Department of Neuroscience, Pfizer Global Research and Development, Groton, CT 06340, USA.
Neurochem Int. 2011 Jan;58(1):78-84. doi: 10.1016/j.neuint.2010.10.015. Epub 2010 Nov 5.
Since a substantial proportion of smokers have comorbid mood disorders, the smoking cessation aid varenicline might occasionally be prescribed to patients who are simultaneously treated with antidepressants. Given that varenicline is a selective nicotinic acetylcholine receptor partial agonist and not a substrate or inhibitor of drug metabolizing enzymes, pharmacokinetic interactions with various classes of antidepressants are highly unlikely. It is, however, conceivable that varenicline may have a pharmacodynamic effect on antidepressant-evoked increases in central monoamine release. Interactions resulting in excessive transmitter release could cause adverse events such as serotonin syndrome, while attenuation of monoamine release could impact the clinical efficacy of antidepressants. To investigate this we examined whether varenicline administration modulates the effects of the selective serotonin reuptake inhibitor sertraline and the monoamine oxidase inhibitor clorgyline, given alone and combined, on extracellular concentrations of the monoamines serotonin, dopamine, and norepinephrine in rat brain by microdialysis. Given the important role attributed to cortical monoamine release in serotonin syndrome as well as antidepressant activity, the effects on extracellular monoamine concentrations were measured in the medial prefrontal cortex. Responses to maximally effective doses of sertraline or clorgyline and of sertraline plus clorgyline were the same in the absence as in the presence of a relatively high dose of varenicline, which by itself had no significant effect on cortical monoamine release. This is consistent with the binding profile of varenicline that has insufficient affinity for receptors, enzymes, or transporters to inhibit or potentiate the pharmacologic effects of antidepressants. Since varenicline neither diminished nor potentiated sertraline- or clorgyline-induced increases in neurotransmitter levels, combining varenicline with serotonergic antidepressants is unlikely to cause excessive serotonin release or to attenuate antidepressant efficacy via effects on cortical serotonin, dopamine or norepinephrine release.
由于相当一部分吸烟者同时患有情绪障碍,因此有时会为同时接受抗抑郁治疗的患者开戒烟辅助药物伐伦克林。鉴于伐伦克林是一种选择性烟碱乙酰胆碱受体部分激动剂,不是药物代谢酶的底物或抑制剂,因此与各种类别的抗抑郁药之间发生药代动力学相互作用的可能性极低。然而,可以想象的是,伐伦克林可能对由抗抑郁药引起的中枢单胺释放增加具有药效学作用。导致过度递质释放的相互作用可能会引起诸如血清素综合征之类的不良事件,而单胺释放的衰减可能会影响抗抑郁药的临床疗效。为了研究这一点,我们通过微透析检查了单独给予和联合给予选择性 5-羟色胺再摄取抑制剂舍曲林和单胺氧化酶抑制剂氯吉林后,伐伦克林给药是否调节这些药物对大鼠脑内单胺类物质 5-羟色胺、多巴胺和去甲肾上腺素细胞外浓度的影响。鉴于皮质单胺释放在血清素综合征以及抗抑郁活性中所起的重要作用,因此在测量了中前额皮质中的细胞外单胺浓度。在存在相对高剂量的伐伦克林的情况下,舍曲林或氯吉林的最大有效剂量以及舍曲林加氯吉林的反应与不存在伐伦克林的情况下相同,伐伦克林本身对皮质单胺释放没有明显影响。这与伐伦克林的结合谱一致,即它对受体、酶或转运蛋白的亲和力不足,无法抑制或增强抗抑郁药的药理作用。由于伐伦克林既没有减弱也没有增强舍曲林或氯吉林引起的神经递质水平的增加,因此将伐伦克林与 5-羟色胺能抗抑郁药合用不太可能导致过度的血清素释放,也不会通过对皮质 5-羟色胺、多巴胺或去甲肾上腺素释放的影响而减弱抗抑郁药的疗效。