Adriamycin-induced nephrotic syndrome in rats: sequence of pathologic events
- PMID: 6172662
Adriamycin-induced nephrotic syndrome in rats: sequence of pathologic events
Abstract
Adriamycin has been suspected of causing experimental nephrotoxicity. We report here that adriamycin induces a nephrotic syndrome in rats, proteinuria beginning 4 to 5 days after a single intravenous injection (7.5 mg. per kg. of body weight). The full expression of the syndrome develops 13 to 15 days later. Minimal alterations at light microscopy, negative immunofluorescence, and only some focal "fusion" of foot processes can be observed by electron microscopy in the early phase after injection (28 hours). At 13 days, loss of foot process architecture, and replacement by flattened epithelial cytoplasm, was invariably found. These ultrastructural findings became extensive at 28 days follow-up. Colloidal iron staining of kidney biopsies revealed loss of glomerular polyanions as early as 3 hours and very marked loss at 28 hours after adriamycin injection. Polyanions were totally absent at 13 days and were still undetectable at 28 days. Thus, the loss of polyanionic charges associated with the sialic acid coat precedes the ultrastructural changes and the onset of proteinuria. These changes appeared similar to those reported in rats treated with daunomycin or puromycin animonucleoside. The present study supports in a different animal model the concept that both morphologic changes and proteinuria are the consequence of a common primary event that is the loss of glomerular fixed negative charges.
Similar articles
-
Changes of glomerular fixed anionic charge sites in adriamycin nephrosis in rats.Chin Med J (Engl). 1991 Feb;104(2):128-31. Chin Med J (Engl). 1991. PMID: 1714805
-
Steroids and Adriamycin nephrosis.Appl Pathol. 1984;2(1):32-8. Appl Pathol. 1984. PMID: 6525317
-
Complement-independent nephrotoxic serum nephritis in Munich Wistar rats. Immunologic and ultrastructural studies.Lab Invest. 1983 May;48(5):585-97. Lab Invest. 1983. PMID: 6341711
-
[Proteinuria and morphological changes of the kidney].Rinsho Byori. 1979;Suppl 36:1-15. Rinsho Byori. 1979. PMID: 372634 Review. Japanese. No abstract available.
-
The experimental model of nephrotic syndrome induced by Doxorubicin in rodents: an update.Inflamm Res. 2015 May;64(5):287-301. doi: 10.1007/s00011-015-0813-1. Epub 2015 Mar 19. Inflamm Res. 2015. PMID: 25788426 Review.
Cited by
-
Current understanding of the molecular mechanisms of circulating permeability factor in focal segmental glomerulosclerosis.Front Immunol. 2023 Sep 19;14:1247606. doi: 10.3389/fimmu.2023.1247606. eCollection 2023. Front Immunol. 2023. PMID: 37795085 Free PMC article. Review.
-
Sanqi Qushi Granule Alleviates Proteinuria and Podocyte Damage in NS Rat: A Network Pharmacology Study and in vivo Experimental Validation.Drug Des Devel Ther. 2023 Jun 19;17:1847-1861. doi: 10.2147/DDDT.S403617. eCollection 2023. Drug Des Devel Ther. 2023. PMID: 37360573 Free PMC article.
-
Renoprotective Effects of Tanshinone IIA: A Literature Review.Molecules. 2023 Feb 20;28(4):1990. doi: 10.3390/molecules28041990. Molecules. 2023. PMID: 36838978 Free PMC article. Review.
-
Characterization and diagnostic value of the gut microbial composition in patients with minimal change disease.Front Physiol. 2022 Dec 6;13:1070569. doi: 10.3389/fphys.2022.1070569. eCollection 2022. Front Physiol. 2022. PMID: 36561217 Free PMC article.
-
Chitin powder enhances growth factor production and therapeutic effects of mesenchymal stem cells in a chronic kidney disease rat model.J Artif Organs. 2023 Sep;26(3):203-211. doi: 10.1007/s10047-022-01346-z. Epub 2022 Aug 17. J Artif Organs. 2023. PMID: 35976577
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources