Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3070089 | Neurobiology of Disease | 2009 | 8 Pages |
Abstract
WIN-55,212-2 (WIN-2) can elicit anti-inflammatory and cognitive-enhancing effect in aged rats. The current study was designed to determine the differential role of the endocannabinoid receptor sub-types 1 (CB1) and 2 (CB2) and transient receptor potential vanilloid 1 receptor (TRPV1) in the reduction of age-associated brain inflammation and their effects on neurogenesis in the dentate gyrus of aged rats. Our results demonstrate that 1) the antagonist actions of WIN-2 at the TRPV1 receptor are responsible for the reduction in microglial activation and 2) the agonist actions of WIN-2 at CB1/2 receptors can trigger neurogenesis in the hippocampus of aged rats. Chronic treatment with WIN-2 established an anti-inflammatory cytokine profile within the hippocampus. Our results provide insight into the role of the endocannabinoid and vanilloid systems upon two different and detrimental aspects of normal and pathological aging, chronic neuroinflammation and decline in neurogenesis.
Keywords
CB1SR 144528SR 141716ASGZCB2N-methyl-d-aspartateNMDAPBSDcxTBSLPSCBRTRPV1NeuroinflammationBrdUbromodeoxyuridineTris buffer salineAlzheimer's diseaseAgingdentate gyrusphosphate buffer salineEntorhinal cortexlipopolysaccharidesubgranular zoneMicrogliaNeurogenesisTransient receptor potential vanilloid 1Vanilloid receptorscannabinoid receptorsCannabinoid receptor 1cannabinoid receptor 2
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Authors
Yannick Marchalant, Holly M. Brothers, Greg J. Norman, Kate Karelina, A. Courtney DeVries, Gary L. Wenk,