Minkkila_2010_Curr.Top.Med.Chem_10_828

Reference

Title : Discovery and development of endocannabinoid-hydrolyzing enzyme inhibitors - Minkkila_2010_Curr.Top.Med.Chem_10_828
Author(s) : Minkkila A , Saario SM , Nevalainen T
Ref : Curr Top Med Chem , 10 :828 , 2010
Abstract :

Fatty acid amide hydrolase (FAAH) and monoglyceride lipase (MGL) are hydrolytic enzymes which degrade the endogenous cannabinoids (endocannabinoids) N-arachidonoylethanolamine (anandamide, AEA) and 2-arachidonoylglycerol (2-AG), respectively. Endocannabinoids are an important class of lipid messenger molecules that are produced on demand in response to elevated intracellular calcium levels. They recognize and activate the cannabinoid CB(1) and CB(2) receptors, the molecular targets for Delta(9)-tetrahydrocannabinol (Delta(9)-THC) in marijuana evoking several beneficial therapeutic effects. However, in vivo the cannabimimetic effects of AEA and 2-AG remain weak owing to their rapid inactivation by FAAH and MGL, respectively. The inactivation of FAAH and MGL by specific enzyme inhibitors increases the levels of AEA and 2-AG, respectively, producing therapeutic effects such as pain relief and depression of anxiety.

PubMedSearch : Minkkila_2010_Curr.Top.Med.Chem_10_828
PubMedID: 20370710

Related information

Citations formats

Minkkila A, Saario SM, Nevalainen T (2010)
Discovery and development of endocannabinoid-hydrolyzing enzyme inhibitors
Curr Top Med Chem 10 :828

Minkkila A, Saario SM, Nevalainen T (2010)
Curr Top Med Chem 10 :828