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钾离子去极化后钙通道阻滞剂对体外血管平滑肌收缩的抑制活性与α2肾上腺素能受体刺激后体内抑制活性之间的相关性。

Correlation between the inhibitory activities of calcium entry blockers on vascular smooth muscle constriction in vitro after K+-depolarisation and in vivo after alpha 2-adrenoceptor stimulation.

作者信息

van Meel J C, Towart R, Kazda S, Timmermans P B, van Zwieten P A

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1983 Feb;322(1):34-7. doi: 10.1007/BF00649349.

Abstract

Calcium entry blockers are known to depress the maximal increase in diastolic pressure induced in pithed rats by selective alpha 2-adrenoceptor stimulation. In order to substantiate the relevance of calcium fluxes in this interaction, a correlation between the potency of calcium entry blockers in pithed rats and their calcium antagonistic potency in vitro was investigated. Accordingly, the inhibition of calcium entry blockers with respect to alpha 2-adrenoceptor-mediated vasoconstriction was quantified in terms of -log ID50 values. As a measure of calcium antagonistic potency, the inhibitory activity of a number of calcium entry blockers on K+-induced contractions of rabbit thoracic aorta strips was determined and the negative logarithms of the 50% inhibitory concentrations, -log IC50, were calculated. A highly significant linear relationship was found between the in vitro, -log IC50, and the in vivo parameter, -log ID50, of the calcium entry blockers. This result suggests a similar type of interaction for the calcium entry blockers in vivo and in vitro, i.e. inhibition of a transmembrane influx of extracellular calcium.

摘要

已知钙通道阻滞剂可抑制选择性α2 -肾上腺素能受体刺激引起的脊髓麻醉大鼠舒张压的最大升高。为了证实钙通量在这种相互作用中的相关性,研究了钙通道阻滞剂在脊髓麻醉大鼠中的效力与其体外钙拮抗效力之间的相关性。因此,根据-log ID50值对钙通道阻滞剂对α2 -肾上腺素能受体介导的血管收缩的抑制作用进行了量化。作为钙拮抗效力的指标,测定了多种钙通道阻滞剂对兔胸主动脉条K +诱导收缩的抑制活性,并计算了50%抑制浓度的负对数-log IC50。发现钙通道阻滞剂的体外-log IC50与体内参数-log ID50之间存在高度显著的线性关系。该结果表明钙通道阻滞剂在体内和体外具有相似类型的相互作用,即抑制细胞外钙的跨膜内流。

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