期刊文献+

神经生长因子在糖尿病神经病理性疼痛大鼠脊髓和背根神经节中的表达 被引量:16

Expression of NGF in dorsal horn and dorsal root ganglion of diabetic rats
下载PDF
导出
摘要 目的观察糖尿病早期大鼠脊髓背角及背根神经节神经生长因子(NGF)的表达及其与疼痛行为的相关性。方法50只SD大鼠随机分为制模组(DM组,n=40)和正常对照组(C组,n=10)。DM组又均分为制模1周组(DM1组)、制模2周组(DM2组)、制模4周组(DM4组)和制模8周组(DM8组)四个亚组。按55mg/kg一次性腹腔注射链脲佐菌素(STZ)建立糖尿病大鼠模型。在制模前及制模后1、2、4、8周利用vonFreyhairs测定大鼠机械痛阈,并通过蛋白质免疫印迹法测定每个时间点大鼠脊髓背角和背根神经节NGF的表达水平。结果糖尿病大鼠机械痛阈在制模1周后即明显下降,并持续至8周;分别在制模2周和1周后脊髓背角和背根神经节内NGF表达水平出现显著下调,并分别持续至4周和8周。大鼠NGF表达水平与机械痛阈存在正相关性。结论糖尿病早期大鼠外周及中枢神经系统NGF表达即出现下调,并与疼痛相关。 Objective To observe the dynamic expression of nerve growth factor (NGF) in spinal dorsal horn and dorsal root ganglion (DRG) of diabetic rats and its correlation with mechanical threshold. Methods Fifty male SD rats were randomly divided into diabetic model group (DM, 40 rats) and control group(C,10 rats). DM group was divided into 4 subgroups of DM1 ,DM2 ,DM4 and DM8 with 10 rats each. The diabetic model was established by a single intraperitoneal injection of streptozocin (STZ 55 mg/kg). Mechanical threshold was assessed using von Frey hairs before and on the 1^st week(DM1),2^nd week(DM2),4^th week(DM4) and 8th week(DM8) after the formation of diabetes model. The NGF expression in spinal dorsal horn and DRG was measured by Western blot at the same time points. Results The mechanical threshold was decreased 1 week after the formation of diabetes model,which lasted for 8 weeks. The NGF expression was reduced in 2 weeks, which lasted for 8 weeks in spinal dorsal horn,and for 4 weeks in the DRG. The NGF protein level was positively correlated with mechanical threshold. Conclusion The NGF expression in peripheral and central nervous system was decreased in the early period of diabetes model and it is correlated with pain.
出处 《临床麻醉学杂志》 CAS CSCD 北大核心 2009年第2期147-150,共4页 Journal of Clinical Anesthesiology
基金 北京大学人民医院发展与研究基金(编号:P610)
关键词 神经生长因子 糖尿病 机械痛阈 Nerve growth factor Diabetes Mechanical threshold
  • 相关文献

参考文献11

  • 1Dixon WJ. Efficient analysis of experimental observations. Annu Rev Pharmacol Toxicol, 1980,20 : 441-462. 被引量:1
  • 2Courteix 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
  • 3Malcangio M, Tomlinson DR. A pharmacologic analysis of mechanical hyperalgesia in streptozotocin/diabetie rats. Pain, 1998,76:151-157. 被引量:1
  • 4Ueno Y, Koike H, Nakamura Y, et al. Effects of beraprost sodium, a prostacyclin analogue, on diabetic neuropathy in streptozotocin induced diabetic rats. Jpn J Pharmacol, 1996, 70:177-182. 被引量:1
  • 5Ossipov MH, Bian D, Malan TP Jr, et al. Lack of involvement of capsaicin sensitive primary afferents in nerve ligation injury induced tactile allodynia in rats. Pain, 1999,79:127- 133. 被引量:1
  • 6Steinbaeher BC Jr, Nadelhaft I. Increased levels of nerve growth factor in the urinary bladder and hypertrophy of dorsal root ganglion neurons in the diabetic rat. Brain Res, 1998,782:255-260. 被引量:1
  • 7Rask CA. Biological actions of nerve growth factor in the peripheral nervous system. Eur Neurol, 1999,41 (Suppl 1 ) : 14-19. 被引量:1
  • 8Anand P, Terenghi G, Warner G, et al. The role of endogenous nerve growth factor in human diabetic neuropathy. Nat Med, 1996,2:703-707. 被引量:1
  • 9Yiangou Y, Facer P, Sinicropi DV, et al. Molecular forms of NGF in human and rat neuropathic tissues: decreased NGF precursor-like immunoreactivity in human diabetic skin. J Peripher Nerv Syst, 2002,7:190 197. 被引量:1
  • 10Kanbayashi H, Itoh H, Kashiwaya T, et al. Spatial distribution of nociceptive neuropeptide and nerve growth factor depletion in experimental diabetic peripheral nervous system.J Int Med Res, 2002,30:512-519. 被引量:1

同被引文献203

引证文献16

二级引证文献121

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部