6-Demethoxynobiletin, a Nobiletin-Analog Citrus Flavonoid, Enhances Extracellular Signal-Regulated Kinase Phosphorylation in PC12D Cells
- 1 January 2013
- journal article
- Published by Pharmaceutical Society of Japan in Biological and Pharmaceutical Bulletin
- Vol. 36 (10) , 1646-1649
Abstract
We previously demonstrated that nobiletin, a polymethoxylated flavone isolated from citrus peels, has the potential to improve cognitive dysfunction in patients with Alzheimer’s disease (AD). Recent studies suggest that the generation of intraneuronal amyloid-beta (Aβ) oligomers is an early event in the pathogenesis of AD. Aβ oligomers cause deficits in the regulation of the extracellular signal-regulated kinase (ERK) signaling which is critical for consolidation of the memory. Our previous studies revealed that nobiletin activated ERK signaling and subsequent cyclic AMP response element-dependent transcription. In this study, the effects of five nobiletin analogs, 6-demethoxynobiletin, tangeretin, 5-demethylnobiletin, sinensetin, and 6-demethoxytangeretin, isolated from citrus peels were assessed on ERK phosphorylation in PC12D cells, and the structure–activity relationships were examined. PC12D cells were treated with nobiletin or its analogs, and the cell extracts were analyzed by Western blotting using an antibody specific to phosphorylated ERK. 6-Demethoxynobiletin markedly enhanced ERK phosphorylation in a concentration-dependent manner. These results may be useful in developing drugs and functional foods using citrus peels for the treatment of dementia including AD.Keywords
This publication has 7 references indexed in Scilit:
- RETRACTED ARTICLE: A specific amyloid-β protein assembly in the brain impairs memoryNature, 2006
- Mechanism of Neurotrophic Action of Nobiletin in PC12D CellsBiochemistry, 2005
- Mitogen-activated protein kinases in synaptic plasticity and memoryCurrent Opinion in Neurobiology, 2004
- Triple-Transgenic Model of Alzheimer's Disease with Plaques and TanglesNeuron, 2003
- Genetic Demonstration of a Role for PKA in the Late Phase of LTP and in Hippocampus-Based Long-Term MemoryCell, 1997
- Induction of CRE-Mediated Gene Expression by Stimuli That Generate Long-Lasting LTP in Area CA1 of the HippocampusNeuron, 1996
- A synaptic model of memory: long-term potentiation in the hippocampusNature, 1993