Couture L, Elie R, Lavoie P A
Département de pharmacologie, Université de Montreal, QC, Canada.
Can J Physiol Pharmacol. 2001 Nov;79(11):946-52.
This study investigated the effect of tricyclic and atypical antidepressants on adenosine triphosphate (ATP) dependent calcium uptake by the endoplasmic reticulum of lysed synaptosomes from rat brain cortex. Tricyclic antidepressants (imipramine, desipramine, clomipramine, amitriptyline) exhibited no effect in the lower range (0.06 to 2 microM) of drug concentrations, and a concentration-dependent inhibition of calcium uptake in the upper range (6 to 200 microM). A concentration-dependent inhibition was observed for atypical antidepressants (mianserin, desmethylmianserin, venlafaxine, desmethylvenlafaxine, fluoxetine) in both the lower and the upper range of drug concentrations. Since no stimulation of calcium uptake was observed in either concentration range, it appears that the tricyclic and atypical antidepressants tested are not capable of normalizing, through their effect on the endoplasmic reticulum, an overactive calcium signal. which is possibly implicated in the etiology of affective disorders. Also, although only marginal inhibition of calcium uptake is expected at brain concentrations of tricyclics and mianserin-desmethylmianserin that are likely to be encountered during clinical use, a more substantial inhibition could occur with fluoxetine.
本研究调查了三环类和非典型抗抑郁药对大鼠大脑皮质裂解突触体的内质网中三磷酸腺苷(ATP)依赖性钙摄取的影响。三环类抗抑郁药(丙咪嗪、地昔帕明、氯米帕明、阿米替林)在较低药物浓度范围(0.06至2微摩尔)内无作用,而在较高浓度范围(6至200微摩尔)内对钙摄取有浓度依赖性抑制作用。对于非典型抗抑郁药(米安色林、去甲米安色林、文拉法辛、去甲文拉法辛、氟西汀),在药物浓度的较低和较高范围内均观察到浓度依赖性抑制作用。由于在任一浓度范围内均未观察到钙摄取的刺激作用,因此所测试的三环类和非典型抗抑郁药似乎无法通过其对内质网的作用来使过度活跃的钙信号正常化,而这种钙信号可能与情感障碍的病因有关。此外,尽管在临床使用中可能遇到的三环类药物以及米安色林 - 去甲米安色林的脑浓度下,预计对钙摄取只有轻微抑制作用,但氟西汀可能会产生更显著的抑制作用。