Literature DB >> 28889264

Metals and Paraoxonases.

Lucio G Costa1,2, Toby B Cole3,4, Jacqueline M Garrick3, Judit Marsillach5, Clement E Furlong5,6.   

Abstract

The paraoxonases (PONs) are a three-gene family which includes PON1, PON2, and PON3. PON1 and PON3 are synthesized primarily in the liver and a portion is secreted in the plasma, where they are associated with high-density lipoproteins (HDLs), while PON2 is an intracellular enzyme, expressed in most tissues and organs, including the brain. PON1 received its name from its ability to hydrolyze paraoxon, the active metabolite of the organophosphorus (OP) insecticide parathion, and also more efficiently hydrolyzes the active metabolites of several other OPs. PON2 and PON3 do not have OP-esterase activity, but all PONs are lactonases and are capable of hydrolyzing a variety of lactones, including certain drugs, endogenous compounds, and quorum-sensing signals of pathogenic bacteria. In addition, all PONs exert potent antioxidant effects. PONs play important roles in cardiovascular diseases and other oxidative stress-related diseases, modulate susceptibility to infection, and may provide neuroprotection (PON2). Hence, significant attention has been devoted to their modulation by a variety of dietary, pharmacological, lifestyle, or environmental factors. A number of metals have been shown in in vitro, animal, and human studies to mostly negatively modulate expression of PONs, particularly PON1, the most studied in this regard. In addition, different levels of expression of PONs may affect susceptibility to toxicity and neurotoxicity of metals due to their aforementioned antioxidant properties.

Entities:  

Keywords:  Cadmium; Lead; Manganese; Mercury; Metals; Oxidative stress; Paraoxonases

Mesh:

Substances:

Year:  2017        PMID: 28889264     DOI: 10.1007/978-3-319-60189-2_5

Source DB:  PubMed          Journal:  Adv Neurobiol


  6 in total

1.  Trace Elements and Paraoxonase-1 Activity in Lower Extremity Artery Disease.

Authors:  Joaquim Rovira; Anna Hernández-Aguilera; Fedra Luciano-Mateo; Noemí Cabré; Gerard Baiges-Gaya; Martí Nadal; Vicente Martín-Paredero; Jordi Camps; Jorge Joven; José L Domingo
Journal:  Biol Trace Elem Res       Date:  2018-03-10       Impact factor: 3.738

Review 2.  PPARγ/PGC1α signaling as a potential therapeutic target for mitochondrial biogenesis in neurodegenerative disorders.

Authors:  Sumit Jamwal; Jennifer K Blackburn; John D Elsworth
Journal:  Pharmacol Ther       Date:  2020-10-09       Impact factor: 12.310

3.  Paraoxonase Activity and Phenotype Distribution in Patients with Chronic Obstructive Pulmonary Disease.

Authors:  Nurhan Sarioglu; Cigdem Bilen; Celalettin Cevik; Nahit Gencer
Journal:  Eurasian J Med       Date:  2020-06-09

4.  Selenium modifies associations between multiple metals and neurologic symptoms in Gulf states residents.

Authors:  Emily J Werder; Lawrence S Engel; Matthew D Curry; Dale P Sandler
Journal:  Environ Epidemiol       Date:  2020-12-04

5.  Serum levels of proinflammatory cytokines and selected bioelements in perimenopausal women with regard to body mass index.

Authors:  Anna Maria Cybulska; Kamila Rachubińska; Małgorzata Szkup; Daria Schneider-Matyka; Irena Baranowska-Bosiacka; Dariusz Chlubek; Anna Lubkowska; Mariusz Panczyk; Joanna Sołek-Pastuszka; Elżbieta Grochans
Journal:  Aging (Albany NY)       Date:  2021-12-10       Impact factor: 5.682

6.  Insights into the role of paraoxonase 2 in human pathophysiology.

Authors:  Fauzia Parween; Rinkoo Devi Gupta
Journal:  J Biosci       Date:  2022       Impact factor: 1.826

  6 in total

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