Watadani Risa, Kotoh Jun, Sasaki Daiki, Someya Azusa, Matsumoto Kozo, Maeda Akihiko
Department of Animal Medical Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Motoyama, Kamigamo, Kita-ku, Kyoto 603-8555, Japan.
J Vet Med Sci. 2017 Sep 29;79(9):1596-1602. doi: 10.1292/jvms.17-0348. Epub 2017 Jul 22.
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.
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。