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Article ; Online: Decrement in Cellular Iron and Reactive Oxygen Species, and Improvement of Insulin Secretion in a Pancreatic Cell Line Using Green Tea Extract.

Koonyosying, Pimpisid / Uthaipibull, Chairat / Fucharoen, Suthat / Koumoutsea, Evangelia Vlachodimitropoulou / Porter, John B / Srichairatanakool, Somdet

Pancreas

2019  Volume 48, Issue 5, Page(s) 636–643

Abstract: Objectives: We have investigated the efficacy of mono- and combined therapy with green tea extract (GTE) in mobilizing redox iron, scavenging reactive oxygen species (ROS), and improving insulin production in iron-loaded pancreatic cells.: Methods: ... ...

Abstract Objectives: We have investigated the efficacy of mono- and combined therapy with green tea extract (GTE) in mobilizing redox iron, scavenging reactive oxygen species (ROS), and improving insulin production in iron-loaded pancreatic cells.
Methods: Rat insulinoma pancreatic β-cells were iron-loaded using culture medium supplemented with either fetal bovine serum or ferric ammonium citrate and treated with various doses of GTE for epigallocatechin-3-gallate (EGCG) equivalence and in combination with iron chelators. Cellular iron, ROS, and secretory insulin were measured.
Results: The rat insulinoma pancreatic cells took up iron from fetal bovine serum more rapidly than ferric ammonium citrate. After treatment with GTE (0.23-2.29 μg EGCG equivalent), cellular levels of iron and ROS were dose dependently decreased. Importantly, secretory insulin levels were increased nearly 2.5-fold with 2.29 μg of EGCG equivalent GTE, indicating a recovery in insulin production.
Conclusions: Green tea EGCG ameliorated oxidative damage of iron-loaded β-cells by removing redox iron and free radicals and attenuating insulin production. The impact can result in the restoration of pancreatic functions and an increase in insulin production. Green tea extract exerts iron-chelating, free-radical scavenging, and pancreato-protective effects in the restoration of β-cell functions, all of which we believe can increase insulin production in diabetic β-thalassemia patients.
MeSH term(s) Animals ; Catechin/analogs & derivatives ; Catechin/pharmacology ; Cell Line, Tumor ; Diabetes Complications/metabolism ; Insulin/metabolism ; Insulin Secretion/drug effects ; Insulin-Secreting Cells/drug effects ; Insulin-Secreting Cells/metabolism ; Insulin-Secreting Cells/pathology ; Iron/metabolism ; Phytotherapy/methods ; Plant Extracts/pharmacology ; Rats ; Reactive Oxygen Species/metabolism ; Tea/chemistry ; beta-Thalassemia/complications ; beta-Thalassemia/metabolism
Chemical Substances Insulin ; Plant Extracts ; Reactive Oxygen Species ; Tea ; Catechin (8R1V1STN48) ; epigallocatechin gallate (BQM438CTEL) ; Iron (E1UOL152H7)
Language English
Publishing date 2019-05-15
Publishing country United States
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 632831-3
ISSN 1536-4828 ; 0885-3177
ISSN (online) 1536-4828
ISSN 0885-3177
DOI 10.1097/MPA.0000000000001320
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