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Protective Effects of Red Wine Flavonols on 4‐Hydroxynonenal‐Induced Apoptosis in PC12 Cells
Author(s) -
Jang Young Jin,
Kang Nam Joo,
Lee Ki Won,
Lee Hyong Joo
Publication year - 2009
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1111/j.1749-6632.2009.04720.x
Subject(s) - 4 hydroxynonenal , flavonols , apoptosis , chemistry , wine , lipid peroxidation , microbiology and biotechnology , biochemistry , food science , oxidative stress , biology , antioxidant , flavonoid
There is accumulating evidence that a moderate consumption of red wine has health benefits, such as the inhibition of neurodegenerative diseases. Although this is generally attributed to resveratrol, the protective mechanisms and the active substance(s) remain unclear. We examined whether and how red wine extract (RWE) and red wine flavonols quercetin and myricetin inhibited 4‐hydroxynonenal (HNE)‐induced apoptosis of rat pheochromocytoma PC12 cells. RWE attenuated HNE‐induced PC12 cell death in a dose‐dependent manner. HNE induced cleavage of poly(ADP‐ribose) polymerase, which is involved in DNA repair in the nucleus, and this was inhibited by RWE treatment. Treatment with RWE also inhibited HNE‐induced nuclear condensation in PC12 cells. Data of 2′,7′‐dichlorofluorescin diacetate showed that RWE protected against apoptosis of PC12 cells by attenuating intracellular reactive oxygen species. The cytoprotective effects on HNE‐induced cell death were stronger for quercetin and myricetin than for resveratrol. HNE‐induced nuclear condensation was attenuated by quercetin and myricetin. These results suggest that the neuroprotective potential of red wine is attributable to flavonols rather than to resveratrol.