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猫离体大脑后交通动脉中的药物诱导收缩反应。

Drug-induced contractile responses in the isolated posterior communicating cerebral artery of the cat.

作者信息

Marín J, Salaices M

出版信息

Rev Esp Fisiol. 1978 Dec;34(4):449-52.

PMID:741068
Abstract

The isolated posterior communicating cerebral artery of the cat has been shown to have the ability to produce a contractile response to the following drugs; norepinephrine (NE), tyramine (Ty), 5-hydroxytryptamine (5-HT), histamine (H), acetylcholine (Ach) and potassium (K+). The changes in the contractile response were dose-dependent. The order of potencies of these vasoactive agents with respect to ED50 was: 5-HT greater than NE greater than Ach = H = Ty greater than K+. With regard to their ability to induce maximal contractile responses the order was: H = Ach greater than 5-HT = Ty greater than NE = K+. These results show that cerebral arteries are more sensitive to 5-HT than to NE, as opposed to extracranial arteries in which NE is generally the most potent vasoconstrictor agent.

摘要

猫的孤立大脑后交通动脉已被证明能够对以下药物产生收缩反应

去甲肾上腺素(NE)、酪胺(Ty)、5-羟色胺(5-HT)、组胺(H)、乙酰胆碱(Ach)和钾(K+)。收缩反应的变化呈剂量依赖性。这些血管活性药物相对于半数有效剂量(ED50)的效力顺序为:5-HT>NE>Ach = H = Ty>K+。就其诱导最大收缩反应的能力而言,顺序为:H = Ach>5-HT = Ty>NE = K+。这些结果表明,脑动脉对5-HT的敏感性高于对NE的敏感性,这与颅外动脉相反,在颅外动脉中,NE通常是最有效的血管收缩剂。

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