Ganry H, Bourin M
Laboratoire de Pharmacologie, Faculté de Médecine, Nantes, France.
Neuropsychobiology. 1988;20(4):187-93. doi: 10.1159/000118497.
Iprindole, an active antidepressant in clinical use, has no effect on norepinephrine reuptake and does not bind to receptors of the noradrenergic system. Iprindole weakly antagonizes reserpine hypothermia and potentiates yohimbine toxicity. This effect is antagonized by propranolol but not by atenolol or metoprolol. In an acute dose, iprindole potentiates the effect of maprotiline on yohimbine toxicity. Beta 2-adrenergic agonists and antagonists specifically modify the effect of iprindole on spontaneous motility. These results indicate that iprindole has an indirect beta 2-mimetic effect.
伊普吲哚是一种临床使用的活性抗抑郁药,对去甲肾上腺素再摄取没有影响,也不与去甲肾上腺素能系统的受体结合。伊普吲哚可轻度拮抗利血平引起的体温过低,并增强育亨宾的毒性。普萘洛尔可拮抗这种作用,但阿替洛尔或美托洛尔则不能。急性给药时,伊普吲哚可增强马普替林对育亨宾毒性的作用。β2-肾上腺素能激动剂和拮抗剂可特异性改变伊普吲哚对自发运动的作用。这些结果表明,伊普吲哚具有间接拟β2效应。