Kim Seung-Jin, Jung Jin Young, Kim Ha Won, Park Taesun
Department of Food and Nutrition, Brain Korea 21 Project, Yonsei University, Seoul, Korea.
Biol Pharm Bull. 2008 Jul;31(7):1415-21. doi: 10.1248/bpb.31.1415.
This study evaluates the protective effect of Juniperus chinensis hot water extract (JCE) against high-fat-diet (HFD)-induced obesity and its molecular mechanisms in the visceral adipose tissue of rats. JCE supplementation significantly lowered body weight gain, visceral fat-pad weights, blood lipid levels, and blood insulin and leptin levels of rats rendered obese by an HFD. Feeding with JCE significantly reversed the HFD-induced down-regulation of the epididymal adipose tissue genes implicated in adipogenesis, such as the peroxisome proliferator-activated receptors gamma2 (PPARgamma2), adipocyte protein 2 (aP2), sterol regulatory element binding protein 1c (SREBP1c), fatty acid synthase (FAS), and HMG-CoA reductase (HMGR), as well as those involved in uncoupled respiration, such as the uncoupling protein 2 (UCP2) and uncoupling protein 3 (UCP3). Dietary supplementation with JCE also reversed the HFD-induced decreases in the AMP-activated protein kinase (AMPK) and the acetyl-CoA carboxylase 2 (ACC2) expressions at both the mRNA and protein levels and restored the HFD-induced inhibitions in the AMPK and ACC2 phosphorylation, which are related to fatty acid beta-oxidation, in the epididymal adipose tissue. This study reports, for the first time, that the JCE can have an anti-obesity effect in a rodent model with HFD-induced obesity through an enhanced gene transcription of the uncoupling protein as well as an elevated AMPK protein expression and phosphorylation in the visceral adipose tissue.
本研究评估了桧柏热水提取物(JCE)对高脂饮食(HFD)诱导的大鼠肥胖的保护作用及其在内脏脂肪组织中的分子机制。补充JCE可显著降低HFD诱导的肥胖大鼠的体重增加、内脏脂肪垫重量、血脂水平、血液胰岛素和瘦素水平。用JCE喂养可显著逆转HFD诱导的附睾脂肪组织中与脂肪生成相关基因的下调,如过氧化物酶体增殖物激活受体γ2(PPARγ2)、脂肪细胞蛋白2(aP2)、固醇调节元件结合蛋白1c(SREBP1c)、脂肪酸合酶(FAS)和HMG-CoA还原酶(HMGR),以及参与解偶联呼吸的基因,如解偶联蛋白2(UCP2)和解偶联蛋白3(UCP3)。饮食中补充JCE还可逆转HFD诱导的附睾脂肪组织中AMP激活蛋白激酶(AMPK)和乙酰辅酶A羧化酶2(ACC2)在mRNA和蛋白水平的表达下降,并恢复HFD诱导的与脂肪酸β氧化相关的AMPK和ACC2磷酸化抑制。本研究首次报道,JCE可通过增强解偶联蛋白的基因转录以及提高内脏脂肪组织中AMPK蛋白表达和磷酸化,对HFD诱导肥胖的啮齿动物模型产生抗肥胖作用。