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Bay K 8644对大鼠门静脉自发电活动和机械活动的影响。

Effects of Bay K 8644 on the spontaneous electrical and mechanical activities of the rat portal vein.

作者信息

Shimamura K, Sunano S

机构信息

Research Institute of Hypertension, Kinki University, Osaka, Japan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1990 Nov;342(5):554-8. doi: 10.1007/BF00169045.

DOI:10.1007/BF00169045
PMID:1708854
Abstract

Effects of Bay K 8644 on the spontaneous electrical and mechanical activities of the rat portal vein were studied. Bay K 8644 enhanced contractions in amplitude and duration. Bay K 8644 prolonged the duration of the spontaneous spike potential bursts and increased the number of spike potentials in a burst. These results indicate that the increase in the amplitude and duration of spontaneous contractions of the rat portal vein induced by Bay K 8644 are mediated mainly by the facilitation of the membrane electrical activity.

摘要

研究了Bay K 8644对大鼠门静脉自发电活动和机械活动的影响。Bay K 8644增强了收缩的幅度和持续时间。Bay K 8644延长了自发尖峰电位爆发的持续时间,并增加了一次爆发中尖峰电位的数量。这些结果表明,Bay K 8644诱导的大鼠门静脉自发收缩幅度和持续时间的增加主要是由膜电活动的促进介导的。

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2
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本文引用的文献

1
ELECTRICAL AND MECHANICAL ACTIVITY OF ISOLATED VASCULAR SMOOTH MUSCLE OF THE RAT.大鼠离体血管平滑肌的电活动和机械活动
Nature. 1964 Jul 11;203:192-4. doi: 10.1038/203192b0.
2
Some effects of sodium nitroprusside, methoxyverapamil (D600) and nifedipine on rat portal vein.硝普钠、甲氧基维拉帕米(D600)和硝苯地平对大鼠门静脉的某些作用。
Br J Pharmacol. 1980 Feb;68(2):311-9. doi: 10.1111/j.1476-5381.1980.tb10420.x.
3
Selectivity of calcium antagonism and serotonin antagonism with respect to venous and arterial tissues.钙拮抗作用和5-羟色胺拮抗作用对静脉和动脉组织的选择性。
Angiology. 1981 Jul;32(7):476-84. doi: 10.1177/000331978103200704.
4
Ionic mechanisms involved in the strontium-induced spike and plateau in the smooth muscle of rat portal vein.参与大鼠门静脉平滑肌中锶诱导的峰电位和平台电位的离子机制。
J Physiol. 1983 Mar;336:199-210. doi: 10.1113/jphysiol.1983.sp014576.
5
Agonist actions of Bay K 8644, a dihydropyridine derivative, on the voltage-dependent calcium influx in smooth muscle cells of the rabbit mesenteric artery.二氢吡啶衍生物 Bay K 8644 对兔肠系膜动脉平滑肌细胞电压依赖性钙内流的激动剂作用。
J Pharmacol Exp Ther. 1984 Dec;231(3):717-23.
6
Novel dihydropyridines with positive inotropic action through activation of Ca2+ channels.通过激活Ca2+通道具有正性肌力作用的新型二氢吡啶类化合物。
Nature. 1983;303(5917):535-7. doi: 10.1038/303535a0.
7
Influence of the ionic environment on spontaneous electrical and mechanical activity of the rat portal vein.离子环境对大鼠门静脉自发电活动和机械活动的影响。
Circ Res. 1967 Nov;21(5):609-18. doi: 10.1161/01.res.21.5.609.
8
Membrane potential and contraction of vascular smooth muscle (portal vein) during application of noradrenaline and high potassium, and selective inhibitory effects of iproveratril (verapamil).去甲肾上腺素和高钾作用期间血管平滑肌(门静脉)的膜电位与收缩,以及维拉帕米的选择性抑制作用
Microvasc Res. 1973 Jan;5(1):73-80. doi: 10.1016/s0026-2862(73)80007-x.
9
Effects of sodium vanadate on the smooth muscle of the rat portal vein.钒酸钠对大鼠门静脉平滑肌的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Mar;337(3):347-53. doi: 10.1007/BF00168849.
10
Effects of the Ca agonists Bay K 8644 and CGP 28392 on vascular smooth muscle tone.钙激动剂Bay K 8644和CGP 28392对血管平滑肌张力的影响。
Gen Pharmacol. 1989;20(6):827-31. doi: 10.1016/0306-3623(89)90338-8.