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Suramin selectively inhibits the non-adrenergic non-cholinergic inhibitory junction potential in the guinea-pig stomach.

作者信息

Ohno N, Ito K M, Yamamoto Y, Suzuki H

机构信息

Department of Physiology, Nagoya City University Medical School, Japan.

出版信息

Eur J Pharmacol. 1993 Nov 2;249(1):121-3. doi: 10.1016/0014-2999(93)90671-4.

DOI:10.1016/0014-2999(93)90671-4
PMID:8282014
Abstract

In smooth muscle cells of the guinea-pig stomach fundus, transmural nerve stimulation evoked a cholinergic excitatory junction potential (e.j.p.) and, in the presence of atropine, a non-adrenergic non-cholinergic (NANC) inhibitory junction potential (i.j.p.). Suramin (> 10(-5) M), a putative inhibitor of the P2 purinoceptor, enhanced the e.j.p. amplitude and inhibited the i.j.p., with no significant effect on the membrane potential. Thus, a possible involvement of ATP in the generation of the NANC i.j.p. has to be considered.

摘要

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2
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引用本文的文献

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The P(2)-purinoceptor antagonist suramin is a competitive antagonist at vasoactive intestinal peptide receptors in the rat gastric fundus.P(2)嘌呤受体拮抗剂苏拉明是大鼠胃底血管活性肠肽受体的竞争性拮抗剂。
Br J Pharmacol. 2000 Aug;130(7):1632-8. doi: 10.1038/sj.bjp.0703482.
3
Properties of the inhibitory junction potential in smooth muscle of the guinea-pig gastric fundus.
豚鼠胃底平滑肌中抑制性连接电位的特性
Br J Pharmacol. 1996 Mar;117(5):974-8. doi: 10.1111/j.1476-5381.1996.tb15290.x.
4
Electrophysiological evidence for different release mechanism of ATP and NO as inhibitory NANC transmitters in guinea-pig colon.豚鼠结肠中ATP和NO作为抑制性非肾上腺素能非胆碱能递质的不同释放机制的电生理证据。
Br J Pharmacol. 1994 Aug;112(4):1077-82. doi: 10.1111/j.1476-5381.1994.tb13193.x.