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Effects of cyclopiazonic acid and thapsigargin on electromechanical activities and intracellular Ca~(2+) in smooth muscle of carotid artery of hypertensive rats

机译:环吡嗪酸和毒胡萝卜素对高血压大鼠颈动脉平滑肌机电活动和细胞内Ca〜(2+)的影响

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摘要

1. The effects of cyclopiazonic acid (CPA) and thapsigargin (TG), both of which are known to inhibit sarcoplasmic reticular Ca~(2+)-ATPase, on the mechanical activities, intracellular Ca~(2+) level and electrical activities of smooth muscle of the carotid artery of stroke-prone spontaneously hypertensive rats (SHRSP) and Wistar Kyoto rats (WKY) were compared. 2. Both CPA and TG induced elevation of tension of the smooth muscle, which was composed of a phasic and a tonic component. The level of tension attained, especially the tonic component, was greater in the preparation from SHRSP. 3. The elevation of tension was associated with an increased intracellular Ca~(2+) level. Both the elevation of tension and the increase in intracellular Ca~(2+) were diminished by the removal of extracellular Ca~(2+) or by the application of verapamil. 4. The resting membrane potential of the preparations from SHRSP were depolarized to a greater extent than those from WKY. CPA depolarized the smooth muscle from both SHRSP and WKY, and the final level was also more depolarized in the preparation from SHRSP. 5. These results indicate that the elevation of tension induced by these drugs is mainly due to increased Ca~(2+) influx through voltage-dependent Ca~(2+) channels, and the difference in the action between the preparation from SHRSP and that from WKY can be explained mainly by the changes in the channels. 6. Thus, differences in the action of these drugs on the tension of smooth muscle between preparations from WKY and SHRSP can mainly be explained by the difference in the membrane potential which is related to the difference in voltage-dependent Ca~(2+) influx.
机译:1.已知都可以抑制肌浆状网状Ca〜(2 +)-ATPase的环吡嗪酸(CPA)和毒胡萝卜素(TG)对机械活性,细胞内Ca〜(2+)水平和电活动的影响比较易发性自发性高血压大鼠(SHRSP)和Wistar Kyoto大鼠(WKY)颈动脉平滑肌的运动状态。 2. CPA和TG均可引起平滑肌张力的升高,平滑肌张力由相和张力成分组成。从SHRSP制备中获得的紧张程度,尤其是滋补成分更大。 3.张力升高与细胞内Ca〜(2+)水平升高有关。通过去除细胞外Ca〜(2+)或使用维拉帕米,可以降低张力的升高和细胞内Ca〜(2+)的增加。 4. SHRSP制剂的静息膜电位比WKY制剂的去极化程度更大。 CPA使SHRSP和WKY的平滑肌去极化,而从SHRSP制备的最终水平也更加去极化。 5.这些结果表明,这些药物引起的张力升高主要归因于通过电压依赖性Ca〜(2+)通道的Ca〜(2+)流入增加,以及SHRSP制剂与SHRSP制剂之间的作用差异。 WKY的观点主要可以通过渠道的变化来解释。 6.因此,WKY和SHRSP制剂之间这些药物对平滑肌张力的作用差异主要可以通过与电位依赖性Ca〜(2+)的差异有关的膜电位差异来解释。涌入。

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