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鞣花酸通过降低肥胖、糖尿病 KK-A(y) 小鼠血清抵抗素水平和肝 ppara 的转录激活,改善肝脏脂肪变性和血清脂质组成。

Ellagic acid improves hepatic steatosis and serum lipid composition through reduction of serum resistin levels and transcriptional activation of hepatic ppara in obese, diabetic KK-A(y) mice.

机构信息

Department of Applied Biological Chemistry, Graduate School of Agricultural Science, Kinki University, 204-3327 Nakamachi, Nara City, Nara 631-8505, Japan.

出版信息

Biochem Biophys Res Commun. 2013 May 10;434(3):486-91. doi: 10.1016/j.bbrc.2013.03.100. Epub 2013 Apr 10.

Abstract

Ellagic acid (EA) is a polyphenol found in a wide variety of plant foods that not only exhibits free radical-scavenging activity, but also confers protective effects against liver injury. Previously, we reported that pomegranate fruit extract (PFE) had an inhibitory effect on resistin secretion from differentiated murine 3T3-L1 adipocytes and identified EA contained in PFE as a potent suppressor of resistin secretion. Resistin, an adipocytokine, is considered the link between obesity and type 2 diabetes. In this study, we explored whether EA supplementation reduces serum resistin and improves hepatic steatosis and serum lipid profile by using KK-A(y) mice fed high-fat diet as a model for obese type 2 diabetes. We found that EA supplementation improved serum lipid profile and hepatic steatosis, and reduced serum resistin levels without altering mRNA expression levels in adipose tissue. Moreover, EA supplementation upregulated mRNA expression of apoa1, ldlr, cpt1a, and ppara genes in the liver. In conclusion, our findings indicate that EA is a potent suppressor of resistin secretion in vivo and a transcriptional activator of ppara in the liver, suggesting a possibility for improving obesity-induced dyslipidemia and hepatic steatosis in KK-A(y) mice.

摘要

鞣花酸(EA)是一种广泛存在于植物性食物中的多酚,不仅具有清除自由基的活性,还能对肝损伤起到保护作用。此前,我们报道过石榴果实提取物(PFE)对分化的鼠 3T3-L1 脂肪细胞中抵抗素分泌具有抑制作用,并鉴定出 PFE 中含有的 EA 是抵抗素分泌的有效抑制剂。抵抗素是一种脂肪细胞因子,被认为是肥胖和 2 型糖尿病之间的联系。在这项研究中,我们使用高脂肪饮食喂养的 KK-A(y) 小鼠作为肥胖 2 型糖尿病模型,探讨了 EA 补充是否可以通过降低血清抵抗素水平、改善肝脂肪变性和血清脂质谱来发挥作用。结果发现,EA 补充改善了血清脂质谱和肝脂肪变性,降低了血清抵抗素水平,而对脂肪组织中的 mRNA 表达水平没有影响。此外,EA 补充还上调了肝脏中 apoA1、LDLR、CPT1A 和 PPARA 基因的 mRNA 表达。综上所述,我们的研究结果表明,EA 是体内抵抗素分泌的有效抑制剂,也是肝脏中 PPARA 的转录激活剂,这提示 EA 有可能改善 KK-A(y) 小鼠肥胖引起的血脂异常和肝脂肪变性。

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