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可乐定与α-肾上腺素能受体阻断药对犬心脏神经刺激所致心动过速反应的相互作用。

Interactions between clonidine and alpha-adrenoceptor blocking drugs on the tachycardic response to stimulation of the cardiac nerve in dogs.

作者信息

Mouillé P, Huchet A M, Lucet B, Chelly J, Schmitt H

出版信息

J Cardiovasc Pharmacol. 1979 Sep-Oct;1(5):515-28. doi: 10.1097/00005344-197909000-00004.

Abstract

In pentobarbital-treated dogs clonidine (10 micrograms/kg) reduced the increase in heart rate caused by electrical stimulation of the cardiac nerve (1-10 Hz). We studied the actions of six alpha-adrenoceptor blocking drugs. Yohimbine (0.3 mg/kg) and phentolamine (1 mg/kg) potentiated the effects of nerve stimulation and antagonized the inhibitory effects of clonidine. Piperoxan (1 mg/kg) increased the response to nerve stimulation but antagonized the effects of clonidine only at the lowest frequency of stimulation. Thymoxamine (1 mg/kg) and prazosin at high doses (1 mg/kg) also antagonized the effects of clonidine but failed to increase the positive chronotropic response to stimulation of the cardiac nerve. AR-C239, a new and potent alpha-adrenoceptor blocking agent, changed neither the response to nerve stimulation nor the inhibitory effect of clonidine. The effects of all these drugs were observed at doses which reduced or reversed the pressor response to adrenaline. Therefore, our results afford further evidence for a dissimilarity between postsynaptic and presynaptic alpha-adrenoceptors in the dog. In addition, they show that the failure of an alpha-adrenoceptor blocking compound to increase the response to nerve stimulation does not necessarily indicate a lack of presynaptic alpha-adrenoceptor blockade.

摘要

在戊巴比妥处理的犬中,可乐定(10微克/千克)可降低电刺激心脏神经(1 - 10赫兹)所引起的心率增加。我们研究了六种α-肾上腺素能受体阻断药物的作用。育亨宾(0.3毫克/千克)和酚妥拉明(1毫克/千克)增强了神经刺激的作用,并拮抗了可乐定的抑制作用。哌罗克生(1毫克/千克)增加了对神经刺激的反应,但仅在最低刺激频率下拮抗可乐定的作用。噻吗洛尔(1毫克/千克)和高剂量(1毫克/千克)的哌唑嗪也拮抗了可乐定的作用,但未能增加对心脏神经刺激的正性变时反应。新型强效α-肾上腺素能受体阻断剂AR-C239既未改变对神经刺激的反应,也未改变可乐定的抑制作用。所有这些药物的作用均在降低或逆转对肾上腺素的升压反应的剂量下观察到。因此,我们的结果为犬突触后和突触前α-肾上腺素能受体之间的差异提供了进一步的证据。此外,它们表明α-肾上腺素能受体阻断化合物未能增加对神经刺激的反应并不一定表明缺乏突触前α-肾上腺素能受体阻断。

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