Morishima So, Abe Aya, Okamoto Saki, Kapoor Mahendra P, Osumi Masahide, Oda Machi, Okubo Tsutomu, Ozeki Makoto, Nishio Masahiro, Inoue Ryo
Laboratory of Food Function, Department of Life Sciences, Graduate School of Bioresources, Mie University, Tsu, Mie, Japan.
Nutrition Division, Taiyo Kagaku Co. Ltd, Yokkaichi, Mie, Japan.
J Gastroenterol Hepatol. 2024 Dec;39(12):2700-2708. doi: 10.1111/jgh.16737. Epub 2024 Sep 23.
Alcohol-associated liver disease (ALD), including alcoholic fatty liver, is a serious problem in many countries, and its economic costs to society are enormous. There is evidence indicating the relations between gut environments and liver disease, and thus, improvement of gut environment is expected to be an effective approach for ALD prevention. In this study, we explored the preventive effect of partially hydrolyzed guar gum (PHGG) on ALD focusing on the gut-liver axis. Two weeks of PHGG pre-feeding suppressed the liver fat accumulation in the experimental binge alcohol model mouse. In cecal microbiome, PHGG pre-feeding increased beneficial Bifidobacterium with its metabolite acetate concentration and suppressed the alcohol-induced increase in the potential pathobiont Streptococcus. PHGG pre-feeding increased colonic gene expression of angiogenin genes, which act as antimicrobial peptides and decreased expression of genes for mast cell protease, which suggests a potential involvement in leaky gut. Correlation network analysis based on evaluated parameters revealed four relations worth noticing. (i) The abundance of Bifidobacterium positively correlated with cecal acetate. (ii) Cecal acetate negatively correlated with Streptococcus via colonic angiogenin expression. (iii) Streptococcus positively correlated with liver fat area. (iv) Cecal acetate had direct negative correlation with liver fat area. Considering these relations comprehensively, acetate produced by Bifidobacterium may be a key mediator in ALD prevention; it inhibited growth of potential pathobiont Streptococcus and also directly regulated liver lipid metabolism reaching through portal vein. This study demonstrated that regularly intake of PHGG may be effective in reducing the risk of alcoholic fatty liver via gut-liver axis.
酒精性肝病(ALD),包括酒精性脂肪肝,在许多国家都是一个严重的问题,其给社会带来的经济成本巨大。有证据表明肠道环境与肝脏疾病之间存在关联,因此,改善肠道环境有望成为预防ALD的有效方法。在本研究中,我们聚焦于肠 - 肝轴,探讨了部分水解瓜尔胶(PHGG)对ALD的预防作用。在实验性暴饮酒精模型小鼠中,提前两周喂食PHGG可抑制肝脏脂肪堆积。在盲肠微生物群中,提前喂食PHGG可增加有益的双歧杆菌及其代谢产物乙酸盐的浓度,并抑制酒精诱导的潜在致病共生菌链球菌的增加。提前喂食PHGG可增加结肠中血管生成素基因的表达,这些基因可作为抗菌肽,同时降低肥大细胞蛋白酶基因的表达,这表明其可能与肠道通透性增加有关。基于评估参数的相关网络分析揭示了四个值得关注的关系。(i)双歧杆菌的丰度与盲肠乙酸盐呈正相关。(ii)盲肠乙酸盐通过结肠血管生成素的表达与链球菌呈负相关。(iii)链球菌与肝脏脂肪面积呈正相关。(iv)盲肠乙酸盐与肝脏脂肪面积呈直接负相关。综合考虑这些关系,双歧杆菌产生的乙酸盐可能是预防ALD的关键介质;它抑制了潜在致病共生菌链球菌的生长,还直接调节了通过门静脉到达肝脏的脂质代谢。本研究表明,定期摄入PHGG可能通过肠 - 肝轴有效降低酒精性脂肪肝的风险。