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1.
Biomed Environ Sci ; 19(2): 96-103, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16827179

RESUMEN

OBJECTIVE: To evaluate the acute toxicity of 2-deoxy-D-glucose (2DG) by oral (p.o.) and intravenous (i.v.) routes, and also the cardio-respiratory effects following high doses of 2DG in animal models. METHODS: The LD50 of 2DG (in water) was determined in rats and mice by p.o. route and in mice by i.v. route. The effect of 2-DG (250 mg/kg, 500 mg/kg, and 1000 mg/kg, i.v.) was studied on various cardio-respiratory parameters viz., mean arterial blood pressure, heart rate and respiratory rate in anaesthetised rats. The effect of 2DG (500 mg/kg, 1000 mg/kg, and 2000 mg/kg, p.o.) was also studied on various respiratory parameters viz., respiratory rate and tidal volume in conscious rats and mice using a computer program. RESULTS: The p.o. LD50 of 2DG was found to be >8000 mg/kg in mice and rats, and at this dose no death was observed. The LD50 in mice by i.v. route was found to be 8000 mg/kg. At this dose 2 out of 4 mice died and the death occurred within 6 h. A significant increase in the body weight was observed after p.o. administration of 2DG in rats at 500 mg/kg, 1000 mg/kg, and 2000 mg/kg doses. There was no significant change in the body weight at 4000 mg/kg and 8000 mg/kg by the p.o. route in rats and up to 8000 mg/kg by p.o. as well as i.v. routes in mice. Intravenous administration of 2DG (250 mg/kg, 500 mg/kg, and 1000 mg/kg) in anaesthetised rats showed a time-dependent decrease in the mean arterial blood pressure. There was no change in the heart rate in any of the treatment groups. The tidal volume was not changed significantly by p.o administration in conscious rats, but a significant decrease in the respiratory frequency at 500 mg/kg and 1000 mg/kg doses was observed. In the mice also there was no change in the tidal volume after p.o, administration, but the respiratory frequency decreased significantly at 2000 mg/kg dose. CONCLUSION: 2DG is a safe compound but can cause a fall in the blood pressure and a decrease in respiratory frequency at high doses.


Asunto(s)
Antimetabolitos/toxicidad , Fenómenos Fisiológicos Cardiovasculares/efectos de los fármacos , Desoxiglucosa/toxicidad , Fármacos Sensibilizantes a Radiaciones/toxicidad , Administración Oral , Animales , Antimetabolitos/administración & dosificación , Presión Sanguínea/efectos de los fármacos , Desoxiglucosa/administración & dosificación , Glucosa , Frecuencia Cardíaca/efectos de los fármacos , Inyecciones Intravenosas , Ratones , Fármacos Sensibilizantes a Radiaciones/administración & dosificación , Ratas , Ratas Wistar , Pruebas de Función Respiratoria
2.
Phys Rev E Stat Nonlin Soft Matter Phys ; 64(2 Pt 2): 026110, 2001 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-11497654

RESUMEN

Based on a Fokker-Planck description of external Ornstein-Uhlenbeck noise and cross-correlated noise processes driving a dynamical system we examine the interplay of the properties of noise processes and the dissipative characteristic of the dynamical system in the steady state entropy production and flux. Our analysis is illustrated with appropriate examples.

3.
Phys Rev E Stat Nonlin Soft Matter Phys ; 63(6 Pt 1): 061111, 2001 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-11415072

RESUMEN

We consider a system-reservoir model where the reservoir is modulated by an external noise. Both the internal noise of the reservoir and the external noise are stationary, Gaussian, and are characterized by arbitrary decaying correlation functions. Based on a relation between the dissipation of the system and the response function of the reservoir driven by external noise, we numerically examine the model using a full bistable potential to show that one can recover the turn-over features of the usual Kramers' dynamics when the external noise modulates the reservoir rather than the system directly. We derive the generalized Kramers' rate for this nonequilibrium open system. The theoretical results are verified by numerical simulation.

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