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一种能够穿过血脑屏障的新型硫醇抗氧化剂在帕金森病实验模型中可保护多巴胺能神经元。

A novel thiol antioxidant that crosses the blood brain barrier protects dopaminergic neurons in experimental models of Parkinson's disease.

作者信息

Bahat-Stroomza Merav, Gilgun-Sherki Yossi, Offen Daniel, Panet Hana, Saada Ann, Krool-Galron Nili, Barzilai Aari, Atlas Daphne, Melamed Eldad

机构信息

Laboratory of Neurosciences, Felsenstein Medical Research Center and Department of Neurology, Rabin Medical Center, Beilinson Campus Tel Aviv University, Sackler School of Medicine, Petah-Tikva 49100, Israel.

出版信息

Eur J Neurosci. 2005 Feb;21(3):637-46. doi: 10.1111/j.1460-9568.2005.03889.x.

Abstract

It is believed that oxidative stress (OS) plays an important role in the loss of dopaminergic nigrostriatal neurons in Parkinson's disease (PD) and that treatment with antioxidants might be neuroprotective. However, most currently available antioxidants cannot readily penetrate the blood brain barrier after systemic administration. We now report that AD4, the novel low molecular weight thiol antioxidant and the N-acytel cysteine (NAC) related compound, is capable of penetrating the brain and protects neurons in general and especially dopaminergic cells against various OS-generating neurotoxins in tissue cultures. Moreover, we found that treatment with AD4 markedly decreased the damage of dopaminergic neurons in three experimental models of PD. AD4 suppressed amphetamine-induced rotational behaviour in rats with unilateral 6-OHDA-induced nigral lesion. It attenuated the reduction in striatal dopamine levels in mice treated with 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine (MPTP). It also reduced the dopaminergic neuronal loss following chronic intrajugular administration of rotenone in rats. Our findings suggest that AD4 is a novel potential new neuroprotective drug that might be effective at slowing down nigral neuronal degeneration and illness progression in patients with PD.

摘要

人们认为氧化应激(OS)在帕金森病(PD)中多巴胺能黑质纹状体神经元的丧失中起重要作用,并且抗氧化剂治疗可能具有神经保护作用。然而,目前大多数可用的抗氧化剂在全身给药后不能轻易穿透血脑屏障。我们现在报告,新型低分子量硫醇抗氧化剂AD4,一种与N-乙酰半胱氨酸(NAC)相关的化合物,能够穿透大脑,并在组织培养中保护神经元,尤其是多巴胺能细胞免受各种产生OS的神经毒素的侵害。此外,我们发现用AD4治疗在三种PD实验模型中显著降低了多巴胺能神经元的损伤。AD4抑制了单侧6-OHDA诱导黑质损伤大鼠中安非他明诱导的旋转行为。它减轻了用1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)治疗的小鼠纹状体多巴胺水平的降低。它还减少了大鼠慢性颈内注射鱼藤酮后多巴胺能神经元的损失。我们的研究结果表明,AD4是一种新型潜在的神经保护药物,可能有效地减缓PD患者黑质神经元变性和疾病进展。

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