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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Serotonin 5-HT receptor activation induces 2-arachidonoylglycerol release through a phospholipase c-dependent mechanism.
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Serotonin 5-HT receptor activation induces 2-arachidonoylglycerol release through a phospholipase c-dependent mechanism.

机译:5-羟色胺5-HT受体激活通过磷脂酶c依赖性机制诱导2-花生四烯酸甘油释放。

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To date, several studies have demonstrated that phospholipase C-coupled receptors stimulate the production of endocannabinoids, particularly 2-arachidonoylglycerol. There is now evidence that endocannabinoids are involved in phospholipase C-coupled serotonin 5-HT(2A) receptor-mediated behavioral effects in both rats and mice. The main objective of this study was to determine whether activation of the 5-HT(2A) receptor leads to the production and release of the endocannabinoid 2-arachidonoylglycerol. NIH3T3 cells stably expressing the rat 5-HT(2A) receptor were first incubated with [(3)H]-arachidonic acid for 24 h. Following stimulation with 10 mum serotonin, lipids were extracted from the assay medium, separated by thin layer chromatography, and analyzed by liquid scintillation counting. Our results indicate that 5-HT(2A) receptor activation stimulates the formation and release of 2-arachidonoylglycerol. The 5-HT(2A) receptor-dependent release of 2-arachidonoylglycerol was partially dependent on phosphatidylinositol-specific phospholipase C activation. Diacylglycerol produced downstream of 5-HT(2A) receptor-mediated phospholipase D or phosphatidylcholine-specific phospholipase C activation did not appear to contribute to 2-arachidonoylglycerol formation in NIH3T3-5HT(2A) cells. In conclusion, our results support a functional model where neuromodulatory neurotransmitters such as serotonin may act as regulators of endocannabinoid tone at excitatory synapses through the activation of phospholipase C-coupled G-protein coupled receptors.
机译:迄今为止,数项研究表明磷脂酶C偶联受体刺激内源性大麻素,特别是2-花生四烯酸甘油酯的产生。现在有证据表明,内源性大麻素与大鼠和小鼠的磷脂酶C偶联的血清素5-HT(2A)受体介导的行为有关。这项研究的主要目的是确定5-HT(2A)受体的激活是否导致内源性大麻素2-花生四烯酸甘油酯的产生和释放。首先将稳定表达大鼠5-HT(2A)受体的NIH3T3细胞与[(3)H]-花生四烯酸孵育24小时。用10羟色胺刺激后,从测定培养基中提取脂质,通过薄层色谱分离,并通过液体闪烁计数进行分析。我们的结果表明5-HT(2A)受体激活刺激2-花生四烯酸甘油酯的形成和释放。 5-花生四烯酸甘油酯的5-HT(2A)受体依赖性释放部分取决于磷脂酰肌醇特异性磷脂酶C的活化。在5-HT(2A)受体介导的磷脂酶D或磷脂酰胆碱特异性磷脂酶C活化的下游产生的二酰基甘油似乎没有促进NIH3T3-5HT(2A)细胞中2-花生四烯酸甘油的形成。总之,我们的结果支持了一种功能模型,其中神经调节性神经递质(如5-羟色胺)可能通过激活磷脂酶C偶联的G蛋白偶联受体来充当兴奋性突触中内源性大麻素的调节剂。

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