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Cellular and molecular mechanisms underlying the treatment of depression: focusing on hippocampal G-protein-coupled receptors and voltage-dependent calcium channels

机译:抑郁症治疗的细胞和分子机制:专注于海马G蛋白偶联受体和电压依赖性钙通道

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摘要

Depression is a brain disorder characterized by severe emotional, cognitive, neuro endocrine and somatic dysfunction. Although the latest generation of antidepressant drugs has improved clinical efficacy and safety, the onset of their clinical effect is significantly delayed after treatment commencement, and a large number of patients exhibit inadequate response to these drugs and/or depression relapse even following initially successful treatment. It is therefore essential to develop new antidepressant drugs and/or adjuncts to existing ones. Recent studies suggest that the beneficial effect of antidepressant drugs is mediated, at least in part, via stimulation of adult hippocampal neurogenesis and subsequent increase in hippocampal plasticity. Since the stimulatory effect of antidepressant drugs on hippocampal neurogenesis involves G-protein coupled receptors (GPCR) and voltage-dependent calcium channels (VDCC), greater efficacy may be available if future antidepressant drugs directly target these specific GPCR and VDCC. The potential advantages and limitations of these treatment strategies are discussed in the article.
机译:抑郁症是一种以严重的情绪,认知,神经内分泌和躯体功能障碍为特征的脑部疾病。尽管最新一代的抗抑郁药具有改善的临床疗效和安全性,但在开始治疗后其临床作用开始明显延迟,并且即使在最初成功的治疗后,许多患者对这些药物的反应仍不充分和/或抑郁症复发。因此,开发新的抗抑郁药和/或现有药物的辅助剂至关重要。最近的研究表明,抗抑郁药的有益作用至少部分是通过刺激成人海马神经发生和随后增加海马可塑性来介导的。由于抗抑郁药对海马神经发生的刺激作用涉及G蛋白偶联受体(GPCR)和电压依赖性钙通道(VDCC),因此,如果将来的抗抑郁药直接针对这些特定的GPCR和VDCC,则可获得更高的疗效。本文讨论了这些治疗策略的潜在优势和局限性。

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