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Cannabidiol reduces neuroinflammation and promotes neuroplasticity and functional recovery after brain ischemia.

Abstract
This study investigated the effects of cannabidiol (CBD), a non-psychotomimetic phytochemical present in Cannabis sativa, on the cognitive and emotional impairments induced by bilateral common carotid artery occlusion (BCCAO) in mice. Using a multi-tiered behavioral testing battery during 21days, we found that BCCAO mice exhibited long-lasting functional deficits reflected by increase in anxiety-like behavior (day 9), memory impairments (days 12-18) and despair-like behavior (day 21). Short-term CBD 10mg/kg treatment prevented the cognitive and emotional impairments, attenuated hippocampal neurodegeneration and white matter (WM) injury, and reduced glial response that were induced by BCCAO. In addition, ischemic mice treated with CBD exhibited an increase in the hippocampal brain derived neurotrophic factor (BDNF) protein levels. CBD also stimulated neurogenesis and promoted dendritic restructuring in the hippocampus of BCCAO animals. Collectively, the present results demonstrate that short-term CBD treatment results in global functional recovery in ischemic mice and impacts multiple and distinct targets involved in the pathophysiology of brain ischemic injury.
AuthorsMarco Aurélio Mori, Erika Meyer, Ligia Mendes Soares, Humberto Milani, Francisco Silveira Guimarães, Rúbia Maria Weffort de Oliveira
JournalProgress in neuro-psychopharmacology & biological psychiatry (Prog Neuropsychopharmacol Biol Psychiatry) Vol. 75 Pg. 94-105 (04 03 2017) ISSN: 1878-4216 [Electronic] England
PMID27889412 (Publication Type: Journal Article)
CopyrightCopyright © 2016 Elsevier Inc. All rights reserved.
Chemical References
  • Aif1 protein, mouse
  • Anti-Inflammatory Agents
  • Calcium-Binding Proteins
  • Doublecortin Domain Proteins
  • Glial Fibrillary Acidic Protein
  • Microfilament Proteins
  • Microtubule-Associated Proteins
  • Neuropeptides
  • Cannabidiol
Topics
  • Animals
  • Anti-Inflammatory Agents (pharmacology, therapeutic use)
  • Brain Ischemia (complications)
  • Calcium-Binding Proteins (metabolism)
  • Cannabidiol (pharmacology, therapeutic use)
  • Disease Models, Animal
  • Doublecortin Domain Proteins
  • Encephalitis (drug therapy, etiology)
  • Exploratory Behavior (drug effects)
  • Glial Fibrillary Acidic Protein (metabolism)
  • Male
  • Maze Learning (drug effects)
  • Mice
  • Mice, Inbred C57BL
  • Microfilament Proteins (metabolism)
  • Microtubule-Associated Proteins (metabolism)
  • Neuronal Plasticity (drug effects)
  • Neuropeptides (metabolism)
  • Recognition, Psychology (drug effects)
  • Recovery of Function (drug effects)
  • Swimming (psychology)
  • Time Factors

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