Polysaccharides from Portulaca oleracea L. regulated insulin secretion in INS-1 cells through voltage-gated Na+ channel

被引:25
作者
Hu, Qingjuan [1 ]
Niu, Qingchuan [1 ]
Song, Hao [1 ]
Wei, Shanshan [1 ]
Wang, Songhua [2 ]
Yao, Lihua [1 ]
Li, Yu-Ping [1 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Sch Life Sci, Nanchang 330013, Jiangxi, Peoples R China
[2] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Polysaccharide; Insulin-secreting beta-cell line cells; Voltage-gated Na (+) channels; Insulin; Tetrodotoxin; ANTITUMOR-ACTIVITY; BETA-CELLS; MODULATION; EXOCYTOSIS; CURRENTS; GLUCOSE;
D O I
10.1016/j.biopha.2018.10.113
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The present study was undertaken to determine the involvement of voltage-gated Na+ channel (VGSC) and other mechanism related to insulin secretion in polysaccharides from Portulaca oleracea L. (POP)-induced secretion of insulin from insulin-secreting beta-cell line cells (INS-1) cells. Our results showed that the concentration of insulin both in culture medium and inside INS-1 cells were increased under the existing of different concentration of glucose by POP or TTX, respectively. However, the effect POP on insulin secretion and production were blocked by TTX, a VGSC blocker. Meanwhile, POP improved the mitochondrial membrane potential (Delta Psi m), increased adenosine triphosphate (ATP) production, depolarized cell membrane potential (MP) and increased intracellular Ca2+ levels ([Ca2+]i). Furthermore, POP treatment increased the expression level of Nav(1.3) and decreased the expression level of Nav(1.7). TTX treatment decreased the expression level of Nav(1.3) and Nav(1.7). On the other hand, POP also elevated the survival of INS-1 cells. These results suggested that POP induced-secretion/production of insulin in INS-1 cells were mediated by VGSC through its change of function and subunits expression and subsequent VGSC-dependent events such as change of intracellular Ca2+ releasing, ATP metabolism, cell membrane and mitochondrial membrane potential, and also improvement of INS-1 cell survival. Meanwhile, our data indicated the potentiality of developing POP to be a drug for diabetes treatment and VGSC as a therapeutic target in diabetes treatment is valuable to be investigated further.
引用
收藏
页码:876 / 885
页数:10
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