Department of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Los Angeles , Los Angeles, CA, USA.
Department of Pathology, University of Washington , Seattle, WA, USA.
Gut Microbes. 2020 Nov 9;12(1):1-16. doi: 10.1080/19490976.2020.1792256.
Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver injury and liver transplantation in Western countries. The pathogenesis of NAFLD includes overnutrition-associated metabolic syndrome or the improper consumption of dietary macro- and micro-nutrients that either support or prevent disease development. This altered nutrient landscape has been linked to shifts within the gut microbiota which can exacerbate liver pathology and the progression of NAFLD. Treatment goals for NAFLD target lifestyle and dietary modifications that restrict calories and adjust macronutrient content. It is not well understood how different macronutrients alter the microbiota and whether the diet-educated microbiota contribute to the resolution of disease. We fed mice a diet high in fat, cholesterol and fructose for 6 weeks and then in two different arms of the study, intervened with either a diet high in saturated and polyunsaturated fats and fiber or low in fats and fiber. In a second set of experiments, we performed microbiota transplants using cecal contents from mice fed one of the intervention diets to assess whether the diet-educated microbiota could impact clinical outcomes in mice fed a NAFLD-inducing diet. Pathology, steatosis, ALT/AST levels, and liver cytokine levels were measured as primary outcomes. We found that despite different microbiota compositions, both of the intervention diets reversed the progression of NAFLD and dampened inflammation. In contrast, transplantation of cecal contents from the intervention diet-fed mice to mice receiving a NAFLD-inducing diet was unable to prevent disease progression, and, in some cases, worsened disease. These data underscore the importance of dietary modifications to treat NAFLD and caution against the use of microbiota transplantation in the absence of dietary and lifestyle modifications.
非酒精性脂肪性肝病(NAFLD)是西方国家慢性肝损伤和肝移植的主要原因。NAFLD 的发病机制包括与营养过剩相关的代谢综合征或饮食宏量和微量营养素的不当摄入,这些营养素或支持或预防疾病的发展。这种改变的营养状况与肠道微生物群的变化有关,这些变化可能会加剧肝病理和 NAFLD 的进展。NAFLD 的治疗目标是针对生活方式和饮食的改变,限制热量和调整宏量营养素含量。目前尚不清楚不同的宏量营养素如何改变微生物群,以及饮食教育的微生物群是否有助于疾病的缓解。我们用高脂肪、高胆固醇和高果糖的饮食喂养小鼠 6 周,然后在研究的两个不同分支中,分别用高饱和脂肪和多不饱和脂肪和纤维或低脂肪和纤维的饮食进行干预。在第二组实验中,我们使用来自喂食干预饮食的小鼠的盲肠内容物进行微生物群移植,以评估饮食教育的微生物群是否可以影响喂食 NAFLD 诱导饮食的小鼠的临床结果。病理学、脂肪变性、ALT/AST 水平和肝细胞因子水平作为主要结果进行测量。我们发现,尽管微生物群组成不同,但两种干预饮食都能逆转 NAFLD 的进展并减轻炎症。相比之下,将喂食干预饮食的小鼠的盲肠内容物移植到喂食 NAFLD 诱导饮食的小鼠中,不能预防疾病的进展,在某些情况下甚至会使疾病恶化。这些数据强调了饮食改变治疗 NAFLD 的重要性,并告诫在没有饮食和生活方式改变的情况下,不要使用微生物群移植。