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凝结魏斯氏菌 JA845 通过调节脂代谢、氧化应激和内皮血管损伤改善维生素 D3 和高脂饮食诱导的大鼠动脉粥样硬化。

Weizmannia coagulans JA845 improves atherosclerosis induced by vitamin D3 and high-fat diet in rats through modulating lipid metabolism, oxidative stress, and endothelial vascular injury.

机构信息

School of Pharmaceutical Sciences, Changchun University of Chinese Medicine, Changchun 130117, P.R. China.

Institute of Agricultural Products Processing Technology, Jilin Academy of Agricultural Sciences /National R&D Center for Milk Processing, Changchun 130033, P.R. China.

出版信息

J Appl Microbiol. 2023 Aug 1;134(8). doi: 10.1093/jambio/lxad165.

Abstract

AIMS

Probiotics have been proved to be strongly linked to the occurrence and progression of atherosclerosis. This study aimed to investigate the improved effects and mechanisms underlying a potential probiotic, Weizmannia coagulans JA845, on atherosclerosis.

METHODS AND RESULTS

Male Sprague-Dawley rats supported on a high-fat diet with vitamin D3 supplementation were subjected to W. coagulans JA845 treatment. W. coagulans JA845 obviously alleviated histological abnormalities of the abdominal aorta. After 6 weeks of W. coagulans JA845 administration, levels of TG, TC, LDL, ox-LDL, ROS, and MDA in the JA845 group decreased significantly, and those of HDL, GSH-Px, and SOD were markedly elevated. Treatment with W. coagulans JA845 also inhibited the secretion of ICAM-1 and VCAM-1 and regulated the plasma NO and eNOS content. In brief, administration of W. coagulans JA845 promoted the expression of the SIRT3/SOD2/FOXO3A pathway, inhibited the lipid metabolism pathway, SREBP-1c/FAS/DGAT2, and suppressed the JNK2/P38 MAPK/VEGF pathway implicated in endothelial injury.

CONCLUSIONS

These results indicated W. coagulans JA845 improved atherosclerosis by regulating lipid metabolism, antioxidative stress, and protecting against endothelial injury.

摘要

目的

益生菌与动脉粥样硬化的发生和发展密切相关。本研究旨在探讨潜在益生菌凝结魏斯氏菌 JA845 对动脉粥样硬化的改善作用及其机制。

方法和结果

雄性 Sprague-Dawley 大鼠给予高脂饮食并补充维生素 D3,同时接受凝结魏斯氏菌 JA845 治疗。JA845 明显减轻了腹主动脉的组织学异常。经过 6 周的 JA845 处理后,JA845 组的 TG、TC、LDL、氧化型 LDL、ROS 和 MDA 水平显著降低,而 HDL、GSH-Px 和 SOD 水平明显升高。JA845 的治疗还抑制了 ICAM-1 和 VCAM-1 的分泌,并调节了血浆 NO 和 eNOS 的含量。总之,JA845 的给药促进了 SIRT3/SOD2/FOXO3A 通路的表达,抑制了脂质代谢通路、SREBP-1c/FAS/DGAT2,并抑制了内皮损伤相关的 JNK2/P38 MAPK/VEGF 通路。

结论

这些结果表明,JA845 通过调节脂质代谢、抗氧化应激和保护内皮损伤来改善动脉粥样硬化。

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