Gloston Gabrielle F, Yoo Seung-Hee, Chen Zheng Jake
Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston , Houston, TX , USA.
Front Neurol. 2017 Mar 15;8:100. doi: 10.3389/fneur.2017.00100. eCollection 2017.
Normal physiological functions require a robust biological timer called the circadian clock. When clocks are dysregulated, misaligned, or dampened, pathological consequences ensue, leading to chronic diseases and accelerated aging. An emerging research area is the development of clock-targeting compounds that may serve as drug candidates to correct dysregulated rhythms and hence mitigate disease symptoms and age-related decline. In this review, we first present a concise view of the circadian oscillator, physiological networks, and regulatory mechanisms of circadian amplitude. Given a close association of circadian amplitude dampening and disease progression, clock-enhancing small molecules (CEMs) are of particular interest as candidate chronotherapeutics. A recent proof-of-principle study illustrated that the natural polymethoxylated flavonoid nobiletin directly targets the circadian oscillator and elicits robust metabolic improvements in mice. We describe mood disorders and aging as potential therapeutic targets of CEMs. Future studies of CEMs will shed important insight into the regulation and disease relevance of circadian clocks.
正常的生理功能需要一个强大的生物钟。当时钟失调、不同步或减弱时,就会产生病理后果,导致慢性疾病和加速衰老。一个新兴的研究领域是开发针对生物钟的化合物,这些化合物可能作为候选药物来纠正失调的节律,从而减轻疾病症状和与年龄相关的衰退。在这篇综述中,我们首先简要介绍昼夜节律振荡器、生理网络以及昼夜节律振幅的调节机制。鉴于昼夜节律振幅减弱与疾病进展密切相关,增强生物钟的小分子(CEMs)作为候选时间治疗药物特别受关注。最近一项原理验证研究表明,天然多甲氧基黄酮川陈皮素直接作用于昼夜节律振荡器,并在小鼠身上引发了显著的代谢改善。我们将情绪障碍和衰老描述为CEMs的潜在治疗靶点。对CEMs的未来研究将为昼夜节律时钟的调节及其与疾病的相关性提供重要见解。