Hwang, J., Adamson, C., Butler, D., Janero, D.R., Makriyannis, A. and Bahr, B.A. (2010) Enhancement of endocannabinoid signaling by fatty acid amide hydrolase inhibition, a neuroprotective therapeutic modality. Life Sciences, 86, 615-623. doi:10.1016/j.lfs.2009.06.003

has been cited by the following article:

• TITLE: Pharmacological manipulation of cannabinoid neurotransmission reduces neuroinflammation associated with normal aging

  AUTHORS: Isabelle Bardou, Nicholas DiPatrizio, Holly M. Brothers, Roxanne M. Kaercher, Kevin Baranger, Mollie Mitchem, Sarah C. Hopp, Gary L. Wenk, Yannick Marchalant

  KEYWORDS: Rats; Memantine; UCM707; Microglia; WIN-55, 212-2; URB597

  JOURNAL NAME: Health, Vol.4 No.9A, September 28, 2012

  ABSTRACT: We have previously demonstrated that antagonism of glutamate NMDA receptors or activation of endocannabinoid receptors could reduce experimentally induced neuroinflammation within the hippocampus of young rats. In the current study, we investigated whether pharmacological manipulation of glutamate or endocannabinoid neurotransmission could reduce naturally-occurring neuroinflammation within the hippocampus of aged rats. We investigated whether UCM707, an inhibitor of endocannabinoid re-uptake, WIN- 55,212-2, an endocannabinoid receptor agonist, and URB597, an inhibitor of endocannabinoid catabolism, or memantine, a non-competitive, low-affinity, inhibitor of the open NMDA receptor channel, could reduce the number of MHC II-IR microglia within the hippocampus. All of the drugs, except URB597, reduced the number of reactive microglia, as compared to vehicle treated rats. The current results suggest potential pharmacological approaches that may mitigate the pathological consequences of chronic brain inflammation associated with numerous neurodegenerative diseases.