Department of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Arkansas Children's Nutrition Center, Little Rock, AR 72202, USA.
Int J Mol Sci. 2022 Aug 25;23(17):9658. doi: 10.3390/ijms23179658.
The gut microbiota plays a critical role in energy homeostasis and its dysbiosis is associated with obesity. Maternal high-fat diet (HFD) and β-adrenergic stimuli alter the gut microbiota independently; however, their collective regulation is not clear. To investigate the combined effect of these factors on offspring microbiota, 20-week-old offspring from control diet (17% fat)- or HFD (45% fat)-fed dams received an injection of either vehicle or β3-adrenergic agonist CL316,243 (CL) for 7 days and then cecal contents were collected for bacterial community profiling. In a follow-up study, a separate group of mice were exposed to either 8 °C or 30 °C temperature for 7 days and blood serum and cecal contents were used for metabolome profiling. Both maternal diet and CL modulated the gut bacterial community structure and predicted functional profiles. Particularly, maternal HFD and CL increased the Firmicutes/Bacteroidetes ratio. In mice exposed to different temperatures, the metabolome profiles clustered by treatment in both the cecum and serum. Identified metabolites were enriched in sphingolipid and amino acid metabolism in the cecum and in lipid and energy metabolism in the serum. In summary, maternal HFD altered offspring's response to CL and altered microbial composition and function. An independent experiment supported the effect of thermogenic challenge on the bacterial function through metabolome change.
肠道微生物群在能量平衡中起着关键作用,其失调与肥胖有关。母体高脂肪饮食(HFD)和β-肾上腺素刺激独立地改变肠道微生物群;然而,它们的集体调节尚不清楚。为了研究这些因素对后代微生物群的综合影响,来自对照饮食(17%脂肪)或 HFD(45%脂肪)喂养的母鼠的 20 周龄后代接受了载体或β3-肾上腺素能激动剂 CL316,243(CL)的注射,持续 7 天,然后收集盲肠内容物进行细菌群落分析。在后续研究中,另一组小鼠暴露于 8°C 或 30°C 温度 7 天,并用血清和盲肠内容物进行代谢组学分析。母体饮食和 CL 均调节肠道细菌群落结构和预测功能谱。特别是,母体 HFD 和 CL 增加了厚壁菌门/拟杆菌门的比例。在暴露于不同温度的小鼠中,盲肠和血清中的处理均通过代谢组学聚类。鉴定出的代谢物在盲肠中的鞘脂和氨基酸代谢以及血清中的脂质和能量代谢中富集。总之,母体 HFD 改变了后代对 CL 的反应,并改变了微生物的组成和功能。一项独立的实验通过代谢组学变化支持了产热挑战对细菌功能的影响。