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汉方制剂当归芍药散和葛根芩连汤对大鼠结肠远端环形平滑肌收缩活动的影响。

Effects of Hange-shashin-to (TJ-14) and Keishi-ka-shakuyaku-to (TJ-60) on contractile activity of circular smooth muscle of the rat distal colon.

机构信息

Department of Pharmacology, Faculty of Medicine, Saga University, Nabeshima, Saga 849-8501, Japan.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2012 Nov 1;303(9):G1059-66. doi: 10.1152/ajpgi.00219.2012. Epub 2012 Aug 23.

Abstract

The Japanese Kampo medicines Hange-shashin-to (TJ-14) and Keishi-ka-shakuyaku-to (TJ-60) have been used to treat symptoms of human diarrhea on an empirical basis as Japanese traditional medicines. However, it remains unclear how these drugs affect smooth muscle tissues in the distal colon. The aim of the present study was to investigate the effects of TJ-14 and TJ-60 on the contractile activity of circular smooth muscle from the rat distal colon. TJ-14 and TJ-60 (both 1 mg/ml) inhibited spontaneous contractions of circumferentially cut preparations with the mucosa intact. Blockade of nitric oxide (NO) synthase or soluble guanylate cyclase activity abolished the inhibitory effects of TJ-60 but only attenuated the inhibitory effects of TJ-14. Apamin (1 μM), a blocker of small-conductance Ca(2+)-activated K(+) channels (SK channels), attenuated the inhibitory effects of 5 mg/ml TJ-60 but not those of 5 mg/ml TJ-14. TJ-14 suppressed contractile responses (phasic contractions and off-contractions) evoked by transmural nerve stimulation and increased basal tone, whereas TJ-60 had little effect on these parameters. These results suggest that 1 mg/ml TJ-14 or TJ-60 likely inhibits spontaneous contractions of the rat distal colon through the production of NO. Activation of SK channels seems to be involved in the inhibitory effects of 5 mg/ml TJ-60. Since TJ-14 has potent inhibitory effects on myogenic and neurogenic contractile activity, TJ-14 may be useful in suppressing gastrointestinal motility.

摘要

日本汉方药 Hange-shashin-to(TJ-14)和 Keishi-ka-shakuyaku-to(TJ-60)已被用作日本传统药物来治疗人类腹泻症状,但这些药物如何影响远端结肠的平滑肌组织尚不清楚。本研究旨在探讨 TJ-14 和 TJ-60 对大鼠远端结肠环形平滑肌收缩活性的影响。TJ-14 和 TJ-60(均为 1mg/ml)抑制完整黏膜的环行肌节段的自发性收缩。一氧化氮(NO)合酶或可溶性鸟苷酸环化酶活性的阻断消除了 TJ-60 的抑制作用,但仅减弱了 TJ-14 的抑制作用。小电导钙激活钾(SK)通道阻断剂阿帕米(1μM)减弱了 5mg/ml TJ-60 的抑制作用,但对 5mg/ml TJ-14 无影响。TJ-14 抑制由肠壁神经刺激引起的收缩反应(相收缩和无收缩)并增加基础张力,而 TJ-60 对这些参数几乎没有影响。这些结果表明,1mg/ml TJ-14 或 TJ-60 可能通过产生 NO 抑制大鼠远端结肠的自发性收缩。SK 通道的激活可能参与了 5mg/ml TJ-60 的抑制作用。由于 TJ-14 对肌源性和神经源性收缩活性具有强烈的抑制作用,因此 TJ-14 可能有助于抑制胃肠道动力。

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