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Mulberry Leaf Regulates Differentially Expressed Genes in Diabetic Mice Liver Based on RNA-Seq Analysis

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Journal Front Physiol
Date 2018 Aug 23
PMID 30131712
Citations 11
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Abstract

The pathogenesis of diabetes mellitus is a complicated process involving much gene regulation. The molecular mechanism of mulberry ( L.) leaf in the treatment of diabetes is not fully understood. In this study, we used the Illumina HiSeq™ 2,500 platform to explore the liver transcriptome of normal mice, STZ-induced diabetic mice, and mulberry leaf-treated diabetic mice, and we obtained 52,542,956, 52,626,414, and 52,780,196 clean reads, respectively. We identified differentially expressed genes (DEGs) during the pathogenesis of diabetes in mice. The functional properties of DEGs were characterized by comparison with the GO and KEGG databases, and the results show that DEGs are mainly involved in the metabolic pathway. qRT-PCR was used to analyse 27 differential genes involved in liver expression in different groups of diabetic mice. Among the DEGs, the expression of , and other genes between the control (C) and diabetic control (DC) groups was significantly upregulated; the expression of , and was significantly downregulated; the expression of the , and genes between the C group and diabetic group treated with mulberry (DD) was significantly upregulated; the expression of , and was significantly downregulated; and the expression of and was significantly upregulated in the DC and DD groups, but , and were significantly downregulated. The results of Western blot validation showed that dynamic changes in proteins, such as IGF2, Ly6a, Grb10, and UBD, occurred to regulate the incidence of diabetes by influencing the insulin receptor substrate (IRS) signaling pathway.

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References
1.
Mu Q, Wang L, Yu F, Gao H, Lei T, Li P . Imp2 regulates GBM progression by activating IGF2/PI3K/Akt pathway. Cancer Biol Ther. 2015; 16(4):623-33. PMC: 4622833. DOI: 10.1080/15384047.2015.1019185. View

2.
Shibata Y, Kume N, Arai H, Hayashida K, Inui-Hayashida A, Minami M . Mulberry leaf aqueous fractions inhibit TNF-alpha-induced nuclear factor kappaB (NF-kappaB) activation and lectin-like oxidized LDL receptor-1 (LOX-1) expression in vascular endothelial cells. Atherosclerosis. 2006; 193(1):20-7. DOI: 10.1016/j.atherosclerosis.2006.08.011. View

3.
Ou T, Hsu M, Chan K, Huang C, Ho H, Wang C . Mulberry extract inhibits oleic acid-induced lipid accumulation via reduction of lipogenesis and promotion of hepatic lipid clearance. J Sci Food Agric. 2011; 91(15):2740-8. DOI: 10.1002/jsfa.4489. View

4.
Kimura T, Nakagawa K, Kubota H, Kojima Y, Goto Y, Yamagishi K . Food-grade mulberry powder enriched with 1-deoxynojirimycin suppresses the elevation of postprandial blood glucose in humans. J Agric Food Chem. 2007; 55(14):5869-74. DOI: 10.1021/jf062680g. View

5.
Huang X, He Y, Ji L, Wang K, Wang Y, Chen D . Hepatoprotective potential of isoquercitrin against type 2 diabetes-induced hepatic injury in rats. Oncotarget. 2017; 8(60):101545-101559. PMC: 5731895. DOI: 10.18632/oncotarget.21074. View