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脊髓P2X4受体在糖尿病大鼠神经病理性痛中的作用 被引量:1

Role of P2X4 receptor in spinal cord in diabetic neuropathic pain in rats
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摘要 目的探讨脊髓P2X4受体在链脲菌素诱导的糖尿病大鼠神经病理性痛中的作用。方法雄性Wistar大鼠84只,3月龄,体重180~220 g,随机分为2组(n=42):对照组(C组)和糖尿病神经病理性痛组(D组)。C组单次腹腔注射等体积(3.25 ml/kg)枸橼酸缓冲液,D组单次腹腔注射链脲菌素65 mg/kg制备糖尿病模型。2组分别于给药前1 d(基础值)、给药后3、7、14、21、28 d各随机选取7只大鼠,测定机械缩足阈值和热痛阈潜伏期,痛阈测定后断头处死大鼠,取L(4,5)脊髓组织,用RT-PCR方法测定P2X4受体mRNA表达水平。结果与C组相比,D组脊髓P2X4受体mRNA表达上调,机械缩足阈值降低(P〈0.05),热痛阈潜伏期差异无统计学意义(P〉0.05);与基础值比较,D组给药后14 d机械缩足阈值逐渐降低,给药后28 d时达最低值;给药后3 d脊髓P2X4受体mRNA表达逐渐上调,给药后7d达峰值(P〈0.05)。结论脊髓P2X4受体表达上调参与了糖尿病大鼠神经病理性痛的发生。 Objective To investigate the role of P2X4 receptor in the spinal cord in diabetes neuropathic pain induced by streptozocin. Methods Eighty-four male Wistar rats weighing 180-220 g were randomly divided into 2 groups ( n = 42 each) : control group and diabetic neuropathic pain group ( D). Diabetes was induced by intraperitoneal streptozocin 65 mg /kg in group D while the animals in control group received equal volume of buffered saline instead. Blood glucose concentration was measured 2 days later. Any rats in group D with blood glucose 〈 16.0 mmol/L were rejected from the study. The paw withdrawal threshold to mechanical stimulus (MWT) and the response of the tail to a thermal nociceptive stimulus (TFL) were measured 1 day before (baseline) and 3 d, 7 d, 14 d,21 d and 28 d after IP streptozocin injection ( n = 7 each). The animals were then killed and the lumbar segment ( L4,5 ) of the spinal cord was removed for determination of P2X4 receptor mRNA expression using RT-PCR. Resttlts The MWT was significantly decreased and the P2X4 receptor mRNA expression in the spinal cord was significantly increased after IP streptozocin injection as compared with the baseline values before streptozocin injection in group D. The MWT was significandy lower and P2X4 receptor mRNA expression in the spinal cord was significantly higher in group D than in control group. Conclusion The P2X4 receptor in the spinal cord is involved in the development of diabetic neuropathic pain in rats.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2007年第9期799-802,共4页 Chinese Journal of Anesthesiology
基金 湖北省教育厅B类资助项目(B200524003)
关键词 受体 细胞表面 脊髓 糖尿病神经病变 神经痛 Receptom, cell surface Spinal cord Diabetic neuropathies Neuralgia
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参考文献19

  • 1李剑波,陈家伟.糖尿病外周神经病变的发病机理研究进展[J].国外医学(内分泌学分册),2004,24(2):82-83. 被引量:87
  • 2Ralevic V, Burnstock G. Receptors for purines and pyrimidines. Pharmacol Rev, 1998, 50:413-492. 被引量:1
  • 3Tsuda M, Inoue K, Salter MW. Neuropathic pain and spinal microglia:a big problem from molecules in "small" glia. Trends Neurosci, 2005, 28: 101-107. 被引量:1
  • 4Guo LH, Trautmann K, Schluesener HJ. Expression of P2X4 receptor by lesional activated microglia during formalin-induced inflammatory pain. J Neuroimmunol, 2005, 163:120-127. 被引量:1
  • 5Colburn RW, DeLeo JA, Rickman A J, et al . Dissociation of microglial activation and neuropathic pain behaviors following peripheral nerve injury in the rat. J Neuroimmunol, 1997,79:163-175. 被引量:1
  • 6孙敬方主编..动物实验方法学[M].北京:人民卫生出版社,2001:530.
  • 7Courteix C, Eschalier A, Lavarenne J. Streptozocin induced diabetic rats: behavioural evidence for a model of chronic pain. Pain, 1993, 53: 81-88. 被引量:1
  • 8Wuarin-Bierman L, Zahnd GR, Kaufmann F, et al. Hyperalgesia in spontaneous and experimental animal models of diabetic neuropathy. Diabetologia, 1987,30: 653-658. 被引量:1
  • 9Fox A, Eastwood C, Gentry C, et al. Critical evaluation of the streptozotocin model of painful diabetic neuropathy in the rat. Pain. 1999, 81:307-316. 被引量:1
  • 10张秀军,郑国光,吴克复.P2X受体研究进展[J].生物物理学报,2003,19(2):125-129. 被引量:14

二级参考文献36

  • 1Abbracchio MP, Williams M. Purinergic and yrimidinergic ignalling I: Molecular, nervos and urogemitary system function[M]. New York: Springer-Verlag Berlin Heidelberg, 2001.47-59. 被引量:1
  • 2Harden TK, Boyer JL, Nicholas RA. P2 purinergic receptor:subtype-associated sionaling responses and structure[J]. Ann Rev Pharmacol Toxicol, 1995,35:541-579. 被引量:1
  • 3Khakh BS, Burnstock G, Kennedy C, et al. International union of pharmacology. XXIV. Current status of the nomenclature and properties of P2X receptors and their subunits[J].Pharmacol Rev, 2001,53:107-118. 被引量:1
  • 4Virgilio D, Chiozzi F, Ferrari O, et al. Nucleotide receptors:an emerging family of regulatory molecules in blood cells[J].Blood, 2001,97:587--600. 被引量:1
  • 5Cseri J, Szappanos H, Szigeti GP, et al. A purinergie signal transduction pathway in mammalian skeletal muscle cells inculture[J]. Pflugers Arch, 2002,443:731-738. 被引量:1
  • 6Endo M, Kurachi Y, Mishina M. Pharmacology of ionicchannel function: Activators and inhibitors[M]. New York:Springer-Verlag Berlin Heidelbeag, 2000. 519--540. 被引量:1
  • 7Khakh BS. Molecular physiology of P2X receptors and ATP signalling at synapses[J]. Nature Reviews Neuroscience, 2001,2:165-174. 被引量:1
  • 8Ramirez AN, Kunze DL. P2X purinergic receptor channel expression and function in bovine aortic endothelium[J]. Am J Physiol Heart Circ Physiol, 2002,282:H2106--2116. 被引量:1
  • 9Amadio S, D'Ambmsi N, Cavaliere F, et al. P2 receptor modulation and cytotoxic function in cultured CNS neurons[J]. Neuropharmacology, 2002,42:489-501. 被引量:1
  • 10Nihei OK, Savino W, Alves LA. Procedures to characterize and study P2Z/P2X7 purinoceptor. Flow cytometry as apromising practical reliable tool[J]. Mere Inst Oswaldo Cruz,2000,95:415--428. 被引量:1

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