Protective Effect of 2-Dodecyl-6-Methoxycyclohexa-2, 5-Diene-1, 4-Dione, Isolated from Averrhoa Carambola L., Against Palmitic Acid-Induced Inflammation and Apoptosis in Min6 Cells by Inhibiting the TLR4-MyD88-NF-κB Signaling Pathway

被引：25

作者：

Xie, Qiuqiao ^{[1
]}

Zhang, Shijun ^{[1
]}

Chen, Chunxia ^{[1
]}

Li, Juman ^{[1
]}

Wei, Xiaojie ^{[1
]}

Xu, Xiaohui ^{[1
]}

Xuan, Feifei ^{[1
]}

Chen, Ning ^{[1
]}

Pham, Thithaihoa ^{[1
]}

Qin, Ni ^{[1
]}

He, Junhui ^{[1
]}

Ye, Fangxing ^{[1
]}

Huang, Wansu ^{[1
]}

Huang, Renbin ^{[1
]}

Wen, Qingwei ^{[1
]}

机构：

[1] Guangxi Med Univ, Pharmaceut Coll, 22 Shuangyong Rd, Nanning 530021, Guangxi, Peoples R China

来源：

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY | 2016年 / 39卷 / 05期

基金：

中国国家自然科学基金;

关键词：

DMDD; Min6; cell; Inflammation; Apoptosis; TLR4; MyD88; NF-kappa B; INSULIN-SECRETION; OXALIDACEAE ROOTS; DOWN-REGULATION; PROTEIN-KINASE; ELIMINATION; EXTRACT; GLP-1;

D O I：

10.1159/000447871

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Background/Aims: Studies have demonstrated that 2-dodecy1-6-methoxycyclohexa-2, 5-diene-1, 4-dione (DMDD), isolated from the roots of Averrhoa carambola L., has significant therapeutic potential for the treatment of diabetes. However, the protective effect of DMDD against pancreatic beta cell dysfunction has never been reported. We investigated whether DMDD protected against palmitic acid-induced dysfunction in pancreatic p-cell line Min6 cells by attenuating the inflammatory response and apoptosis and to shed light on its possible mechanism. Methods: Cell viability was assessed by CCK-8. Glucose-stimulated insulin secretion levels and inflammatory cytokines levels were examined by ELISA. Apoptosis was assessed by Annexin V-FITC/PI Flow cytometry assay, Hoechst 33342/PI double-staining assay, and Transmission electron microscopy assay. Relative quantitative real-time PCR and western blot were used to determine the expressions of genes and proteins. Results: Cell viability and glucose -stimulated insulin secretion levels were increased in DMDD-pretreated Min6 cells. DMDD inhibited inflammatory cytokines IL-6, TNF-alpha and MCP-1 generations in palmitic acid (PA)-induced Min6 cells. Moreover. DMDD protected against PA -induced Min6 cells apoptosis and the expression of Cleaved-Caspase-3, -8 and -9 were down-regulated and the BcI-2/Bax ratio was increased in DMDD-pretreated Min6 cells. In addition, the expression of TLR4, MyD88 and NF-kappa B were down-regulated in DMDD-pretreated Min6 cells and TAK-242-pretreated group cells. Conclusions: DMDD protected Min6 cells against PA -induced dysfunction by attenuating the inflammatory response and apoptosis, and its mechanism of this protection was associated with inhibiting the TLR4-MyD88-NF-kappa B signaling pathway. (C) 2016 The Author(s) Published by S. Karger AG, Basel

引用

页码：1705 / 1715

页数：11

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