The influence of chronic ethanol administration on adriamycin-induced nephrotic syndrome in rats
Language English Country Great Britain, England Media print
Document type Comparative Study, Journal Article
PubMed
7748275
Knihovny.cz E-resources
- MeSH
- Aspartate Aminotransferases metabolism MeSH
- Cholesterol blood MeSH
- Doxorubicin adverse effects blood urine MeSH
- Ethanol administration & dosage pharmacology MeSH
- Kidney Glomerulus MeSH
- Cholesterol, HDL MeSH
- Hyperglycemia MeSH
- Creatine blood urine MeSH
- Rats MeSH
- Kidney cytology drug effects physiopathology MeSH
- Nephrotic Syndrome chemically induced physiopathology MeSH
- Rats, Wistar * MeSH
- Dose-Response Relationship, Drug * MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Aspartate Aminotransferases MeSH
- Cholesterol MeSH
- Doxorubicin MeSH
- Ethanol MeSH
- Cholesterol, HDL MeSH
- Creatine MeSH
Alcoholic liver disease may be frequently complicated by mesangial proliferation with the deposition of IgA in glomeruli and glomerulosclerosis, but these glomerular lesions are usually mild and without greater impact on renal function. To evaluate the putative role of ethanol in glomerular pathology we studied the influence of chronic ethanol administration on the development of experimental adriamycin nephropathy in rats. Nephrotic syndrome was induced by a single i.v. dose of adriamycin (5 mg/kg body wt) both in rats given ethanol at a dose of 4 g/day for 3 months and control rats given standard chow. Further controls on both diets without adriamycin administration were also studied. Blood and urine were examined before and 3 and 6 weeks after adriamycin administration. All rats were killed and examined histologically 6 weeks after adriamycin administration. Ethanol fed nephrotic rats were more catabolic than control nephrotic rats (with higher free fatty acids, lower glycaemia, higher urea with similar creatinine) and had lower proteinuria (0.55 +/- 0.34 versus 5.79 +/- 3.15 g of protein/nmol of creatinine, P < 0.05), higher albuminaemia (5.41 +/- 2.62 versus 1.92 +/- 1.94 g/l, P < 0.01), lower plasma cholesterol (6.54 +/- 2.6 versus 10.57 +/- 2.92 mmol/l, P < 0.01) and triglycerides. The development of nephrotic syndrome and renal morphological changes after adriamycin administration in rats seemed to be ameliorated, or at least delayed by chronic ethanol feeding with much milder and focal glomerulosclerosis as compared with more severe and diffuse glomerulosclerosis in control nephrotic animals. The mechanism of this effect of chronic ethanol feeding remains to be elucidated.(ABSTRACT TRUNCATED AT 250 WORDS)