Zarrindast Mohammed-Reza, Sahebgharani Mousa
Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Pharmacology. 2002 Apr;64(4):201-7. doi: 10.1159/000056172.
In this study, the effect of central administration of the alpha-adrenoceptor agents on the antinociception induced by imipramine in the formalin test has been investigated. Intraperitoneal (IP) administration of different doses of imipramine (10-80 mg/kg) and intracerebroventricular (ICV) administration of the alpha(2)-adrenoceptor agonist clonidine (0.05-0.8 microg/rat) elicited a dose-dependent antinociception in the both phases of the test. Furthermore, different doses of clonidine (0.05-0.2 microg/rat) increased the antinociception induced by imipramine (10 and 20 mg/kg). The alpha(2)-adrenoceptor antagonist yohimbine (2 microg/rat, ICV) reduced the response of a low dose imipramine (10 mg/kg, IP) plus different doses of clonidine (0.05, 0.1 and 0.2 microg/rat, ICV), but did not alter the response induced by higher doses of imipramine (20 and 40 mg/kg) alone or in combination with clonidine. Yohimbine by itself elicited no effect. The alpha(1)-adrenoceptor agonist phenylephrine (0.07-1.5 microg/rat) induced antinociception in both phases of the formalin test, but did not alter the imipramine-induced antinociception. The alpha(1)-adrenoceptor antagonist prazosin neither elicited antinociception nor altered the imipramine response. Yohimbine (2 microg/ rat, ICV) in combination with prazosin (0.5 microg/rat, ICV) caused more inhibition of the response of imipramine or imipramine plus clonidine. Therefore, it is concluded that alpha(2)-adrenoceptor mechanism may be involved in the imipramine-induced antinociception.
在本研究中,已对中枢给予α-肾上腺素能受体药物对丙咪嗪在福尔马林试验中诱导的抗伤害感受作用进行了研究。腹腔注射(IP)不同剂量的丙咪嗪(10 - 80毫克/千克)以及脑室内(ICV)注射α₂-肾上腺素能受体激动剂可乐定(0.05 - 0.8微克/大鼠)在试验的两个阶段均引发了剂量依赖性的抗伤害感受作用。此外,不同剂量的可乐定(0.05 - 0.2微克/大鼠)增强了丙咪嗪(10和20毫克/千克)诱导的抗伤害感受作用。α₂-肾上腺素能受体拮抗剂育亨宾(2微克/大鼠,ICV)减弱了低剂量丙咪嗪(10毫克/千克,IP)加不同剂量可乐定(0.05、0.1和0.2微克/大鼠,ICV)的反应,但未改变高剂量丙咪嗪(20和40毫克/千克)单独或与可乐定联合诱导的反应。育亨宾单独使用无作用。α₁-肾上腺素能受体激动剂去氧肾上腺素(0.07 - 1.5微克/大鼠)在福尔马林试验的两个阶段均诱导了抗伤害感受作用,但未改变丙咪嗪诱导的抗伤害感受作用。α₁-肾上腺素能受体拮抗剂哌唑嗪既未引发抗伤害感受作用,也未改变丙咪嗪的反应。育亨宾(2微克/大鼠,ICV)与哌唑嗪(0.5微克/大鼠,ICV)联合使用对丙咪嗪或丙咪嗪加可乐定的反应产生了更强的抑制作用。因此,得出结论:α₂-肾上腺素能受体机制可能参与了丙咪嗪诱导的抗伤害感受作用。