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M1受体在猫回肠一氧化氮途径中的作用。

Participation of M1 receptors in NO pathway in cat ileum.

作者信息

Kortezova N, Shikova L, Papasova M

机构信息

Institute of Physiology, Bulgarian Academy ofSciences, Sofia.

出版信息

Acta Physiol Pharmacol Bulg. 1998;23(1):1-4.

Abstract

Electrical field stimulation (EFS) elicited two types of responses from longitudinal muscle strips of the distal cat ileum: contraction at switching on the stimulation (in 62% of the strips) and inhibition of the phasic contractions at switching on the stimulation followed by contraction in 38% of the strips. In all strips the muscarinic acetylcholine subtype M1-receptor agonist (4-Hydroxy-2-butynyl)-1-trimethylammonium-m-chlorocarbanilate chloride (McN-A-343) increased the tone and amplitude of the spontaneous contractions. On this background EFS elicited an inhibition of the phasic contractions at switching on the stimulation followed by contraction. Blockade of nitric oxide (NO)-synthase by Nw-nitro-L-arginine (L-NNA) transformed the inhibitory response into contraction and this transformation was partly overcome by L-arginine. The results suggest that presynaptically situated M1 receptors are involved in the NO pathway.

摘要

电场刺激(EFS)可引起猫远端回肠纵肌条产生两种类型的反应:在开启刺激时收缩(62%的肌条),以及在开启刺激时抑制相性收缩,随后38%的肌条出现收缩。在所有肌条中,毒蕈碱型乙酰胆碱M1受体激动剂(4-羟基-2-丁炔基)-1-三甲基氯化铵间氯卡巴腙(McN-A-343)可增加自发性收缩的张力和幅度。在此背景下,EFS在开启刺激时引起相性收缩的抑制,随后出现收缩。Nω-硝基-L-精氨酸(L-NNA)对一氧化氮(NO)合酶的阻断将抑制性反应转变为收缩,而L-精氨酸可部分克服这种转变。结果表明,突触前的M1受体参与了NO通路。

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