Please use this identifier to cite or link to this item:
|標題:||Synergistic effects of homocysteine, S-adenosylhomocysteine and adenosine on apoptosis in BV-2 murine microglial cells||作者:||胡淼琳
|關鍵字:||Homocysteine;S-adenosylhomocysteine;adenosine;apoptosis;synergy;parkinsons-disease;plasma homocysteine;alzheimers-disease;endothelial-cells;extracellular atp;dna-damage;rat-liver;hypomethylation;adenosylmethionine;metabolism||Project:||Biofactors||期刊/報告no：:||Biofactors, Volume 34, Issue 2, Page(s) 81-95.||摘要:||
Homocysteine (Hcy), S-adenosylhomocysteine (SAH) and adenosine (Ado) are methionine metabolism intermediates that may act synergistically in certain disease. In this study, we examined whether HCy, SAH and Ado may synergistically induce neuronal apoptosis of BV-2 microglial cells. We found that an incubation of BV-2 cells with 1 mM Hcy, 1 mu M SAH and 100 mu M Ado (SAH + Hcy + Ado) led to marked apoptosis of BV-2 cells, as evidenced by several markers of apoptosis. A synergistic effect of SAH + Hcy + Ado on apoptosis (2.55-fold, P < 0.05) was obtained, as calculated using the data of Annexin V-positive cells. This combination markedly induced intracellular levels of reactive oxygen species (ROS) starting at 6 h and significantly decreased the mitochondrial potential starting at 12 h. The combination significantly elevated caspase-9 and caspase-3 activities at 24 and 48 h. The combination also induced hypomethylation (at 24 and 48 h), as indicated by significantly decreased 5-methyldeoxycytidine levels and SAM/SAH ratios. Pre-incubation of cells with a-tocopherol (30 mu M) reduced the increase of ROS (at 6 h) and significantly restored cell viability (at 24 and 48 h) in the SAH + Hcy + Ado group. Overall, the present study demonstrates that SAH, Hcy and Ado synergistically induce BV-2 apoptosis, possibly by generation of ROS and induction of intracellular hypomethylation.
|Appears in Collections:||食品暨應用生物科技學系|
Show full item record
TAIR Related Article
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.