Center for Advanced Biotechnology and Medicine, Rutgers University, Piscataway, NJ, USA.
Department of Medicine: Metabolism, Endocrinology, and Nutrition, Seattle, WA, USA; Diabetes Institute, University of Washington, Seattle, WA, USA.
Mol Metab. 2024 Nov;89:102029. doi: 10.1016/j.molmet.2024.102029. Epub 2024 Sep 16.
Obesity continues to be a major problem, despite known treatment strategies such as lifestyle modifications, pharmaceuticals, and surgical options, necessitating the development of novel weight loss approaches. The naturally occurring fatty acid, 10,12 conjugated linoleic acid (10,12 CLA), promotes weight loss by increasing fat oxidation and browning of white adipose tissue, leading to increased energy expenditure in obese mice. Coincident with weight loss, 10,12 CLA also alters the murine gut microbiota by enriching for microbes that produce short chain fatty acids (SCFAs), with concurrent elevations in fecal butyrate and plasma acetate.
To determine if the observed microbiota changes are required for 10,12 CLA-mediated weight loss, adult male mice with diet-induced obesity were given broad-spectrum antibiotics (ABX) to perturb the microbiota prior to and during 10,12 CLA-mediated weight loss. Conversely, to determine whether gut microbes were sufficient to induce weight loss, conventionally-raised and germ-free mice were transplanted with cecal contents from mice that had undergone weight loss by 10,12 CLA supplementation.
While body weight was minimally modulated by ABX-mediated perturbation of gut bacterial populations, adult male mice given ABX were more resistant to the increased energy expenditure and fat loss that are induced by 10,12 CLA supplementation. Transplanting cecal contents from donor mice losing weight due to oral 10,12 CLA consumption into conventional or germ-free mice led to improved glucose metabolism with increased butyrate production.
These data suggest a critical role for the microbiota in diet-modulated changes in energy balance and glucose metabolism, and distinguish the metabolic effects of orally delivered 10,12 CLA from cecal transplantation of the resulting microbiota.
尽管存在生活方式改变、药物和手术等已知的治疗策略,但肥胖仍然是一个主要问题,因此需要开发新的减肥方法。天然存在的脂肪酸 10,12 共轭亚油酸(10,12 CLA)通过增加脂肪氧化和白色脂肪组织的褐变来促进体重减轻,从而导致肥胖小鼠的能量消耗增加。与体重减轻同时发生的是,10,12 CLA 还通过富集产生短链脂肪酸(SCFAs)的微生物来改变小鼠的肠道微生物群,同时粪便丁酸和血浆乙酸盐升高。
为了确定观察到的微生物群变化是否是 10,12 CLA 介导的体重减轻所必需的,在给予 10,12 CLA 介导的体重减轻之前和期间,用广谱抗生素(ABX)处理饮食诱导肥胖的成年雄性小鼠以扰乱微生物群。相反,为了确定肠道微生物是否足以引起体重减轻,用来自因 10,12 CLA 补充而减轻体重的小鼠的盲肠内容物移植常规饲养和无菌小鼠。
尽管 ABX 介导的肠道细菌种群扰动对体重的影响很小,但给予 ABX 的成年雄性小鼠对 10,12 CLA 补充诱导的能量消耗增加和脂肪损失的抵抗力更强。将因口服 10,12 CLA 消耗而减轻体重的供体小鼠的盲肠内容物移植到常规或无菌小鼠中,可导致葡萄糖代谢改善,丁酸生成增加。
这些数据表明微生物群在饮食调节的能量平衡和葡萄糖代谢变化中起关键作用,并将口服 10,12 CLA 与盲肠移植产生的微生物群的代谢作用区分开来。