» Articles » PMID: 33147856

A Comprehensive Review on Source, Types, Effects, Nanotechnology, Detection, and Therapeutic Management of Reactive Carbonyl Species Associated with Various Chronic Diseases

Abstract

Continuous oxidation of carbohydrates, lipids, and amino acids generate extremely reactive carbonyl species (RCS). Human body comprises some important RCS namely hexanal, acrolein, 4-hydroxy-2-nonenal, methylglyoxal, malondialdehyde, isolevuglandins, and 4-oxo-2- nonenal etc. These RCS damage important cellular components including proteins, nucleic acids, and lipids, which manifests cytotoxicity, mutagenicity, multitude of adducts and crosslinks that are connected to ageing and various chronic diseases like inflammatory disease, atherosclerosis, cerebral ischemia, diabetes, cancer, neurodegenerative diseases and cardiovascular disease. The constant prevalence of RCS in living cells suggests their importance in signal transduction and gene expression. Extensive knowledge of RCS properties, metabolism and relation with metabolic diseases would assist in development of effective approach to prevent numerous chronic diseases. Treatment approaches for RCS associated diseases involve endogenous RCS metabolizers, carbonyl metabolizing enzyme inducers, and RCS scavengers. Limited bioavailability and bio efficacy of RCS sequesters suggest importance of nanoparticles and nanocarriers. Identification of RCS and screening of compounds ability to sequester RCS employ several bioassays and analytical techniques. Present review describes in-depth study of RCS sources, types, properties, identification techniques, therapeutic approaches, nanocarriers, and their role in various diseases. This study will give an idea for therapeutic development to combat the RCS associated chronic diseases.

Citing Articles

The role of potential oxidative biomarkers in the prognosis of intracerebral hemorrhage and the exploration antioxidants as possible preventive and treatment options.

Yao J, Dai X, Yv X, Zheng L, Zheng J, Kuang B Front Mol Biosci. 2025; 12:1541230.

PMID: 39967652 PMC: 11832355. DOI: 10.3389/fmolb.2025.1541230.


A mechanistic overview on green assisted formulation of nanocomposites and their multifunctional role in biomedical applications.

Mahnoor , Malik K, Kazmi A, Sultana T, Raja N, Bibi Y Heliyon. 2025; 11(3):e41654.

PMID: 39916856 PMC: 11800088. DOI: 10.1016/j.heliyon.2025.e41654.


Chemoselective Stabilized Triphenylphosphonium Probes for Capturing Reactive Carbonyl Species and Regenerating Covalent Inhibitors with Acrylamide Warheads in Cellulo.

Chen A, Lin Z, Chang H, Wang T J Am Chem Soc. 2024; 147(2):1518-1528.

PMID: 39730301 PMC: 11744745. DOI: 10.1021/jacs.4c09727.


Exploring Secondary Amine Carnosine Derivatives: Design, Synthesis, and Properties.

Artasensi A, Mazzotta S, Sanz I, Lin L, Vistoli G, Fumagalli L Molecules. 2024; 29(21).

PMID: 39519724 PMC: 11547551. DOI: 10.3390/molecules29215083.


Sanger Sequencing Reveals Novel Variants in , , and Genes in Patients of Early and Severe Diabetic Nephropathy.

Shah S, Rashid A, Majeed A, Ghafoor T, Azam N Medicina (Kaunas). 2024; 60(9).

PMID: 39336582 PMC: 11433688. DOI: 10.3390/medicina60091540.


References
1.
Janssen B, Hohenadel D, Brinkkoetter P, Peters V, Rind N, Fischer C . Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1. Diabetes. 2005; 54(8):2320-7. DOI: 10.2337/diabetes.54.8.2320. View

2.
Vasiliou V, Pappa A, Estey T . Role of human aldehyde dehydrogenases in endobiotic and xenobiotic metabolism. Drug Metab Rev. 2004; 36(2):279-99. DOI: 10.1081/dmr-120034001. View

3.
Gao D, Willard B, Podrez E . Analysis of covalent modifications of proteins by oxidized phospholipids using a novel method of peptide enrichment. Anal Chem. 2013; 86(2):1254-62. PMC: 4084736. DOI: 10.1021/ac4035949. View

4.
Novoselov K, Geim A, Morozov S, Jiang D, Zhang Y, Dubonos S . Electric field effect in atomically thin carbon films. Science. 2004; 306(5696):666-9. DOI: 10.1126/science.1102896. View

5.
Keller J, Schmitt F, Scheff S, Ding Q, Chen Q, Butterfield D . Evidence of increased oxidative damage in subjects with mild cognitive impairment. Neurology. 2005; 64(7):1152-6. DOI: 10.1212/01.WNL.0000156156.13641.BA. View