Polydatin combined with hawthorn flavonoids alleviate high fat diet induced atherosclerosis by remodeling the gut microbiota and glycolipid metabolism.

IF 4.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2025-03-03 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1515485
Dan Li, Yujuan Li, Shengjie Yang, Xiaonan Zhang, Yu Cao, Ran Zhao, Yixi Zhao, Xiao Jin, Jing Lu, Xinyue Wang, Qiutao Wang, Longtao Liu, Min Wu
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Abstract

Background: Atherosclerosis is a widely studied pathophysiological foundation of cardiovascular diseases. Inflammation and dyslipidemia are risk factors that promote the formation of atherosclerotic plaques. The gut microbiota and their metabolites are considered independent risk factors for atherosclerosis. Polydatin combined with hawthorn flavonoids, as the extracts of Polygonum cuspidatum Sieb. et Zucc. and Crataegus pinnatifida Bunge, have shown excellent cardiovascular protective effects. However, the underlying mechanism requires further investigation. Our study aimed to explore the anti-atherosclerotic mechanism through gut microbiota and their metabolites.

Methods: ApoE-/- mice were fed either a normal-chow diet or a high-fat diet. The polydatin combined with hawthorn flavonoids group received varied doses of polydatin and hawthorn flavonoids: a high dose (polydatin 200 mg/kg daily; hawthorn flavonoids 100 mg/kg daily), a medium dose (polydatin 100 mg/kg daily; hawthorn flavonoids 50 mg/kg daily), and a low dose (polydatin 50 mg/kg daily; hawthorn flavonoids 25 mg/kg daily). The control and model groups were administered distilled water (0.2 mL daily). The experiment lasted for 24 weeks.

Results: Polydatin combined with hawthorn flavonoids administration significantly reduced lipid and inflammatory cytokine levels, meanwhile, the atherosclerotic lesions in a high-fat diet-induced ApoE-/- mice were significantly decreased. Additionally, polydatin combined with hawthorn flavonoids also inhibited the enhancement of trimethylamine N-oxide (TMAO), trimethylamine (TMA) levels of HFD-induced ApoE-/- mice by regulating the expression of hepatic flavin-containing enzyme monooxygenase 3 (FMO3). 16S rRNA sequencing results demonstrated that high-dose polydatin combined with hawthorn flavonoids treatment increased the abundance of Actinobacteriota, Atopobiaceae and Coriobacteriaea_UCG-002, and decreased the abundance of Desulfobacterota. Norank_f_Muribaculaceae was enriched in the medium-dose polydatin combined with hawthorn flavonoids and simvastatin groups, and Lactobacillus was mainly increased in the simvastatin and the low-dose polydatin combined with hawthorn flavonoids groups. According to the metagenetic results, functional annotations also suggested that the biological processes of each group mainly focused on metabolism-related processes. Specifically, polydatin combined with hawthorn flavonoids may regulate the abundance of TMA-producing bacteria (Coriobacteriaceae, Desulfovibrio, Muribaculum, and Clostridium) and related enzymes in glycolipid metabolic pathways to exert an important effect on the prevention of atherosclerosis.

Conclusion: Our results suggested that polydatin combined with hawthorn flavonoids could regulate the glucolipid metabolism-related pathway, attenuate inflammatory cytokine levels, and reduce atherosclerotic plaques by remodeling gut microbiota.

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多柚素联合山楂黄酮通过重塑肠道菌群和糖脂代谢减轻高脂饮食诱导的动脉粥样硬化。
背景:动脉粥样硬化是一个被广泛研究的心血管疾病的病理生理基础。炎症和血脂异常是促进动脉粥样硬化斑块形成的危险因素。肠道菌群及其代谢产物被认为是动脉粥样硬化的独立危险因素。虎杖黄酮与山楂黄酮结合,作为虎杖提取物。调查。山楂、山楂等具有良好的心血管保护作用。然而,潜在的机制需要进一步研究。我们的研究旨在通过肠道菌群及其代谢物探讨抗动脉粥样硬化的机制。方法:ApoE-/-小鼠分别饲喂正常饮食和高脂饮食。多果苷联合山楂黄酮组给予不同剂量的多果苷和山楂黄酮:高剂量组(多果苷200 mg/kg每日;山楂黄酮100 mg/kg每日),中剂量(聚葡苷100 mg/kg每日;山楂黄酮50 mg/kg /天),低剂量(聚葡苷50 mg/kg /天;山楂黄酮25 mg/kg每日)。对照组和模型组灌胃蒸馏水(0.2 mL / d)。试验期24周。结果:多果苷联合山楂黄酮可显著降低高脂饮食诱导的ApoE-/-小鼠的脂质和炎性细胞因子水平,同时可显著降低ApoE-/-小鼠的动脉粥样硬化病变。此外,多柚素联合山楂黄酮还可通过调节肝脏含黄素酶单加氧酶3 (FMO3)的表达,抑制hfd诱导的ApoE-/-小鼠三甲胺n-氧化物(TMAO)、三甲胺(TMA)水平的升高。16S rRNA测序结果显示,大剂量聚葡苷联合山楂黄酮处理可增加放线菌群、Atopobiaceae和Coriobacteriaea_UCG-002的丰度,降低Desulfobacterota的丰度。Norank_f_Muribaculaceae在辛伐他汀和中剂量多聚糖联合山楂黄酮组富集,Lactobacillus在辛伐他汀和低剂量多聚糖联合山楂黄酮组主要增加。根据元遗传学结果,功能注释也表明各组的生物学过程主要集中在代谢相关过程。其中,多柚素联合山楂黄酮可调节糖脂代谢途径中产生tma的细菌(Coriobacteriaceae, Desulfovibrio, Muribaculum, Clostridium)及相关酶的丰度,对预防动脉粥样硬化发挥重要作用。结论:多柚素联合山楂黄酮可通过重塑肠道菌群,调节糖脂代谢相关通路,降低炎症细胞因子水平,减少动脉粥样硬化斑块。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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