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Thalidomide reduces MPTP-induced decrease in striatal dopamine levels in mice.

机译:沙利度胺降低了MPTP诱导的小鼠纹状体多巴胺水平的降低。

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摘要

The effects of thalidomide, a sedative, anti-inflammatory and immunosuppressive agent were studied in the MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) murine model of Parkinson's disease. The striatal levels of dopamine (DA) and of its main metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were measured both in the MPTP control group (3 x 15 mg/kg intraperitoneally) and in the thalidomide groups (repeated treatments at 25 mg/kg or 50 mg/kg postoperatively). For mice treated with thalidomide, a dose-dependent protection was observed against the MPTP-induced decrease in DA. The decrease in HVA levels was totally antagonized by thalidomide at both doses. That thalidomide has activity in this model suggests that an inflammatory process may be involved in the induction of lesions by MPTP in DAergic neurons.
机译:在帕金森氏病的MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)小鼠模型中研究了沙利度胺的镇静,抗炎和免疫抑制剂的作用。在MPTP对照组(3 x 15 mg / kg腹膜内)和沙利度胺中测量多巴胺(DA)及其主要代谢物3,4-二羟基苯基乙酸(DOPAC)和高香草酸(HVA)的纹状体水平组(术后25 mg / kg或50 mg / kg的重复治疗)。对于用沙利度胺治疗的小鼠,观察到针对MPTP诱导的DA降低的剂量依赖性保护。两种剂量的沙利度胺都完全抑制了HVA水平的降低。沙利度胺在该模型中具有活性,表明炎症过程可能与DA能神经元中MPTP诱导的损伤有关。

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