The role of fatty acid amide hydrolase enzyme inhibitors in Alzheimer's disease.
Smita JainAkansha BishtKanika VermaSwarnima NegiSarvesh PaliwalSwapnil SharmaPublished in: Cell biochemistry and function (2021)
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.
Keyphrases
- fatty acid
- cerebral ischemia
- sleep quality
- cognitive decline
- poor prognosis
- chronic pain
- human health
- white matter
- pain management
- working memory
- lipopolysaccharide induced
- multiple sclerosis
- neuropathic pain
- binding protein
- blood brain barrier
- long non coding rna
- lps induced
- mild cognitive impairment
- postoperative pain