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Anandamide and noladin ether prevent neurotoxicity of the human amyloid-beta peptide.

Abstract
Cannabinoid receptor agonists including anandamide and noladin either have recently been suggested to exhibit neuroprotective properties. The amyloid-beta (Abeta) peptide is thought to be responsible for the neurodegenerative changes associated with Alzheimer's disease pathology. This study characterizes the effects of anandamide and noladin ether on the neurotoxicity of Abeta in differentiated human teratocarcinoma cell line, Ntera 2/cl-D1 neurons. Anandamide and noladin ether, at nanomolar concentrations, showed concentration dependent inhibition of Abeta toxicity. A CB(1) cannabinoid receptor antagonist, AM251, prevented the protective effects of anandamide and noladin ether. The mitogen activated protein kinase (MAPK) pathway inhibitor PD98059 also prevented the protective effects of cannabinoids and corticotrophin-releasing hormone. These results suggest that activation of the MAPK pathway by either cannabinoids or corticotrophin-releasing hormone could be used to prevent Abeta peptide induced neurodegeneration.
AuthorsNathaniel G N Milton
JournalNeuroscience letters (Neurosci Lett) Vol. 332 Issue 2 Pg. 127-30 (Oct 31 2002) ISSN: 0304-3940 [Print] Ireland
PMID12384227 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2002 Elsevier Science Ireland Ltd.
Chemical References
  • Amyloid beta-Peptides
  • Arachidonic Acids
  • Cannabinoids
  • Endocannabinoids
  • Enzyme Inhibitors
  • Flavonoids
  • Glycerides
  • Neuroprotective Agents
  • Neurotoxins
  • Peptide Fragments
  • Polyunsaturated Alkamides
  • Receptors, Cannabinoid
  • Receptors, Drug
  • amyloid beta-protein (1-40)
  • noladin ether
  • Corticotropin-Releasing Hormone
  • corticotropin releasing hormone (9-41)
  • Mitogen-Activated Protein Kinases
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one
  • anandamide
Topics
  • Amyloid beta-Peptides (antagonists & inhibitors, toxicity)
  • Arachidonic Acids (pharmacology)
  • Cannabinoids (pharmacology)
  • Corticotropin-Releasing Hormone (pharmacology)
  • Endocannabinoids
  • Enzyme Inhibitors (pharmacology)
  • Flavonoids (pharmacology)
  • Glycerides (pharmacology)
  • Humans
  • Mitogen-Activated Protein Kinases (antagonists & inhibitors)
  • Nervous System Diseases (chemically induced, prevention & control)
  • Neurons (drug effects, pathology)
  • Neuroprotective Agents
  • Neurotoxins (antagonists & inhibitors, toxicity)
  • Oxidation-Reduction
  • Peptide Fragments (antagonists & inhibitors, pharmacology, toxicity)
  • Polyunsaturated Alkamides
  • Receptors, Cannabinoid
  • Receptors, Drug (antagonists & inhibitors)

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