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光暴露影响生物钟系统相位移动反应的药物的系统评价。

Systematic review of drugs that modify the circadian system's phase-shifting responses to light exposure.

机构信息

Department of Psychology, University of Arizona, Tucson, AZ, USA.

Department of Neurology, University of Arizona, Tucson, AZ, USA.

出版信息

Neuropsychopharmacology. 2022 Mar;47(4):866-879. doi: 10.1038/s41386-021-01251-8. Epub 2021 Dec 27.

Abstract

We searched PubMed for primary research quantifying drug modification of light-induced circadian phase-shifting in rodents. This search, conducted for work published between 1960 and 2018, yielded a total of 146 papers reporting results from 901 studies. Relevant articles were those with any extractable data on phase resetting in wildtype (non-trait selected) rodents administered a drug, alongside a vehicle/control group, near or at the time of exposure. Most circadian pharmacology experiments were done using drugs thought to act directly on either the brain's central pacemaker, the suprachiasmatic nucleus (SCN), the SCN's primary relay, the retinohypothalamic tract, secondary pathways originating from the medial/dorsal raphe nuclei and intergeniculate leaflet, or the brain's sleep-arousal centers. While the neurotransmitter systems underlying these circuits were of particular interest, including those involving glutamate, gamma-aminobutyric acid, serotonin, and acetylcholine, other signaling modalities have also been assessed, including agonists and antagonists of receptors linked to dopamine, histamine, endocannabinoids, adenosine, opioids, and second-messenger pathways downstream of glutamate receptor activation. In an effort to identify drugs that unduly influence circadian responses to light, we quantified the net effects of each drug class by ratioing the size of the phase-shift observed after administration to that observed with vehicle in a given experiment. This allowed us to organize data across the literature, compare the relative efficacy of one mechanism versus another, and clarify which drugs might best suppress or potentiate phase resetting. Aggregation of the available data in this manner suggested that several candidates might be clinically relevant as auxiliary treatments to suppress ectopic light responses during shiftwork or amplify the circadian effects of timed bright light therapy. Future empirical research will be necessary to validate these possibilities.

摘要

我们在 PubMed 上搜索了定量研究啮齿动物光诱导生物钟相位移动药物修饰的原始研究。这项从 1960 年到 2018 年期间发表的工作进行的搜索,共产生了 146 篇论文,报道了 901 项研究的结果。相关文章是指那些在给予药物的野生型(非特征选择)啮齿动物中提取到任何生物钟相位重置数据的文章,同时有药物处理组和载体/对照组,接近或在暴露时给药。大多数生物钟药理学实验是使用被认为直接作用于大脑中央起搏器、视交叉上核(SCN)、SCN 的主要中继、视网膜下丘脑束、起源于中/背缝核和正中核的次级途径,或大脑的睡眠觉醒中心的药物进行的。虽然这些回路的神经递质系统特别受关注,包括涉及谷氨酸、γ-氨基丁酸、血清素和乙酰胆碱的系统,但也评估了其他信号转导方式,包括与多巴胺、组胺、内源性大麻素、腺苷、阿片类药物和谷氨酸受体激活下游第二信使途径相关的受体激动剂和拮抗剂。为了确定药物对光诱导生物钟反应的不当影响,我们通过将给药后观察到的相位移动大小与给定实验中载体观察到的相位移动大小进行比较,对每种药物类别进行了净效应的量化。这使我们能够跨文献组织数据,比较一种机制与另一种机制的相对疗效,并阐明哪些药物可能最能抑制或增强相位重置。以这种方式汇总可用数据表明,一些候选药物可能具有临床相关性,可作为辅助治疗手段,抑制轮班工作期间的异位光反应,或放大定时强光治疗的生物钟效应。未来的实证研究将有必要验证这些可能性。

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