» Articles » PMID: 15317907

Catecholamine Metabolism: a Contemporary View with Implications for Physiology and Medicine

Overview
Journal Pharmacol Rev
Specialty Pharmacology
Date 2004 Aug 20
PMID 15317907
Citations 319
Authors
Affiliations
Soon will be listed here.
Abstract

This article provides an update about catecholamine metabolism, with emphasis on correcting common misconceptions relevant to catecholamine systems in health and disease. Importantly, most metabolism of catecholamines takes place within the same cells where the amines are synthesized. This mainly occurs secondary to leakage of catecholamines from vesicular stores into the cytoplasm. These stores exist in a highly dynamic equilibrium, with passive outward leakage counterbalanced by inward active transport controlled by vesicular monoamine transporters. In catecholaminergic neurons, the presence of monoamine oxidase leads to formation of reactive catecholaldehydes. Production of these toxic aldehydes depends on the dynamics of vesicular-axoplasmic monoamine exchange and enzyme-catalyzed conversion to nontoxic acids or alcohols. In sympathetic nerves, the aldehyde produced from norepinephrine is converted to 3,4-dihydroxyphenylglycol, not 3,4-dihydroxymandelic acid. Subsequent extraneuronal O-methylation consequently leads to production of 3-methoxy-4-hydroxyphenylglycol, not vanillylmandelic acid. Vanillylmandelic acid is instead formed in the liver by oxidation of 3-methoxy-4-hydroxyphenylglycol catalyzed by alcohol and aldehyde dehydrogenases. Compared to intraneuronal deamination, extraneuronal O-methylation of norepinephrine and epinephrine to metanephrines represent minor pathways of metabolism. The single largest source of metanephrines is the adrenal medulla. Similarly, pheochromocytoma tumor cells produce large amounts of metanephrines from catecholamines leaking from stores. Thus, these metabolites are particularly useful for detecting pheochromocytomas. The large contribution of intraneuronal deamination to catecholamine turnover, and dependence of this on the vesicular-axoplasmic monoamine exchange process, helps explain how synthesis, release, metabolism, turnover, and stores of catecholamines are regulated in a coordinated fashion during stress and in disease states.

Citing Articles

Widespread and Heterologous Effects of L-DOPA on Monoaminergic Tissue Metabolism in Newborn Rats Expressing Air-Stepping.

Barriere G, Pelloquin-Mvogo Z, Boulain M, Khsime I, Bharatiya R, Riquier M Int J Mol Sci. 2025; 26(5).

PMID: 40076918 PMC: 11901079. DOI: 10.3390/ijms26052298.


SVHRSP protects against rotenone-induced neurodegeneration in mice by inhibiting TLR4/NF-κB-mediated neuroinflammation via gut microbiota.

Chen M, Zhang Y, Hou L, Zhao Z, Tang P, Sun Q NPJ Parkinsons Dis. 2025; 11(1):43.

PMID: 40050294 PMC: 11885645. DOI: 10.1038/s41531-025-00892-6.


Effects of the stress hormone norepinephrine on the probiotic properties of : antibacterial colonization, anti-inflammation, and antioxidation.

Niu L, Gao M, Li Y, Wang C, Zhang C, Duan H Front Microbiol. 2025; 16:1526362.

PMID: 39996081 PMC: 11849050. DOI: 10.3389/fmicb.2025.1526362.


Viral infections of the central nervous system increase the risk of knee osteoarthritis: a two-sample mendelian randomization study.

Yang M, Su Y, Xu K, Wen P, Xie J, Wan X Aging Clin Exp Res. 2025; 37(1):30.

PMID: 39836329 PMC: 11750930. DOI: 10.1007/s40520-025-02927-7.


Small Molecules in Parkinson's Disease Therapy: From Dopamine Pathways to New Emerging Targets.

Lee H, Elkamhawy A, Rakhalskaya P, Lu Q, Nada H, Quan G Pharmaceuticals (Basel). 2025; 17(12.

PMID: 39770531 PMC: 11677913. DOI: 10.3390/ph17121688.