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丁香酚对大鼠离体回肠的抑制作用。

Inhibitory actions of eugenol on rat isolated ileum.

作者信息

Leal-Cardoso José H, Lahlou Saad, Coelho-de-Souza Andrelina N, Criddle David N, Pinto Duarte Glória I B, Santos Marcia A V, Magalhães Pedro J C

出版信息

Can J Physiol Pharmacol. 2002 Sep;80(9):901-6. doi: 10.1139/y02-117.

Abstract

The effects of eugenol (1-2000 microM) on rat isolated ileum were studied. Eugenol relaxed the basal tonus (IC50 83 microM) and the ileum precontracted with 60 mM KCl (IC50 162 microM), an action unaltered by 0.5 microM tetrodotoxin, 0.2 mM N(G)-nitro-L-arginine methyl ester, 0.5 mM hexamethonium, and 1 microM indomethacin. Eugenol did not alter the resting transmembrane potential (Em) of the longitudinal muscle layer under normal conditions (5.0 mM K+) or in depolarised tissues. Eugenol reversibly inhibited contractions induced by submaximal concentrations of acetylcholine (ACh) and K+ (40 mM) with IC50 values of approximately 228 and 237 microM, respectively. Eugenol blocked the component of ACh-induced contraction obtained in Ca(2+)-free solution (0.2 mM EGTA) or in the presence of nifedipine (1 microM). Our results suggest that eugenol induces relaxation of rat ileum by a direct action on smooth muscle via a mechanism largely independent of alterations of Em and extracellular Ca2+ influx.

摘要

研究了丁香酚(1 - 2000微摩尔)对大鼠离体回肠的作用。丁香酚可使基础张力(半数抑制浓度[IC50]为83微摩尔)以及用60毫摩尔氯化钾预收缩的回肠松弛(IC50为162微摩尔),该作用不受0.5微摩尔河豚毒素、0.2毫摩尔N(G)-硝基-L-精氨酸甲酯、0.5毫摩尔六甲铵和1微摩尔吲哚美辛的影响。在正常条件下(5.0毫摩尔钾离子)或去极化组织中,丁香酚不会改变纵肌层的静息跨膜电位(Em)。丁香酚可逆性抑制由亚最大浓度的乙酰胆碱(ACh)和钾离子(40毫摩尔)诱导的收缩,其IC50值分别约为228和237微摩尔。丁香酚阻断了在无钙溶液(0.2毫摩尔乙二醇双四乙酸)或硝苯地平(1微摩尔)存在下获得的ACh诱导收缩的成分。我们的结果表明,丁香酚通过对平滑肌的直接作用诱导大鼠回肠松弛,其机制在很大程度上独立于Em和细胞外钙离子内流的改变。

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