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Acute oral sodium propionate supplementation raises resting energy expenditure and lipid oxidation in fasted humans

机译:急性口服丙酸钠补充提高了禁食人类的休息能源支出和脂质氧化

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摘要

Short‐chain fatty acids (SCFAs), produced from fermentation of dietary fibre by the gut microbiota, have been suggested to modulate energy metabolism. Previous work using rodent models has demonstrated that oral supplementation of the SCFA propionate raises resting energy expenditure (REE) by promoting lipid oxidation. The objective of the present study was to investigate the effects of oral sodium propionate on REE and substrate metabolism in humans. Eighteen healthy volunteers (9 women and 9 men; age 25?±?1 years; body mass index 24.1?±?1.2 kg/m 2 ) completed 2 study visits following an overnight fast. Tablets containing a total of 6845?mg sodium propionate or 4164?mg sodium chloride were provided over the 180‐minute study period in random order. REE and substrate oxidation were assessed by indirect calorimetry. Oral sodium propionate administration increased REE (0.045?±?0.020?kcal/min; P ?=?.036); this was accompanied by elevated rates of whole‐body lipid oxidation (0.012?±?0.006?g/min; P ?=?.048) and was independent of changes in glucose and insulin concentrations. Future studies are warranted to determine whether the acute effects of oral sodium propionate on REE translate into positive improvements in long‐term energy balance in humans.
机译:提出了由肠道微生物发酵产生的短链脂肪酸(SCFA),以调节能量代谢。以前使用啮齿动物模型的工作表明,通过促进脂质氧化来促进SCFA丙种的口服补充。本研究的目的是研究口服钠丙酸钠对人类REE和底物代谢的影响。十八个健康的志愿者(9名女性和9名男子;年龄25岁?±1年;体重指数24.1?±1.2千克/平方米)完成了2次研究访问过夜。以随机顺序在180分钟的研究期内提供含有总共6845μl丙酸钠或4164毫克氯化钠的片剂。通过间接量热法评估REE和底物氧化。口服钠丙酸钠给药克雷(0.045?±0.020?Kcal / min; p?= 036);这伴随着全身脂质氧化率的升高(0.012?±0.006Ω·克/分钟; p?= 048),并且与葡萄糖和胰岛素浓度的变化无关。未来的研究是有必要确定口服钠丙酸的急性作用是否转化为人类长期能量平衡的积极改善。

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