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一种新型2-哌嗪基四氢萘对离体大鼠输精管α-1和α-2肾上腺素能受体的作用。

Effects of a new 2-piperazinotetralin on alpha-1 and alpha-2 adrenergic receptors in isolated rat vas deferens.

作者信息

Mutafova-Yambolieva V, Staneva-Stoytcheva D, Ivanov D

出版信息

Methods Find Exp Clin Pharmacol. 1985 Jun;7(6):291-6.

PMID:2997557
Abstract

The pharmacological action of a newly synthesized piperazine derivative of 2-aminotetralin (P11) on pre- and postsynaptic alpha-adrenoceptors of isolated rat vas deferens has been investigated. P11 shifted noradrenaline concentration-effect curves to the right. The pA2 value was 5.88 for P11, 5.38 for phentolamine, and 7.73 for prazosin. The maximum effect of the agonist was enhanced by P11 and phentolamine, but this enhancement was less pronounced in the presence of 1 X 10(-5) M cocaine and 1 X 10(-6) M propranolol. 1 X 10(-6) M to 1 X 10(-5) M P11 increased the contractions of a field-stimulated vas deferens and antagonized the effects of clonidine (1 X 10(-9) M on the same preparation. The IC50 values of P11, phentolamine and prazosin were 0.40 microM, 0.03 microM and greater than 10.0 microM, respectively. The results show that P11 possesses alpha 1-and alpha 2-adrenolytic activity. The effect of P11 on these receptors most likely participates in the mechanisms of its hypotensive action.

摘要

研究了新合成的2-氨基四氢萘哌嗪衍生物(P11)对离体大鼠输精管突触前和突触后α-肾上腺素能受体的药理作用。P11使去甲肾上腺素浓度-效应曲线右移。P11的pA2值为5.88,酚妥拉明为5.38,哌唑嗪为7.73。P11和酚妥拉明增强了激动剂的最大效应,但在存在1×10⁻⁵M可卡因和1×10⁻⁶M普萘洛尔时,这种增强作用不太明显。1×10⁻⁶M至1×10⁻⁵M的P11增加了场刺激输精管的收缩,并拮抗了可乐定(1×10⁻⁹M)对同一制剂的作用。P11、酚妥拉明和哌唑嗪的IC50值分别为0.40μM、0.03μM和大于10.0μM。结果表明,P11具有α1和α2肾上腺素能阻断活性。P11对这些受体的作用很可能参与了其降压作用机制。

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