Endocannabinoid signalling in Alzheimer's disease

Author:

Maroof Nazia1,Pardon Marie Christine2,Kendall David A.2

Affiliation:

1. Sheffield Institute for Translational Neuroscience (SITraN), 385a Glossop Road, University of Sheffield, Sheffield S10 2HQ, U.K.

2. University of Nottingham Medical School, School of Life Sciences, Queen's Medical Centre, Nottingham NG7 2UH, U.K.

Abstract

The ECs (endocannabinoids) AEA (anandamide) and 2-AG (2-arachidonoylglycerol) and their lipid congeners OEA (N-oleoylethanolamide) and PEA (N-palmitoylethanolamide) are multifunctional lipophilic signalling molecules. The ECs, OEA and PEA have multiple physiological roles including involvement in learning and memory, neuroinflammation, oxidative stress, neuroprotection and neurogenesis. They have also been implicated in the pathology of, or perhaps protective responses to, neurodegenerative diseases. This is particularly the case with Alzheimer's disease, the most common age-related dementia associated with impairments in learning and memory accompanied by neuroinflammation, oxidative stress and neurodegeneration. The present mini-review examines the evidence supporting the roles that ECs appear to play in Alzheimer's disease and the potential for beneficial therapeutic manipulation of the EC signalling system.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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