Anti-obesity effects of galacto-oligosaccharides in obese rats

被引:8
|
作者
Kong, Shang [1 ,2 ]
Huang, Xingjun [3 ,4 ]
Cao, Hua [5 ]
Bai, Yan [6 ]
Che, Qishi [7 ]
Nie, Hong [1 ,2 ]
Su, Zhengquan [3 ]
机构
[1] Jinan Univ, Coll Pharm, Guangdong Prov Key Lab Pharmacodynam Constituents, Guangzhou 510632, Peoples R China
[2] Jinan Univ, Coll Pharm, Chinese Minist Educ MOE, Int Cooperat Lab Tradit Chinese Med Modernizat &, Guangzhou 510632, Peoples R China
[3] Guangdong Pharmaceut Univ, Guangdong Prov Univ, Engn Technol Res Ctr Nat Prod & Drugs, Guangdong Engn Res Ctr Nat Prod & New Drugs, Guangzhou 510006, Peoples R China
[4] Guangdong Pharmaceut Univ, Guangdong Metab Dis Res Ctr Integrated Chinese &, Guangzhou 510006, Peoples R China
[5] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Guangdong Cosmet Engn & Technol Res Ctr, Guangzhou 510006, Peoples R China
[6] Guangdong Pharmaceut, Sch Publ Hlth, Guangzhou 510310, Peoples R China
[7] Guangzhou Rainhome Pharm & Tech Co Ltd, Guangzhou 510663, Peoples R China
关键词
Obesity; Galacto-oligosaccharides; Browning; Thermogenesis; Lipid metabolism; BROWN ADIPOSE-TISSUE; CHITOSAN OLIGOSACCHARIDE; ADIPOCYTES; RECEPTOR;
D O I
10.1016/j.ejphar.2021.174728
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Galacto-oligosaccharides (GOS) are commonly used as prebiotic with a variety of known metabolic benefits; however, whether GOS plays a protective role in obesity remains unknown. Here, we demonstrate that GOS prevented obesity in a rat model of obesity induced by a high-fat diet. Our results showed that GOS effectively slowed weight gain in diet-induced obese rats without affecting energy intake. GOS significantly suppressed the hypertrophy and hyperplasia of white adipose tissue and markedly reduced the ratio of the fat/body. Consistently, GOS significantly improved serum total cholesterol, triglycerides, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol levels, indicating the weight loss activity of GOS. Interestingly, GOS also significantly increased the expression levels of browning proteins, including uncoupling protein 1, peroxisome proliferator-activated receptor-gamma, peroxisome proliferator-activated receptor-gamma coactivator 1 alpha, and PR domain 16, in both white and brown adipose tissue. Furthermore, we found that GOS markedly increased the expression levels of liver X receptor alpha, peroxisome proliferation-activated receptor-alpha, low-density lipoprotein receptor, and cholesterol 7 alpha-hydroxylase proteins in the liver of obese rats. Taken together, we concluded that GOS inhibits obesity by accelerating the browning of white fat cells and the thermogenesis of brown fat cells and that GOS improves host lipid homeostasis by promoting cholesterol catabolism.
引用
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页数:10
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