Jang Kyoung Ok, Choi Jung Seo, Choi Kyeong Hun, Kim Seongjae, Kim Hangeun, Chung Dae Kyun
Graduate School of Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea.
Research and Development Center, Skin Biotechnology Center Co., Ltd., Yongin, 17104, Republic of Korea.
Heliyon. 2023 Jan 13;9(1):e12926. doi: 10.1016/j.heliyon.2023.e12926. eCollection 2023 Jan.
Probiotics exert anti-obesity effects in high-fat diet (HFD) obese mice, but there are few studies on anti-obesity using heat-killed probiotics. Here, we investigated the effect of heat-killed K8 (K8HK) on the anti-differentiation of 3T3-L1 preadipocytes and on anti-obesity in HFD mice. K8HK decreased triglyceride (TG) accumulation in 3T3-L1 cells. Specifically, 1 × 10 CFU/mL K8HK showed the greatest anti-obesity effect, while the same concentration of live K8 (K8 Live) showed cytotoxicity. K8HK increased suppressor of cytokine signaling (SOCS)-1, which might affect the JAK2-STAT3 signaling pathway activated during differentiation. As a result, the levels of transcription factors of adipogenesis such as Peroxisome proliferator-activated receptor γ (PPARγ) and CCAAT/enhancer binding protein α (C/EBPα) decreased in K8HK-treated cells. We also observed a decrease in the lipogenic enzymes and fatty acid binding protein 4 (FABP4). In the mouse study, oral ingestion of K8 Live and K8HK showed weight reduction and decrease in blood TG content at 12 weeks of feeding. In addition, TG synthesis was suppressed in liver and adipose tissues, and genes related to fat metabolism were suppressed. This study suggests that K8HK could be a good material to prevent obesity by inhibiting adipogenesis genes related to fat metabolism.
益生菌对高脂饮食(HFD)诱导的肥胖小鼠具有抗肥胖作用,但关于使用热灭活益生菌进行抗肥胖的研究较少。在此,我们研究了热灭活的K8(K8HK)对3T3-L1前脂肪细胞抗分化及对HFD小鼠抗肥胖的影响。K8HK降低了3T3-L1细胞内甘油三酯(TG)的积累。具体而言,1×10 CFU/mL的K8HK显示出最大的抗肥胖效果,而相同浓度的活K8(K8 Live)则表现出细胞毒性。K8HK增加了细胞因子信号转导抑制因子(SOCS)-1的表达,这可能影响分化过程中激活的JAK2-STAT3信号通路。结果,在K8HK处理的细胞中,过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT/增强子结合蛋白α(C/EBPα)等脂肪生成转录因子的水平降低。我们还观察到生脂酶和脂肪酸结合蛋白4(FABP4)减少。在小鼠研究中,口服K8 Live和K8HK在喂养12周时体重减轻且血液TG含量降低。此外,肝脏和脂肪组织中的TG合成受到抑制,与脂肪代谢相关的基因也受到抑制。本研究表明,K8HK可能是一种通过抑制与脂肪代谢相关的脂肪生成基因来预防肥胖的良好物质。