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S-烯丙半胱氨酸,一种大蒜化合物,可预防 1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的小鼠帕金森病的氧化应激。

S-Allylcysteine, a garlic compound, protects against oxidative stress in 1-methyl-4-phenylpyridinium-induced parkinsonism in mice.

机构信息

Laboratory of Neurotoxicology, National Institute of Neurology and Neurosurgery, "Manuel Velasco Suárez," SS, Mexico City, D.F., Mexico.

出版信息

J Nutr Biochem. 2011 Oct;22(10):937-44. doi: 10.1016/j.jnutbio.2010.08.005. Epub 2010 Dec 28.

Abstract

S-Allylcysteine (SAC), the most abundant organosulfur compound in aged garlic extract, has multifunctional activity via different mechanisms and neuroprotective effects that are exerted probably via its antioxidant or free radical scavenger action. The 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated mouse has been the most widely used model for assessing neuroprotective agents for Parkinson's disease. 1-Methyl-4-phenylpyridinium (MPP(+)) is the stable metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, and it causes nigrostriatal dopaminergic neurotoxicity. Previous studies suggest that oxidative stress, via free radical production, is involved in MPP(+)-induced neurotoxicity. Here, we report on the neuroprotective effect of SAC against oxidative stress induced by MPP(+) in the striatum of C57BL/6J mice. Mice were pretreated with SAC (125 mg/kg ip) daily for 17 days, followed by administration of MPP(+) (0.72 mg/kg icv), and were sacrificed 24 h later to evaluate lipid peroxidation, different antioxidant enzyme activities, spontaneous locomotor activity and dopamine (DA) content. MPP(+) administration resulted in a significant decrease in DA levels in the striatum. Mice receiving SAC (125 mg/kg ip) had significantly attenuated MPP(+)-induced loss of striatal DA levels (32%). The neuroprotective effect of SAC against MPP(+) neurotoxicity was associated with blocked (100% of protection) of lipid peroxidation and reduction of superoxide radical production - indicated by an up-regulation of Cu-Zn-superoxide dismutase activity - both of which are indices of oxidative stress. Behavioral analyses showed that SAC improved MPP(+)-induced impairment of locomotion (35%). These findings suggest that in mice, SAC attenuates MPP(+)-induced neurotoxicity in the striatum and that an antioxidant effect against oxidative stress may be partly responsible for its observed neuroprotective effects.

摘要

S-烯丙半胱氨酸(SAC)是陈年大蒜提取物中含量最丰富的有机硫化合物,通过不同的机制具有多功能活性和神经保护作用,可能是通过其抗氧化或自由基清除作用发挥作用。1-甲基-4-苯基-1,2,3,6-四氢吡啶处理的小鼠已成为评估帕金森病神经保护剂的最广泛使用的模型。1-甲基-4-苯基吡啶(MPP(+)) 是 1-甲基-4-苯基-1,2,3,6-四氢吡啶的稳定代谢物,它会导致黑质纹状体多巴胺能神经毒性。先前的研究表明,氧化应激通过自由基产生参与 MPP(+)-诱导的神经毒性。在这里,我们报告了 SAC 对 C57BL/6J 小鼠纹状体中 MPP(+)诱导的氧化应激的神经保护作用。小鼠每天用 SAC(125 mg/kg ip)预处理 17 天,然后给予 MPP(+)(0.72 mg/kg icv),24 小时后处死以评估脂质过氧化、不同抗氧化酶活性、自发运动活动和多巴胺(DA) 含量。MPP(+)给药导致纹状体中 DA 水平显着降低。接受 SAC(125 mg/kg ip)的小鼠显着减弱了 MPP(+)-诱导的纹状体 DA 水平降低(32%)。SAC 对 MPP(+)神经毒性的神经保护作用与脂质过氧化的阻断(100%保护)和超氧自由基产生的减少有关-通过上调 Cu-Zn-超氧化物歧化酶活性来表示-两者都是氧化应激的指标。行为分析表明,SAC 改善了 MPP(+)-诱导的运动障碍(35%)。这些发现表明,在小鼠中,SAC 减弱了 MPP(+)-诱导的纹状体神经毒性,并且对氧化应激的抗氧化作用可能部分负责其观察到的神经保护作用。

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