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WB - 4101和哌唑嗪对豚鼠乳头肌的直接变力作用。与ATP敏感性钾通道新激活剂HOE - 234的比较。

Direct inotropic action of WB-4101 and prazosin in the guinea pig papillary muscle. Comparison with HOE-234, the new activator of ATP-sensitive K+ channels.

作者信息

Kocić I

机构信息

Department of Pharmacology, School of Medicine, Gdańsk, Poland.

出版信息

Gen Pharmacol. 1994 Oct;25(6):1191-5. doi: 10.1016/0306-3623(94)90137-6.

Abstract
  1. The alpha-1a adrenoceptor antagonist WB-4101, the alpha-1 adrenoceptor antagonist prazosin and the new activator of ATP-sensitive K+ channels HOE-234 were examined. The force of contraction and the rate of rise of contraction force were measured. 2. WB-4101 and HOE-234 were found to produce negative inotropic action in a dose dependent manner. This effect was attenuated by glibenclamide. On the other hand prazosin increased slightly the force of contraction and the rate of rise of contraction force in the same tissue. 3. The direct inotropic effects of above mentioned substances are compared and discussed.
摘要
  1. 对α-1a肾上腺素能受体拮抗剂WB-4101、α-1肾上腺素能受体拮抗剂哌唑嗪以及ATP敏感性钾通道的新型激活剂HOE-234进行了研究。测量了收缩力和收缩力上升速率。2. 发现WB-4101和HOE-234以剂量依赖性方式产生负性肌力作用。该效应被格列本脲减弱。另一方面,哌唑嗪使同一组织中的收缩力和收缩力上升速率略有增加。3. 比较并讨论了上述物质的直接肌力作用。

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