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Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation

Paraoxonase 1 (PON1) is a high-density lipoprotein (HDL)-associated protein that endows its carrier with (lipo-)lactonase-dependent antioxidative features. Low levels of PON1 activity have been observed in association with obesity, a major risk factor for cardiovascular disease (CVD). Considering th...

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Autores principales: Tisato, Veronica, Romani, Arianna, Tavanti, Elisa, Melloni, Elisabetta, Milani, Daniela, Bonaccorsi, Gloria, Sanz, Juana M., Gemmati, Donato, Passaro, Angelina, Cervellati, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719214/
https://www.ncbi.nlm.nih.gov/pubmed/31390816
http://dx.doi.org/10.3390/antiox8080287
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author Tisato, Veronica
Romani, Arianna
Tavanti, Elisa
Melloni, Elisabetta
Milani, Daniela
Bonaccorsi, Gloria
Sanz, Juana M.
Gemmati, Donato
Passaro, Angelina
Cervellati, Carlo
author_facet Tisato, Veronica
Romani, Arianna
Tavanti, Elisa
Melloni, Elisabetta
Milani, Daniela
Bonaccorsi, Gloria
Sanz, Juana M.
Gemmati, Donato
Passaro, Angelina
Cervellati, Carlo
author_sort Tisato, Veronica
collection PubMed
description Paraoxonase 1 (PON1) is a high-density lipoprotein (HDL)-associated protein that endows its carrier with (lipo-)lactonase-dependent antioxidative features. Low levels of PON1 activity have been observed in association with obesity, a major risk factor for cardiovascular disease (CVD). Considering the well-recognized atheroprotective role of PON1, exogenous/endogenous factors that might modulate its levels/activity are raising great interest. Since adipokines represent a molecular link between obesity and CVD, we here explored the possible impact of these substances on PON1 activity/expression. The levels of interleukin (IL)-6, IL-8, tumor necrosis factor alpha, monocyte chemoattractant protein-1, hepatocyte growth factor, resistin, leptin, and adiponectin were measured along with arylesterase, paraoxonase, and lactonase activities of PON1 in 107 postmenopausal women. Moreover, the direct effect of resistin on PON1 expression was evaluated in vitro. Multivariate analysis revealed that only resistin was significantly and inversely correlated with PON1-lactonase activities (r = −0.346, p < 0.001) regardless of confounding factors such as age or HDL-cholesterol. It is worth noting that no statistical link was found between adipokine and arylesterase or paraoxonase, the two promiscuous activities of PON1. Notably, resistin down-regulated PON1 expression occurred in hepatocellular carcinoma cultures. Our study suggests that resistin might be a negative modulator of PON1 expression and anti-oxidative activity.
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spelling pubmed-67192142019-09-10 Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation Tisato, Veronica Romani, Arianna Tavanti, Elisa Melloni, Elisabetta Milani, Daniela Bonaccorsi, Gloria Sanz, Juana M. Gemmati, Donato Passaro, Angelina Cervellati, Carlo Antioxidants (Basel) Article Paraoxonase 1 (PON1) is a high-density lipoprotein (HDL)-associated protein that endows its carrier with (lipo-)lactonase-dependent antioxidative features. Low levels of PON1 activity have been observed in association with obesity, a major risk factor for cardiovascular disease (CVD). Considering the well-recognized atheroprotective role of PON1, exogenous/endogenous factors that might modulate its levels/activity are raising great interest. Since adipokines represent a molecular link between obesity and CVD, we here explored the possible impact of these substances on PON1 activity/expression. The levels of interleukin (IL)-6, IL-8, tumor necrosis factor alpha, monocyte chemoattractant protein-1, hepatocyte growth factor, resistin, leptin, and adiponectin were measured along with arylesterase, paraoxonase, and lactonase activities of PON1 in 107 postmenopausal women. Moreover, the direct effect of resistin on PON1 expression was evaluated in vitro. Multivariate analysis revealed that only resistin was significantly and inversely correlated with PON1-lactonase activities (r = −0.346, p < 0.001) regardless of confounding factors such as age or HDL-cholesterol. It is worth noting that no statistical link was found between adipokine and arylesterase or paraoxonase, the two promiscuous activities of PON1. Notably, resistin down-regulated PON1 expression occurred in hepatocellular carcinoma cultures. Our study suggests that resistin might be a negative modulator of PON1 expression and anti-oxidative activity. MDPI 2019-08-06 /pmc/articles/PMC6719214/ /pubmed/31390816 http://dx.doi.org/10.3390/antiox8080287 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tisato, Veronica
Romani, Arianna
Tavanti, Elisa
Melloni, Elisabetta
Milani, Daniela
Bonaccorsi, Gloria
Sanz, Juana M.
Gemmati, Donato
Passaro, Angelina
Cervellati, Carlo
Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title_full Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title_fullStr Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title_full_unstemmed Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title_short Crosstalk Between Adipokines and Paraoxonase 1: A New Potential Axis Linking Oxidative Stress and Inflammation
title_sort crosstalk between adipokines and paraoxonase 1: a new potential axis linking oxidative stress and inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719214/
https://www.ncbi.nlm.nih.gov/pubmed/31390816
http://dx.doi.org/10.3390/antiox8080287
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