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Biogenic Aldehydes as Therapeutic Targets for Cardiovascular Disease
Journal article   Open access   Peer reviewed

Biogenic Aldehydes as Therapeutic Targets for Cardiovascular Disease

Margaret-Ann M Nelson, Shahid P Baba and Ethan J Anderson
Current opinion in pharmacology, Vol.33, pp.56-63
04/2017
DOI: 10.1016/j.coph.2017.04.004
PMCID: PMC5563970
PMID: 28528297
url
https://www.ncbi.nlm.nih.gov/pmc/articles/5563970View
Open Access

Abstract

Aldehydes are continuously formed in biological systems through enzyme-dependent and spontaneous oxidation of lipids, glucose, and primary amines. These highly reactive, biogenic electrophiles can become toxic via covalent modification of proteins, lipids and DNA. Thus, agents that scavenge aldehydes through conjugation have therapeutic value for a number of major cardiovascular diseases. Several commonly-prescribed drugs (e.g., hydralazine) have been shown to have potent aldehyde-conjugating properties which may contribute to their beneficial effects. Herein, we briefly describe the major sources and toxicities of biogenic aldehydes in cardiovascular system, and provide an overview of drugs that are known to have aldehyde-conjugating effects. Some compounds of phytochemical origin, and histidyl-dipeptides with emerging therapeutic value in this area are also discussed.
Animals Dipeptides - therapeutic use Phytochemicals - therapeutic use Aldehydes - pharmacology Cardiovascular Diseases - drug therapy Dipeptides - pharmacology Humans Oxidation-Reduction - drug effects Aldehydes - therapeutic use Phytochemicals - pharmacology

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