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Medicinas Complementárias
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1.
Toxicol Appl Pharmacol ; 96(2): 380-92, 1988 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-2461606

RESUMEN

Male rats administered unleaded gasoline rapidly develop nephropathy characterized by accumulation of hyaline droplets in cells of the proximal convoluted tubules (PCT). This acute response is implicated in development of renal carcinoma in male rats exposed chronically to wholly volatilized gasoline. A major constituent of hyaline droplets is alpha 2 mu-globulin, a protein of hepatic origin for which the rate of synthesis declines during aging. Little information, however, is presently available on possible age-dependent susceptibility of male rats to hydrocarbon-induced nephropathy. In kidneys of untreated male Fischer 344 rats the number of constitutive hyaline droplets declined progressively with increasing age. Electrophoresis of renal cortical homogenates revealed a protein with Mr about 18 X 10(3), probably alpha 2 mu-globulin, in young (3.5 months old) male rats and total absence of this protein in aged (26 months old) males. RIA confirmed that constitutive levels of renal and hepatic alpha 2 mu-globulin in old rats were less than 1.5% of those in young adults. Unleaded gasoline (0.4 ml/kg/day, po, 5 days) caused accumulation of hyaline droplets in renal PCT of 3.5-month-old males accompanied by a marked increase (about twofold) in the renal content of alpha 2 mu-globulin, whereas the same treatment was without effect in 26-month-old rats. Finally, in the renal cortex of young rats the activities of the lysosomal proteases cathepsin B and D were increased following gasoline administration, presumably in response to protein accumulation. However, in 26-month-old rats cathepsin B activity was unaffected, while cathepsin D was increased by gasoline administration. Thus, we conclude that animal age is an important determinant in the development of hydrocarbon-induced nephropathy and only rats which produce large amounts of alpha 2 mu-globulin are susceptible to development of this pathology.


Asunto(s)
Envejecimiento , Gasolina/toxicidad , Enfermedades Renales/inducido químicamente , Riñón/efectos de los fármacos , Petróleo/toxicidad , alfa-Globulinas/análisis , Animales , Catepsina B/metabolismo , Catepsina D/metabolismo , Enfermedades Renales/patología , Hígado/análisis , Hígado/efectos de los fármacos , Masculino , Azul de Metileno , Ratas , Ratas Endogámicas F344 , Colorantes de Rosanilina
2.
Toxicol Appl Pharmacol ; 90(1): 43-51, 1987 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-2442852

RESUMEN

Saturated branched-chain aliphatic hydrocarbons, found in motor fuels, induce nephrotoxicity in male rats. Treatment of male rats with unleaded gasoline (0.04-2.0 ml/kg body wt, po) for 9 days increased markedly the number and size of hyaline (protein resorption) droplets in epithelial cells of the renal proximal convoluted tubules (PCT) and enhanced cellular exfoliation at high dose levels. No other treatment-related pathological effects were observed in the glomeruli, distal tubules, or medulla. The renal content of alpha 2u-globulin, a major urinary protein of male rats, was increased maximally by about 4.4-fold after gasoline administration (1.0 ml/kg, po, 9 days); no further increase was observed at higher doses. Immunoperoxidase staining of kidney tissue sections for alpha 2u-globulin revealed large accumulations of antigen localized in many of the PCT epithelial cells which contained hyaline droplets. The hepatic content of alpha 2u-globulin and its mRNA were not altered by gasoline administration. These data show, for the first time, that alpha 2u-globulin is accumulated in the kidneys of gasoline-intoxicated male rats and sequestered specifically in some of the hyaline droplets characteristic of gasoline-induced nephropathy. A hydrocarbon-induced defect in the renal lysosomal degradation of low-molecular-weight urinary proteins, rather than increased synthesis of these proteins, appears to cause hyaline droplet accumulation.


Asunto(s)
alfa-Globulinas/metabolismo , Gasolina/toxicidad , Túbulos Renales Proximales/metabolismo , Petróleo/toxicidad , Administración Oral , alfa-Globulinas/genética , Animales , Cromatografía de Gases , Histocitoquímica , Técnicas Inmunológicas , Túbulos Renales Proximales/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/metabolismo , Masculino , ARN Mensajero/análisis , Ratas , Ratas Endogámicas F344
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