http://www.sciencedirect.com/science/article/pii/S0027510708002595
- a Department of Agricultural Biotechnology and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Republic of Korea
- b Department of Bioscience and Biotechnology, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul 143-701, Republic of Korea
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Neurodegenerative
disorders such as Alzheimer's disease (AD) are strongly associated with
oxidative stress, which is induced by reactive oxygen species (ROS)
including hydrogen peroxide (H2O2). Recent studies
suggest that moderate coffee consumption may reduce the risk of
neurodegenerative diseases such as AD, but the molecular mechanisms
underlying this effect remain to be clarified. In this study, we
investigated the protective effects of chlorogenic acid (5-O-caffeoylquinic
acid; CGA), a major phenolic phytochemical found in instant
decaffeinated coffee (IDC), and IDC against oxidative PC12 neuronal cell
death. IDC (1 and 5 μg/ml) or CGA (1 and 5 μM) attenuated H2O2-induced PC12 cell death. H2O2-induced
nuclear condensation and DNA fragmentation were strongly inhibited by
pretreatment with IDC or CGA. Pretreatment with IDC or CGA also
inhibited the H2O2-induced cleavage of poly(ADP-ribose) polymerase (PARP), and downregulation of Bcl-XL and caspase-3. The accumulation of intracellular ROS in H2O2-treated
PC12 cells was dose-dependently diminished by IDC or CGA. The
activation of c-Jun N-terminal protein kinase (JNK) and p38
mitogen-activated protein kinase (MAPK) by H2O2 in PC12 cells was also inhibited by IDC or CGA. Collectively, these results indicate that IDC and CGA protect PC12 cells from H2O2-induced apoptosis by blocking the accumulation of intracellular ROS and the activation of MAPKs.
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