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揭示肌肽的隐藏治疗潜力,一种具有多模式作用机制的分子:立场文件。

Unveiling the Hidden Therapeutic Potential of Carnosine, a Molecule with a Multimodal Mechanism of Action: A Position Paper.

机构信息

Department of Drug and Health Sciences, University of Catania, 95125 Catania, Italy.

Unit of Neuropharmacology and Translational Neurosciences, Oasi Research Institute-IRCCS, 94018 Troina, Italy.

出版信息

Molecules. 2022 May 20;27(10):3303. doi: 10.3390/molecules27103303.

DOI:10.3390/molecules27103303
PMID:35630780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9143376/
Abstract

Carnosine (β-alanyl-L-histidine) is a naturally occurring endogenous dipeptide and an over-the-counter food supplement with a well-demonstrated multimodal mechanism of action that includes the detoxification of reactive oxygen and nitrogen species, the down-regulation of the production of pro-inflammatory mediators, the inhibition of aberrant protein formation, and the modulation of cells in the peripheral (macrophages) and brain (microglia) immune systems. Since its discovery more than 100 years ago, a plethora of in vivo preclinical studies have been carried out; however, there is still substantial heterogeneity regarding the route of administration, the dosage, the duration of the treatment, and the animal model selected, underlining the urgent need for "coordinated/aligned" preclinical studies laying the foundations for well-defined future clinical trials. The main aim of the present position paper is to critically and concisely consider these key points and open a discussion on the possible "alignment" for future studies, with the goal of validating the full therapeutic potential of this intriguing molecule.

摘要

肌肽(β-丙氨酰-L-组氨酸)是一种天然存在的内源性二肽,也是一种非处方食品补充剂,具有经过充分证明的多模式作用机制,包括解毒活性氧和氮物种、下调促炎介质的产生、抑制异常蛋白质形成,以及调节外周(巨噬细胞)和大脑(小神经胶质细胞)免疫系统中的细胞。自 100 多年前发现以来,已经进行了大量的体内临床前研究;然而,关于给药途径、剂量、治疗持续时间和所选动物模型,仍然存在很大的异质性,这突出表明迫切需要“协调/一致”的临床前研究,为明确的未来临床试验奠定基础。本立场文件的主要目的是批判性和简洁地考虑这些要点,并就未来研究的可能“调整”展开讨论,目标是验证这种有趣分子的全部治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c9/9143376/e846c646baed/molecules-27-03303-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c9/9143376/5c063ff73725/molecules-27-03303-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c9/9143376/e846c646baed/molecules-27-03303-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c9/9143376/5c063ff73725/molecules-27-03303-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0c9/9143376/e846c646baed/molecules-27-03303-g002.jpg

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