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禁食疗法通过激活内皮祖细胞的自噬,有助于改善超重和肥胖个体的内皮功能,并降低血管损伤相关标志物水平。

Fasting Therapy Contributes to the Improvement of Endothelial Function and Decline in Vascular Injury-Related Markers in Overweight and Obese Individuals via Activating Autophagy of Endothelial Progenitor Cells.

作者信息

Sun Jiapan, Zhang Tingying, Zhang Li, Ke Bin, Qin Jian

机构信息

Department of Traditional Chinese Medicine, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong 510080, China.

Department of Traditional Chinese Medicine, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, Guangdong 518107, China.

出版信息

Evid Based Complement Alternat Med. 2020 Jul 27;2020:3576030. doi: 10.1155/2020/3576030. eCollection 2020.

Abstract

BACKGROUND

High body mass index- (BMI-) related vascular injury contributes to the pathogenesis of the atherosclerotic cardiovascular disease (ASCVD). Rigorous calorie restriction is one of the major lifestyle interventions to reduce vascular risk in overweight or obese individuals. However, the effects of fasting therapy (FT) on vascular function and the mechanism are still unclear. This study was aimed to investigate the impacts of FT on endothelial function, arterial stiffness, and circulating arterial damage parameters in overweight and obese individuals and possible mechanism.

METHODS

Overweight and obese individuals participated in FT intervention (7-day very low calorie diet). Arterial function including brachial arterial flow-mediated dilation (FMD), brachial-ankle pulse wave velocity (baPWV), vascular injury-related markers including trimethylamine N-oxide (TMAO), and leptin and endothelial microparticles (EMPs) were assessed. Endothelial progenitor cells (EPCs) of these participants were isolated and cultured to investigate EPCs function. mRFP-GFP-LC3 confocal microscopy scanning and western blot were carried out to determine autophagy.

RESULTS

After FT, body weight and BMI significantly decreased (81.76 ± 12.04 vs. 77.51 ± 12.06 kg, < 0.01; 29.93 ± 2.82 vs. 28.47 ± 2.83 kg/m, < 0.01). FT remarkably improved FMD (5.26 ± 1.34 vs. 6.25 ± 1.60%, =0.01) while baPWV kept unchanged. TMAO and leptin levels decreased (3.96 ± 1.85 vs. 2.73 ± 1.33 mol/L, =0.044; 6814 ± 2639 vs. 3563 ± 2668 mol/L, < 0.01). EMPs showed a decreased tendency. EPCs function was significantly improved, autophagy fluorescence intensity was enhanced, and the level of Beclin1, Atg5, LC3 II/I also increased after starvation in vitro, and the effects were blocked by autophagy inhibitor.

CONCLUSIONS

Our present study demonstrated for the first time that FT markedly improves endothelial function and reduces the levels of arterial injury markers through improving EPCs function via activating autophagy. These findings provide a novel insight into FT as a lifestyle intervention strategy to promote the maintenance of vascular homeostasis in overweight or obese individuals. The trial was registered with ChiCTR1900024290.

摘要

背景

高体重指数(BMI)相关的血管损伤促成了动脉粥样硬化性心血管疾病(ASCVD)的发病机制。严格的热量限制是超重或肥胖个体降低血管风险的主要生活方式干预措施之一。然而,禁食疗法(FT)对血管功能的影响及其机制仍不清楚。本研究旨在探讨FT对超重和肥胖个体内皮功能、动脉僵硬度及循环动脉损伤参数的影响及其可能机制。

方法

超重和肥胖个体参与FT干预(7天极低热量饮食)。评估动脉功能,包括肱动脉血流介导的舒张功能(FMD)、臂踝脉搏波速度(baPWV);血管损伤相关标志物,包括氧化三甲胺(TMAO)、瘦素和内皮微粒(EMPs)。分离并培养这些参与者的内皮祖细胞(EPCs)以研究EPCs功能。进行mRFP-GFP-LC3共聚焦显微镜扫描和蛋白质印迹法以确定自噬情况。

结果

FT后,体重和BMI显著降低(81.76±12.04 vs. 77.51±12.06 kg,P<0.01;29.93±2.82 vs. 28.47±2.83 kg/m²,P<0.01)。FT显著改善了FMD(5.26±1.34 vs. 6.25±1.60%,P=0.01),而baPWV保持不变。TMAO和瘦素水平降低(3.96±1.85 vs. 2.73±1.33 μmol/L,P=0.044;6814±2639 vs. 3563±2668 μmol/L,P<0.01)。EMPs呈下降趋势。EPCs功能显著改善,自噬荧光强度增强,体外饥饿后Beclin1、Atg5、LC3 II/I水平也升高,且这些作用被自噬抑制剂阻断。

结论

我们目前的研究首次表明,FT通过激活自噬改善EPCs功能,显著改善内皮功能并降低动脉损伤标志物水平。这些发现为FT作为一种生活方式干预策略促进超重或肥胖个体维持血管稳态提供了新的见解。该试验已在中国临床试验注册中心注册,注册号为ChiCTR1900024290。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1418/7403908/6cae450a1d3f/ECAM2020-3576030.001.jpg

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