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10-羟基-2-癸烯酸,一种天然产物,可改善肥胖/糖尿病KK-Ay小鼠的高血糖和胰岛素抵抗,但不能预防肥胖。

10-Hydroxy-2-decenoic acid, a natural product, improves hyperglycemia and insulin resistance in obese/diabetic KK-Ay mice, but does not prevent obesity.

作者信息

Watadani Risa, Kotoh Jun, Sasaki Daiki, Someya Azusa, Matsumoto Kozo, Maeda Akihiko

机构信息

Department of Animal Medical Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Motoyama, Kamigamo, Kita-ku, Kyoto 603-8555, Japan.

出版信息

J Vet Med Sci. 2017 Sep 29;79(9):1596-1602. doi: 10.1292/jvms.17-0348. Epub 2017 Jul 22.

DOI:10.1292/jvms.17-0348
PMID:28740028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5627335/
Abstract

10-Hydroxy-2-decenoic acid (10H2DA) is a fatty acid found in royal jelly (RJ). In healthy mice, it activates 5'-AMP-activated protein kinase (AMPK) and increases glucose transporter 4 (GLUT4) translocation. Therefore, we examined whether 10H2DA has a potential therapeutic effect against type 2 diabetes in obese/diabetic KK-Ay mice. 10H2DA (3 mg/kg body weight) was administered to female KK-Ay mice for 4 weeks by oral gavage. Phenotypes for body weight, plasma glucose by oral glucose tolerance test and insulin levels were measured. mRNA and protein levels were determined using qRT-PCR and Western blot analyses, respectively. Long-term administration of 10H2DA significantly improved hyperglycemia and insulin resistance in KK-Ay mice, but did not prevent obesity. 10H2DA increased the expression of phosphorylated AMPK (pAMPK) protein in skeletal muscles; however, this expression did not correlate with increased GLUT4 translocation. Furthermore, 10H2DA neither enhanced the expression of adiponectin receptor mRNA nor activated the insulin signaling cascade, such as GSK-3β phosphorylation, in the liver. We found that 10H2DA-treated mice had a significant increase in the expression of peroxisome proliferator-activated receptor gamma coactivator 1 alpha (Pgc-1α) mRNA in skeletal muscles compared with non-treated group (P=0.0024). These findings suggest that 10H2DA is involved in the improvement of type 2 diabetes, at least in part via activation of Pgc-1α expression, but does not prevent obesity.

摘要

10-羟基-2-癸烯酸(10H2DA)是一种存在于蜂王浆(RJ)中的脂肪酸。在健康小鼠中,它可激活5'-AMP激活的蛋白激酶(AMPK)并增加葡萄糖转运蛋白4(GLUT4)的易位。因此,我们研究了10H2DA对肥胖/糖尿病KK-Ay小鼠的2型糖尿病是否具有潜在治疗作用。通过口服灌胃法给雌性KK-Ay小鼠施用10H2DA(3毫克/千克体重),持续4周。测量体重、口服葡萄糖耐量试验的血浆葡萄糖和胰岛素水平的表型。分别使用qRT-PCR和蛋白质印迹分析来测定mRNA和蛋白质水平。长期施用10H2DA可显著改善KK-Ay小鼠的高血糖和胰岛素抵抗,但不能预防肥胖。10H2DA增加了骨骼肌中磷酸化AMPK(pAMPK)蛋白的表达;然而,这种表达与GLUT4易位增加无关。此外,10H2DA既没有增强脂联素受体mRNA的表达,也没有激活肝脏中的胰岛素信号级联反应,如GSK-3β磷酸化。我们发现,与未处理组相比,10H2DA处理的小鼠骨骼肌中过氧化物酶体增殖物激活受体γ共激活因子1α(Pgc-1α)mRNA的表达显著增加(P = 0.0024)。这些发现表明,10H2DA至少部分通过激活Pgc-1α的表达参与2型糖尿病的改善,但不能预防肥胖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/11d2a1b40c6a/jvms-79-1596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/90780828810a/jvms-79-1596-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/a49dec15fcce/jvms-79-1596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/a57354e781bf/jvms-79-1596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/11d2a1b40c6a/jvms-79-1596-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/90780828810a/jvms-79-1596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/64fcff240c31/jvms-79-1596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/a49dec15fcce/jvms-79-1596-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/a57354e781bf/jvms-79-1596-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5627335/11d2a1b40c6a/jvms-79-1596-g005.jpg

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