Tsai You-Shan, Lin Shih-Wei, Chen Yen-Lien, Chen Chin-Chu
Biotech Research Institute, Grape King Bio Ltd, Taoyuan 32542, Taiwan.
Institute of Food Science and Technology, National Taiwan University, Taipei 10617, Taiwan.
Nutr Res Pract. 2020 Aug;14(4):299-308. doi: 10.4162/nrp.2020.14.4.299. Epub 2020 May 18.
BACKGROUND/OBJECTIVES: Heavy alcohol consumption causes the development of alcoholic liver disease (ALD), a neglected but important public health problem. Many studies have pointed out that probiotics could improve gut health, which is also considered to be a cause of ALD. Therefore, this study screened the probiotics, GKC1 (GKC1), GKF3 (GKF3), GKK2 (GKK2), GKLC1 (GKLC1), GKS6 (GKS6), and GKM3 (GKM3), for their potential benefits in alleviating ALD for applications to disease prevention.
SUBJECTS/METHODS: C57BL/6N mice were divided into 8 groups (n = 6 in each): normal control, positive control (alcohol-diet fed), and treatments of feeding probiotics GKC1, GKF3, GKK2, GKLC1, GKS6, and GKM3 under an oral dose 0.82 g/kg B.W. per day by oral gavage. The experiment was conducted for 8 weeks, and the concentrations of alanine aminotransferase (ALT), aspartate aminotransferase, triglyceride (TG), and total cholesterol (TC) in mice were measured. The glutathione (GSH), catalase (CAT), and histology were analyzed after sacrifice.
The results showed a decrease in the serum ALT, liver TG, and liver TC levels in the GKS6, GKM3, and GKLC1 groups compared to the positive control. In addition, the decreasing GSH and CAT levels were inhibited in the GKS6 and GKM3 groups. The histopathological results showed that all probiotics could reduce the accumulation of liver fat. Furthermore, there was a significant difference in GKLC1 with lower stomach damage compared to the alcohol-fed mice without any addition of probiotics.
GKLC1, GKS6, and GKM3 can be used as supplements for alleviating the development of ALD.
背景/目的:大量饮酒会导致酒精性肝病(ALD)的发生,这是一个被忽视但很重要的公共卫生问题。许多研究指出,益生菌可以改善肠道健康,而肠道健康也被认为是ALD的一个病因。因此,本研究筛选了益生菌GKC1、GKF3、GKK2、GKLC1、GKS6和GKM3,以探究它们在缓解ALD方面的潜在益处,用于疾病预防。
受试者/方法:将C57BL/6N小鼠分为8组(每组n = 6):正常对照组、阳性对照组(给予酒精饮食),以及通过灌胃给予剂量为0.82 g/kg体重/天的益生菌GKC1、GKF3、GKK2、GKLC1、GKS6和GKM3的处理组。实验进行8周,测量小鼠体内丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶、甘油三酯(TG)和总胆固醇(TC)的浓度。处死小鼠后分析谷胱甘肽(GSH)、过氧化氢酶(CAT)水平及组织学情况。
结果显示与阳性对照组相比,GKS6、GKM3和GKLC1组小鼠血清ALT、肝脏TG和肝脏TC水平降低。此外,GKS6和GKM3组中GSH和CAT水平降低受到抑制。组织病理学结果表明,所有益生菌均可减少肝脏脂肪堆积。此外与未添加任何益生菌的酒精喂养小鼠相比,GKLC1组胃损伤程度较低,存在显著差异。
GKLC1、GKS6和GKM3可作为缓解ALD发展的补充剂。