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内源性MAO-B抑制因子-靛红预防MPTP对多巴胺神经递质的耗竭作用(英文) 被引量:11

Endogenous MAO-B inhibitor, isatin,prevents the MPTP-induced depletion of dopamine in C57BL/6J mice
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摘要 研究内源性单胺氧化酶B抑制因子 靛红 (2 ,3 吲哚醌 ,isatin)对MPTP引起的小鼠纹状体DA含量降低的影响。用高效液相色谱配电化学检测器测定纹状体DA ,DOPAC和HVA水平。MPTP 30mg/kgip使纹状体DA ,DOPAC和HVA含量与各自对照组比较显著降低 (P <0 .0 1) ,预先靛红 (2 0 0mg/kg·d ,× 4d ,ig)几乎完全抑制了上述效应 ,并减少了MPTP对DA更新率的升高 ,说明靛红有预防MPTP对中枢DA能神经元的毒性。 The present study was designed to examine the effects of isatin(indole 2,3 dione), an endogenous selective monoamine oxidase type B(MAO B) inhibitor, on the 1 methyl 4 phenyl 1,2,3,6 tetrahydropyridine (MPTP) induced reduction of dopamine (DA) and its metabolites in striatum of C57BL/6J mice. The amount of DA, dihydroxy phenylacetic acid (DOPAC) and homovanillic acid (HVA) in striatum of C57BL/6J mice was measured by high performance liquid chromatography coupled with electrochemical detection. It was found that, administration of MPTP (30 mg/kg, ip) caused significant decrease of striatal DA,DOPAC and HVA ( P <0.01, compared with the control group) , while isatin (200 mg/kg·d,×4d, ig) almost completely inhibited the MPTP induced reduction of these parameters in the striatum, and reduced the increase of DA turnover induced by MPTP. In conclusion, isatin is able to prevent the depletive action of MPTP on central dopaminergic neurons, and therefore exerts a protective effect on the central dopaminergic system.
出处 《中国神经科学杂志》 CSCD 2002年第4期690-693,共4页
基金 国家自然科学基金 (3 0 0 76867) 国家卫生部基金 (96 2 3 2 3 )资助项目
关键词 MAO-B抑制因子 预防 单胺氧化酶B抑制因子 靛红 多巴胺 1-甲基-4-苯基-1 2 3 6-四氢吡啶 高效液相色谱 电化学检测器 monoamine oxidase type B inhibitor isatin dopamine 1 methyl 4 phenyl 1,2,3,6 tetrahydropyridine
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  • 1M. Gerlach,P. Riederer. Animal models of Parkinson’s disease: An empirical comparison with the phenomenology of the disease in man[J] 1996,Journal of Neural Transmission(8-9):987~1041
  • 2Dr. A. Ueki,Jane Willoughby,Vivette Glover,M. Sandler,K. Stibbe,G. M. Stern. Endogenous urinary monoamine oxidase inhibitor excretion in Parkinson’s disease and other neurological disorders[J] 1989,Journal of Neural Transmission - Parkinson’s Disease and Dementia Section(4):263~268

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