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酮体对细胞生物化学、表观遗传学和代谢组学的调节。生酮饮食在生物体生理和病理状态中的意义。

Modulation of Cellular Biochemistry, Epigenetics and Metabolomics by Ketone Bodies. Implications of the Ketogenic Diet in the Physiology of the Organism and Pathological States.

机构信息

Department of Molecular Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.

INSERM Unit 1060, CarMeN Laboratory, 165 Chemin du Grand Revoyet - BP12, F-69495 Pierre Bénite CEDEX, Lyon, France.

出版信息

Nutrients. 2020 Mar 17;12(3):788. doi: 10.3390/nu12030788.

DOI:10.3390/nu12030788
PMID:32192146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7146425/
Abstract

Ketone bodies (KBs), comprising β-hydroxybutyrate, acetoacetate and acetone, are a set of fuel molecules serving as an alternative energy source to glucose. KBs are mainly produced by the liver from fatty acids during periods of fasting, and prolonged or intense physical activity. In diabetes, mainly type-1, ketoacidosis is the pathological response to glucose malabsorption. Endogenous production of ketone bodies is promoted by consumption of a ketogenic diet (KD), a diet virtually devoid of carbohydrates. Despite its recently widespread use, the systemic impact of KD is only partially understood, and ranges from physiologically beneficial outcomes in particular circumstances to potentially harmful effects. Here, we firstly review ketone body metabolism and molecular signaling, to then link the understanding of ketone bodies' biochemistry to controversies regarding their putative or proven medical benefits. We overview the physiological consequences of ketone bodies' consumption, focusing on (i) KB-induced histone post-translational modifications, particularly β-hydroxybutyrylation and acetylation, which appears to be the core epigenetic mechanisms of activity of β-hydroxybutyrate to modulate inflammation; (ii) inflammatory responses to a KD; (iii) proven benefits of the KD in the context of neuronal disease and cancer; and (iv) consequences of the KD's application on cardiovascular health and on physical performance.

摘要

酮体(KBs)由β-羟丁酸、乙酰乙酸和丙酮组成,是一组燃料分子,可作为葡萄糖的替代能源。在禁食和长时间或剧烈运动期间,肝脏主要从脂肪酸中产生 KBs。在糖尿病中,主要是 1 型糖尿病,酮症酸中毒是葡萄糖吸收不良的病理反应。酮体的内源性产生是通过消耗生酮饮食(KD)来促进的,KD 几乎不含碳水化合物。尽管 KD 最近得到了广泛的应用,但它对全身的影响仅部分被理解,范围从特定情况下对生理有益的结果到可能有害的影响。在这里,我们首先回顾了酮体代谢和分子信号转导,然后将对酮体生物化学的理解与关于其推测或已证明的医学益处的争议联系起来。我们综述了酮体消耗的生理后果,重点关注(i)KB 诱导的组蛋白翻译后修饰,特别是β-羟丁酸介导炎症的核心表观遗传机制β-羟丁酸和乙酰化;(ii)KD 引起的炎症反应;(iii)KD 在神经疾病和癌症方面的已证实益处;以及(iv)KD 在心血管健康和运动表现方面应用的后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/c9b983094812/nutrients-12-00788-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/0eb8e8584595/nutrients-12-00788-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/185eed5a2377/nutrients-12-00788-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/c9b983094812/nutrients-12-00788-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/0eb8e8584595/nutrients-12-00788-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/185eed5a2377/nutrients-12-00788-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/379b/7146425/c9b983094812/nutrients-12-00788-g003.jpg

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