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Ro 5-4864和PK 11195,但地西泮不会,在离体工作大鼠心脏模型中会抑制心脏功能。

Ro 5-4864 and PK 11195, but not diazepam, depress cardiac function in an isolated working rat heart model.

作者信息

Edoute Y, Giris J, Ben-Haim S A, Lochner A, Weizman A, Hayam G, Katz Y, Gavish M

机构信息

Rappaport Family Institute for Research, Medical Sciences, Haifa, Israel.

出版信息

Pharmacology. 1993 Apr;46(4):224-30. doi: 10.1159/000139049.

Abstract

The present study was designed to investigate the effects of diazepam, a benzodiazepine (BZ) with high affinity to central BZ receptors and moderate affinity to mitochondrial BZ receptors, and of Ro 5-4864 and PK 11195, ligands specific for mitochondrial BZ receptors, on cardiac function in the isolated working rat heart model. Five concentrations of these drugs (10(-9)-10(-5) mol/l) were used, and the chronotropic (heart rate) and inotropic [maximum elastance of the left ventricle at end systole (Emax), maximal first derivative of left ventricular (LV) pressure (dP/dtmax), LV pressure at dP/dtmax (pressure at dP/dtmax), aortic flow, stroke work, and total pressure-volume area] cardiac parameters were measured. Diazepam, Ro 5-4864, and PK 11195 showed no significant chronotropic activity up to 10(-5) mol/l. Diazepam did not alter the inotropic properties of the heart. Ro 5-4864 at 10(-5) mol/l significantly decreased the indices of contractility, namely, Emax, dP/dtmax, and pressure at dP/dtmax. Aortic flow, stroke work, and total pressure-volume area were significantly depressed at the same concentration. The negative inotropism of PK 11195 appeared to be identical, by most indices, to that of Ro 5-4864, both qualitatively (same pattern) and quantitatively (similar maximal variations); however, for some indices a depressant effect was also found at 10(-7) mol/l. These results show that at high concentrations Ro 5-4864 and PK 11195, but not diazepam, have a depressant effect on mechanical function.

摘要

本研究旨在探讨地西泮(一种对中枢苯二氮䓬(BZ)受体具有高亲和力且对线粒体BZ受体具有中等亲和力的苯二氮䓬类药物)以及线粒体BZ受体特异性配体Ro 5-4864和PK 11195对离体工作大鼠心脏模型心功能的影响。使用了这三种药物的五种浓度(10(-9)-10(-5) mol/l),并测量了变时性(心率)和变力性[收缩末期左心室最大弹性(Emax)、左心室(LV)压力的最大一阶导数(dP/dtmax)、dP/dtmax时的LV压力(dP/dtmax时的压力)、主动脉流量、搏功和总压力-容积面积]心脏参数。地西泮、Ro 5-4864和PK 11195在浓度高达10(-5) mol/l时均未表现出明显的变时活性。地西泮未改变心脏的变力特性。10(-5) mol/l的Ro 5-4864显著降低了收缩性指标,即Emax、dP/dtmax和dP/dtmax时的压力。在相同浓度下,主动脉流量、搏功和总压力-容积面积均显著降低。PK 11195的负性变力作用在大多数指标上似乎与Ro 5-4864相同,在定性(相同模式)和定量(相似的最大变化)方面均如此;然而,对于某些指标,在10(-7) mol/l时也发现了抑制作用。这些结果表明,高浓度时Ro 5-4864和PK 11195对机械功能有抑制作用,而地西泮则没有。

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