毛螺菌科
山梨醇
肠道菌群
内分泌学
葡萄糖稳态
内科学
生物
微生物群
糖耐量试验
山梨醇脱氢酶
胰岛素
胰岛素抵抗
食品科学
医学
生物化学
基因
生物信息学
厚壁菌
16S核糖体RNA
作者
Chung‐Hao Li,Chung-Teng Wang,Ying-Ju Lin,Hsin‐Yu Kuo,Juei-Seng Wu,Tzu‐Chun Hong,Chih‐Jen Chang,Hung‐Tsung Wu
出处
期刊:Life Sciences
[Elsevier BV]
日期:2022-07-02
卷期号:305: 120770-120770
被引量:25
标识
DOI:10.1016/j.lfs.2022.120770
摘要
Epidemic obesity and diabetes have led to increased use of low-calorie sweeteners. Although several studies have suggested that consumption of artificial sweeteners, such as aspartame and saccharin, might have negative effects, the potential impacts of natural sweeteners on human health remain largely unknown.The deferential effects of short term and long term consumption of sorbitol on glucose homeostasis in mice by oral gavage. The glucose homeostasis and utility were evaluated by both oral or intraperitoneal glucose tolerance tests. Insulin levels were determined using enzyme-linked immunosorbent assay. Changes of gut microbiome were evaluated by 16S rRNA gene sequencing, and analyzed by principal components analysis.Bolus feeding of sorbitol by gavage significantly increased plasma insulin concentrations and decreased fasting blood glucose levels. Intriguingly, long-term sorbitol gavage for four weeks showed no significant effects on intraperitoneal glucose tolerance test outcomes, but it induced glucose intolerance according to the oral glucose tolerance test. Thus, we tested whether long-term sorbitol gavage might alter the relative abundances of gut microbiome constituents in mice. Principal components analysis indicated that long-term sorbitol intake indeed caused significant changes to the gut microbiome. In particular, we found that long-term sorbitol intake significantly decreased the relative abundances of Bifidobacterium, Lachnospiraceae UCG 001, Lachnospiraceae NK4A136, Eubacterium ventriosum, Candidatus Arthromitus, and Ruminococcus torques. We also found that long-term sorbitol increased the relative abundances of Helicobacter, Tyzzerella, Alistipes, and Prevotella 9.Long-term sorbitol consumption may change the composition of the gut microbiome and potentially induce glucose intolerance.
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