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1.
Toxicol In Vitro ; 44: 142-153, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28700953

RESUMO

Hand hygiene plays a key role in nosocomial infection prevention. To achieve users' adherence, products' dermal tolerance is essential. We aimed at making a comparative assessment of skin irritation and phototoxicity of the 3 alcohols commonly used in alcohol-based hand rubs (Ethanol, Propan-2-ol, Propan-1-ol) at 60, 70, 80 or 85% w/w in water or with co-formulates (hydrating, emollient and skin protective agents). In vitro validated OECD methods 439 and 432 were used. For irritation, EpiSkin™ Small Model was the chosen Reconstructed Human Epidermis (RhE). For phototoxicity, co-formulates alone or in mixture with and without alcohol were tested using BALB/c 3T3 cell cultures. Whilst Ethanol and Propan-2-ol could not be differentiated and displayed good skin tolerance profiles, Propan-1-ol based products lead to significant viability impairments of RhE at 60, 70 or 80% and at 60% in the presence of co-formulates. However, these results could not be reproduced in another RhE model. Taking also into account bibliographic data on Propan-1-ol, this suggests that our results are probably related to a lack of specificity of the used RhE. Therefore, it can be relevant in case of significant results to use two different RhE models before performing any classification and/or performing any complementary tests.


Assuntos
Álcoois/toxicidade , Anti-Infecciosos Locais/toxicidade , Pele/efeitos dos fármacos , Animais , Células 3T3 BALB , Dermatite Fototóxica , Higiene das Mãos , Humanos , Técnicas In Vitro , Camundongos , Testes de Irritação da Pele
2.
Toxicol Lett ; 222(2): 132-8, 2013 Oct 24.
Artigo em Inglês | MEDLINE | ID: mdl-23916686

RESUMO

Environmental exposure to pollutants such as heavy metal(s) is responsible for various altered physiological functions which are detrimental for health. The gut microbiota is critical for intestinal homeostasis but its role on xenobiotic handling is not fully understood, especially when continuous sub-chronic exposure is addressed. We first confirmed the essential role of the intestinal microbiome to limit heavy metal body burden by using germ-free mice following 6-weeks oral exposure. Significant increases of cadmium and lead absorption and dissemination in blood and target organs were measured in germ-free mice when compared with conventional specific pathogen free (SPF) mice. Besides the "barrier" function of the luminal microbiota, this may involve specific host-genes such as metallothioneins, which are differentially expressed in the gastrointestinal tract of each group of mice. Considering genes relevant for divalent metal transporters and oxidative pathways, significant differences in basal gene expression were measured between control and germ-free mice. Moreover, the magnitude of induction of these genes upon stimulation by heavy metals varied greatly depending on the dose and type of metal as well as the microbial status of the animal. Collectively, these data illustrate the complex host-microbes interplay occurring with environmental pollutants inside the gut.


Assuntos
Intoxicação por Cádmio/prevenção & controle , Poluentes Ambientais/toxicidade , Intestinos/microbiologia , Intoxicação por Chumbo/prevenção & controle , Administração Oral , Animais , Cloreto de Cádmio/administração & dosagem , Cloreto de Cádmio/análise , Cloreto de Cádmio/farmacocinética , Cloreto de Cádmio/toxicidade , Intoxicação por Cádmio/sangue , Intoxicação por Cádmio/metabolismo , Intoxicação por Cádmio/microbiologia , Relação Dose-Resposta a Droga , Poluentes Ambientais/administração & dosagem , Poluentes Ambientais/análise , Poluentes Ambientais/farmacocinética , Fezes/química , Feminino , Regulação da Expressão Gênica/efeitos dos fármacos , Vida Livre de Germes , Bactérias Gram-Negativas/crescimento & desenvolvimento , Bactérias Gram-Positivas/crescimento & desenvolvimento , Absorção Intestinal , Mucosa Intestinal/metabolismo , Intestinos/efeitos dos fármacos , Chumbo/administração & dosagem , Chumbo/análise , Chumbo/farmacocinética , Chumbo/toxicidade , Intoxicação por Chumbo/sangue , Intoxicação por Chumbo/metabolismo , Intoxicação por Chumbo/microbiologia , Camundongos , Camundongos Endogâmicos C57BL , Organismos Livres de Patógenos Específicos , Distribuição Tecidual
3.
Arch Toxicol ; 87(10): 1787-95, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23503628

