Brindley Rebecca L, Bauer Mary Beth, Blakely Randy D, Currie Kevin P M
Department of Anesthesiology, Vanderbilt University Medical Center , Nashville, Tennessee 37232, United States.
Department of Biomedical Science, Charles E. Schmidt College of Medicine, and Florida Atlantic University Brain Institute, Florida Atlantic University , Jupiter, Florida 33458, United States.
ACS Chem Neurosci. 2017 May 17;8(5):943-954. doi: 10.1021/acschemneuro.7b00026. Epub 2017 Apr 13.
Serotonin (5-HT) is an important neurotransmitter in the central nervous system where it modulates circuits involved in mood, cognition, movement, arousal, and autonomic function. The 5-HT transporter (SERT; SLC6A4) is a key regulator of 5-HT signaling, and genetic variations in SERT are associated with various disorders including depression, anxiety, and autism. This review focuses on the role of SERT in the sympathetic nervous system. Autonomic/sympathetic dysfunction is evident in patients with depression, anxiety, and other diseases linked to serotonergic signaling. Experimentally, loss of SERT function (SERT knockout mice or chronic pharmacological block) has been reported to augment the sympathetic stress response. Alterations to serotonergic signaling in the CNS and thus central drive to the peripheral sympathetic nervous system are presumed to underlie this augmentation. Although less widely recognized, SERT is robustly expressed in chromaffin cells of the adrenal medulla, the neuroendocrine arm of the sympathetic nervous system. Adrenal chromaffin cells do not synthesize 5-HT but accumulate small amounts by SERT-mediated uptake. Recent evidence demonstrated that 5-HT receptors inhibit catecholamine secretion from adrenal chromaffin cells via an atypical mechanism that does not involve modulation of cellular excitability or voltage-gated Ca channels. This raises the possibility that the adrenal medulla is a previously unrecognized peripheral hub for serotonergic control of the sympathetic stress response. As a framework for future investigation, a model is proposed in which stress-evoked adrenal catecholamine secretion is fine-tuned by SERT-modulated autocrine 5-HT signaling.
血清素(5-羟色胺,5-HT)是中枢神经系统中一种重要的神经递质,它调节参与情绪、认知、运动、觉醒和自主功能的神经回路。5-羟色胺转运体(SERT;SLC6A4)是5-羟色胺信号传导的关键调节因子,SERT的基因变异与包括抑郁症、焦虑症和自闭症在内的多种疾病相关。本综述重点关注SERT在交感神经系统中的作用。自主神经/交感神经功能障碍在抑郁症、焦虑症和其他与血清素能信号传导相关的疾病患者中很明显。在实验中,据报道SERT功能丧失(SERT基因敲除小鼠或长期药物阻断)会增强交感应激反应。中枢神经系统中血清素能信号的改变以及由此对周围交感神经系统的中枢驱动被认为是这种增强的基础。尽管认识程度较低,但SERT在肾上腺髓质的嗜铬细胞中大量表达,肾上腺髓质是交感神经系统的神经内分泌分支。肾上腺嗜铬细胞不合成5-羟色胺,但通过SERT介导的摄取积累少量5-羟色胺。最近的证据表明,5-羟色胺受体通过一种不涉及调节细胞兴奋性或电压门控钙通道的非典型机制抑制肾上腺嗜铬细胞分泌儿茶酚胺。这增加了肾上腺髓质是交感应激反应的血清素能控制中一个以前未被认识的外周枢纽的可能性。作为未来研究的框架,提出了一个模型,其中应激诱发的肾上腺儿茶酚胺分泌通过SERT调节的自分泌5-羟色胺信号进行微调。