PMID- 37017445 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230407 IS - 1424-8247 (Print) IS - 1424-8247 (Electronic) IS - 1424-8247 (Linking) VI - 16 IP - 2 DP - 2023 Jan 19 TI - Endocannabinoid System: Chemical Characteristics and Biological Activity. LID - 10.3390/ph16020148 [doi] LID - 148 AB - The endocannabinoid system (eCB) has been studied to identify the molecular structures present in Cannabis sativa. eCB consists of cannabinoid receptors, endogenous ligands, and the associated enzymatic apparatus responsible for maintaining energy homeostasis and cognitive processes. Several physiological effects of cannabinoids are exerted through interactions with various receptors, such as CB1 and CB2 receptors, vanilloid receptors, and the recently discovered G-protein-coupled receptors (GPR55, GPR3, GPR6, GPR12, and GPR19). Anandamide (AEA) and 2-arachidoylglycerol (2-AG), two small lipids derived from arachidonic acid, showed high-affinity binding to both CB1 and CB2 receptors. eCB plays a critical role in chronic pain and mood disorders and has been extensively studied because of its wide therapeutic potential and because it is a promising target for the development of new drugs. Phytocannabinoids and synthetic cannabinoids have shown varied affinities for eCB and are relevant to the treatment of several neurological diseases. This review provides a description of eCB components and discusses how phytocannabinoids and other exogenous compounds may regulate the eCB balance. Furthermore, we show the hypo- or hyperfunctionality of eCB in the body and how eCB is related to chronic pain and mood disorders, even with integrative and complementary health practices (ICHP) harmonizing the eCB. FAU - Rezende, Bismarck AU - Rezende B AUID- ORCID: 0000-0002-4005-6493 AD - Department of Pharmacology and Psychobiology, Roberto Alcantara Gomes Institute Biology (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro 20551-030, Brazil. FAU - Alencar, Allan Kardec Nogueira AU - Alencar AKN AUID- ORCID: 0000-0002-3072-6270 AD - Department of Biomedical Engineering, Tulane University, New Orleans, LA 70118, USA. FAU - de Bem, Graziele Freitas AU - de Bem GF AD - Department of Pharmacology and Psychobiology, Roberto Alcantara Gomes Institute Biology (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro 20551-030, Brazil. FAU - Fontes-Dantas, Fabricia Lima AU - Fontes-Dantas FL AUID- ORCID: 0000-0002-5201-0927 AD - Department of Pharmacology and Psychobiology, Roberto Alcantara Gomes Institute Biology (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro 20551-030, Brazil. FAU - Montes, Guilherme Carneiro AU - Montes GC AUID- ORCID: 0000-0003-4946-9056 AD - Department of Pharmacology and Psychobiology, Roberto Alcantara Gomes Institute Biology (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro 20551-030, Brazil. LA - eng GR - E-26/211.795/2021/Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro/ PT - Journal Article PT - Review DEP - 20230119 PL - Switzerland TA - Pharmaceuticals (Basel) JT - Pharmaceuticals (Basel, Switzerland) JID - 101238453 PMC - PMC9966761 OTO - NOTNLM OT - chronic pain OT - endocannabinoid ligands OT - endocannabinoid system OT - integrative and complementary health practices OT - mood disorders OT - phytocannabinoids OT - receptor cannabinoid COIS- The authors declare no conflict of interest. EDAT- 2023/04/06 06:00 MHDA- 2023/04/06 06:01 PMCR- 2023/01/19 CRDT- 2023/04/05 09:13 PHST- 2022/11/15 00:00 [received] PHST- 2023/01/11 00:00 [revised] PHST- 2023/01/13 00:00 [accepted] PHST- 2023/04/06 06:01 [medline] PHST- 2023/04/05 09:13 [entrez] PHST- 2023/04/06 06:00 [pubmed] PHST- 2023/01/19 00:00 [pmc-release] AID - ph16020148 [pii] AID - pharmaceuticals-16-00148 [pii] AID - 10.3390/ph16020148 [doi] PST - epublish SO - Pharmaceuticals (Basel). 2023 Jan 19;16(2):148. doi: 10.3390/ph16020148.