PMID- 20698744 OWN - NLM STAT- MEDLINE DCOM- 20110112 LR - 20101201 IS - 1362-3095 (Electronic) IS - 0955-3002 (Linking) VI - 86 IP - 12 DP - 2010 Dec TI - Purple sweet potato pigments protect murine thymocytes from (6)(0)Co gamma-ray-induced mitochondria-mediated apoptosis. PG - 1061-9 LID - 10.3109/09553002.2010.501840 [doi] AB - PURPOSE: Purple sweet potato (PSP) pigments have been widely accepted as antioxidants but their radioprotective effect still remains unclear. In this study we investigated the effect of PSP pigments on (6)(0)Co gamma-ray-induced mitochondria-mediated apoptosis in murine thymocytes. MATERIALS AND METHODS: The murine thymocytes were pretreated by PSP pigments before exposure to 4 Gy (6)(0)Co gamma-rays. Flow cytometry analysis was used to measure apoptotic cells and mitochondrial membrane potential. Reactive oxygen species (ROS) were detected using 2',7',-dichlorofluorescein diacetate (DCFH-DA) probe and the activity of antioxidant enzymes was tested by biochemical assay after irradiation. Cytochrome c, caspase-3 and poly ADP-ribose polymerase (PARP) were measured by Western blotting. RESULTS: After treatment with PSP pigments and exposure to 4 Gy radiation the apoptosis of thymocytes was reduced and the mitochondrial transmembrane potential was maintained compared to control cells. In the presence of PSP pigments, ROS were reduced and the activities of glutathione peroxidase (GSH-px) and superoxide dismutase (SOD) were protected and in some cases increased. All the pro-apoptotic proteins (cytochrome oxidase, caspase 3 and PARP) decreased in PSP pigments pretreated thymocytes compared to irradiated cells in the absence of PSP pigments. CONCLUSIONS: Pre-treatment with PSP pigments significantly inhibited (6)(0)Co gamma-ray-induced mitochondria-mediated apoptosis. This radioprotective effect might be related to ROS scavenging, the enhancement of the activity of antioxidant enzymes, the maintenance of mitochondrial transmembrane potential, and the sequential inhibition of cytochrome c release and downstream caspase and PARP cleavage. FAU - Xie, Jing AU - Xie J AD - Department of Pharmacochemistry, Ocean University of China, Qingdao, PR China. FAU - Han, Yan-Tao AU - Han YT FAU - Wang, Chun-Bo AU - Wang CB FAU - Yu, Wen-Gong AU - Yu WG LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100810 PL - England TA - Int J Radiat Biol JT - International journal of radiation biology JID - 8809243 RN - 0 (Cobalt Radioisotopes) RN - 0 (Pigments, Biological) RN - 0 (Radiation-Protective Agents) RN - 0 (Reactive Oxygen Species) RN - 9007-43-6 (Cytochromes c) RN - EC 1.11.1.9 (Glutathione Peroxidase) RN - EC 1.15.1.1 (Superoxide Dismutase) RN - EC 2.4.2.30 (Poly(ADP-ribose) Polymerases) RN - EC 3.4.22.- (Casp3 protein, mouse) RN - EC 3.4.22.- (Caspase 3) SB - IM MH - Animals MH - Apoptosis/drug effects/radiation effects MH - Caspase 3/metabolism MH - Cell Survival/drug effects/radiation effects MH - Cells, Cultured MH - Cobalt Radioisotopes/toxicity MH - Cytochromes c/metabolism MH - Gamma Rays/adverse effects MH - Glutathione Peroxidase/metabolism MH - Ipomoea batatas MH - Membrane Potential, Mitochondrial/drug effects/radiation effects MH - Mice MH - Mitochondria/drug effects/metabolism/radiation effects MH - Pigments, Biological/*pharmacology MH - Poly(ADP-ribose) Polymerases/metabolism MH - Radiation-Protective Agents/*pharmacology MH - Reactive Oxygen Species/metabolism MH - Superoxide Dismutase/metabolism MH - T-Lymphocytes/*drug effects/metabolism/pathology/*radiation effects EDAT- 2010/08/12 06:00 MHDA- 2011/01/13 06:00 CRDT- 2010/08/12 06:00 PHST- 2010/08/12 06:00 [entrez] PHST- 2010/08/12 06:00 [pubmed] PHST- 2011/01/13 06:00 [medline] AID - 10.3109/09553002.2010.501840 [doi] PST - ppublish SO - Int J Radiat Biol. 2010 Dec;86(12):1061-9. doi: 10.3109/09553002.2010.501840. Epub 2010 Aug 10.