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一氧化氮合酶的定位表明一氧化氮具有神经作用。

Localization of nitric oxide synthase indicating a neural role for nitric oxide.

作者信息

Bredt D S, Hwang P M, Snyder S H

机构信息

Department of Neuroscience, John Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

Nature. 1990 Oct 25;347(6295):768-70. doi: 10.1038/347768a0.

Abstract

Nitric oxide (NO), apparently identical to endothelium-derived relaxing factor in blood vessels, is also formed by cytotoxic macrophages, in adrenal gland and in brain tissue, where it mediates the stimulation by glutamate of cyclic GMP formation in the cerebellum. Stimulation of intestinal or anococcygeal nerves liberates NO, and the resultant muscle relaxation is blocked by arginine derivatives that inhibit NO synthesis. It is, however, unclear whether in brain or intestine, NO released following nerve stimulation is formed in neurons, glia, fibroblasts, muscle or blood cells, all of which occur in proximity to neurons and so could account for effects of nerve stimulation on cGMP and muscle tone. We have now localized NO synthase protein immunohistochemically in the rat using antisera to the purified enzyme. We demonstrate NO synthase in the brain to be exclusively associated with discrete neuronal populations. NO synthase is also concentrated in the neural innervation of the posterior pituitary, in autonomic nerve fibres in the retina, in cell bodies and nerve fibres in the myenteric plexus of the intestine, in adrenal medulla, and in vascular endothelial cells. These prominent neural localizations provide the first conclusive evidence for a strong association of NO with neurons.

摘要

一氧化氮(NO),显然与血管中内皮衍生的舒张因子相同,也由细胞毒性巨噬细胞、肾上腺和脑组织产生,在脑组织中它介导谷氨酸对小脑环磷酸鸟苷(cGMP)形成的刺激作用。刺激肠神经或肛门尾骨神经可释放NO,而由此产生的肌肉松弛会被抑制NO合成的精氨酸衍生物所阻断。然而,目前尚不清楚在脑或肠道中,神经刺激后释放的NO是在神经元、神经胶质细胞、成纤维细胞、肌肉还是血细胞中形成的,所有这些细胞都与神经元相邻,因此都可能解释神经刺激对cGMP和肌张力的影响。我们现在使用针对纯化酶的抗血清,通过免疫组织化学方法在大鼠中定位了NO合酶蛋白。我们证明脑中的NO合酶仅与离散的神经元群体相关。NO合酶还集中在后叶垂体的神经支配、视网膜的自主神经纤维、肠肌间神经丛的细胞体和神经纤维、肾上腺髓质以及血管内皮细胞中。这些显著的神经定位为NO与神经元的紧密关联提供了首个确凿证据。

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