Yin Chao, Fan Peizhi, Mou Xiangyu, Zhao Wenjing
Shenzhen Key Laboratory for Systems Medicine for Inflammatory Diseases, School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen 518107, China.
Microorganisms. 2025 May 27;13(6):1220. doi: 10.3390/microorganisms13061220.
Dysbiosis of the gut microbiota is strongly implicated in atherosclerosis (AS), thus prompting microbial modulation to be explored as a therapeutic strategy. However, limited evidence exists for probiotic interventions capable of alleviating AS. Here, we focused on (; CB), a probiotic known for its production of short-chain fatty acids (SCFAs). We found that administration of to high-fat diet (HFD)-fed deficient () mice reduced plaque area by improving blood lipid profiles, decreasing macrophage infiltration in the aortic roots, and lowering the levels of circulating pro-inflammatory monocytes and macrophages. By non-targeted serum metabolomics analysis, treatment significantly reduced the levels of both linoleic acid and its downstream metabolites. Collectively, these findings establish -mediated amelioration of AS through modulation of linoleic acid metabolism.
肠道微生物群失调与动脉粥样硬化(AS)密切相关,因此促使人们探索微生物调节作为一种治疗策略。然而,能够缓解AS的益生菌干预的证据有限。在这里,我们重点研究了(;CB),一种以产生短链脂肪酸(SCFAs)而闻名的益生菌。我们发现,给高脂饮食(HFD)喂养的缺乏()小鼠施用可通过改善血脂谱、减少主动脉根部的巨噬细胞浸润以及降低循环促炎单核细胞和巨噬细胞水平来减少斑块面积。通过非靶向血清代谢组学分析,治疗显著降低了亚油酸及其下游代谢物的水平。总的来说,这些发现通过调节亚油酸代谢建立了介导的AS改善作用。