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用MPTP处理后,人α-突触核蛋白转基因小鼠黑质线粒体病理增强。

Enhanced substantia nigra mitochondrial pathology in human alpha-synuclein transgenic mice after treatment with MPTP.

作者信息

Song David D, Shults Clifford W, Sisk Abbyann, Rockenstein Edward, Masliah Eliezer

机构信息

Neurology Service, VA San Diego Healthcare System, San Diego, CA 92161-9127, USA.

出版信息

Exp Neurol. 2004 Apr;186(2):158-72. doi: 10.1016/S0014-4886(03)00342-X.

Abstract

Recent studies have implicated alpha-synuclein (alpha-S) in the pathogenesis of Parkinson's disease (PD). The mechanisms underlying PD are not completely understood; however, mitochondrial complex I inhibition and oxidative injury may be involved. Because the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is a potent complex I inhibitor that can cause oxidative injury and mimic many aspects of PD in treated animals, we sought to determine whether the overexpression of alpha-S in transgenic (tg) mice (alpha-S-tg) would enhance the substantia nigra (SN) pathology resulting from treatment with MPTP. For this purpose, alpha-S-tg mice were produced expressing high levels of wild-type (wt) human alpha-S under the control of the neuron-specific Thy-1 promoter. Alpha-S-tg mice and non-tg controls were treated with MPTP (15 mg/kg ip, twice a week for 2 weeks) or saline (Sal) and then examined 2 weeks after completion of treatment by transmission electron microscopy (EM). We found that alpha-S-tg mice treated with MPTP had extensive mitochondrial alterations, increases in mitochondrial size, filamentous neuritic aggregations, axonal degeneration, and formation of electron dense perinuclear cytoplasmic inclusions in the SN that did not occur in the hippocampus or neocortex, nor in MPTP-treated non-tg mice or Sal-treated alpha-S-tg mice. These findings support the potential involvement of alpha-S expression in the vulnerability of SN neurons to toxicity from mitochondrial complex I inhibitors and the subsequent development of neurodegenerative pathology.

摘要

最近的研究表明,α-突触核蛋白(α-S)与帕金森病(PD)的发病机制有关。PD的潜在机制尚未完全明确;然而,线粒体复合体I抑制和氧化损伤可能与之相关。由于神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)是一种有效的复合体I抑制剂,可导致氧化损伤,并在接受治疗的动物中模拟PD的许多方面,因此我们试图确定转基因(tg)小鼠(α-S-tg)中α-S的过表达是否会加重MPTP治疗导致的黑质(SN)病变。为此,我们制备了在神经元特异性Thy-1启动子控制下高水平表达野生型(wt)人α-S的α-S-tg小鼠。将α-S-tg小鼠和非tg对照小鼠用MPTP(15mg/kg腹腔注射,每周两次,共2周)或生理盐水(Sal)处理,然后在治疗结束后2周通过透射电子显微镜(EM)检查。我们发现,用MPTP处理的α-S-tg小鼠出现广泛的线粒体改变、线粒体大小增加、丝状神经突聚集、轴突退变以及在SN中形成电子致密的核周细胞质包涵体,而这些改变在海马体或新皮层中未出现,在用MPTP处理的非tg小鼠或用Sal处理的α-S-tg小鼠中也未出现。这些发现支持α-S表达可能参与SN神经元对线粒体复合体I抑制剂毒性的易感性以及随后神经退行性病变的发展。

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