PMID- 22644639 OWN - NLM STAT- MEDLINE DCOM- 20121106 LR - 20240109 IS - 1559-0291 (Electronic) IS - 0273-2289 (Linking) VI - 167 IP - 7 DP - 2012 Aug TI - Bioactive compounds extracted from Ecklonia cava by using enzymatic hydrolysis protects high glucose-induced damage in INS-1 pancreatic beta-cells. PG - 1973-85 LID - 10.1007/s12010-012-9695-7 [doi] AB - Pancreatic beta-cells are very sensitive to oxidative stress and this might play an important role in beta-cell death in diabetes. In the present study, we investigated whether the brown alga Ecklonia cava has protective effects against high glucose-induced damage in INS-1 pancreatic beta-cells. For that purpose, we prepared an enzymatic hydrolysate from E. cava (EHE) by using the carbohydrase, Celluclast. High-glucose (30 mM) treatment induced glucotoxicity, whereas EHE prevented cells from high glucose-induced damage then restoring cell viability was significantly increased. Furthermore, lipid peroxidation, intracellular reactive oxygen species (ROS) and nitric oxide (NO) were overproduced as the result of the treatment by high glucose; however, these lipid peroxidation, ROS and NO generations were effectively inhibited by addition of EHE in a dose-dependent manner. Moreover, EHE treatment increased activities of antioxidant enzymes including catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-px) in high glucose pretreated INS-1 pancreatic beta-cells. EHE slightly reduced the expression of pro-apoptotic protein Bax induced by high glucose but increased the expression of Bcl-2, an anti-apoptotic protein. These findings indicate that EHE might be used as potential nutraceutical agent which will protect the glucotoxicity caused by hyperglycemia-induced oxidative stress associated with diabetes. FAU - Lee, Seung-Hong AU - Lee SH AD - Department of Marine Life Science, Jeju National University, Jeju 690-756, South Korea. FAU - Park, Mi-Hwa AU - Park MH FAU - Park, Sun-Joo AU - Park SJ FAU - Kim, Jaeil AU - Kim J FAU - Kim, Yong-Tae AU - Kim YT FAU - Oh, Myung-Cheol AU - Oh MC FAU - Jeong, Yoonhwa AU - Jeong Y FAU - Kim, Misook AU - Kim M FAU - Han, Ji-Sook AU - Han JS FAU - Jeon, You-Jin AU - Jeon YJ LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120529 PL - United States TA - Appl Biochem Biotechnol JT - Applied biochemistry and biotechnology JID - 8208561 RN - 0 (Antioxidants) RN - 0 (Biological Products) RN - 0 (Polyphenols) RN - 0 (Polysaccharides) RN - 0 (Protective Agents) RN - 0 (Reactive Oxygen Species) RN - 0 (Thiobarbituric Acid Reactive Substances) RN - 0 (bcl-2-Associated X Protein) RN - 31C4KY9ESH (Nitric Oxide) RN - EC 3.2.1.- (Glycoside Hydrolases) RN - EC 3.2.1.- (carbohydrase) RN - IY9XDZ35W2 (Glucose) SB - IM MH - Animals MH - Antioxidants/metabolism MH - Apoptosis/drug effects MH - Biological Products/*isolation & purification/*pharmacology MH - Cell Line, Tumor MH - Cell Survival/drug effects MH - Cytoprotection/*drug effects MH - Enzyme Assays MH - Glucose/*toxicity MH - Glycoside Hydrolases/*metabolism MH - Hydrolysis/drug effects MH - Insulin-Secreting Cells/drug effects/metabolism/*pathology MH - Intracellular Space/drug effects/metabolism MH - Lipid Peroxidation/drug effects MH - Nitric Oxide/biosynthesis MH - Phaeophyceae/*chemistry MH - Polyphenols/pharmacology MH - Polysaccharides/pharmacology MH - Protective Agents/pharmacology MH - Rats MH - Reactive Oxygen Species/metabolism MH - Staining and Labeling MH - Thiobarbituric Acid Reactive Substances/metabolism MH - bcl-2-Associated X Protein/metabolism EDAT- 2012/05/31 06:00 MHDA- 2012/11/07 06:00 CRDT- 2012/05/31 06:00 PHST- 2011/09/19 00:00 [received] PHST- 2012/04/12 00:00 [accepted] PHST- 2012/05/31 06:00 [entrez] PHST- 2012/05/31 06:00 [pubmed] PHST- 2012/11/07 06:00 [medline] AID - 10.1007/s12010-012-9695-7 [doi] PST - ppublish SO - Appl Biochem Biotechnol. 2012 Aug;167(7):1973-85. doi: 10.1007/s12010-012-9695-7. Epub 2012 May 29.