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1.
Part Fibre Toxicol ; 13: 10, 2016 Feb 24.
Artículo en Inglés | MEDLINE | ID: mdl-26911867

RESUMEN

BACKGROUND: Particulate matter (PM) is one of the six criteria pollutant classes for which National Ambient Air Quality Standards have been set by the United States Environmental Protection Agency. Exposures to PM have been correlated with increased cardio-pulmonary morbidity and mortality. Butadiene soot (BDS), generated from the incomplete combustion of 1,3-butadiene (BD), is both a model PM mixture and a real-life example of a petrochemical product of incomplete combustion. There are numerous events, including wildfires, accidents at refineries and tank car explosions that result in sub-acute exposure to high levels of airborne particles, with the people exposed facing serious health problems. These real-life events highlight the need to investigate the health effects induced by short-term exposure to elevated levels of PM, as well as to assess whether, and if so, how well these adverse effects are resolved over time. In the present study, we investigated the extent of recovery of mouse lungs 10 days after inhalation exposures to environmentally-relevant levels of BDS aerosols had ended. METHODS: Female BALB/c mice exposed to either HEPA-filtered air or to BDS (5 mg/m(3) in HEPA filtered air, 4 h/day, 21 consecutive days) were sacrificed immediately, or 10 days after the final BDS exposure. Bronchoalveolar lavage fluid (BALF) was collected for cytology and cytokine analysis. Lung proteins and RNA were extracted for protein and gene expression analysis. Lung histopathology evaluation also was performed. RESULTS: Sub-acute exposures of mice to hydrocarbon-rich ultrafine particles induced: (1) BALF neutrophil elevation; (2) lung mucosal inflammation, and (3) increased BALF IL-1ß concentration; with all three outcomes returning to baseline levels 10 days post-exposure. In contrast, (4) lung connective tissue inflammation persisted 10 days post-exposure; (5) we detected time-dependent up-regulation of biotransformation and oxidative stress genes, with incomplete return to baseline levels; and (6) we observed persistent particle alveolar load following 10 days of recovery. CONCLUSION: These data show that 10 days after a 21-day exposure to 5 mg/m(3) of BDS has ended, incomplete lung recovery promotes a pro-biotransformation, pro-oxidant, and pro-inflammatory milieu, which may be a starting point for potential long-term cardio-pulmonary effects.


Asunto(s)
Butadienos/toxicidad , Contaminantes Ambientales/toxicidad , Pulmón/efectos de los fármacos , Neumonía/inducido químicamente , Hollín/toxicidad , Administración por Inhalación , Aerosoles , Animales , Líquido del Lavado Bronquioalveolar/química , Butadienos/administración & dosificación , Contaminantes Ambientales/administración & dosificación , Femenino , Regulación de la Expresión Génica , Redes Reguladoras de Genes , Mediadores de Inflamación/metabolismo , Interleucina-1beta/metabolismo , Pulmón/metabolismo , Pulmón/patología , Ratones Endogámicos BALB C , Infiltración Neutrófila/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Tamaño de la Partícula , Neumonía/genética , Neumonía/metabolismo , Neumonía/patología , Recuperación de la Función , Medición de Riesgo , Hollín/administración & dosificación , Factores de Tiempo
2.
Zentralbl Veterinarmed A ; 37(4): 247-52, 1990 May.
Artículo en Inglés | MEDLINE | ID: mdl-2116703

RESUMEN

Disposition kinetics, renal clearance and urinary excretion of ampicillin were determined after oral administration of 10 mg/kg in 8 goats. Peak plasma concentration 1.86 +/- 0.14 mumol/l was attained at 117 +/- 11 min after oral administration. Half-time of absorption was 28.7 +/- 5.8 minutes and that of elimination was 135 +/- 15 minutes. Total area under plasma concentration versus time curve was 9.16 +/- 0.97 mumol.h/l. Total body clearance of ampicillin was 52.1 +/- 4.2 and renal clearance was 0.07 +/- 0.008 ml/min.kg. The renal handling of ampicillin involved glomerular filtration and back diffusion.


Asunto(s)
Ampicilina/farmacocinética , Cabras/metabolismo , Riñón/metabolismo , Absorción , Administración Oral , Ampicilina/administración & dosificación , Animales , Creatinina/orina , Femenino , Semivida
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