Suppr超能文献

豚鼠肠道神经刺激诱发一氧化氮的释放。

Release of nitric oxide evoked by nerve stimulation in guinea-pig intestine.

作者信息

Wiklund N P, Leone A M, Gustafsson L E, Moncada S

机构信息

Department of Urology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Neuroscience. 1993 Apr;53(3):607-11. doi: 10.1016/0306-4522(93)90609-j.

Abstract

Non-adrenergic non-cholinergic nerves provide the main inhibitory autonomic supply to intestinal smooth muscle and other organ systems. Nitric oxide is likely to act as a neurotransmitter in these nerves and a nitric oxide synthase has been demonstrated in autonomic neurons. However, there are as yet no biochemical measurements of nerve-induced release of nitric oxide or its breakdown products nitrite and nitrate. We have examined the possibility that nitric oxide is released by stimulation of autonomic nerves in the guinea-pig intestine by studying the release of nitric oxide, nitrite and nitrate. The biological activity of a vascular relaxing factor released by the activation of these nerves was compared with that of nitric oxide using a bioassay system as previously described. Nitrite and nitrate release were measured by high-performance liquid chromatography using UV absorbance. The relaxation of the bioassay tissues to nerve stimulation was indistinguishable from the relaxation induced by nitric oxide. Both relaxations were equally unstable and inhibited to a similar degree by haemoglobin and enhanced by superoxide dismutase. Furthermore, the release of the relaxing factor was attenuated by treatment with the nitric oxide synthase inhibitor N omega-nitro-L-arginine. Concomitant with the release of the relaxing factor, which was frequency dependent, there was a frequency-dependent release of nitrite and nitrate in amounts sufficient to explain the vascular relaxations observed during nerve stimulation. The release of nitrite and nitrate was also inhibited by treatment with the nitric oxide synthase inhibitor.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

非肾上腺素能非胆碱能神经为肠道平滑肌和其他器官系统提供主要的自主抑制性神经支配。一氧化氮可能在这些神经中充当神经递质,并且在自主神经元中已证实存在一氧化氮合酶。然而,目前尚无关于神经诱导释放一氧化氮或其分解产物亚硝酸盐和硝酸盐的生化测量。我们通过研究一氧化氮、亚硝酸盐和硝酸盐的释放,探讨了豚鼠肠道自主神经刺激是否释放一氧化氮的可能性。使用先前描述的生物测定系统,将这些神经激活释放的血管舒张因子的生物活性与一氧化氮的生物活性进行比较。亚硝酸盐和硝酸盐的释放通过高效液相色谱法利用紫外吸收进行测量。生物测定组织对神经刺激的舒张作用与一氧化氮诱导的舒张作用无法区分。两种舒张作用同样不稳定,且均被血红蛋白以相似程度抑制,并被超氧化物歧化酶增强。此外,用一氧化氮合酶抑制剂Nω-硝基-L-精氨酸处理可减弱舒张因子的释放。与频率依赖性的舒张因子释放同时,存在频率依赖性的亚硝酸盐和硝酸盐释放,其释放量足以解释神经刺激期间观察到的血管舒张。用一氧化氮合酶抑制剂处理也可抑制亚硝酸盐和硝酸盐的释放。(摘要截短于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验