Chiba S, Ogiwara Y, Furukawa Y, Akahane K
Department of Pharmacology, Shinshu University School of Medicine, Matsumoto, Japan.
Jpn Heart J. 1989 Nov;30(6):895-902. doi: 10.1536/ihj.30.895.
Cross-perfused canine atrial preparations were used to investigate the direct and indirect cardiac actions of clonidine and alinidine. Intravenous injections of clonidine (0.1-3 micrograms/kg) produced an initial brief pressor response and bradycardia followed by hypotension in the intact dog. Chronotropic and inotropic responses were absent in the isolated atrium perfused with the intact dog's blood. Intravenous clonidine (10-300 micrograms) also induced negative chronotropic and inotropic effects in isolated atria. On the other hand, alinidine, at doses which caused a depressor action and bradycardia in the intact dog, consistently produced negative chronotropic and inotropic effects in the isolated atrium. Therefore, it was confirmed that a relatively small dose of clonidine has a selective vascular action, while alinidine has direct cardiac depressant properties at all effective doses. Negative chronotropic and inotropic effects of peripheral vagal stimulation, carbachol and adenosine were not significantly modified by 100 or 300 micrograms doses of intraarterial clonidine. On the other hand, the effects of vagal stimulation and carbachol were significantly inhibited by 100 and 300 micrograms of alinidine, without affecting adenosine-induced cardiac actions. Therefore, it was demonstrated that alinidine has anti-muscarinic properties.
采用交叉灌注犬心房标本研究可乐定和阿利尼定对心脏的直接和间接作用。静脉注射可乐定(0.1 - 3微克/千克)可使完整犬产生最初的短暂升压反应和心动过缓,随后出现低血压。在用完整犬血液灌注的离体心房中未出现变时性和变力性反应。静脉注射可乐定(10 - 300微克)也可在离体心房中诱导负性变时性和变力性作用。另一方面,阿利尼定在完整犬中引起降压作用和心动过缓的剂量下,始终在离体心房中产生负性变时性和变力性作用。因此,证实了相对小剂量的可乐定具有选择性血管作用,而阿利尼定在所有有效剂量下均具有直接的心脏抑制特性。外周迷走神经刺激、卡巴胆碱和腺苷的负性变时性和变力性作用在动脉内注射100或300微克可乐定时未受到显著影响。另一方面,100和300微克阿利尼定显著抑制了迷走神经刺激和卡巴胆碱的作用,而不影响腺苷诱导的心脏作用。因此,证明阿利尼定具有抗毒蕈碱特性。