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Neuropeptides as possible targets in sleep disorders.

机译:神经肽可能是睡眠障碍的靶标。

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摘要

Insomnia and hypersomnia are frequent sleep disorders, and they are most often treated pharmacologically with hypnotics and wake-promoting compounds. These compounds act on classical neurotransmitter systems, such as benzodiazepines on GABA-A receptors, and amfetamine-like stimulants on monoaminergic terminals to modulate neurotransmission. In addition, acetylcholine, amino acids, lipids and proteins (cytokines) and peptides, are known to significantly modulate sleep and are, therefore, possibly involved in the pathophysiology of some sleep disorders. Due to the recent developments of molecular biological techniques, many neuropeptides have been newly identified, and some are found to significantly modulate sleep. It was also discovered that the impairment of the hypocretin/orexin neurotransmission (a recently isolated hypothalamic neuropeptide system) is the major pathophysiology of narcolepsy, and hypocretin replacement therapy is anticipated to treat the disease in humans. In this article, the authors briefly review the history of neuropeptide research, followed by the sleep modulatory effects of various neuropeptides. Finally, general strategies for the pharmacological therapeutics targeting the peptidergic systems for sleep disorders are discussed.
机译:失眠和失眠是常见的睡眠障碍,最常使用催眠药和促醒化合物进行药理治疗。这些化合物可作用于经典的神经递质系统,例如GABA-A受体上的苯并二氮杂卓,单胺能末端上的安非他明样兴奋剂可调节神经传递。另外,已知乙酰胆碱,氨基酸,脂质和蛋白质(细胞因子)和肽可显着调节睡眠,因此可能与某些睡眠障碍的病理生理有关。由于分子生物学技术的最新发展,许多神经肽已被新发现,并且发现其中一些显着调节睡眠。还发现,降钙素/食欲神经传递(最近分离的下丘脑神经肽系统)受损是发作性睡病的主要病理生理学,并且降钙素替代疗法有望治疗人类疾病。在本文中,作者简要回顾了神经肽研究的历史,然后介绍了各种神经肽的睡眠调节作用。最后,讨论了针对针对睡眠障碍的肽能系统的药理疗法的一般策略。

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