Journal
ONCOTARGET
Volume 7, Issue 14, Pages 17380-17392Publisher
IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.8041
Keywords
resveratrol; beta amyloid peptide; learning and memory; PDE4; apoptosis; Gerotarget
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Funding
- Medicine and Health Science and Technology Plan Projects in Zhejiang Province [2012KYA151]
- Natural Science Foundation of Zhejiang Province [LY15H090003]
- Science Technology Department Foundation of Zhejiang Province [2012C33118]
- National Natural Science Foundation for the Youth (NSFY) [81400600]
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Resveratrol, a natural polyphenol found in red wine, has wide spectrum of pharmacological properties including antioxidative and antiaging activities. Beta amyloid peptides (A beta) are known to involve cognitive impairment, neuroinflammatory and apoptotic processes in Alzheimer's disease (AD). Activation of cAMP and/or cGMP activities can improve memory performance and decrease the neuroinflammation and apoptosis. However, it remains unknown whether the memory enhancing effect of resveratrol on AD associated cognitive disorders is related to the inhibition of phosphodiesterase 4 (PDE4) subtypes and subsequent increases in intracellular cAMP and/or cGMP activities. This study investigated the effect of resveratrol on A beta 1-42-induced cognitive impairment and the participation of PDE4 subtypes related cAMP or cGMP signaling. Mice microinfused with A beta 1-42 into bilateral CA1 subregions displayed learning and memory impairment, as evidenced by reduced memory acquisition and retrieval in the water maze and retention in the passive avoidance tasks; it was also significant that neuroinflammatory and pro-apoptotic factors were increased in A beta 1-42-treated mice. A beta 1-42-treated mice also increased in PDE4A, 4B and 4D expression, and decreased in PKA level. However, PKA inhibitor H89, but not PKG inhibitor KT5823, prevented resveratrol's effects on these parameters. Resveratrol also reversed A beta 1-42-induced decreases in phosphorylated cAMP response-element binding protein (pCREB), brain derived neurotrophic factor (BDNF) and anti-apoptotic factor BCl-2 expression, which were reversed by H89. These findings suggest that resveratrol reversing A beta-induced learning and memory disorder may involve the regulation of neuronal inflammation and apoptosis via PDE4 subtypes related cAMP-CREB-BDNF signaling.
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