Yuan Haidan, Chung Sunghyun, Ma Qianqian, Ye L I, Piao Guangchun
Department of Pharmacognosy, College of Pharmacy, Yanbian University, Yanji, Jilin 133000, P.R. China; Key Laboratory of Natural Resources of Changbai Mountain and Functional Molecules, Ministry of Education, Yanbian University, Yanji, Jilin 133000, P.R. China.
Department of Pharmacology, College of Pharmacy, Kyung Hee University, Seoul 130701, Republic of Korea.
Exp Ther Med. 2016 Jan;11(1):338-344. doi: 10.3892/etm.2015.2852. Epub 2015 Nov 10.
The aim of the present study was to evaluate the protective effects of a combination of deep sea water (DSW) and Sesamum indicum leaf extract (SIE) against high-fat diet (HFD)-induced obesity and investigate its molecular mechanisms in adipose tissue. ICR mice were randomly divided into three groups: HFD control (HFC), DSW and DSW + 125 mg/kg SIE (DSS) groups. The mice in the HFC group had free access to drinking water while those in the DSW and DSS groups had free access to DSW. The mice in the DSS group were treated with SIE once per day for 8 weeks. The mice in all three groups were allowed to freely access a HFD. Compared with the HFC group, the DSS group showed lower body weight gain and serum levels of glucose, triglycerides and leptin. Histological analyses of the epididymal white, retroperitoneal white and scapular brown adipose tissue of mice in the DSS group revealed that the adipocytes were markedly decreased in size compared with those in the HFC group. Moreover, DSS significantly increased the levels of phosphorylated adenosine monophosphate-activated protein kinase (AMPK) and its substrate, acetyl-CoA carboxylase (ACC) in mice epididymal adipose tissues. Furthermore, DSS upregulated the expression levels of lipolysis-associated mRNA, specifically peroxisome proliferator-activated receptor-α (PPAR-α) and cluster of differentiation 36 (CD36), and energy expenditure-associated mRNA, namely uncoupling protein 2 (UCP2) and carnitine palmitoyltransferase-1 (CPT1) in the epididymal adipose tissues. By contrast, DSS suppressed the expression of the lipogenesis-related gene sterol regulatory element-binding protein-1 (SREBP1) at the mRNA level. These results suggest that DSS is effective for suppressing body weight gain and enhancing the lipid profile.
本研究的目的是评估深海水(DSW)和芝麻叶提取物(SIE)联合使用对高脂饮食(HFD)诱导的肥胖的保护作用,并研究其在脂肪组织中的分子机制。将ICR小鼠随机分为三组:HFD对照组(HFC)、DSW组和DSW + 125 mg/kg SIE组(DSS)。HFC组小鼠可自由饮用普通水,而DSW组和DSS组小鼠可自由饮用深海水。DSS组小鼠每天接受一次SIE处理,持续8周。三组小鼠均自由摄取高脂饮食。与HFC组相比,DSS组小鼠体重增加、血糖、甘油三酯和瘦素血清水平较低。对DSS组小鼠附睾白色、腹膜后白色和肩胛棕色脂肪组织的组织学分析显示,与HFC组相比,其脂肪细胞大小明显减小。此外,DSS显著提高了小鼠附睾脂肪组织中磷酸化的腺苷单磷酸激活蛋白激酶(AMPK)及其底物乙酰辅酶A羧化酶(ACC)的水平。此外,DSS上调了附睾脂肪组织中脂解相关mRNA的表达水平,特别是过氧化物酶体增殖物激活受体-α(PPAR-α)和分化簇36(CD36),以及能量消耗相关mRNA,即解偶联蛋白2(UCP2)和肉碱棕榈酰转移酶-1(CPT1)。相比之下,DSS在mRNA水平上抑制了脂肪生成相关基因固醇调节元件结合蛋白-1(SREBP1)的表达。这些结果表明,DSS对抑制体重增加和改善血脂状况有效。