Caffeine: a potential mechanism for anti-obesity.

IF 3 4区 医学 Q2 NEUROSCIENCES
Meng Wang, Wei Guo, Jiang-Fan Chen
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引用次数: 0

Abstract

Obesity refers to the excessive accumulation of fat caused by a long-term imbalance between energy intake (EI) and energy expenditure (EE). Over recent years, obesity has become a major public health challenge. Caffeine is a natural product that has been demonstrated to exert anti-obesity effects; however, the mechanisms responsible for the effect of caffeine on weight loss have yet to be fully elucidated. Most obesity-related deaths are due to cardiovascular disease. Recent research has demonstrated that caffeine can reduce the risk of death from cardiovascular disease; thus, it can be hypothesized that caffeine may represent a new therapeutic agent for weight loss. In this review, we synthesize data arising from clinical and animal studies over the last decade and discuss the potential mechanisms by which caffeine may induce weight loss, focusing particularly on increasing energy consumption, suppressing appetite, altering lipid metabolism, and influencing the gut microbiota. Finally, we summarize the major challenges associated with caffeine and anti-obesity research and highlight possible directions for future research and development.

Abstract Image

咖啡因:抗肥胖的潜在机制。
肥胖症是指由于能量摄入(EI)和能量消耗(EE)长期失衡而导致的脂肪过度堆积。近年来,肥胖已成为一项重大的公共卫生挑战。咖啡因是一种天然产品,已被证实具有抗肥胖作用;然而,咖啡因对减肥作用的机制尚未完全阐明。大多数与肥胖有关的死亡都是由心血管疾病造成的。最近的研究表明,咖啡因可以降低心血管疾病导致死亡的风险;因此,可以假设咖啡因可能是一种新的减肥治疗药物。在这篇综述中,我们综合了过去十年中临床和动物研究的数据,讨论了咖啡因诱导减肥的潜在机制,尤其侧重于增加能量消耗、抑制食欲、改变脂质代谢和影响肠道微生物群。最后,我们总结了咖啡因和抗肥胖研究面临的主要挑战,并强调了未来研究和发展的可能方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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