Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Dambrova 2022 Pharmacol Rev

From Bioblast
Publications in the MiPMap
Dambrova M, Makrecka-Kuka M, Kuka J, Vilskersts R, Nordberg D, Attwood MM, Smesny S, Sen ZD, Guo AC, Oler E, Tian S, Zheng J, Wishart DS, Liepinsh E, Schioth HB. (2022) Acylcarnitines: Nomenclature, Biomarkers, Therapeutic Potential, Drug Targets, and Clinical Trials. https://doi.org/10.1124/pharmrev.121.000408

Β» PMID: 35710135 Open Access

Dambrova Maija, Makrecka-Kuka Marina, Kuka Janis, Vilskersts Reinis, Nordberg Didi, Attwood Misty M, Smesny Stefan, Sen Zumrut Duygu, Guo An Chi, Oler Eponine, Tian Siyang, Zheng Jiamin, Wishart David S, Liepinsh Edgars, Schioth Helgi B (2022) Pharmacol Rev

Abstract: Acylcarnitines are fatty acid metabolites that play important roles in many cellular energy metabolism pathways. They have historically been used as important diagnostic markers for inborn errors of fatty acid oxidation and are being intensively studied as markers of energy metabolism, deficits in mitochondrial and peroxisomal Ξ² -oxidation activity, insulin resistance, and physical activity. Acylcarnitines are increasingly being identified as important indicators in metabolic studies of many diseases, including metabolic disorders, cardiovascular diseases, diabetes, depression, neurologic disorders, and certain cancers. The US Food and Drug Administration-approved drug L-carnitine, along with short-chain acylcarnitines (acetylcarnitine and propionylcarnitine), is now widely used as a dietary supplement. In light of their growing importance, we have undertaken an extensive review of acylcarnitines and provided a detailed description of their identity, nomenclature, classification, biochemistry, pathophysiology, supplementary use, potential drug targets, and clinical trials. We also summarize these updates in the Human Metabolome Database, which now includes information on the structures, chemical formulae, chemical/spectral properties, descriptions, and pathways for 1240 acylcarnitines. This work lays a solid foundation for identifying, characterizing, and understanding acylcarnitines in human biosamples. We also discuss the emerging opportunities for using acylcarnitines as biomarkers and as dietary interventions or supplements for many wide-ranging indications. The opportunity to identify new drug targets involved in controlling acylcarnitine levels is also discussed. SIGNIFICANCE STATEMENT: This review provides a comprehensive overview of acylcarnitines, including their nomenclature, structure and biochemistry, and use as disease biomarkers and pharmaceutical agents. We present updated information contained in the Human Metabolome Database website as well as substantial mapping of the known biochemical pathways associated with acylcarnitines, thereby providing a strong foundation for further clarification of their physiological roles.

β€’ Bioblast editor: Cecatto C β€’ O2k-Network Lab: LV Riga Liepins E


Labels: MiParea: Pharmacology;toxicology  Pathology: Cardiovascular, Diabetes, Inherited 



Regulation: Fatty acid 



FAT4BRAIN, Publication:FAT4BRAIN