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酮体 3-羟基丁酸通过 Nrf2 激活剂富马酸模拟热量限制在视网膜中的作用。

Ketone body 3-hydroxybutyrate mimics calorie restriction via the Nrf2 activator, fumarate, in the retina.

机构信息

Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.

Department of Developmental Anatomy and Regenerative Biology, National Defense Medical College, Tokorozawa, Japan.

出版信息

Aging Cell. 2018 Feb;17(1). doi: 10.1111/acel.12699. Epub 2017 Nov 9.

Abstract

Calorie restriction (CR) being the most robust dietary intervention provides various health benefits. D-3-hydroxybutyrate (3HB), a major physiological ketone, has been proposed as an important endogenous molecule for CR. To investigate the role of 3HB in CR, we investigated potential shared mechanisms underlying increased retinal 3HB induced by CR and exogenously applied 3HB without CR to protect against ischemic retinal degeneration. The repeated elevation of retinal 3HB, with or without CR, suppressed retinal degeneration. Metabolomic analysis showed that the antioxidant pentose phosphate pathway and its limiting enzyme, glucose-6-phosphate dehydrogenase (G6PD), were concomitantly preserved. Importantly, the upregulation of nuclear factor erythroid 2 p45-related factor 2 (Nrf2), a regulator of G6PD, and elevation of the tricarboxylic acid cycle's Nrf2 activator, fumarate, were also shared. Together, our findings suggest that CR provides retinal antioxidative defense by 3HB through the antioxidant Nrf2 pathway via modification of a tricarboxylic acid cycle intermediate during 3HB metabolism.

摘要

热量限制(CR)是最有效的饮食干预措施,可带来多种健康益处。D-3-羟基丁酸(3HB),一种主要的生理酮体,已被提议作为 CR 诱导的增加视网膜 3HB 的重要内源性分子。为了研究 3HB 在 CR 中的作用,我们研究了 CR 诱导的和无 CR 时外源性应用 3HB 增加视网膜 3HB 以防止缺血性视网膜变性的潜在共同机制。无论是否存在 CR,视网膜 3HB 的反复升高均可抑制视网膜变性。代谢组学分析表明,抗氧化戊糖磷酸途径及其限速酶葡萄糖-6-磷酸脱氢酶(G6PD)同时得到了保护。重要的是,核因子红细胞 2 p45 相关因子 2(Nrf2)的上调,G6PD 的调节剂,以及三羧酸循环的 Nrf2 激活物富马酸的升高,也是共同的。总之,我们的研究结果表明,CR 通过 3HB 代谢过程中对三羧酸循环中间产物的修饰,通过抗氧化 Nrf2 途径为视网膜提供抗氧化防御。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103c/5770878/26f6b35fb024/ACEL-17-na-g001.jpg

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