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在用二乙基二硫代氨基甲酸盐抑制超氧化物歧化酶后,超氧阴离子会阻断牛阴茎退缩肌中的非肾上腺素能非胆碱能神经传递。

NANC neurotransmission in the bovine retractor penis muscle is blocked by superoxide anion following inhibition of superoxide dismutase with diethyldithiocarbamate.

作者信息

Martin W, McAllister K H, Paisley K

机构信息

Department of Pharmacology, University of Glasgow, Scotland, U.K.

出版信息

Neuropharmacology. 1994 Nov;33(11):1293-301. doi: 10.1016/0028-3908(94)90029-9.

Abstract

This study examined the effects of inhibiting Cu/Zn superoxide dismutase with diethyldithiocarbamate (DETCA) on the ability of superoxide generating agents such as pyrogallol, hypoxanthine/xanthine oxidase and LY 83583, to influence NANC relaxation of strips of bovine retractor penis (BRP) muscle. Although pyrogallol (100 microM) and hypoxanthine (0.3 mM)/xanthine oxidase (64 mU ml-1) had little effect on NANC relaxation in control strips, both induced almost complete inhibition following treatment with DETCA (3 mM) for 1 h. Inhibition was due to the actions of superoxide anion since it was blocked by the addition of exogenous superoxide dismutase (250 U ml-1). LY 83583 (0.1-30 microM) produced a concentration-dependent inhibition of NANC relaxation even in control strips and this too was blocked by exogenous superoxide dismutase, but sensitivity to inhibition was enhanced 10-fold following treatment with DETCA. The data suggest that under normal circumstances the NANC neurotransmitter is protected by high levels of tissue superoxide dismutase, and inhibition of this enzyme increases its susceptibility to destruction by superoxide anions. An important impediment to accepting free nitric oxide as the NANC neurotransmitter in the BRP on the basis that superoxide anion-generating agents inhibit the actions of authentic nitric oxide but not those of NANC nerve stimulation has thus been removed.

摘要

本研究检测了用二乙基二硫代氨基甲酸盐(DETCA)抑制铜/锌超氧化物歧化酶对诸如连苯三酚、次黄嘌呤/黄嘌呤氧化酶和LY 83583等超氧化物生成剂影响牛阴茎退缩肌(BRP)肌条非肾上腺素能非胆碱能(NANC)舒张能力的作用。尽管连苯三酚(100微摩尔)和次黄嘌呤(0.3毫摩尔)/黄嘌呤氧化酶(64毫国际单位/毫升)对对照肌条的NANC舒张作用很小,但在用DETCA(3毫摩尔)处理1小时后二者均几乎完全抑制。抑制是由于超氧阴离子的作用,因为加入外源性超氧化物歧化酶(250单位/毫升)可阻断这种抑制。即使在对照肌条中,LY 83583(0.1 - 30微摩尔)也产生浓度依赖性的NANC舒张抑制,并且这也被外源性超氧化物歧化酶阻断,但在用DETCA处理后对抑制的敏感性增强了10倍。数据表明,在正常情况下,NANC神经递质受到高水平组织超氧化物歧化酶的保护,抑制该酶会增加其被超氧阴离子破坏的敏感性。因此,基于超氧阴离子生成剂抑制真正一氧化氮的作用但不抑制NANC神经刺激的作用,接受游离一氧化氮作为BRP中NANC神经递质的一个重要障碍已被消除。

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