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在犬脑动脉中研究了各种血管舒张剂对快速拉伸诱导的肌源性收缩的抑制作用。

Inhibitory actions of various vasorelaxants on the myogenic contraction induced by quick stretch studied in canine cerebral artery.

作者信息

Tanaka Y, Shigenobu K, Nakayama K

机构信息

Department of Pharmacology, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.

出版信息

Eur J Pharmacol. 1998 Sep 4;356(2-3):225-30. doi: 10.1016/s0014-2999(98)00547-0.

Abstract

Quick stretch at a rate of 10 cm/s with the amount of 30% of the initial muscle length (= 100%) produced a myogenic contraction in canine cerebral artery. The inhibitory actions of various vasorelaxants on the stretch-induced contraction were investigated. Ca2+ channel blockers (nicardipine, D-cis-diltiazem) inhibited the stretch-induced contraction by 50-60% at the concentrations which abolished high KCl-induced contraction. Inhibitions of the stretch-induced contraction by nitro-compounds (nitroglycerin, sodium nitroprusside) were about 50%. In contrast, inhibitions by the compounds which activate ATP-sensitive K+ channels (cromakalim, nicorandil, pinacidil) of the myogenic contraction in response to quick stretch were only 20%. Papaverine totally abolished the stretch-induced contraction. It is likely that all the vasorelaxant compounds tested in the present study except papaverine are beneficial in the sense that they do not suppress the intrinsic myogenic contraction, which may be related to the autoregulation of local blood flow.

摘要

以10厘米/秒的速度快速拉伸,拉伸量为初始肌肉长度(=100%)的30%,可在犬脑动脉中产生肌源性收缩。研究了各种血管舒张剂对拉伸诱导收缩的抑制作用。钙通道阻滞剂(尼卡地平、D-顺式地尔硫䓬)在消除高钾诱导收缩的浓度下,可将拉伸诱导收缩抑制50%-60%。硝基化合物(硝酸甘油、硝普钠)对拉伸诱导收缩的抑制率约为50%。相比之下,激活ATP敏感性钾通道的化合物(克罗卡林、尼可地尔、吡那地尔)对快速拉伸引起的肌源性收缩的抑制率仅为20%。罂粟碱可完全消除拉伸诱导的收缩。本研究中测试的除罂粟碱外的所有血管舒张剂可能都是有益的,因为它们不会抑制内在的肌源性收缩,而这可能与局部血流的自动调节有关。

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