High resolution light microscopic morphological and microvascular changes in an acutely induced renal papillary necrosis.

Abstract

Morphological changes were followed in semi-thin glycolmethacrylate sections, after treating male Wistar rats with a single ip dose of 2-bromoethanamine (BEA) hydrobromide (100 mg/kg) to induce renal papillary necrosis. Medullary interstitial cells had irregular nuclei at 4 hr and focal necrosis by 8 hr which spread from the papilla tip to the cortico-medullary junction from 12 hr. Increased mucopolysaccharide staining was observed in the papilla tip at 4 hr, and was lost from those regions where necrosis had developed by 48 hr. Endothelial platelet adhesion, first seen at 8 hr, was very marked at 18 hr, but affected capillaries in necrotic regions only, up to 144 hr. The absence of extravasated Monastral Blue B demonstrated the integrity of the medullary microvascular endothelia. The distal nephron showed degenerative changes at 12 hr and cell exfoliation at 18 hr. Cortical changes were confined to PAS-positive casts in the collecting duct and loop of Henle from 8 hr and dilatation of distal and proximal tubules at 8 and 72 hr, respectively. There was active repair at the junction between viable and necrotic tissue in the papilla from 24 hr with mitoses in the collecting ducts and loops of Henle. Normally the urothelium is less than 3-4 cells thick, but upper urothelial proliferation followed BEA administration. Hyperplasia was especially marked at the mouth of the ureter and in the pelvis opposite the region of necrosis (7-8 cells thick at 18 hr) and had only partially resolved by 144 hr.(ABSTRACT TRUNCATED AT 250 WORDS)

• Authors: N J Gregg, E A Courtauld, P H Bach
• Journal: Toxicologic pathology (Toxicol Pathol) Vol. 18 Issue 1 Pt 1 Pg. 47-55 ( 1990) ISSN: 0192-6233 [Print] United States
• PMID: 2194275 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Ethylamines
• 2-bromoethylamine

Topics

• Animals
• Ethylamines (toxicity)
• Histological Techniques
• Kidney (blood supply, pathology, physiopathology)
• Kidney Cortex (blood supply, pathology, physiopathology)
• Kidney Medulla (blood supply, drug effects, pathology)
• Kidney Papillary Necrosis (chemically induced, pathology, physiopathology)
• Male
• Microcirculation (drug effects)
• Rats
• Rats, Inbred Strains
• Time Factors