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梦想更佳治疗方法:睡眠医学与时间疗法的药物研发进展

Dreaming of Better Treatments: Advances in Drug Development for Sleep Medicine and Chronotherapy.

作者信息

Prakash Brooke A, Shah Ishani, Ni Guohao, Vasudevan Sridhar, Jagannath Aarti, Foster Russell G

机构信息

Department of Pharmacology, University of Oxford, Oxford, UK.

Nuffield Department of Clinical Neurosciences, Sleep and Circadian Neuroscience Institute (SCNi), University of Oxford, Oxford, UK.

出版信息

J Sleep Res. 2025 Oct;34(5):e70087. doi: 10.1111/jsr.70087. Epub 2025 May 10.

Abstract

Throughout history, the development of new sleep medicines has been driven by progress in our understanding of the mechanisms underlying sleep. Ancient civilisations used their understanding of the sedative nature of natural herbs and compounds to induce sleep. The discovery of barbiturates and bromides heralded a new era of synthetic sleep medicine in the 19th century. This was followed by the development of benzodiazepines that were used to inhibit signalling throughout the brain by promoting gamma-amino butyric acid release and thereby produce loss of consciousness. As our understanding of sleep has deepened, newer therapies have more specifically targeted the wake-inducing neurotransmitter orexin with fewer side effects. Given the newly highlighted role of kinases in sleep/wake regulation, we predict that the next breakthroughs in sleep medicine will likely target these kinases. Given the fundamental role that sleep plays in maintaining brain health through processes such as glymphatic clearance, sleep medicine has therapeutic potential beyond just sleep. Recent evidence suggests that sleep disruptions directly contribute to the build-up of pathological neuronal proteins in neurodegenerative disorders. Therefore, sleep medicine could improve prognosis in disorders such as these. Great attention must be paid to the mechanism of action of each sleep medicine, however, as sleep medicines which do not fully mimic sleep could actually worsen disease progression.

摘要

纵观历史,新型睡眠药物的研发一直受到我们对睡眠潜在机制理解的推动。古代文明利用对天然草药和化合物镇静特性的了解来诱导睡眠。巴比妥类药物和溴化物的发现开创了19世纪合成睡眠药物的新时代。随后是苯二氮䓬类药物的研发,这类药物通过促进γ-氨基丁酸释放来抑制全脑信号传导,从而导致意识丧失。随着我们对睡眠的理解不断深入,更新的疗法更有针对性地作用于诱导清醒的神经递质食欲素,副作用更少。鉴于激酶在睡眠/觉醒调节中 newly highlighted 的作用,我们预测睡眠医学的下一个突破可能会针对这些激酶。鉴于睡眠通过类淋巴清除等过程在维持大脑健康方面发挥的基本作用,睡眠医学的治疗潜力不仅限于睡眠。最近的证据表明,睡眠中断直接导致神经退行性疾病中病理性神经元蛋白的积累。因此,睡眠医学可以改善这类疾病的预后。然而,必须高度关注每种睡眠药物的作用机制,因为不能完全模拟睡眠的睡眠药物实际上可能会使疾病进展恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/debc/12426713/05772dc5002f/JSR-34-e70087-g003.jpg

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