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Featured researches published by P. Fernández Freire.


Mutation Research-genetic Toxicology and Environmental Mutagenesis | 2012

Toxicological evaluation of three contaminants of emerging concern by use of the Allium cepa test.

Óscar Herrero; J.M. Pérez Martín; P. Fernández Freire; L. Carvajal López; Ana Peropadre; M.J. Hazen

Di(2-ethylhexyl)phthalate, triclosan and propylparaben are contaminants of emerging concern that have been subjected to extensive toxicological studies, but for which limited information is currently available concerning adverse effects on terrestrial plant systems. The Allium cepa test, which is considered one of the most efficient approaches to assess toxic effects of environmental chemicals, was selected to evaluate the potential risks of these ubiquitous pollutants. Our data demonstrate that all three compounds studied may in some way be considered toxic, but different effects were noted depending on the chemical and the end point analysed. Results derived from the analysis of macroscopic parameters used in testing for general toxicity, revealed that while di(2-ethylhexyl)phthalate had no apparent effects, the other two chemicals inhibited A. cepa root growth in a dose-dependent manner. On the other hand, although all three compounds caused alterations in the mitotic index of root-tip cells, propylparaben was the only one that did not show evidence of genotoxicity in assays for chromosome aberrations and micronuclei. The results of the present study clearly indicate that sensitive plant bioassays are useful and complementary tools to determine environmental impact of contaminants of emerging concern.


Toxicology in Vitro | 2008

In vitro assessment of the cytotoxic and mutagenic potential of perfluorooctanoic acid.

P. Fernández Freire; J.M. Pérez Martín; Óscar Herrero; Ana Peropadre; E. De la Peña; M.J. Hazen

Perfluorooctanoic acid (PFOA) is a perfluorinated compound ubiquitously detected in the environment, including wildlife and humans. Despite the available information, research on the cytotoxicity of PFOA in non-tumoral mammalian cells is relatively limited. In this work, two in vitro toxicity systems were employed to provide further insight into the cytotoxic and mutagenic potential of PFOA. The cytotoxicity of the chemical towards Vero cells was assessed using biochemical and morphological parameters, while mutagenicity was evaluated according to Ames test. High doses of PFOA cause oxidative stress in Vero cells, that was closely linked to cell cycle arrest at the G1 phase and induction of apoptosis. Our results corroborate previous findings in human tumoral cells and suggest that the mode of action of this perfluorinated compound is not a peculiarity among mammalian cell types. On the other hand, the compound was not mutagenic in the Ames test, using four strains of Salmonella typhimurium in the presence or absence of rat S9 metabolic activation system.


Cell Biology and Toxicology | 2007

Cytotoxicity of butylated hydroxyanisole in Vero cells

V. Labrador; P. Fernández Freire; J.M. Pérez Martín; M.J. Hazen

Butylated hydroxyanisole (BHA) is perhaps the most extensively used synthetic antioxidant in the food and cosmetic industry, although considerable controversy exists in the literature regarding the safety of this compound. Most in vitro studies describing the effects of BHA have been performed in cancer cells, but it is unclear whether normal cells are equally susceptible to BHA exposure.The present study investigate the toxic potential of BHA in mammalian cells, using biochemical and morphological parameters, which reveal interference with structures essential for cell survival, proliferation and/or function. Cell growth inhibition was assessed by using colorimetric assays, whereas cellular alterations after BHA exposure, were evaluated using conventional light and fluorescence microscopy. Low doses of BHA exerted a significant cytotoxic effect, associated with loss of mitochondrial function. As the concentration of BHA was increased, morphological alterations in critical subcellular targets such as lysosomes, mitochondria and actin cytoskeleton, were observed. In parallel, BHA induced an irreversible loss of cell proliferative capacity, preceding apoptosis induction.Thus, the dose-dependent activity of BHA on Vero cells appears to be cytotoxic as well as cytostatic. Our observations, although simplified with respect to the in vivo situations, allowed the assessment of the specific damage at the cellular level, and provide some clue about the effects of BHA in non-tumoral mammalian cells.


Toxicology in Vitro | 2009

An integrated cellular model to evaluate cytotoxic effects in mammalian cell lines

P. Fernández Freire; Ana Peropadre; J.M. Pérez Martín; Óscar Herrero; M.J. Hazen

The ever growing anthropogenic pressure to the environment has lead in 2007 to the revision of the existing legislation and the approval of the new European law regarding the production and importation of chemicals, known as REACH. This new legal framework supports the development of alternative methods to animal experimentation encouraging the improvement and/or design of new methodological strategies for the toxicological evaluation of chemical compounds. Even though cytotoxicity studies are a reductionist approach to acute toxicity in vivo, they offer the best agreement between obtaining relevant information about the mechanism of toxic action and the use of alternative methods. Following this trend, this work presents an integrated cellular strategy in order to know the toxicity and mechanism of action of chemical compounds, using simple and reproducible in vitro systems. The experimental procedures are performed in two steps. The first one involves the systematic analysis of the main cellular targets using proliferation, viability and morphological probes. The second step relies upon the results obtained in the first step, including specific assays that focus on the mechanism of toxic action and the cellular response. The benefits of this strategy are exemplified with two real cases: pentachlorophenol and rotenone.


Toxicology | 2005

Cytotoxic effects in mammalian Vero cells exposed to pentachlorophenol

P. Fernández Freire; V. Labrador; J.M. Pérez Martín; M.J. Hazen


Mutation Research | 2008

Carbamazepine induces mitotic arrest in mammalian Vero cells.

J.M. Pérez Martín; P. Fernández Freire; V. Labrador; M.J. Hazen


Journal of Applied Toxicology | 2004

Ultrastructural Changes Induced in HeLa Cells after Phototoxic Treatment with Harmine

J.M. Pérez Martín; V. Labrador; P. Fernández Freire; M.L. Molero; M.J. Hazen


Revista de toxicología | 2014

Cytotoxic evaluation of a mixture of eight pollutants at environmental relevant concentrations

J.M. Pérez Martín; P. Fernández Freire; Ana Peropadre; M.J. Hazen


Toxicology Letters | 2016

Exposure to low doses of triclosan induces DNA-damage and increased proliferation in human keratinocytes

Ana Peropadre; L. Blanco; P. Fernández Freire; G. Repetto; M.J. Hazen


Toxicology Letters | 2016

Carbendazim induces cytotoxic and cytostatic effects in non-tumoral human cells

P. Fernández Freire; J. Paredes; Ana Peropadre; G. Repetto; M.J. Hazen

Collaboration


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M.J. Hazen

Autonomous University of Madrid

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J.M. Pérez Martín

Autonomous University of Madrid

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Ana Peropadre

Autonomous University of Madrid

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V. Labrador

Autonomous University of Madrid

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Óscar Herrero

Autonomous University of Madrid

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E. De la Peña

Spanish National Research Council

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J. Paredes

Autonomous University of Madrid

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L. Carvajal López

Autonomous University of Madrid

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M.L. Molero

Autonomous University of Madrid

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