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犬回结肠连接处一氧化氮与含氮能神经递质之间的药理学相似性。

Pharmacological similarity between nitric oxide and the nitrergic neurotransmitter in the canine ileocolonic junction.

作者信息

Boeckxstaens G E, De Man J G, De Winter B Y, Herman A G, Pelckmans P A

机构信息

Division of Gastroenterology, Faculty of Medicine, University of Antwerp (UIA), Belgium.

出版信息

Eur J Pharmacol. 1994 Oct 13;264(1):85-9. doi: 10.1016/0014-2999(94)90640-8.

Abstract

In organ bath experiments, pyrogallol (30-100 microM), and to a lesser extent L-cysteine (3 microM), reduced nitric oxide (NO)-induced relaxation, but not the NO-mediated non-adrenergic non-cholinergic (NANC) relaxation elicited by field stimulation of the canine ileocolonic junction. In contrast, in a superfusion bioassay, pyrogallol (10-30 microM) and L-cysteine (1 microM) inhibited the biological activity of both the transferable nitrergic factor released from the canine ileocolonic junction in response to NANC nerve stimulation and NO, but not that of S-nitroso-L-cysteine, S-nitrosoglutathione or S-nitroso-N-acetyl-D,L-penicillamine. Based on the bioassay experiments, it is concluded that the nitrergic NANC neurotransmitter in the canine ileocolonic junction behaves pharmacologically like NO.

摘要

在器官浴实验中,连苯三酚(30 - 100微摩尔),以及程度较轻的L-半胱氨酸(3微摩尔),可降低一氧化氮(NO)诱导的舒张作用,但不影响由犬回结肠交界处的场刺激引发的NO介导的非肾上腺素能非胆碱能(NANC)舒张。相比之下,在灌注生物测定中,连苯三酚(10 - 30微摩尔)和L-半胱氨酸(1微摩尔)抑制了犬回结肠交界处因NANC神经刺激和NO释放的可转移硝化因子的生物活性,但不影响S-亚硝基-L-半胱氨酸、S-亚硝基谷胱甘肽或S-亚硝基-N-乙酰-D,L-青霉胺的生物活性。基于生物测定实验,得出结论:犬回结肠交界处的硝化NANC神经递质在药理学上表现得与NO相似。

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