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首页> 外文期刊>Biological & pharmaceutical bulletin >Neuroprotective Effects of Phenylethanoid Glycosides from Cistanches salsa against 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-Induced Dopaminergic Toxicity in C57 Mice.
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Neuroprotective Effects of Phenylethanoid Glycosides from Cistanches salsa against 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-Induced Dopaminergic Toxicity in C57 Mice.

机译:肉Ci蓉的苯乙醇类苷对C57小鼠对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的多巴胺能毒性的神经保护作用。

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The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) has been employed to create a Parkinson's disease-like model in both rodents and primates based primarily on its ability to create a striatal dopamine deficit due to the loss of dopaminergic neurons in the substantia nigra compacta. The present study was carried out to determine the possible effects of phenylethanoid glycosides (PhGs) from Cistanches salsa (C. A. MEY, G. BECK) on attenuating the serious behavioral disorder and increasing dopamine (DA) levels in the striata of MPTP-lesioned C57 mice. MPTP (30 mg/kg i.p. for 4 d) induced serious behavioral disorders and significantly reduced striatal DA levels in C57 mice. In spontaneous motor activity and rotarod tests, obvious behavioral differences were seen between control and model groups. PhGs (10, 50 mg/kg) significantly increased the spontaneous movement number and latent period of mice on the rotating rod (p<0.01). Injections of MPTP 30 mg/kg for 4 d caused a significant reduction in DA, 3,4-dihydroxyphenyl acetic acid, and homovanillic acid in striata analyzed by HPLC-electrochemistry (p<0.01). The neurotoxic effects of MPTP were attenuated by pretreatment with PhGs (10, 50 mg/kg) in a dose-dependent fashion. The apparent neuroprotective effects of PhGs on nigral dopaminergic neurons were also confirmed by the results of immunohistochemical staining. The present in vivo data clearly demonstrate that PhGs can protect dopaminergic neurons against dopamine neurotoxicity induced by MPTP, as suggested by an earlier in vitro study. The neuroprotective effects of PhGs were the first reported for a natural product.
机译:神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)已被用于在啮齿动物和灵长类动物中建立帕金森氏病样模型,主要是基于其产生纹状体多巴胺缺陷的能力。对黑质致密部中多巴胺能神经元的损失。进行本研究,以确定肉Ci蓉(CA MEY,G。BECK)中苯乙醚类苷(PhGs)对减轻MPTP损伤的C57小鼠纹状体中的严重行为障碍和增加多巴胺(DA)水平的可能作用。 。 MPTP(30 mg / kg i.p.,持续4 d)可引起严重的行为障碍,并显着降低C57小鼠的纹状体DA水平。在自发的运动活动和旋转试验中,对照组和模型组之间存在明显的行为差异。 PhG(10,50 mg / kg)显着增加了旋转棒上小鼠的自发运动次数和潜伏期(p <0.01)。通过HPLC-电化学分析,注射MPTP 30 mg / kg持续4 d导致纹状体中的DA,3,4-二羟苯基乙酸和高香草酸显着降低(p <0.01)。用PhGs(10,50 mg / kg)预处理以剂量依赖的方式减弱了MPTP的神经毒性作用。免疫组化染色的结果也证实了PhGs对黑色素多巴胺能神经元的明显神经保护作用。目前的体内数据清楚地表明,正如较早的一项体外研究表明的那样,PhG可以保护多巴胺能神经元免受MPTP诱导的多巴胺神经毒性。 PhGs的神经保护作用是首次报道天然产物。

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