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Difference between revisions of "Magnifico 2018 Oxid Med Cell Longev"

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{{Publication
{{Publication
|title=Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M (2018) Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling. Oxid Med Cell Longev [Epub ahead of print].
|title=Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M (2018) Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling. Oxid Med Cell Longev 2018:1684827.
|info=[https://www.hindawi.com/journals/omcl/aip/1684827/ Open Access]
|info=[https://www.ncbi.nlm.nih.gov/pubmed/29805728 PMID: 29805728 Open Access]
|authors=Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M
|authors=Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M
|year=2018
|year=2018
Line 7: Line 7:
|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 μM 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 (p NP vs CTR = 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 (p NP vs CTR = 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 (p NP vs CTR ≤ 0.01) and the endothelial NOS (p OP vs CTR ≤ 0.05), with a significant variation of the coupling efficiency of the latter (p NP vs CTR ≤ 0.05), a finding that may provide a novel clue to understand the specific xenoestrogenic properties of OP and NP.
|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 μM 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 (p NP vs CTR = 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 (p NP vs CTR = 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 (p NP vs CTR ≤ 0.01) and the endothelial NOS (p OP vs CTR ≤ 0.05), with a significant variation of the coupling efficiency of the latter (p NP vs CTR ≤ 0.05), a finding that may provide a novel clue to understand the specific xenoestrogenic properties of OP and NP.
|editor=[[Kandolf G]],
|editor=[[Kandolf G]],
|mipnetlab=IT Roma Sarti P
}}
}}
{{Labeling
{{Labeling
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|couplingstates=ROUTINE, OXPHOS
|couplingstates=ROUTINE, OXPHOS
|pathways=N, S, CIV, ROX
|pathways=N, S, CIV, ROX
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k, NO
|additional=Labels, 2018-03,
|additional=Labels, 2018-03,
}}
}}

Revision as of 09:08, 29 May 2019

Publications in the MiPMap
Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M (2018) Nonylphenol and octylphenol differently affect cell redox balance by modulating the nitric oxide signaling. Oxid Med Cell Longev 2018:1684827.

» PMID: 29805728 Open Access

Magnifico MC, Xhani M, Popov M, Saso L, Sarti P, Arese M (2018) Oxid Med Cell Longev

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 μM 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 (p NP vs CTR = 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 (p NP vs CTR = 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 (p NP vs CTR ≤ 0.01) and the endothelial NOS (p OP vs CTR ≤ 0.05), with a significant variation of the coupling efficiency of the latter (p NP vs CTR ≤ 0.05), a finding that may provide a novel clue to understand the specific xenoestrogenic properties of OP and NP.

Bioblast editor: Kandolf G O2k-Network Lab: IT Roma Sarti P


Labels: MiParea: Respiration 


Organism: Human  Tissue;cell: Liver, Other cell lines  Preparation: Intact cells, Permeabilized cells 


Coupling state: ROUTINE, OXPHOS  Pathway: N, S, CIV, ROX  HRR: Oxygraph-2k, NO 

Labels, 2018-03