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α-肾上腺素能受体在清醒家兔血浆钾控制中的作用

Role of alpha-adrenoceptors in control of plasma potassium in conscious rabbits.

作者信息

Reverte M, García-Barrado M J, Moratinos J

机构信息

Department of Pharmacology, School of Medicine, University of Salamanca, Spain.

出版信息

J Auton Pharmacol. 1991 Oct;11(5):305-13. doi: 10.1111/j.1474-8673.1991.tb00254.x.

Abstract
  1. In conscious fed rabbits the intravenous infusion of amidephrine (10 micrograms kg-1 min-1), an alpha 1-adrenoceptor agonist, caused a significant increase in plasma potassium levels that was blunted by prazosin (50 micrograms kg-1, s.c.). Idazoxan failed to modify this response. 2. Clonidine (2 micrograms kg-1 min-1, i.v.), an alpha 2-adrenoceptor agonist, also evoked a hyperkalaemic response which was antagonized by idazoxan (1 microgram kg-1, s.c.), yohimbine (0.45 mg kg-1, s.c.) and prazosin (50 micrograms kg-1, s.c.). Apamin (40 micrograms kg-1, i.v. bolus) also suppressed the clonidine-mediated hyperkalaemia. 3. Verapamil (5 micrograms kg-1, s.c.) prevented both alpha 1- and alpha 2-adrenoceptor-mediated increase in plasma potassium levels. 4. It is concluded that in conscious fed rabbits both alpha 1- and alpha 2-adrenoceptor stimulation induce hyperkalaemia by activation of hepatic Ca(2+)-activated K(+)-channels.
摘要
  1. 在清醒食饵兔中,静脉输注α1肾上腺素能受体激动剂去氧肾上腺素(10微克/千克·分钟)可使血浆钾水平显著升高,而哌唑嗪(50微克/千克,皮下注射)可减弱此效应。育亨宾未能改变这种反应。2. α2肾上腺素能受体激动剂可乐定(2微克/千克·分钟,静脉注射)也引发高钾血症反应,该反应可被育亨宾(1微克/千克,皮下注射)、育亨宾(0.45毫克/千克,皮下注射)和哌唑嗪(50微克/千克,皮下注射)拮抗。蜂毒明肽(40微克/千克,静脉推注)也可抑制可乐定介导的高钾血症。3. 维拉帕米(5微克/千克,皮下注射)可防止α1和α2肾上腺素能受体介导的血浆钾水平升高。4. 得出结论:在清醒食饵兔中,α1和α2肾上腺素能受体刺激均通过激活肝脏钙激活钾通道诱导高钾血症。

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