Laboratory of Animal Physiology, Department of Animal Science and Technology, National Taiwan University, Taipei, 10617, Taiwan.
Laboratory of Hormonal Regulation, Cardiovascular and Metabolic Disorders Program, Duke-National University of Singapore Medical School, Singapore, 16987, Singapore.
Sci Rep. 2017 Oct 25;7(1):13999. doi: 10.1038/s41598-017-14376-y.
Previous studies have demonstrated that saturated fatty acids (SFAs) are more lipotoxic than unsaturated fatty acids (UFAs) in inhibiting hepatic autophagy and promoting non-alcoholic steatohepatitis (NASH). However, there have been few studies have investigated the effects of carbon chain length on SFA-induced autophagy impairment and lipotoxicity. To investigate whether SFAs with shorter carbon chain lengths have differential effects on hepatic autophagy and NASH development, we partially replaced lard with coconut oil to elevate the ratio of medium-chain fatty acids (MCFAs) to long-chain fatty acids (LCFAs) in a mouse high-fat diet (HFD) and fed mice for 16 weeks. In addition, we treated HepG2 cells with different combinations of fatty acids to study the mechanisms of MCFAs-mediated hepatic protections. Our results showed that increasing dietary MCFA/LCFA ratio mitigated HFD-induced Type 2 diabetes and NASH in mice. Importantly, we demonstrated that increased MCFA ratio exerted its protective effects by restoring Rubicon-suppressed autophagy. Our study suggests that the relative amount of LCFAs and MCFAs in the diet, in addition to the amount of SFAs, can significantly contribute to autophagy impairment and hepatic lipotoxicity. Collectively, we propose that increasing dietary MCFAs could be an alternative therapeutic and prevention strategy for Type 2 diabetes and NASH.
先前的研究表明,与不饱和脂肪酸(UFAs)相比,饱和脂肪酸(SFAs)在抑制肝自噬和促进非酒精性脂肪性肝炎(NASH)方面更具脂毒性。然而,很少有研究调查碳链长度对 SFA 诱导的自噬损伤和脂毒性的影响。为了研究链长较短的 SFAs 是否对肝自噬和 NASH 发展有不同的影响,我们用椰子油部分替代猪油,以提高高脂肪饮食(HFD)中小鼠中中链脂肪酸(MCFAs)与长链脂肪酸(LCFAs)的比例,并喂养小鼠 16 周。此外,我们用不同的脂肪酸组合处理 HepG2 细胞,以研究 MCFAs 介导的肝保护机制。我们的结果表明,增加饮食中 MCFA/LCFA 比例可减轻 HFD 诱导的 2 型糖尿病和 NASH 小鼠的发病。重要的是,我们证明增加 MCFA 比例通过恢复 Rubicon 抑制的自噬发挥其保护作用。我们的研究表明,饮食中 LCFAs 和 MCFAs 的相对量,除了 SFAs 的量之外,可显著导致自噬损伤和肝脂毒性。总之,我们提出增加饮食中的 MCFAs 可能是 2 型糖尿病和 NASH 的一种替代治疗和预防策略。