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哌唑嗪、酚妥拉明和酚苄明对豚鼠离体回肠中抑制性α-肾上腺素能受体的作用。

The effects of prazosin, phentolamine and phenoxybenzamine on inhibitory alpha-adrenoceptors in the guniea-pig isolated ileum.

作者信息

Fagbemi S O, Salako L A

出版信息

Br J Pharmacol. 1982 Jun;76(2):235-43. doi: 10.1111/j.1476-5381.1982.tb09212.x.

Abstract

1 The relaxant effect of noradrenaline on strips of guinea-pig isolated terminal ileum was blocked by pretreatment with prazosin, phentolamine, yohimbine and phenoxybenzamine. 2 The presence of a very high concentration of noradrenaline (50 micrometers) during exposure to the blocking agent protected against the blocking effect of the drugs. 3 Yohimbine, prazosin and phentolamine partially protected against irreversible blockade by phenoxybenzamine. 4 Spontaneous release of acetylcholine in the unstimulated ileum was blocked by noradrenaline (0.05-5.9 micrometers) this effect of noradrenaline was antagonized by phentolamine (0.13-26 micrometers) and yohimbine (0.051-0.51 micrometers) but not prazosin (0.53-5.3 micrometers) or phenoxybenzamine (4.2-42 nm). All four antagonists reversed the noradrenaline-induced relaxation of the ileum. 5 Acetylcholine output in the transmurally stimulated ileum was inhibited by noradrenaline. This effect of noradrenaline was antagonized by phentolamine and yohimbine but not by prazosin or phenoxybenzamine. The first two antagonists blocked the noradrenaline-induced inhibition of evoked twitches of the ileum while the last two had no effect. 6 The results show (a) that prazosin has no effect on presynaptic alpha-adrenoceptor located on cholinergic nerve endings in the guinea-pig ileum and (b) that prazosin, phentolamine and phenoxybenzamine act on the same subgroup of postsynaptic alpha-adrenoceptors on the smooth muscle of the guniea-pig ileum.

摘要

1 用哌唑嗪、酚妥拉明、育亨宾和酚苄明预处理可阻断去甲肾上腺素对豚鼠离体终末回肠条的松弛作用。2 在暴露于阻断剂期间存在非常高浓度的去甲肾上腺素(50微摩尔)可防止药物的阻断作用。3 育亨宾、哌唑嗪和酚妥拉明可部分防止酚苄明引起的不可逆阻断。4 去甲肾上腺素(0.05 - 5.9微摩尔)可阻断未受刺激的回肠中乙酰胆碱的自发释放,酚妥拉明(0.13 - 26微摩尔)和育亨宾(0.051 - 0.51微摩尔)可拮抗去甲肾上腺素的这种作用,但哌唑嗪(0.53 - 5.3微摩尔)或酚苄明(4.2 - 42纳米)则不能。所有四种拮抗剂均可逆转去甲肾上腺素引起的回肠松弛。5 去甲肾上腺素可抑制经壁刺激的回肠中乙酰胆碱的释放。酚妥拉明和育亨宾可拮抗去甲肾上腺素的这种作用,但哌唑嗪或酚苄明则不能。前两种拮抗剂可阻断去甲肾上腺素引起的回肠诱发抽搐的抑制作用,而后两种则无此作用。6 结果表明:(a)哌唑嗪对豚鼠回肠胆碱能神经末梢上的突触前α - 肾上腺素能受体无作用;(b)哌唑嗪、酚妥拉明和酚苄明作用于豚鼠回肠平滑肌上同一亚组的突触后α - 肾上腺素能受体。

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The effect of prazosin on the guinea-pig ileum.哌唑嗪对豚鼠回肠的作用。
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本文引用的文献

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The effect of prazosin on the guinea-pig ileum.哌唑嗪对豚鼠回肠的作用。
Br J Pharmacol. 1980 Nov;70(3):395-402. doi: 10.1111/j.1476-5381.1980.tb08715.x.
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Cardiovascular effects of prazosin in dogs.
Clin Sci Mol Med Suppl. 1976 Dec;3:609s-612s. doi: 10.1042/cs051609s.

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