RESUMO

Chronic ingestion of environmental heavy metals such as lead (Pb) and cadmium (Cd) causes various well-documented pathologies in specific target organs following their intestinal absorption and subsequent accumulation. However, little is known about the direct impact of the non-absorbed heavy metals on the small intestine and the colon homeostasis. The aim of our study was to compare the specific bioaccumulation and retention of Cd and Pb and their effect on the essential metal balance in primary organs, with those occurring specifically in the gastrointestinal tract of mice. Various doses of Cd (5, 20 and 100 mg l(-1)) and Pb (100 and 500 mg l(-1)) chloride salts were provided in drinking water for subchronic to chronic exposures (4, 8 and 12 weeks). In contrast to a clear dose- and time-dependent accumulation in target organs, results showed that intestines are poor accumulators for Cd and Pb. Notwithstanding, changes in gene expression of representative intestinal markers revealed that the transport-, oxidative- and inflammatory status of the gut epithelium of the duodenum, ileum and colon were specifically affected by both heavy metal species. Additionally, in vivo comet assay used to evaluate the impact of heavy metals on DNA damage showed clear genotoxic activities of Cd, on both the upper and distal parts of the gastrointestinal tract. Altogether, these results outline the resilience of the gut which balances the various effects of chronic Cd and Pb in the intestinal mucosa. Collectively, it provides useful information for the risk assessment of heavy metals in gut homeostasis and further disease's susceptibility.


Assuntos
Cloreto de Cádmio/toxicidade , Intestinos/efeitos dos fármacos , Chumbo/toxicidade , Metais Pesados/toxicidade , Animais , Disponibilidade Biológica , Cloreto de Cádmio/administração & dosagem , Cloreto de Cádmio/farmacocinética , Dano ao DNA/efeitos dos fármacos , Relação Dose-Resposta a Droga , Feminino , Trato Gastrointestinal/efeitos dos fármacos , Trato Gastrointestinal/metabolismo , Regulação da Expressão Gênica/efeitos dos fármacos , Absorção Intestinal , Mucosa Intestinal/efeitos dos fármacos , Mucosa Intestinal/metabolismo , Chumbo/administração & dosagem , Chumbo/farmacocinética , Metais Pesados/administração & dosagem , Metais Pesados/farmacocinética , Camundongos , Camundongos Endogâmicos BALB C , Mutagênicos/administração & dosagem , Mutagênicos/farmacocinética , Mutagênicos/toxicidade , Fatores de Tempo , Distribuição Tecidual
4.
Biochem Biophys Res Commun ; 322(3): 734-9, 2004 Sep 24.
Artigo em Inglês | MEDLINE | ID: mdl-15336525

RESUMO

CDC25 enzymes are dual-specificity phosphatases involved in the regulation of the cell cycle. No CDC25 enzymes have been described in higher plant organisms. We report here the characterization of an Arabidopsis thaliana CDC25 enzyme, constituted by a sole catalytic domain and devoid of the N-terminal regulatory region found in the human CDC25. We describe the recombinant expression in Escherichia coli of the Arath;CDC25 and its purification for activity assay and structure determination by NMR. The recombinant enzyme has a tyrosine phosphatase activity towards an artificial substrate, a NMR characterization equally concludes to its correct folding. The secondary structure of the protein was predicted on the basis of the assigned chemical shift of (1)H, (15)N, and (13)C backbone atoms of the protein. The presence of a metal ion in the C-terminus of this new protein points to a zinc finger, and sequence homology indicates that this new structural element might be conserved in related plant homologs.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/enzimologia , Proteínas Tirosina Fosfatases/metabolismo , Fosfatases cdc25/metabolismo , Sequência de Aminoácidos , Substituição de Aminoácidos , Arginina , Sequência de Bases , Clonagem Molecular , Códon/genética , Sequência Conservada , Cisteína , Primers do DNA , Escherichia coli/genética , Espectroscopia de Ressonância Magnética , Dados de Sequência Molecular , Mutação de Sentido Incorreto , Estrutura Secundária de Proteína , Proteínas Recombinantes/metabolismo , Serina
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