Hypoxylonol F Isolated from Annulohypoxylon annulatum Improves Insulin Secretion by Regulating Pancreatic beta-cell Metabolism

Authors
Lee, DahaeHwang, Buyng SuChoi, PiljuKim, TaejungKim, YoungseokSong, Bong GeunYamabe, NorikoHwang, Gwi SeoKang, Ki SungHam, Jungyeob
Issue Date
2019-08
Publisher
MDPI
Citation
BIOMOLECULES, v.9, no.8
Abstract
Insulin plays a key role in glucose homeostasis and is hence used to treat hyperglycemia, the main characteristic of diabetes mellitus. Annulohypoxylon annulatum is an inedible ball-shaped wood-rotting fungus, and hypoxylon F is one of the major compounds of A. annulatum. The aim of this study is to evaluate the effects of hypoxylonol F isolated from A. annulatum on insulin secretion in INS-1 pancreatic beta-cells and demonstrate the molecular mechanisms involved. Glucose-stimulated insulin secretion (GSIS) values were evaluated using a rat insulin ELISA kit. Moreover, the expression of proteins related to pancreatic beta-cell metabolism and insulin secretion was evaluated using Western blotting. Hypoxylonol F isolated from A. annulatum was found to significantly enhance glucose-stimulated insulin secretion without inducing cytotoxicity. Additionally, hypoxylonol F enhanced insulin receptor substrate-2 (IRS-2) levels and activated the phosphatidylinositol 3-kinase/protein kinase B (PI3K/Akt) pathway. Interestingly, it also modulated the expression of peroxisome proliferator-activated receptor gamma (PPAR gamma) and pancreatic and duodenal homeobox 1 (PDX-1). Our findings showed that A. annulatum and its bioactive compounds are capable of improving insulin secretion by pancreatic beta-cells. This suggests that A. annulatum can be used as a therapeutic agent to treat diabetes.
Keywords
GLUCOSE; PIOGLITAZONE; METFORMIN; SAFETY; RISK; PDX1; MASS; GLUCOSE; PIOGLITAZONE; METFORMIN; SAFETY; RISK; PDX1; MASS; Annulohypoxylon annulatum; insulin; PI3K; Akt; PPAR gamma; PDX-1
ISSN
2218-273X
URI
https://pubs.kist.re.kr/handle/201004/119735
DOI
10.3390/biom9080335
Appears in Collections:
KIST Article > 2019
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