Grassland and Forage Division, National Institute of Animal Science, Rural Development Administration, Cheonan, Republic of Korea.
Research Center of Bioactive Materials, Institute of Molecular Biology and Genetics, Chonbuk National University, Jeonju, Republic of Korea.
FASEB J. 2020 Sep;34(9):12289-12307. doi: 10.1096/fj.202000971R. Epub 2020 Jul 23.
Given the rising evidence that gut malfunction including changes in the gut microbiota composition, plays a major role in the development of obesity and associated metabolic diseases, the exploring of novel probiotic bacteria with potential health benefits has attracted great attention. Recently Lactobacillus spp., exert potent anti-obesity effects by regulating key transcriptional and translational factors in adipose tissues. However, the molecular mechanism behind the anti-obesity effect of probiotics is not yet fully understood. Therefore, we investigated the effect of Lactobacillus plantarum A29 on the expression of adipogenic and lipogenic genes in 3T3-L1 adipocytes and high-fat diet (HFD)-fed mice. We observed that the treatment of 3T3-L1 adipocytes with the cell-free metabolites of L plantarum inhibited their differentiation and fat depositions via downregulating the key adipogenic transcriptional factors (PPAR-γ, C/EBP-α, and C/EBP-β) and their downstream targets (FAS, aP2, ACC, and SREBP-1). Interestingly, supplementation with L plantarum reduced the fat mass and serum lipid profile concurrently with downregulation of lipogenic gene expression in the adipocytes, resulting in reductions in the bodyweight of HFD-fed obese mice. L plantarum treatment attenuated the development of obesity in HFD-fed mice via the activation of p38MAPK, p44/42, and AMPK-α by increasing their phosphorylation. Further analysis revealed that A29 modulated gut-associated microbiota composition. Thus, A 29 potential probiotic strain may alleviate the obesity development and its associated metabolic disorders via inhibiting PPARγ through activating the p38MAPK and p44/42 signaling pathways.
鉴于肠道功能障碍(包括肠道微生物群落组成的变化)在肥胖及其相关代谢性疾病的发展中起着重要作用的证据不断增加,探索具有潜在健康益处的新型益生菌已引起极大关注。最近,乳杆菌属通过调节脂肪组织中的关键转录和翻译因子,发挥出强大的抗肥胖作用。然而,益生菌的抗肥胖作用的分子机制尚不完全清楚。因此,我们研究了植物乳杆菌 A29 对 3T3-L1 脂肪细胞和成脂基因表达的影响,以及高脂肪饮食(HFD)喂养的小鼠。我们观察到,植物乳杆菌的无细胞代谢产物处理 3T3-L1 脂肪细胞,通过下调关键的成脂转录因子(PPAR-γ、C/EBP-α 和 C/EBP-β)及其下游靶标(FAS、aP2、ACC 和 SREBP-1),抑制其分化和脂肪沉积。有趣的是,补充植物乳杆菌同时降低了脂肪细胞中脂肪生成基因的表达,减少了肥胖 HFD 喂养小鼠的脂肪量和血清脂质谱,导致肥胖 HFD 喂养小鼠的体重减轻。植物乳杆菌通过增加 p38MAPK、p44/42 和 AMPK-α 的磷酸化来激活它们,从而减轻 HFD 喂养小鼠肥胖的发展。进一步分析表明,A29 调节了与肠道相关的微生物群落组成。因此,A29 可能是一种潜在的益生菌株,通过激活 p38MAPK 和 p44/42 信号通路抑制 PPARγ,从而缓解肥胖的发展及其相关的代谢紊乱。