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红曲米、植物甾醇酯和番茄红素的饮食组合通过调节肠道微生物群和激活小鼠肝脏中的FXR-LDLR/ABCG途径来改善高胆固醇血症。

A dietary combination of red yeast rice, phytosterol ester and lycopene ameliorates hypercholesterolemia by regulating gut microbiota and activating hepatic FXR-LDLR/ABCG pathway in mice.

作者信息

Xu Jingxian, Huang Xin, Pei Fei, Chen Yuzhu, Zhang Cunzheng, Zhao Lingling, Zhang Hua, Zhang Jindong, Duan Liping

机构信息

Department of Gastroenterology, Peking University Third Hospital, Beijing, China.

Beijing Key Laboratory for Helicobacter pylori Infection and Upper Gastrointestinal Diseases, Beijing, China.

出版信息

Front Microbiol. 2025 Aug 7;16:1622818. doi: 10.3389/fmicb.2025.1622818. eCollection 2025.

DOI:10.3389/fmicb.2025.1622818
PMID:40851863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12369415/
Abstract

BACKGROUND

Excessive nutrition intake is a well-established contributor to obesity and hypercholesterolemia, both of which pose substantial risks to cardiovascular health. Statins, which are widely prescribed for managing serum cholesterol levels, are sometimes discontinued owing to adverse reactions. In contrast, dietary components have shown promise in lowing lipid lowering potential with a relatively higher safety profile, although the underlying mechanisms remains incompletely understood.

OBJECTIVES

This study aimed to investigate the role and underlying mechanism of a dietary combination comprising red yeast rice (RYR), phytosterol ester, and lycopene (RPL), in mitigating hypercholesterolemia.

METHODS

High-fat, high-cholesterol (HFHC)-fed C57BL/6J mice were administered either the RPL combination (low and high dose) or simvastatin. The effects of these interventions on obesity, serum cholesterol, and glucose tolerance were evaluated. Mechanistic insights were gained through fecal 16S rRNA sequencing, targeted metabolomic profiling, and molecular analysis of liver and intestinal tissues using western blotting, qPCR, and immunofluorescence techniques.

RESULTS

Compared to the HFHC group, low and high doses of the RPL combination reduced serum low-density lipoprotein cholesterol (LDL-C) levels by 33 and 20%, respectively, whereas simvastatin achieved a 22% reduction. Both doses of RPL significantly lowered serum total cholesterol (TC) levels and alleviated obesity in mice, effects not observed with simvastatin. Mechanistically, the RPL combination reshaped the gut microbiota, specifically increasing the abundance of and decreasing that of , and . Additionally, the RPL combination modulated bile acids profiles, leading to an increased proportion of hyodeoxycholic acid (HDCA) and a decreased level of omega-muricholic acid (ω-MCA). Furthermore, the altered gut microbiota and ω-MCA levels activated the hepatic FXR-LDLR/ABCG5/8 pathway, promoting cholesterol excretion into feces and thereby alleviating hypercholesterolemia. The increased proportion of HDCA suppressed lipid absorption, further facilitating its excretion in feces.

CONCLUSION

The dietary combination of RPL effectively lowers serum cholesterol by regulating gut microbiota, influencing bile acid metabolism, and enhancing cholesterol excretion. This study offers a novel and promising strategy for the clinical management of hypercholesterolemia.

摘要

背景

营养摄入过多是导致肥胖和高胆固醇血症的公认因素,这两者都会对心血管健康构成重大风险。他汀类药物被广泛用于控制血清胆固醇水平,但有时会因不良反应而停药。相比之下,饮食成分在降低血脂方面显示出潜力,且安全性相对较高,尽管其潜在机制仍未完全明确。

目的

本研究旨在探讨红曲米(RYR)、植物甾醇酯和番茄红素(RPL)的饮食组合在减轻高胆固醇血症中的作用及潜在机制。

方法

给高脂高胆固醇(HFHC)喂养的C57BL/6J小鼠给予RPL组合(低剂量和高剂量)或辛伐他汀。评估这些干预措施对肥胖、血清胆固醇和葡萄糖耐量的影响。通过粪便16S rRNA测序、靶向代谢组学分析以及使用蛋白质印迹法、qPCR和免疫荧光技术对肝脏和肠道组织进行分子分析来深入了解其机制。

结果

与HFHC组相比,低剂量和高剂量的RPL组合分别使血清低密度脂蛋白胆固醇(LDL-C)水平降低了33%和20%,而辛伐他汀降低了22%。两种剂量的RPL均显著降低了小鼠血清总胆固醇(TC)水平并减轻了肥胖,辛伐他汀未观察到这些效果。从机制上讲,RPL组合重塑了肠道微生物群,具体表现为增加了[未提及的微生物名称1]的丰度,降低了[未提及的微生物名称2]、[未提及的微生物名称3]和[未提及的微生物名称4]的丰度。此外,RPL组合调节了胆汁酸谱,导致猪去氧胆酸(HDCA)比例增加,ω-鼠胆酸(ω-MCA)水平降低。此外,肠道微生物群和ω-MCA水平的改变激活了肝脏FXR-LDLR/ABCG5/8通路,促进胆固醇排泄到粪便中,从而减轻高胆固醇血症。HDCA比例的增加抑制了脂质吸收,进一步促进其在粪便中的排泄。

结论

RPL饮食组合通过调节肠道微生物群、影响胆汁酸代谢和增强胆固醇排泄有效降低血清胆固醇。本研究为高胆固醇血症的临床管理提供了一种新颖且有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/f410f246a753/fmicb-16-1622818-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/e6162122d814/fmicb-16-1622818-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/5cad4467ef47/fmicb-16-1622818-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/ef9a3f9563e9/fmicb-16-1622818-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/ede197533a74/fmicb-16-1622818-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/d57ab0aba189/fmicb-16-1622818-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/9d39566b3fe4/fmicb-16-1622818-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/b667d0fadae5/fmicb-16-1622818-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/f410f246a753/fmicb-16-1622818-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/e6162122d814/fmicb-16-1622818-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/5cad4467ef47/fmicb-16-1622818-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/ef9a3f9563e9/fmicb-16-1622818-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/ede197533a74/fmicb-16-1622818-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/d57ab0aba189/fmicb-16-1622818-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/9d39566b3fe4/fmicb-16-1622818-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/b667d0fadae5/fmicb-16-1622818-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/12369415/f410f246a753/fmicb-16-1622818-g008.jpg

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