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(-)-S-贝前列素K 8644、(±)-贝前列素W 5035和(±)-贝前列素T 5006对离体大鼠心脏血流动力学及异硫氰酸荧光素-葡聚糖3洗脱动力学的影响。

Influence of (-)-S-Bay K 8644, (+/-)-Bay W 5035 and (+/-)-Bay T 5006 on hemodynamics and FITC-dextran 3 elution kinetics in isolated rat hearts.

作者信息

Rump A F, Ratke R, Fricke U, Klaus W

机构信息

Institut für Pharmakologie, Universität Köln, Germany.

出版信息

Gen Pharmacol. 1993 May;24(3):631-6. doi: 10.1016/0306-3623(93)90222-j.

DOI:10.1016/0306-3623(93)90222-j
PMID:7689998
Abstract
  1. We investigated the effects of the new calcium-agonists (+/-)-Bay W 5035 and (+/-)-Bay T 5006 in comparison to (-)-S-Bay K 8644 on hemodynamics and epimyocardial perfusion in Langendorff rat hearts. 2. At equieffective inotropic concentration, vasoconstriction of coronary resistance vessels was significantly less after (+/-)-Bay W 5035 or (+/-)-Bay T 5006 than after (-)-S-Bay K 8644 application. 3. FITC-Dextran 3 elution kinetics indicated that the epimyocardial vascular volume was significantly reduced only by (-)-S-Bay K 8644. 4. Moreover, (-)-S-Bay K 8644 enhanced transcoronary exchange more markedly than (+/-)-Bay W 5035 or (+/-)-Bay T 5006, reflecting the differences in coronary constrictor activity. 5. We conclude that in comparison to (-)-S-Bay K 8644 the relation between inotropy and vasoconstriction is more favorable for (+/-)-Bay W 5035 or (+/-)-Bay T 5006.
摘要
  1. 我们研究了新型钙激动剂(±)-Bay W 5035和(±)-Bay T 5006与(-)-S-Bay K 8644相比,对Langendorff大鼠心脏血流动力学和心外膜灌注的影响。2. 在等效应性肌力浓度下,(±)-Bay W 5035或(±)-Bay T 5006应用后冠状动脉阻力血管的血管收缩明显小于(-)-S-Bay K 8644应用后。3. FITC-葡聚糖3洗脱动力学表明,仅(-)-S-Bay K 8644可使心外膜血管容积显著降低。4. 此外,(-)-S-Bay K 8644比(±)-Bay W 5035或(±)-Bay T 5006更显著地增强了跨冠状动脉交换,反映了冠状动脉收缩活性的差异。5. 我们得出结论,与(-)-S-Bay K 8644相比,(±)-Bay W 5035或(±)-Bay T 5006在肌力作用和血管收缩之间的关系更为有利。

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Influence of (-)-S-Bay K 8644, (+/-)-Bay W 5035 and (+/-)-Bay T 5006 on hemodynamics and FITC-dextran 3 elution kinetics in isolated rat hearts.(-)-S-贝前列素K 8644、(±)-贝前列素W 5035和(±)-贝前列素T 5006对离体大鼠心脏血流动力学及异硫氰酸荧光素-葡聚糖3洗脱动力学的影响。
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