Rotenberg F A, Verrier R L, Lown B, Sole M J
Eur J Pharmacol. 1978 Jan 1;47(1):71-9. doi: 10.1016/0014-2999(78)90376-x.
Clonidine infusion (10 microgram/kg, i.v.) elicited a 30% increase in repetitive extrasystole (RE) threshold in 6 chloralose-anesthetized dogs. A reduction in heart rate and arterial blood pressure accompanied the increased threshold. Intracisternal injection of clonidine (2 microgram/kg) in 6 dogs caused similar alterations in these parameters. Bilateral vagotomy, performed in 6 dogs prior to intravenous clonidine, prevented the increase in RE threshold but did not prevent the drug-induced bradycardia. Atropine (0.2 and 0.6 mg/kg), however, did not attenuate the effect of clonidine on RE threshold. Clonidine administration did not prevent the reduction in ventricular fibrillation threshold associated with a 10 min occlusion of the left anterior descending coronary artery or following reperfusion. We conclude that: (1) clonidine reduces ventricular vulnerability in the normal but not the ischemic heart, and (2) its protective effect is mediated by enhanced afferent vagal input to midbrain cardiovascular regulatory centers. This central nervous system action causes a reduction in sympathetic tone to the heart.
在6只氯醛糖麻醉的犬中,静脉输注可乐定(10微克/千克)使重复性期外收缩(RE)阈值升高30%。阈值升高的同时伴有心率和动脉血压降低。在6只犬中脑池内注射可乐定(2微克/千克)导致这些参数出现类似变化。在静脉注射可乐定之前,对6只犬实施双侧迷走神经切断术可防止RE阈值升高,但不能防止药物引起的心动过缓。然而,阿托品(0.2和0.6毫克/千克)并未减弱可乐定对RE阈值的作用。给予可乐定不能防止与左前降支冠状动脉闭塞10分钟或再灌注后相关的心室颤动阈值降低。我们得出结论:(1)可乐定降低正常心脏而非缺血心脏的心室易损性,(2)其保护作用是通过增强迷走神经向中脑心血管调节中枢的传入输入介导的。这种中枢神经系统作用导致心脏交感神经张力降低。