Finberg J P, Kopin I J
Eur J Pharmacol. 1987 Jun 12;138(1):95-100. doi: 10.1016/0014-2999(87)90342-6.
Rats were treated chronically with clonidine by osmotic minipump (500 micrograms/kg daily for 14 days). One day after the end of the infusion period, the animals were pithed, and alpha 2-presynaptic and -postsynaptic adrenoceptor responses evaluated using inhibition of cardioaccelerator response to sympathetic stimulation by guanabenz, and pressor response to guanabenz respectively. Chronic clonidine treatment had no effect on the presynaptic effect of guanabenz, but the postsynaptic response to this agonist was decreased. In a separate group of pithed rats treated chronically with clonidine, there was no alteration in the increment in plasma noradrenaline concentration produced by sympathetic stimulation, and no alteration in the yohimbine-induced enhancement of plasma noradrenaline response to sympathetic stimulation. These data argue against desensitisation of peripheral presynaptic alpha 2-adrenoceptors by chronic administration of alpha 2-adrenoceptor agonist. Sympathetic hyperactivity following withdrawal of chronic clonidine treatment may be mediated by down-regulation of postsynaptic alpha 2-adrenoceptors in the CNS.
通过渗透微型泵对大鼠进行可乐定长期治疗(每日500微克/千克,持续14天)。输注期结束后一天,将动物处死,分别使用胍那苄抑制交感神经刺激引起的心脏加速反应以及胍那苄的升压反应来评估α2突触前和突触后肾上腺素能受体反应。可乐定长期治疗对胍那苄的突触前效应无影响,但对该激动剂的突触后反应降低。在另一组长期接受可乐定治疗的处死大鼠中,交感神经刺激引起的血浆去甲肾上腺素浓度增量没有改变,育亨宾诱导的血浆去甲肾上腺素对交感神经刺激反应增强也没有改变。这些数据表明,长期给予α2肾上腺素能受体激动剂不会使外周突触前α2肾上腺素能受体脱敏。长期可乐定治疗停药后的交感神经过度活跃可能是由中枢神经系统中突触后α2肾上腺素能受体的下调介导的。