Czarnecka E, Tymczyszyn W, Pietrzak B
Department of Pharmacology, Medical University of Lódź, Poland.
Pol J Pharmacol. 1998 May-Jun;50(3):193-201.
The present study examined the influence of nifedipine and verapamil on clonidine-induced hypotension in the rabbits. Clonidine was given intravenously (i.v.) (0.2 mg/kg) or intracerebroventricularly (icv) (0.03 mg). Nifedipine (0.3 mg/kg and 0.45 mg/kg) and verapamil (0.2 mg/kg and 0.3 mg/kg) were injected i.v. 15 min before clonidine administration or icv (nifedipine 0.03 mg, verapamil 0.1 mg) 10 min before clonidine. It has been shown that nifedipine administered i.v. increases whereas injected icv prevents the hypotensive action of clonidine administered in the same way. Verapamil injected i.v. and icv did not change the hypotensive action of clonidine. It seems that nifedipine has alpha 2-adrenoceptor blocking properties.
本研究考察了硝苯地平和维拉帕米对家兔可乐定诱导的低血压的影响。可乐定通过静脉注射(i.v.)(0.2mg/kg)或脑室内注射(icv)(0.03mg)给药。硝苯地平(0.3mg/kg和0.45mg/kg)和维拉帕米(0.2mg/kg和0.3mg/kg)在可乐定给药前15分钟静脉注射,或在可乐定给药前10分钟脑室内注射(硝苯地平0.03mg,维拉帕米0.1mg)。结果表明,静脉注射硝苯地平会增强,而脑室内注射则会阻止以相同方式给药的可乐定的降压作用。静脉注射和脑室内注射维拉帕米均未改变可乐定的降压作用。硝苯地平似乎具有α2 -肾上腺素能受体阻断特性。