Zhu Boran, Zhai Yi, Ji Mengjiao, Wei Yanan, Wu Jiafei, Xue Wenda, Tao Wei Wei, Wu Haoxin
School of Chinese Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Front Pharmacol. 2020 Sep 25;11:570555. doi: 10.3389/fphar.2020.570555. eCollection 2020.
beverage (AOB) is a Chinese traditional medicine formulated with a diversity of medicinal plants and used for treating metabolic syndrome and atherosclerosis (AS) since time ago. Given the current limited biological research on AOB, the mechanism by which AOB treats AS is unknown. This study investigats the role of AOB-induced gut microbiota regulation in the expansion of AS.
We established an AS model in male apolipoprotein E-deficient (ApoE) mice that are fed with a high-fat diet (HFD), treated with numerous interventions, and evaluated the inflammatory cytokines and serum biochemical indices. The root of the aorta was stained with oil red O, and the proportion of the lesion area was quantified. Trimethylamine N-oxide (TMAO) and trimethylamine (TMA) levels in serum were evaluated through liquid chromatography with mass spectrometry. Flavin-containing monooxygenase 3 (FMO3) liver protein expression was assessed by Western blotting. 16S rDNA sequencing technique was adopted to establish the changes in the microbiota structure.
After 8 weeks of HFD feeding, an inflammatory cytokine, and AS development expression were significantly decreased in mice treated with AOB; the same parameters in the mice treated with the antibiotics cocktail did not change. In the gut microbiota study, mice treated with AOB had a markedly different gut microbiota than the HFD-fed mice. Additionally, AOB also decreased serum TMAO and hepatic FMO3 expression.
The antiatherosclerotic effects of AOB were found associated with changes in the content of gut microbiota and a reduction in TMAO, a gut microbiota metabolite, suggesting that AOB has potential therapeutic value in the treatment of AS.
中药复方制剂(AOB)是一种由多种药用植物配制而成的中药,长期以来一直用于治疗代谢综合征和动脉粥样硬化(AS)。鉴于目前对AOB的生物学研究有限,AOB治疗AS的机制尚不清楚。本研究探讨AOB诱导的肠道微生物群调节在AS发展中的作用。
我们在喂食高脂饮食(HFD)的雄性载脂蛋白E缺陷(ApoE)小鼠中建立AS模型,进行多种干预处理,并评估炎症细胞因子和血清生化指标。用油红O对主动脉根部进行染色,并对病变面积的比例进行量化。通过液相色谱-质谱联用技术评估血清中的三甲胺N-氧化物(TMAO)和三甲胺(TMA)水平。通过蛋白质免疫印迹法评估肝脏中含黄素单加氧酶3(FMO3)的蛋白表达。采用16S rDNA测序技术确定微生物群结构的变化。
喂食HFD 8周后,接受AOB治疗的小鼠体内炎症细胞因子和AS发展表达显著降低;接受抗生素鸡尾酒治疗的小鼠的相同参数没有变化。在肠道微生物群研究中,接受AOB治疗的小鼠的肠道微生物群与喂食HFD的小鼠明显不同。此外,AOB还降低了血清TMAO和肝脏FMO3的表达。
发现AOB的抗动脉粥样硬化作用与肠道微生物群含量的变化以及肠道微生物群代谢产物TMAO的减少有关,这表明AOB在治疗AS方面具有潜在的治疗价值。