褪黑激素与视网膜细胞损伤:分子和生物功能。

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Jingwen Sun, Yan Liu, Zhangming Chen
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引用次数: 0

摘要

吲哚胺激素--褪黑激素由松果体产生,在许多生理功能中发挥着重要作用。松果体被认为是产生褪黑激素的最重要器官。不过,需要指出的是,眼睛也能产生褪黑激素,并且有自己产生这种激素的昼夜节律。褪黑激素主要由感光器的一个亚群以昼夜节律产生。大量体外和体内研究表明,褪黑激素对眼部相关疾病有益。这些疾病主要影响视网膜细胞,凸显了褪黑激素的治疗潜力,尤其是对视网膜的治疗潜力。褪黑激素能够调节氧化应激反应途径并调节抗氧化基因的表达,因此有望成为减轻视网膜细胞损伤的候选药物。此外,褪黑激素还能调节NF-кB等炎症通路,进一步减轻视网膜损伤,并影响视网膜细胞的程序性细胞死亡,如细胞凋亡和自噬。因此,本综述旨在探讨褪黑激素保护视网膜细胞免受损伤和缺血的方法。我们讨论其中涉及的机制,以便对褪黑激素在保护视网膜细胞和治疗视网膜疾病方面可能的治疗应用获得有价值的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Melatonin and retinal cell damage: molecular and biological functions.

The indoleamine hormone, melatonin, is produced in the pineal gland and has an essential role in many physiological functions. The pineal gland is considered to be the most important organ for producing melatonin. Nevertheless, it is important to point out that the eye is also capable of producing melatonin, and has its own circadian rhythm in producing this hormone. Melatonin is mainly produced by a subpopulation of photoreceptors in a diurnal rhythm. Numerous in vitro and in vivo studies have shown the beneficial effects of melatonin in eye-related disorders. These diseases primarily affect retinal cells, highlighting the therapeutic potential of melatonin, especially in the retina. Melatonin's ability to regulate oxidative stress response pathways and modulate the expression of antioxidant genes makes it a promising candidate for mitigating retinal cell damage. Moreover, melatonin can modulate inflammatory pathways such as NF-кB and further reduce retinal damage, as well as affecting programmed cell death such as apoptosis and autophagy in retinal cells. Therefore, the goal of this review is to explore the ways in which melatonin protects retinal cells from damage and ischemia. We discuss the mechanisms involved in order to gain valuable understanding of the possible therapeutic applications of melatonin in protection of retinal cells and treatment of retinal disorders.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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