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章鱼胺异构体对大鼠血管平滑肌体外反应性的影响。

Effect of isomers of octopamine on in vitro reactivity of vascular smooth muscle of rats.

作者信息

Ress R J, Rahmani M A, Fregly M J, Field F P, Williams C M

出版信息

Pharmacology. 1980;21(5):342-7. doi: 10.1159/000137450.

Abstract

The vascular reactivity to DL-ortho-, meta-, and para-octopamine was tested in vitro in aortic smooth muscle of the rat. When reactivities were compared on a molar basis with L-phenylephrine, an alpha-adrenergic agonist, the potencies of the three isomers were: 0.7500, 0.0075 and 0.0038 times that of phenylephrine for the m-, p- and o-isomer, respectively, Thus, of the three isomers, DL-m-octopamine had the greatest alpha-adrenergic activity in vitro as it did in vivo in earlier studies. Additional studies showed L-phenylephrine to induce about one-third the vascular response induced by L-norepinephrine.

摘要

在大鼠主动脉平滑肌中对DL-邻、间、对去甲辛福林的血管反应性进行了体外测试。当将三种异构体与α-肾上腺素能激动剂L-去氧肾上腺素按摩尔基础比较反应性时,三种异构体的效价分别为:间位、对位和邻位异构体相对于去氧肾上腺素的效价分别为0.7500、0.0075和0.0038倍。因此,在这三种异构体中,DL-间去甲辛福林在体外具有最大的α-肾上腺素能活性,正如早期研究中其在体内的情况一样。额外的研究表明,L-去氧肾上腺素诱导的血管反应约为L-去甲肾上腺素诱导的血管反应的三分之一。

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