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

Authors :
Hu Q
Niu Q
Song H
Wei S
Wang S
Yao L
Li YP
Source :
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2019 Jan; Vol. 109, pp. 876-885. Date of Electronic Publication: 2018 Nov 05.
Publication Year :
2019

Abstract

The present study was undertaken to determine the involvement of voltage-gated Na <superscript>+</superscript> channel (VGSC) and other mechanism related to insulin secretion in polysaccharides from Portulaca oleracea L. (POP)-induced secretion of insulin from insulin-secreting β-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 (Δψm), increased adenosine triphosphate (ATP) production, depolarized cell membrane potential (MP) and increased intracellular Ca <superscript>2+</superscript> levels ([Ca <superscript>2+</superscript> ] <subscript>i</subscript> ). Furthermore, POP treatment increased the expression level of Nav <subscript>1.3</subscript> and decreased the expression level of Nav <subscript>1.7.</subscript> TTX treatment decreased the expression level of Nav <subscript>1.3</subscript> and Nav <subscript>1.7</subscript> . 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 Ca <superscript>2+</superscript> 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.<br /> (Copyright © 2018. Published by Elsevier Masson SAS.)

Details

Language :
English
ISSN :
1950-6007
Volume :
109
Database :
MEDLINE
Journal :
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Publication Type :
Academic Journal
Accession number :
30551541
Full Text :
https://doi.org/10.1016/j.biopha.2018.10.113