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突触后α2肾上腺素能受体介导对2-N,N-二甲基氨基-5,6-二羟基-1,2,3,4-四氢萘(M-7)的升压反应。

Postsynaptic alpha 2-adrenoceptors mediate pressor responses to 2-N,N-dimethylamino-5,6-dihydroxy-1,2,3,4-tetrahydronaphthalene (M-7).

作者信息

Drew G M

出版信息

Eur J Pharmacol. 1980 Jul 11;65(1):85-7. doi: 10.1016/0014-2999(80)90212-5.

Abstract

M-7 (2-N,N-dimethylamino-5,6-dihydroxy-1,2,3,4-tetrahydronaphthalene) is a potent agonist at presynaptic alpha 2-adrenoceptors in the pithed rat heart, it is also a potent vasopressor agent. The pressor effects of M-7 were unaffected by prazosin in doses much higher than were required to antagonise the pressor effects of phenylephrine, but were antagonised by yohimbine in doses lower than were effective against phenylephrine. The results suggest that the pressor responses to M-7 are mediated via postsynaptic alpha 2-adrenoceptors.

摘要

M-7(2-N,N-二甲基氨基-5,6-二羟基-1,2,3,4-四氢萘)是去脑大鼠心脏中突触前α2肾上腺素能受体的强效激动剂,也是一种强效升压剂。M-7的升压作用不受比拮抗去氧肾上腺素升压作用所需剂量高得多的哌唑嗪的影响,但可被低于对抗去氧肾上腺素有效剂量的育亨宾所拮抗。结果表明,对M-7的升压反应是通过突触后α2肾上腺素能受体介导的。

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