Drug induced contraction and relaxation in mouse isolated aorta.

Artery Pub Date : 1997-01-01
K K Wong
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Abstract

Possibility of using mouse isolated aorta to evaluate the effect of vasoactive agents was demonstrated. The results suggested that aortic contraction induced by the alpha adrenoceptor agonist norepinephrine was sensitive to prazosin, and the contraction induced by the membrane depolarization agent KCl was sensitive to verapamil. Clonidine acting as a partial agonist attenuated the norepinephrine or methoxamine induced contraction. Both IBMX and nitroprusside relaxed the aortic contraction. These vascular changes induced by the above vasoactive agents in mouse isolated aorta were similar to those of rat described elsewhere. The present findings suggested that mouse isolated aorta can be used as a tool to test the effect of vasoactive agents.

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药物诱导小鼠离体主动脉收缩舒张。
证明了用小鼠离体主动脉评价血管活性药物作用的可能性。结果表明,肾上腺素受体激动剂去甲肾上腺素诱导的主动脉收缩对哌唑嗪敏感,而膜去极化剂KCl诱导的主动脉收缩对维拉帕米敏感。可乐定作为部分激动剂可减弱去甲肾上腺素或甲氧胺引起的收缩。IBMX和硝普塞均能缓解主动脉收缩。上述血管活性药物在小鼠离体主动脉中引起的血管变化与其他文献中描述的大鼠血管变化相似。本研究结果提示,小鼠离体主动脉可以作为检测血管活性药物作用的工具。
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