered Saline Tween-20 (TBST andincubat

40、ed for 1 h with the secondary antibody conjugatedwith alkaline phosphatase (AP at room temperature. Theimmune complexes were detected by using a NBT/BCIPassay kit (Promega, Shanghai, China. The scanned im-ages were imported into Adobe Photoshop software (Adobe,California, USA. Scanning densitometry

41、was used forsemiquantitative analysis of the data.1.7 Experimental groupsTo study the effect of intrathecal injection of SB203580 onCCI-induced thermal hyperalgesia and mechanicalallodynia, rats were divided into six groups as following:rats without any treatment + intrathecal injection ofSB203580 5

42、 g (naive + SB5 group, CCI + intrathecalinjection of DMSO (CCI + DMSO group, CCI + intrath-ecal injection of SB203580 0.1, 0.5, 2.5 or 5 g (CCI +SB0.1 group, CCI + SB0.5 group, CCI + SB2.5 group,CCI + SB5 group. To study the time course of p-p38MAPK expression in the spinal cord of CCI rats, rats we

43、redivided into five groups: naive group, sham group, CCI 5 dgroup, CCI 10 d group and CCI 15 d group. To explorethe effect of intrathecal injection of SB203580 on CCI-induced p-p38 MAPK and p-CREB expression, the fol-lowing six groups were included: sham group, CCI group,CCI + DMSO group, CCI + SB0.

44、1 group, CCI + SB0.5group and CCI + SB5 group. The rat spinal cord was ex-tracted 6 h post-drug.1.8 Statistical analysisAll data are expressed as meanSD. Statistical analysis wascarried out using one-way ANOVA or Students t -test. P 0.05 was considered statistically significant.Acta Physiologica Sin

45、ica, October 25, 2005, 57 (5: 545-5515482 RESULTS2.1 CCI increased the expression of p-p38 MAPKin the spinal cord of ratsCCI, and not sham surgery, produced significant mechani-cal allodynia and thermal hyperalgesia. The time coursesof PWT and PWL were presented in Fig.1A and B . Com-pared with naiv

46、e or sham group, the protein levels of bothcytosolic and nuclear p-p38 MAPK were increased in thespinal cord of CCI rats. The expression of p-p38 MAPK,especially in the nuclear fraction, reached a peak level onday 10 post-CCI. The time course of changes of p-p38MAPK, at least in part, correlated sig

47、nificantly with CCI-induced mechanical allodynia and thermal hyperalgesia (Fig.1C .2.2 Intrathecal injection of SB203580 reversed CCI-ABCFig.1. Time courses of CCI-induced mechanical allodynia (A andthermal hyperalgesia (B and the p38 MAPK (38 kDa activation inthe spinal cord (C in rats. All data we

48、re expressed as meanSD. n =8, *P 0.05, * P 0.01 vs d 0 in behavior test; n = 4, *P 0.05, *P 0.01vs naive group in Western blot test.Fig.2. Intrathecal injection of SB203580 reversed CCI-induced me-chanical allodynia (A and thermal hyperalgesia (B and the spinalp38 MAPK activation (C . All data were

49、expressed as meanSD. n = 8, *P 0.05, *P 0.01 vs CCI+DMSO in behavior test; n = 4, *P 0.05, *P 0.01 vs CCI in Western blot test.A BC549 ZHANG Fei-E et al: Activation of p38 MAPK in Spinal Cord Contributes to CCI-induced-neuropathic Paininduced mechanical allodynia and thermal hyperal-gesia and the sp

50、inal p38 MAPK activation Intrathecal administration of SB203580 did not affect the mechanical PWT, the thermal PWL, or motor function in the rats implanted with intrathecal catheters. Intrathecal administration of SB203580, not DMSO, reversed the es-tablished mechanical allodynia and thermal hyperal

51、gesia in a dose-dependent manner. The inhibitory effect on me-chanical allodynia was better than that on thermal hyperalgesia. The time courses of the mechanical PWT and thermal PWL after SB203580 injection were presented in Fig.2A and B . Inhibition of p38 MAPK activation by SB203580 was confirmed

52、by quantification of the expres-sion of cytosolic and nuclear p-p38 MAPK in the spinal cord. SB203580 dose-dependently reversed the CCI-in-duced increase of the expression of cytosolic and nuclear p-p38 MAPK, compared to vehicle-treated rats (Fig.2C . 2.3 Intrathecal injection of SB203580 inhibited

53、the CCI-induced increase of nuclear pCREB expression in the spinal cordThe Western blot results revealed that, compared with sham group, CCI significantly increased the expression of nuclear pCREB in the spinal cord. Intrathecal administration of SB203580 dose-dependently inhibited the increase of n

54、uclear pCREB expression in the spinal cord (Fig.3. related with behavior hyperalgesia. Furthermore, intrathe-cal injection of SB203580, a p38 MAPK inhibitor, remark-ably reversed CCI-induced mechanical allodynia and ther-mal hyperalgesia and activation of p38 MAPK in a dose-dependent manner. Another

55、 finding in the present study was that intrathecal injection of SB203580 also dose-de-pendently inhibited the CCI-induced increase of pCREB expression in the spinal cord. These results suggest that activation of p38 MAPK pathway contributes to the devel-opment of neuropathic pain induced by CCI, and

56、 that the function of p-p38 MAPK might partly be accomplished via the CREB-dependent gene expression.The mechanisms underlying p-p38 MAPK mediated neu-ropathic pain are unknown. Nerve fibers produce abnor-mal ectopic excitability at or near the site of nerve ligation after CCI. The local persistent

57、abnormal excitability of sen-sory nerve can spread to distant parts of the peripheral including the peripheral nerve bodies in the dorsal root gan-glion (DRG and central nervous system. Repeated or pro-longed noxious stimulations and the persistent abnormal input following nerve injury increase the

58、release of nocice-ptive neurotransmitters, such as glutamate, ATP , substance P, calcitonin gene-related peptide (CGRP, and BDNF in the central terminals of primary sensory afferents and then activate NMDA and NK receptors in the spinal cord. Cal-cium influx through NMDA receptor triggers Ras-raf/ M

59、APK cascades responses. Several reports demonstrated that the phosphorylation of p38 MAPK was increased by Ca 2+ influx 20-22.Phospho-p38 MAPK could translocate from cytoplasm into nuclear and in turn phosphorylate transcriptional fac-tor CREB on Ser-133. In agreement with this view, we found that CCI significantly increased the nuclear fraction p-p38 MAPK expression. Moreover, th