期刊文献+

褪黑素对脑缺血再灌注后脑内抗氧化酶及MDA的影响 被引量:7

Effects of melatonin on some antioxidant enzymes and MDA in brain of global ischemic gerbils
暂未订购
导出
摘要 目的 研究褪黑素 (melatonin ,MT)对脑缺血再灌注沙土鼠脑组织谷胱甘肽过氧化物酶 (GPx)、超氧化物歧化酶(SOD)活性及丙二醛 (MDA)含量的影响 ,探讨MT的脑保护作用机制。方法 采用沙土鼠双侧颈总动脉结扎法制作前脑缺血再灌注损伤的模型 ,缺血前 30min腹腔注射MT ,测定脑缺血再灌注 1h沙土鼠大脑皮层和纹状体GPx、SOD活性及MDA含量。结果 脑缺血再灌注后大脑皮层和纹状体GPx、SOD活性降低 ,MDA含量升高 ;MT预处理能部分反转这种变化。结论 MT对脑缺血再灌注损伤有保护作用 ,其机制可能与保护GPx、SOD活性 。 AIM To investigate the effects of melatonin (MT) on glutathione peroxidase(GPx), superoxide dismutase(SOD) activities and malondialdehyde(MDA) contents in the cerebrum of cerebral ischemia-reperfusion gerbils, so as to explore the protective mechanisms of MT. METHODS Cerebral ischemia-reperfusion model was made by 10 min occlusion of bilateral carotid arteries of gerbil. MT was administered intraperitoneally 30 min prior to the onset of ischemia. After 1 h reperfusion, bilateral cortex and striatum were taken out for measurement of GPx, SOD and MDA. RESULTS Ischemia-reperfusion lowered the activities of GPx and SOD in cerebral cortex and striatum. Conversely, it elevated the contents of MDA in both areas. Treatment with MT at 5, 10, or 20 mg·kg -1 partly reversed these effects. CONCLUSION MT provides protective effect against cerebral ischemia-reperfusion injury by protecting GPx and SOD activities and reducing the lipid peroxidation.
出处 《中国药理学通报》 CAS CSCD 北大核心 2003年第11期1284-1286,共3页 Chinese Pharmacological Bulletin
关键词 褪黑素 脑缺血再灌注损伤 谷胱甘肽过氧化物酶 超氧化物歧化酶 丙二醛 melatonin cerebral ischemia-reperfusion glutathione peroxidase superoxide dismutase malondialdehyde
  • 相关文献

参考文献11

  • 1王洁,张均田.脑缺血、氧自由基清除剂与脑保护[J].中国药理学通报,1998,14(1):8-10. 被引量:36
  • 2张晶,郭继东,邢淑华,谷淑玲,戴体俊.褪黑素对沙土鼠脑缺血再灌注损伤的保护作用[J].药学学报,2002,37(5):329-333. 被引量:9
  • 3Reiter RJ, Tan DX, Qi W et al. Pharmacology and physiology of melatonin in the reduction of oxidative stress in vivo. Biol Signals Recept, 2000;9 (3 - 4):160 - 71.
  • 4Reiter RJ. Oxidative damage in the central nervous system: Protection by melatonin. Prog Neurobiol, 1998;56(3) :359-84.
  • 5Pei Z, Pang SF, Cheung RT. Pretreatment with melatonin reduces volume of cerebral infarction in a rat middle cerebral artery occlusion stroke model. J Pineal Res, 2002;32(3):168-72.
  • 6Shuaib A, Mahmood RH, Wishart T et al. Neuroprotective effects of lamotrigine in global iscbemia in gerbils. A histological, in vlvo microdialysis and behavioral study. Brain Res,1995 ;702(1 -2) : 199-206.
  • 7Kondoh T, Uneyama H, Nishino H, Torii K. Melatonin reduces cerebral edema formation caused by transient forebrain iscbemia in rats. Life Sc1,2002;72(4-5) :583-90.
  • 8Kotler M, Rodriguez C, Sainz RM et al. Melatonon increases gene expression for antioxidant enzymes in rat brain cortex. J Pineal Res, 1998 ; 24(2) : 83-9.
  • 9Pablos MI, Reiter RJ, Ortiz GG et al. Rhythms of glutathione peroxidase and glutathione reductase in brain of chick and their inhibition by light. Neurochem Int, 1998;32(1):69-75.
  • 10Seabra ML, Bignotto M, Pinto LR Jr, Tufik S. Randomized, double-blind clinical trial, controlled with placebo, of the toxicology of chronic melatonin treatment. J Pineal Res, 2000;29(4):193-200.

二级参考文献1

共引文献43

同被引文献63

  • 1周文鹏,吴金民,张行,潘宏铭,方勇,曹厚军,王宏,张俊平,张在云.抗氧化剂和NF-κB对大肠癌细胞IL-8表达的作用及机制[J].中国病理生理杂志,2005,21(9):1779-1782. 被引量:1
  • 2张艳淑,阎立成,姚林.茶多酚对DNA损伤保护作用的机制[J].华北煤炭医学院学报,2005,7(3):320-321. 被引量:5
  • 3Nicotera P, Hartzell P, Baldi C. Cystamine induces toxicity in hepatocytes through the elevation of cystosolic Ca2+ and the stimulation of a nonlysosomal protoclytic system[J]. J Biol Chem, 1986, 261(31): 14628-35.
  • 4Jaeschke H. Molecular mechanisms of hepatic ischemia-reperfusion injury and preconditioning[J]. Am J Physiol Gastrointest Liver Physiol, 2003, 284(1):G15-26.
  • 5Kaneda K, Ekataksin W, Sogawa M et al. Endothelin-1-induced vasoconstriction causes a significant increase in portal pressure of rat liver: localized constrictive effect on the distal segment of preterminal portal venules as revealed by light and electron microscopy and serial reconstruction[J]. Hepatology, 1998,27(3): 735-47.
  • 6Peralta C, Rull R, Rimola A et al. Endogenous nitric oxide and exogenous nitric oxide supplementation in hepatic ischemia-reperfusion injury in the rat[J]. Transplantation, 2001, 71(4): 529-35.
  • 7Rudiger HA, Clavien PA. Tumor necrosis factor-alpha, but not Fas, mediates hepatocellular apoptosis in the murine ischemic liver[J]. Gastroenterology, 2002, 122(1): 202-10.
  • 8Muller JM, Vollmar B, Menger MD. Pentoxifylline reduces venular leukocyte adherence ('Rellow paradox') but not microvascular 'No rellow' in hepatic ischemia/reperfusion[J]. J Surg Res, 1997, 71(1): 1-6.
  • 9Rodriguez-Reynoso S, Leal C, Portilla E et al. Effect of exogenous melatonin on hepatic energetic status during ischemia/reperfusion: possible role of tumor necrosis factor-α and nitric oxide[J]. J Surg Res, 2001, 100(2): 141-9.
  • 10Petra. Pharmacokinetically guided melatonin schedulin in rats with circadian system suppression[J]. Eur J Pharmacol, 1996, 312(2): 171-8.

引证文献7

二级引证文献43

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