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简单酯的制备及临床前特征:同时外源性供给乳酸和 β-羟基丁酸。

Preparation and Preclinical Characterization of a Simple Ester for Dual Exogenous Supply of Lactate and Beta-hydroxybutyrate.

机构信息

Department of Chemistry, Aarhus University, Langelandsgade 140, Aarhus C DK-8000, Denmark.

Department of Cardiology, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, Aarhus N DK-8200, Denmark.

出版信息

J Agric Food Chem. 2024 Sep 11;72(36):19883-19890. doi: 10.1021/acs.jafc.4c04849. Epub 2024 Aug 30.

DOI:10.1021/acs.jafc.4c04849
PMID:39214666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11403612/
Abstract

Elevation of the plasma levels of ()-lactate (Lac) and/or ()-beta-hydroxybutyrate (BHB) occurs naturally in response to strenuous exercise and prolonged fasting, respectively, resulting in millimolar concentrations of these two metabolites. It is increasingly appreciated that Lac and BHB have wide-ranging beneficial physiological effects, suggesting that novel nutritional solutions, compatible with high-level and/or sustained consumption, which allow direct control of plasma levels of Lac and BHB, are of strong interest. In this study, we present a molecular hybrid between ()-lactate and the BHB-precursor ()-1,3-butanediol in the form of a simple ester referred to as . We show that can be readily prepared on the kilogram scale and undergoes rapid hydrolytic conversion under a variety of physiological conditions to release its two constituents. Oral ingestion of , in rats, resulted in dose-dependent elevation of plasma levels of Lac and BHB triggering expected physiological responses such as reduced lipolysis and elevation of the appetite-suppressing compound -L-lactoyl-phenylalanine (Lac-Phe).

摘要

血浆中 - 乳酸 (Lac) 和/或 - 羟丁酸 (BHB) 水平升高分别是剧烈运动和长时间禁食的自然反应,导致这两种代谢物的浓度达到毫摩尔水平。越来越多的人认识到 Lac 和 BHB 具有广泛的有益的生理作用,这表明新型营养解决方案,与高水平和/或持续消耗兼容,并允许直接控制 Lac 和 BHB 的血浆水平,具有很强的吸引力。在这项研究中,我们以一种简单的酯的形式展示了 ()- 乳酸和 BHB 前体 ()-1,3-丁二醇的分子杂交体,称为 。我们表明可以在公斤级规模上很容易地制备 ,并且在各种生理条件下迅速发生水解转化,释放出其两种成分。在大鼠中口服摄入 ,可使血浆 Lac 和 BHB 水平呈剂量依赖性升高,引发预期的生理反应,如减少脂肪分解和升高抑制食欲的化合物 -L- 乳酰 - 苯丙氨酸 (Lac-Phe)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/54ea9400bad1/jf4c04849_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/c0a3de247489/jf4c04849_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/54c46a5e98fb/jf4c04849_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/54ea9400bad1/jf4c04849_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/c0a3de247489/jf4c04849_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/141939f90660/jf4c04849_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/2e33a0d212ae/jf4c04849_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/40afa615b652/jf4c04849_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/66afaf1aded8/jf4c04849_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/0f9b4cdb2116/jf4c04849_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/54c46a5e98fb/jf4c04849_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e1d/11403612/54ea9400bad1/jf4c04849_0008.jpg

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