A PON for All Seasons: Comparing Paraoxonase Enzyme Substrates, Activity and Action including the Role of PON3 in Health and Disease.

HIV cancer cardiovascular disease lactones paraoxonase substrates

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
19 Mar 2022
Historique:
received: 24 02 2022
revised: 15 03 2022
accepted: 17 03 2022
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 26 3 2022
Statut: epublish

Résumé

Paraoxonases (PONs) are a family of hydrolytic enzymes consisting of three members, PON1, PON2, and PON3, located on human chromosome 7. Identifying the physiological substrates of these enzymes is necessary for the elucidation of their biological roles and to establish their applications in the biomedical field. PON substrates are classified as organophosphates, aryl esters, and lactones based on their structure. While the established native physiological activity of PONs is its lactonase activity, the enzymes' exact physiological substrates continue to be elucidated. All three PONs have antioxidant potential and play an important anti-atherosclerotic role in several diseases including cardiovascular diseases. PON3 is the last member of the family to be discovered and is also the least studied of the three genes. Unlike the other isoforms that have been reviewed extensively, there is a paucity of knowledge regarding PON3. Thus, the current review focuses on PON3 and summarizes the PON substrates, specific activities, kinetic parameters, and their association with cardiovascular as well as other diseases such as HIV and cancer.

Identifiants

pubmed: 35326240
pii: antiox11030590
doi: 10.3390/antiox11030590
pmc: PMC8945423
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL137004
Pays : United States
Organisme : National Institute of Health
ID : HL-137004

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Auteurs

Chrysan J Mohammed (CJ)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Sabitri Lamichhane (S)

Department of Chemistry and Biochemistry, University of Toledo, Toledo, OH 43606, USA.

Jacob A Connolly (JA)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Sophia M Soehnlen (SM)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Fatimah K Khalaf (FK)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.
Department of Clinical Pharmacy, College of Pharmacy, University of Alkafeel, Najaf 61001, Iraq.

Deepak Malhotra (D)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Steven T Haller (ST)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Dragan Isailovic (D)

Department of Chemistry and Biochemistry, University of Toledo, Toledo, OH 43606, USA.

David J Kennedy (DJ)

Department of Medicine, University of Toledo College of Medicine and Life Sciences, Toledo, OH 43614, USA.

Classifications MeSH