抗生素诱导的肠道微生物群破坏通过减少短链脂肪酸乙酸减少血管化,促进了血管化
Shi-Yu Zeng1, Yi-Fu Liu2,3, Zhao-Lin Zeng1
1Department of Metabolism and Endocrinology, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.
抗生素通过破坏肠道细菌和短链脂肪酸 (SCFA) 来恶化血管化. 乙酸补充剂可以缓解这种情况,为血管化提供潜在的治疗点.
科学领域:
- 心血管研究研究心血管研究
- 微生物组科学 微生物组科学
- 代谢研究 代谢研究
背景情况:
- 血管化是心血管事件的重要危险因素.
- 抗生素可以改变肠道微生物群 (GM),但它们对血管化的影响尚不清楚.
研究的目的:
- 研究抗生素诱导的转基因破坏对血管化的影响.
- 探索短链脂肪酸 (SCFA) 的潜力,特别是酸,减轻血管化.
主要方法:
- 对小鼠进行了抗生素尾酒 (ABX) 和万科米辛治疗,以诱导转基因破坏.
- 使用16S rRNA基因测序和向代谢学来分析转基因组合和血清SCFA水平.
- 蛋白质组学被用来阐明乙酸对血管光滑肌细胞 (VSMCs) 的作用机制.
主要成果:
- 抗生素治疗加剧了血管化,与减少Bacteroidetes丰度和较低的血清SCFA水平相关.
- 乙酸补充剂减少了大动脉沉积,并抑制了VSMC的骨质变化.
- 乙酸对VSMCs的抑制作用涉及谷氨代谢,正如BSO干预所证明的那样.
结论:
- 抗生素诱导的肠道失生症,其特点是减少了Bacteroidetes和SCFA,加剧了血管化.
- 乙酸作为血管化的潜在治疗剂出现,准VSMC骨质变化.
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