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用吲哚美辛预处理可调节选择性腺苷受体激动剂对豚鼠心脏收缩性和有效不应期的影响。

Pretreatment with indomethacin modulates the effects of selective adenosine receptor agonists on the contractility and effective refractory period in the guinea pig heart.

作者信息

Kocić I

机构信息

Department of Pharmacology, Medical University of Gdańsk, Poland.

出版信息

Acta Physiol Hung. 1996;84(4):421-3.

PMID:9328620
Abstract

The effects of selective adenosine receptor agonists N6-Cyclohexyladenosine (CHA, A1-agonist) and 5'-(N-ethylcarboxamido)-adenosine (NECA, A2-agonist) on the force of contraction (Fc) and effective refractory period (ERP) of isolated guinea pig papillary muscle were measured. Additionally, the influence of potent cycloxygenase inhibitor indomethacin on above mentioned parameters as well as on the effects of CHA and NECA were studied. It was found that CHA induced negative inotropic action and a shortening of ERP, opposite to NECA and indomethacin. The pretreatment with 10 microM of indomethacin shifted to the right the CHA effects and abolished the NECA effects.

摘要

测定了选择性腺苷受体激动剂N6-环己基腺苷(CHA,A1激动剂)和5'-(N-乙基甲酰胺基)腺苷(NECA,A2激动剂)对离体豚鼠乳头肌收缩力(Fc)和有效不应期(ERP)的影响。此外,还研究了强效环氧化酶抑制剂吲哚美辛对上述参数以及CHA和NECA作用的影响。结果发现,与NECA和吲哚美辛相反,CHA可诱导负性肌力作用并缩短ERP。用10微摩尔的吲哚美辛预处理可使CHA的作用向右偏移,并消除NECA的作用。

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