Li Jing, Luo Mei, Hu Minghua, Guo An-Yuan, Yang Xiangliang, Zhang Qiong, Zhu Yanhong
National Engineering Research Center for Nano medicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Key Laboratory of Molecular Biophysics of the Ministry of Education, Department of Bioinformatics and Systems Biology, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Front Pharmacol. 2018 Aug 9;9:912. doi: 10.3389/fphar.2018.00912. eCollection 2018.
Diabetes is generally regarded as a metabolic disorder disease caused by various reasons, including pancreas islet injury and lipid metabolism disorders. The aqueous extract of leaves (CPAE) was reported to be anti-diabetic. However, the possible molecular mechanisms have not been investigated. To elucidate the anti-diabetic effects of CPAE and the underlying potential mechanisms, we performed transcriptome profiling (RNA-Seq and miRNA-Seq) on the pancreas and liver from non-diabetic, diabetic and diabetic-CPAE rats. Our results demonstrated the CPAE could reduce excessive oxidative stress and inflammation in the pancreas, and maintain the balance of glucose and lipid metabolism in the liver. Transcriptome profiling and regulatory network analysis indicated that CPAE may ameliorate diabetes through improving β-cell survival and strengthening insulin secretion in the pancreas. Meanwhile, CPAE could improve impaired lipid metabolism and reduce excessive oxidative damage in the liver probably through miR-200/375-/- co-regulatory network. Taken together, our biochemical experiments combined with transcriptome profiling showed that the effects of CPAE on anti-diabetes may work through protecting pancreatic β-cell, improving dyslipidaemia and lipid metabolism disorders.
糖尿病通常被认为是一种由多种原因引起的代谢紊乱疾病,包括胰岛损伤和脂质代谢紊乱。据报道,叶水提取物(CPAE)具有抗糖尿病作用。然而,其可能的分子机制尚未得到研究。为了阐明CPAE的抗糖尿病作用及其潜在机制,我们对非糖尿病、糖尿病和糖尿病-CPAE大鼠的胰腺和肝脏进行了转录组分析(RNA测序和miRNA测序)。我们的结果表明,CPAE可以减轻胰腺中的过度氧化应激和炎症,并维持肝脏中葡萄糖和脂质代谢的平衡。转录组分析和调控网络分析表明,CPAE可能通过改善胰腺中β细胞的存活和增强胰岛素分泌来改善糖尿病。同时,CPAE可能通过miR-200/375-/-共同调控网络改善肝脏中受损的脂质代谢并减少过度的氧化损伤。综上所述,我们的生化实验与转录组分析表明,CPAE的抗糖尿病作用可能是通过保护胰腺β细胞、改善血脂异常和脂质代谢紊乱来实现的。