Eriksson L, Tuomisto L
Acta Pharmacol Toxicol (Copenh). 1983 Apr;52(4):241-5. doi: 10.1111/j.1600-0773.1983.tb01094.x.
The possible involvement of opioid receptors in the effects of clonidine was studied in conscious, normotensive goats. Clonidine was infused intravenously followed by an intravenous injection of naloxone. Blood pressure was recorded through an intraarterial catheter. All doses of clonidine (0.2-7 micrograms/kg) significantly lowered blood pressure and decreased heart rate. Hypotension after 0.2-0.7 micrograms/kg of clonidine was significantly reduced by naloxone (1 mg/kg), while naloxone did not antagonize hypotension induced by the larger doses of clonidine. The bradycardiac effect of 0.7-2 micrograms/kg of clonidine was reduced by naloxone while that of 0.2 and 7 micrograms/kg was not. Clonidine also induced sedation and respiratory irregularity, but these changes were not modified by naloxone. Opioid mechanisms possibly participate in the hypotensive action of clonidine, but less in the normotensive animal than in spontaneously hypertensive animals.
在清醒的正常血压山羊中研究了阿片受体在可乐定作用中的可能参与情况。静脉注射可乐定,随后静脉注射纳洛酮。通过动脉内导管记录血压。所有剂量的可乐定(0.2 - 7微克/千克)均显著降低血压并减慢心率。纳洛酮(1毫克/千克)可显著减轻0.2 - 0.7微克/千克可乐定引起的低血压,而纳洛酮不能拮抗较大剂量可乐定引起的低血压。纳洛酮可减轻0.7 - 2微克/千克可乐定的心动过缓作用,而对0.2和7微克/千克可乐定引起的心动过缓无影响。可乐定还可引起镇静和呼吸不规则,但这些变化不受纳洛酮影响。阿片机制可能参与可乐定的降压作用,但在正常血压动物中比在自发性高血压动物中参与程度小。