Anti-diabetic and hypolipidemic effects of Sargassum yezoense in db/db mice

被引:23
作者
Kim, Su-Nam [1 ]
Lee, Woojung [1 ]
Bae, Gyu-Un [2 ,3 ]
Kim, Yong Kee [2 ]
机构
[1] KIST Gangneung Inst, Nat Med Ctr, Kangnung 210340, South Korea
[2] Sookmyung Womens Univ, Coll Pharm, Seoul 140742, South Korea
[3] Sookmyung Womens Univ, Res Ctr Cell Fate Control, Seoul 140742, South Korea
关键词
Sargassum yezoense; PPAR alpha/gamma; Type 2 diabetes mellitus; Dyslipidemia; PPAR-ALPHA/GAMMA AGONIST; MISCELLANEOUS MECHANISMS; ANTIVIRAL ACTIVITIES; MARINE PHARMACOLOGY; LIPID-METABOLISM; NERVOUS SYSTEMS; EXPRESSION; OBESITY; WEIGHT; RISK;
D O I
10.1016/j.bbrc.2012.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peroxisome proliferator-activated receptors (PPARs) have been considered to be desirable targets for metabolic syndrome, even though their specific agonists have several side effects including body weight gain, edema and tissue failure. Previously, we have reported in vitro effects of Sargassum yezoense (SY) and its ingredients, sargaquinoic acid (SQA) and sargahydroquinoic acid (SHQA), on PPAR alpha/gamma dual transcriptional activation. In this study, we describe in vivo pharmacological property of SY on metabolic disorders. SY treatment significantly improved glucose and lipid impairment in db/db mice model. More importantly, there are no significant side effects such as body weight gain and hepatomegaly in SY-treated animals, indicating little side effects of SY in liver and lipid metabolism. In addition, SY led to a decrease in the expression of G6Pase for gluconeogenesis in liver responsible for lowering blood glucose level and an increase in the expression of UCP3 in adipose tissue for the reduction of total and LDL-cholesterol level. Altogether, our data suggest that SY would be a potential therapeutic agent against type 2 diabetes and related metabolic disorders by ameliorating the glucose and lipid metabolism. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:675 / 680
页数:6
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