Matsuda Y, Masuda Y, Blattberg B, Levy M N
Eur J Pharmacol. 1980 Apr 11;63(1):25-33. doi: 10.1016/0014-2999(80)90113-2.
The effects of cocaine (COC), chlorpheniramine (CHL), and tripelennamine (TRI) on the cardiac responses to sympathetic neural stimulation were compared in open-chest, anesthetized dogs. The amplitudes of the chronotropic responses were not significantly altered by any of these drugs. Similarly, the amplitudes of the inotropic responses were not affected significantly by either COC or TRI, but they were increased moderately by CHL. All three drugs prolonged the inotropic and especially the chronotropic responses. CHL and TRI, in addition to being antihistaminics, are inhibitors of the neuronal uptake of norepinephrine. Therefor, the similarity of the effects of CHL, TRI, and COC on the cardiac responses to sympathetic stimulation is probably ascribable to their inhibitory activities on the neuronal uptake mechanism.
在开胸麻醉犬中比较了可卡因(COC)、氯苯那敏(CHL)和曲普利啶(TRI)对交感神经刺激所致心脏反应的影响。这些药物中的任何一种均未显著改变变时反应的幅度。同样,COC或TRI均未显著影响变力反应的幅度,但CHL使其适度增加。所有这三种药物均延长了变力反应,尤其是变时反应。CHL和TRI除具有抗组胺作用外,还是去甲肾上腺素神经元摄取的抑制剂。因此,CHL、TRI和COC对交感神经刺激所致心脏反应的影响相似,可能归因于它们对神经元摄取机制的抑制活性。