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1.
Biomarkers ; 24(5): 492-498, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31099265

RESUMEN

Objective: The aim of the present work is to evaluate the toxicity of titanium dioxide nanoparticles (TiO2NPs) according to their doses and particle sizes. Materials and methods: The effect of five days oral administration of TiO2NPs (21 and 80 nm) with different doses (50, 250 and 500 mg/kg body weight) was assessed in mice via measurement of oxidative stress markers; glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), malondialdehyde (MDA) and nitric oxide (NO), liver function indices; aspartate and alanine aminotransferases (AST and ALT), chromosomal aberrations and liver histopathological pattern. Results: The results revealed drastic alterations in all the measured parameters and showed positive correlation with the gradual dose increment. In addition, the smaller particle size of TiO2NPS (21 nm) had more adverse effect in all the selected biochemical parameters, genetic aberrations and histological investigations. Conclusions: Toxicity of TiO2NPs increases in a dose-dependent manner and vice versa with particles size. The evaluated biomarkers are good indicators for TiO2NPs toxicity. More detailed studies are required before the recommendation of TiO2NPS as food additives.


Asunto(s)
Biomarcadores/sangre , Nanopartículas/toxicidad , Titanio/toxicidad , Alanina Transaminasa/sangre , Animales , Aspartato Aminotransferasas/sangre , Catalasa/sangre , Aberraciones Cromosómicas/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Glutatión/sangre , Hígado/metabolismo , Hígado/patología , Malondialdehído/sangre , Ratones , Nanopartículas/metabolismo , Óxido Nítrico/metabolismo , Estrés Oxidativo/efectos de los fármacos , Tamaño de la Partícula , Superóxido Dismutasa/sangre , Titanio/metabolismo
2.
Mutat Res ; 516(1-2): 1-9, 2002 Apr 26.
Artículo en Inglés | MEDLINE | ID: mdl-11943604

RESUMEN

The protective effect of calcium given orally by gavage with two doses (40 and 80mg/kg body weight) was evaluated against clastogenecity induced by lead acetate with two concentrations (200 and 400mg/kg diet) on bone marrow and spermatocyte cells of mice in vivo. The parameter screened was percentage of chromosomal aberrations with and without gaps and sperm abnormalities. Statistical analyses indicated the protection efficacy of calcium with the high dose rather than the other in both types of mouse cells. The observation from the laboratory tests, dealing that lead acetate can be considered as an environmental genotoxic material. We recommended that it must be administered of calcium (as calcium chloride) as a protective agent to reduce the genotoxic effect of lead in the somatic and germ cells.


Asunto(s)
Médula Ósea/efectos de los fármacos , Calcio/uso terapéutico , Aberraciones Cromosómicas/efectos de los fármacos , Plomo/toxicidad , Espermatocitos/efectos de los fármacos , Animales , Cromosomas/efectos de los fármacos , Masculino , Meiosis/efectos de los fármacos , Ratones , Pruebas de Mutagenicidad , Compuestos Organometálicos , Espermatocitos/patología
3.
Mutat Res ; 516(1-2): 11-7, 2002 Apr 26.
Artículo en Inglés | MEDLINE | ID: mdl-11943605

RESUMEN

The protective effect of Nigella sativa seed extract and its main constituents thymoquinone (TQ) was studied on mouse cells infected with schistosomiasis. Bone marrow cells in the in vivo experiments and spleen cells in the in vitro one were used to evaluate the potentially protective effect of these natural compounds on the induction of chromosomal aberrations. Karyotyping of the mice cells illustrated that the main abnormalities were gaps, fragments and deletions especially in chromosomes 2, 6 and some in chromosomes 13 and 14. Both N. sativa extract and TQ were considered as protective agents against the chromosomal aberrations induced as a result of schistosomiasis.


Asunto(s)
Benzoquinonas/farmacología , Células de la Médula Ósea/parasitología , Extractos Vegetales/farmacología , Aceites de Plantas/metabolismo , Esquistosomiasis/tratamiento farmacológico , Bazo/parasitología , Animales , Antineoplásicos/farmacología , Células de la Médula Ósea/citología , Células de la Médula Ósea/efectos de los fármacos , Aberraciones Cromosómicas/efectos de los fármacos , Cromosomas/efectos de los fármacos , Cariotipificación , Masculino , Ratones , Esquistosomiasis/transmisión , Semillas/química , Bazo/citología , Bazo/efectos de los fármacos
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