Faculty of Agriculture, Kagawa University.
Faculty of Human Sciences, Hokkaido Bunkyo University.
J Oleo Sci. 2024 Oct 1;73(10):1329-1337. doi: 10.5650/jos.ess24099. Epub 2024 Sep 20.
We investigated the effects of a single and simultaneous intake of allitol and d-allulose on body fat accumulation and cecal short-chain fatty acid (SCFA) production and accurately assessed the contribution of rare sugars to body fat in rats fed a high-fat diet that led to obesity. Thirty-two male 3-week-old Wistar rats were randomly divided into four groups: control, allitol, d-allulose, and allitol + d-allulose. The rats were fed experimental diets and water ad libitum for 11 weeks. High doses of allitol or d-allulose can induce diarrhea in rat; hence, each group of rats was acclimated to 1-5% allitol and d-allulose incrementally for the initial 20 days. After the feeding period, all rats were euthanized and collected tissues. Perirenal, mesenteric, and total intra-abdominal adipose tissue weights were significantly reduced by dietary d-allulose, whereas dietary allitol tended to decrease these adipose tissue weights. Both allitol and d-allulose significantly decreased carcass and total body fat mass. We confirmed that both dietary allitol and d-allulose inhibited body fat accumulation; however, d-allulose did not inhibit hepatic lipogenesis and no synergy was observed between dietary allitol and d-allulose in terms of anti-obesity effects. Dietary allitol significantly increased cecal SCFA levels and these effects were more potent than those of dietary d-allulose. The antiobesity effect of allitol may be due to the action of SCFAs, especially butyric acid, produced by the gut microbiota. Many of the effects of allitol as an alternative sweetener remain unknown, and further research is required.
我们研究了单独和同时摄入山梨醇和 d-阿洛酮糖对体脂肪积累和盲肠短链脂肪酸(SCFA)产生的影响,并准确评估了在导致肥胖的高脂肪饮食中,稀有糖对大鼠体脂肪的贡献。32 只 3 周龄雄性 Wistar 大鼠被随机分为四组:对照组、山梨醇组、d-阿洛酮糖组和山梨醇+d-阿洛酮糖组。大鼠自由进食实验饮食和水 11 周。高剂量的山梨醇或 d-阿洛酮糖可引起大鼠腹泻;因此,每组大鼠在前 20 天内逐渐适应 1-5%的山梨醇和 d-阿洛酮糖。喂养期结束后,处死所有大鼠并收集组织。饮食 d-阿洛酮糖显著降低肾周、肠系膜和总腹腔内脂肪组织重量,而饮食山梨醇则倾向于降低这些脂肪组织重量。山梨醇和 d-阿洛酮糖均显著降低了胴体和总体脂质量。我们证实,饮食山梨醇和 d-阿洛酮糖均抑制体脂肪积累;然而,d-阿洛酮糖并未抑制肝内脂肪生成,且饮食山梨醇和 d-阿洛酮糖在抗肥胖作用方面无协同作用。饮食山梨醇显著增加盲肠 SCFA 水平,其作用比饮食 d-阿洛酮糖更强。山梨醇的抗肥胖作用可能归因于肠道微生物产生的 SCFA(特别是丁酸)的作用。山梨醇作为替代甜味剂的许多作用仍不清楚,需要进一步研究。