The role of fatty acid amide hydrolase enzyme inhibitors in Alzheimer's disease

Cell Biochem Funct. 2022 Mar;40(2):106-117. doi: 10.1002/cbf.3680. Epub 2021 Dec 21.

Abstract

Fatty acid amide hydrolase (FAAH) is a prominent enzyme of the endocannabinoid system that degrades endogenous cannabinoid anandamide and oleamide. These lipid amides are involved in reducing neuroinflammation, pain and regulation of other neurological-related activities including feeding behaviours, sleep patterns, body temperature, memory processes and locomotory activity. Many of these activities are affected in most neurological disorders. Increased levels of brain FAAH expressions are speculated to correlate with decreased levels of lipid amides and increased AD-related symptoms. Thus, inhibition of FAAH shows promising potential in amelioration of symptoms associated with Alzheimer's disease (AD). The review aims at establishing the detrimental role of increased FAAH expression in AD and highlights the translational potential and therapeutic application of FAAH inhibitors in AD.

Keywords: Alzheimer's disease; cognition; fatty acid amide hydrolase; neuroinflammation; synaptic plasticity.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease* / drug therapy
  • Amidohydrolases / metabolism
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Humans
  • Memory

Substances

  • Enzyme Inhibitors
  • Amidohydrolases
  • fatty-acid amide hydrolase