Nonylphenol (NP) and octylphenol (OP) are pervasive environmental contaminants belonging to the broader class of compounds known as alkylphenols, with potential human toxic effects. Classified as "xenoestrogens," NP and OP are able to interfere with the cell endocrine physiology via a direct interaction with the estrogen receptors. Here, using HepG2 cells in culture, the changes of the cell redox balance and mitochondrial activity induced by OP and NP have been investigated at mu M concentrations, largely below those provoking acute toxicity, as those typical of environmental contaminants. Following 24 h cell exposure to both OP and NP, ROS production appeared significantly increased (p <= 0.01), together with the production of higher NO oxides (p = 0.003) and peroxynitrated protein-derivatives (NP versus CTR, p = 0.003). The mitochondrial proton electrochemical potential gradient instead was decreased (p <= 0.05), as the oxygen consumption by complex IV, particularly following incubation with NP (NP versus CTR, p = 0.017). Consistently, the RT-PCR and Western blot analyses proved that the OP and NP can modulate to a different extent the expression of the inducible NOS (NP versus CTR, p <= 0.01) and the endothelial NOS (OP versus CTR, p <= 0.05), with a significant variation of the coupling efficiency of the latter (NP versus CTR, p <= 0.05), a finding that may provide a novel clue to understand the specific xenoestrogenic properties of OP and NP.

Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling / Magnifico, Maria Chiara; Xhani, Marla; Popov, Milica; Saso, Luciano; Sarti, Paolo; Arese, Marzia. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - ELETTRONICO. - 2018:(2018). [10.1155/2018/1684827]

Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling

Chiara Magnifico
Writing – Original Draft Preparation
;
Marla Xhani
Investigation
;
Luciano Saso
Membro del Collaboration Group
;
Paolo Sarti
Supervision
;
Marzia Arese
Writing – Original Draft Preparation
2018

Abstract

Nonylphenol (NP) and octylphenol (OP) are pervasive environmental contaminants belonging to the broader class of compounds known as alkylphenols, with potential human toxic effects. Classified as "xenoestrogens," NP and OP are able to interfere with the cell endocrine physiology via a direct interaction with the estrogen receptors. Here, using HepG2 cells in culture, the changes of the cell redox balance and mitochondrial activity induced by OP and NP have been investigated at mu M concentrations, largely below those provoking acute toxicity, as those typical of environmental contaminants. Following 24 h cell exposure to both OP and NP, ROS production appeared significantly increased (p <= 0.01), together with the production of higher NO oxides (p = 0.003) and peroxynitrated protein-derivatives (NP versus CTR, p = 0.003). The mitochondrial proton electrochemical potential gradient instead was decreased (p <= 0.05), as the oxygen consumption by complex IV, particularly following incubation with NP (NP versus CTR, p = 0.017). Consistently, the RT-PCR and Western blot analyses proved that the OP and NP can modulate to a different extent the expression of the inducible NOS (NP versus CTR, p <= 0.01) and the endothelial NOS (OP versus CTR, p <= 0.05), with a significant variation of the coupling efficiency of the latter (NP versus CTR, p <= 0.05), a finding that may provide a novel clue to understand the specific xenoestrogenic properties of OP and NP.
2018
Nitric oxide synthesis; cell signalling; NOS uncoupling; inflammation; oxidative stress; environmental contaminants; endocrine disruptors
01 Pubblicazione su rivista::01a Articolo in rivista
Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling / Magnifico, Maria Chiara; Xhani, Marla; Popov, Milica; Saso, Luciano; Sarti, Paolo; Arese, Marzia. - In: OXIDATIVE MEDICINE AND CELLULAR LONGEVITY. - ISSN 1942-0900. - ELETTRONICO. - 2018:(2018). [10.1155/2018/1684827]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1115040
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