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Antidepressant stimulation of CDP-diacylglycerol synthesis does not require monoamine reuptake inhibition

机译:抗抑郁药刺激CDP-二酰甘油合成不需要单胺再摄取抑制

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摘要

BackgroundRecent studies demonstrate that diverse antidepressant agents increase the cellular production of the nucleolipid CDP-diacylglycerol and its synthetic derivative, phosphatidylinositol, in depression-relevant brain regions. Pharmacological blockade of downstream phosphatidylinositide signaling disrupted the behavioral antidepressant effects in rats. However, the nucleolipid responses were resistant to inhibition by serotonin receptor antagonists, even though antidepressant-facilitated inositol phosphate accumulation was blocked. Could the neurochemical effects be additional to the known effects of the drugs on monoamine transmitter transporters? To examine this question, we tested selected agents in serotonin-depleted brain tissues, in PC12 cells devoid of serotonin transporters, and on the enzymatic activity of brain CDP-diacylglycerol synthase - the enzyme that catalyzes the physiological synthesis of CDP-diacylglycerol.
机译:背景技术最近的研究表明,在与抑郁症相关的大脑区域中,多种抗抑郁药会增加细胞核磷脂CDP-二酰甘油及其合成衍生物磷脂酰肌醇的产量。下游磷脂酰肌醇信号传导的药理学阻断破坏了大鼠的行为抗抑郁作用。然而,即使抗抑郁药促进的肌醇磷酸积累被阻滞,核苷反应仍能抵抗5-羟色胺受体拮抗剂的抑制作用。神经化学作用是否可以与药物对单胺递质转运蛋白的已知作用相补充?为了检查这个问题,我们测试了5-羟色胺缺乏脑组织中,不含5-羟色胺转运蛋白的PC12细胞中选定的药物,以及脑CDP-二甘油甘油合酶(催化CDP-二甘油甘油生理合成的酶)的酶活性。

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