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大鼠局灶性脑缺血后铜/锌超氧化物歧化酶和锰超氧化物歧化酶的免疫组织化学研究

An immunohistochemical study of copper/zinc superoxide dismutase and manganese superoxide dismutase following focal cerebral ischemia in the rat.

作者信息

Liu X H, Kato H, Araki T, Itoyama Y, Kato K, Kogure K

机构信息

Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Brain Res. 1994 May 2;644(2):257-66. doi: 10.1016/0006-8993(94)91688-8.

Abstract

We investigated immunohistochemically the localization and changes of copper/zinc superoxide dismutase (CuZn-SOD) and manganese superoxide dismutase (Mn-SOD) in the rat brain following 1 h of middle cerebral artery (MCA) occlusion. In normal brain, immunoreactivity to both SODs was observed in medium-sized neurons in the striatum and in many neurons in the neocortex. Mn-SOD was predominantly stained in cortical interneurons. The immunostaining of both SODs rapidly decreased or disappeared in neurons in the lateral segment of the striatum (ischemic center) 4 h after MCA occlusion, when the neurons were degenerating. Most neurons in the neocortex (ischemic penumbra) decreased their CuZn-SOD immunoreactivity but not Mn-SOD immunoreactivity 4 h after ischemia, when only a few neurons showed histopathological changes. CuZn-SOD immunoreactivity in almost all cortical neurons disappeared 1 day after ischemia, but Mn-SOD immunoreactivity was still preserved in interneurons, when cortical neurons showed typical pathological changes. Some cortical neurons in the boundary zone between normal and infarcted areas showed intense immunostaining to both SODs and glial SOD immunoreactivity appeared after 3 and 7 days. These results suggest that early loss of the scavenging system of free radicals may lead to neuronal damage after ischemic insult, and that induced SODs in the boundary zone between the normal and infarcted areas may act as a defense mechanism against damage.

摘要

我们采用免疫组织化学方法研究了大脑中动脉(MCA)闭塞1小时后大鼠脑内铜/锌超氧化物歧化酶(CuZn-SOD)和锰超氧化物歧化酶(Mn-SOD)的定位及变化。在正常脑中,纹状体中型神经元和新皮层许多神经元均观察到对两种超氧化物歧化酶的免疫反应性。Mn-SOD主要在皮层中间神经元中染色。MCA闭塞4小时后,当纹状体外侧段(缺血中心)的神经元发生变性时,两种超氧化物歧化酶的免疫染色在这些神经元中迅速降低或消失。缺血4小时后,新皮层(缺血半暗带)的大多数神经元CuZn-SOD免疫反应性降低,但Mn-SOD免疫反应性未降低,此时仅有少数神经元出现组织病理学改变。缺血1天后,几乎所有皮层神经元的CuZn-SOD免疫反应性消失,但当皮层神经元出现典型病理改变时,Mn-SOD免疫反应性仍保留在中间神经元中。正常与梗死区域边界带的一些皮层神经元对两种超氧化物歧化酶均显示强烈免疫染色,且3天和7天后出现胶质超氧化物歧化酶免疫反应性。这些结果表明,自由基清除系统的早期丧失可能导致缺血性损伤后神经元损伤,并且正常与梗死区域边界带诱导产生的超氧化物歧化酶可能作为一种防御机制抵抗损伤。

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