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多发性硬化症脑白质脱髓鞘区域一氧化氮合酶的诱导。

Induction of nitric oxide synthase in demyelinating regions of multiple sclerosis brains.

作者信息

Bö L, Dawson T M, Wesselingh S, Mörk S, Choi S, Kong P A, Hanley D, Trapp B D

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.

出版信息

Ann Neurol. 1994 Nov;36(5):778-86. doi: 10.1002/ana.410360515.

Abstract

The amount of messenger RNA encoding human inducible nitric oxide synthase and the presence and distribution of NADPH diaphorase were determined in tissue sections from multiple sclerosis (MS) and control brains. Levels of human nitric oxide synthase messenger RNA were markedly elevated in MS brains when compared to normal control brains. NADPH diaphorase activity, a histochemical stain reflecting nitric oxide synthase catalytic activity, was detected in reactive astrocytes in active demyelinating MS lesions and at the edge of chronic active demyelinating lesions. Control brains did not contain NADPH diaphorase-positive astrocytes. These results implicate the free radical nitric oxide in the pathogenesis of demyelinating MS lesions.

摘要

在取自多发性硬化症(MS)患者及对照者大脑的组织切片中,测定了编码人诱导型一氧化氮合酶的信使核糖核酸的量以及还原型辅酶Ⅱ黄递酶的存在情况和分布。与正常对照大脑相比,MS大脑中人类一氧化氮合酶信使核糖核酸的水平显著升高。还原型辅酶Ⅱ黄递酶活性是一种反映一氧化氮合酶催化活性的组织化学染色,在活动性脱髓鞘MS病灶中的反应性星形胶质细胞以及慢性活动性脱髓鞘病灶边缘被检测到。对照大脑中未含有还原型辅酶Ⅱ黄递酶阳性星形胶质细胞。这些结果表明自由基一氧化氮参与了脱髓鞘MS病灶的发病机制。

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