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麻黄碱和甲基麻黄碱光学异构体对离体大鼠输精管抽搐反应的影响及α2-肾上腺素能受体的参与

Effects of optical isomers of ephedrine and methylephedrine on the twitch response in the isolated rat vas deferens and the involvement of alpha 2-adrenoceptors.

作者信息

Kawasuji T, Koike K, Saito H

机构信息

Toyama Prefectural Institute for Pharmaceutical Research, Japan.

出版信息

J Smooth Muscle Res. 1996 Aug;32(4):155-63. doi: 10.1540/jsmr.32.155.

Abstract

The effects of optical isomers of ephedrine (EPH) and methylephedrine (MEP) on the twitch response to electrical stimulation (1 msec, 1 Hz) in the isolated rat vas deferens were investigated to clarify the action on alpha 2-adrenoceptors. l-EPH (10(-7) 3 x 10(-5) M) and d-EPH (10(-6)-10(-4) M) markedly inhibited the twitch response in the presence of prazosin (10(-6) M). l-MEP also inhibited the twitch response at high concentrations (3 x 10(-5)-10(-3) M). The rank order of inhibitory potency was 1-EPH > d-EPH >> l-MEP. Yohimbine (3 x 10(-7) M), a selective alpha 2-adrenoceptor antagonist, attenuated the twitch-inhibitory effects of EPH isomers and l-MEP. Furthermore, the twitch-inhibitory effects of EPH isomers and l-MEP were attenuated by reserpine treatment (8 mg/kg, s.c.). On the other hand, d-MEP showed the potentiation of twitch response, and competitively antagonized the twitch-inhibitory effect of clonidine (10(-9)-10(-6) M) with the pA2 value of 4.3 in the presence of prazosin. The results suggest that EPH isomers and l-MEP have stimulating activity for presynaptic alpha 2-adrenoceptors. In addition, the twitch-inhibitory effect of EPH isomers and l-MEP may be at least partly mediated through the release of noradrenaline. It is also suggested that d-MEP has competitive alpha 2-adrenoceptor antagonist activity.

摘要

研究了麻黄碱(EPH)和甲基麻黄碱(MEP)的光学异构体对离体大鼠输精管电刺激(1毫秒,1赫兹)引起的抽搐反应的影响,以阐明其对α2肾上腺素能受体的作用。在存在哌唑嗪(10(-6) M)的情况下,左旋EPH(10(-7)-3×10(-5) M)和右旋EPH(10(-6)-10(-4) M)显著抑制抽搐反应。左旋MEP在高浓度(3×10(-5)-10(-3) M)时也抑制抽搐反应。抑制效力的顺序为:左旋EPH>右旋EPH>>左旋MEP。育亨宾(3×10(-7) M),一种选择性α2肾上腺素能受体拮抗剂,减弱了EPH异构体和左旋MEP的抽搐抑制作用。此外,利血平处理(8毫克/千克,皮下注射)减弱了EPH异构体和左旋MEP的抽搐抑制作用。另一方面,右旋MEP表现出抽搐反应增强,并在存在哌唑嗪的情况下竞争性拮抗可乐定(10(-9)-10(-6) M)的抽搐抑制作用,pA2值为4.3。结果表明,EPH异构体和左旋MEP对突触前α2肾上腺素能受体具有刺激活性。此外,EPH异构体和左旋MEP的抽搐抑制作用可能至少部分通过去甲肾上腺素的释放介导。还表明,右旋MEP具有竞争性α2肾上腺素能受体拮抗剂活性。

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