Hong Brian V, Rhodes Christopher H, Agus Joanne K, Tang Xinyu, Zhu Chenghao, Zheng Jack Jingyuan, Zivkovic Angela M
Department of Nutrition, University of California, Davis, Davis, CA, United States.
Front Cardiovasc Med. 2023 Sep 7;10:1251122. doi: 10.3389/fcvm.2023.1251122. eCollection 2023.
Prolonged fasting, characterized by restricting caloric intake for 24 h or more, has garnered attention as a nutritional approach to improve lifespan and support healthy aging. Previous research from our group showed that a single bout of 36-h water-only fasting in humans resulted in a distinct metabolomic signature in plasma and increased levels of bioactive metabolites, which improved macrophage function and lifespan in .
This secondary outcome analysis aimed to investigate changes in the plasma lipidome associated with prolonged fasting and explore any potential links with markers of cardiometabolic health and aging.
We conducted a controlled pilot study with 20 male and female participants (mean age, 27.5 ± 4.4 years; mean BMI, 24.3 ± 3.1 kg/m) in four metabolic states: (1) overnight fasted (baseline), (2) 2-h postprandial fed state (fed), (3) 36-h fasted state (fasted), and (4) 2-h postprandial refed state 12 h after the 36-h fast (refed). Plasma lipidomic profiles were analyzed using liquid chromatography and electrospray ionization mass spectrometry.
Several lipid classes, including lysophosphatidylcholine (LPC), lysophosphatidylethanolamine (LPE), phosphatidylethanolamine, and triacylglycerol were significantly reduced in the 36-h fasted state, while free fatty acids, ceramides, and sphingomyelin were significantly increased compared to overnight fast and fed states ( < 0.05). After correction for multiple testing, 245 out of 832 lipid species were significantly altered in the fasted state compared to baseline ( < 0.05). Random forest models revealed that several lipid species, such as LPE(18:1), LPC(18:2), and FFA(20:1) were important features in discriminating the fasted state from both the overnight fasted and postprandial state.
Our findings indicate that prolonged fasting vastly remodels the plasma lipidome and markedly alters the concentrations of several lipid species, which may be sensitive biomarkers of prolonged fasting. These changes in lipid metabolism during prolonged fasting have important implications for the management of cardiometabolic health and healthy aging, and warrant further exploration and validation in larger cohorts and different population groups.
长时间禁食的特点是将热量摄入限制24小时或更长时间,作为一种改善寿命和支持健康衰老的营养方法,已受到关注。我们团队之前的研究表明,人类单次36小时只饮水禁食会导致血浆中出现独特的代谢组学特征,并提高生物活性代谢物水平,这改善了巨噬细胞功能和线虫的寿命。
这项次要结果分析旨在研究与长时间禁食相关的血浆脂质组变化,并探索与心脏代谢健康和衰老标志物之间的潜在联系。
我们对20名男性和女性参与者(平均年龄27.5±4.4岁;平均BMI 24.3±3.1kg/m²)进行了一项对照试验研究,分为四种代谢状态:(1)过夜禁食(基线),(2)餐后2小时进食状态(进食),(3)36小时禁食状态(禁食),以及(4)36小时禁食后12小时的餐后2小时再进食状态(再进食)。使用液相色谱和电喷雾电离质谱法分析血浆脂质组谱。
在36小时禁食状态下,包括溶血磷脂酰胆碱(LPC)、溶血磷脂酰乙醇胺(LPE)、磷脂酰乙醇胺和三酰甘油在内的几种脂质类别显著减少,而与过夜禁食和进食状态相比,游离脂肪酸、神经酰胺和鞘磷脂显著增加(P<0.05)。在进行多重检验校正后,与基线相比,832种脂质中有245种在禁食状态下有显著变化(P<0.05)。随机森林模型显示,几种脂质,如LPE(18:1)、LPC(18:2)和FFA(20:1)是区分禁食状态与过夜禁食和餐后状态的重要特征。
我们的研究结果表明,长时间禁食会极大地重塑血浆脂质组,并显著改变几种脂质的浓度,这些脂质可能是长时间禁食的敏感生物标志物。长时间禁食期间脂质代谢的这些变化对心脏代谢健康管理和健康衰老具有重要意义,值得在更大的队列和不同人群中进一步探索和验证。