Weinstock M, Zavadil A P, Kopin I J
Eur J Pharmacol. 1979 Nov 16;59(3-4):187-93. doi: 10.1016/0014-2999(79)90281-4.
The effects of l-propranolol, d-propranolol and clonidine on homovanillic acid (HVA) concentrations in the corpus striatum and nucleus accumbens of rats were studied under normal conditions and after treatment with oxotremorine or haloperidol. Thile propranolol and clonidine given alone had no significant effect on HVA levels in either area, l-propranolol (1--10 mg/kg) and clonidine (0.1 mg/kg), both significantly inhibited the elevation of striatal HVA, found 60 min after oxotremorine administration. Both l- and d-propranolol (2.5 mg/kg), reduced the effect of oxotremorine in the nucleus accumbens. Neither l-propranolol no clonidine affected the rise in HVA in either brain area seen after haloperidol. Our results suggest that propranolol may reduce cholinergic activation of dopaminergic pathways by two different mechanisms. One is stereospecific for the l-isomer and operates in the striatum and another, which is shared by both isomers, occurs in the nucleus accumbens.
在正常条件下以及用毒蕈碱或氟哌啶醇处理后,研究了左旋普萘洛尔、右旋普萘洛尔和可乐定对大鼠纹状体和伏隔核中高香草酸(HVA)浓度的影响。单独给予普萘洛尔和可乐定对这两个区域的HVA水平均无显著影响,但左旋普萘洛尔(1 - 10毫克/千克)和可乐定(0.1毫克/千克)均能显著抑制毒蕈碱给药60分钟后纹状体HVA的升高。左旋和右旋普萘洛尔(2.5毫克/千克)均能降低毒蕈碱对伏隔核的作用。左旋普萘洛尔和可乐定均未影响氟哌啶醇处理后任一脑区HVA的升高。我们的结果表明,普萘洛尔可能通过两种不同机制降低多巴胺能通路的胆碱能激活。一种对左旋异构体具有立体特异性,作用于纹状体,另一种为两种异构体所共有,发生在伏隔核。