Literature DB >> 6674670

Early functional and morphological changes in renal tubular necrosis due to p-aminophenol.

J M Davis, K R Emslie, R S Sweet, L L Walker, R J Naughton, S L Skinner, J D Tange.   

Abstract

Functional and morphological changes developed rapidly in rats after the intravenous administration of the organic nephrotoxin p-aminophenol. Proximal intratubular pressure remained close to its mean control value of 14.9 +/- 0.9 mm Hg up to 40 min after injection of the nephrotoxin then rose rapidly over the following 50 min to a maximum of 38.7 +/- 7.4 mm Hg. Distal tubular pressure also rose in the same manner. Renal blood flow remained constant, but GFR fell to 11% of control values while fractional excretion of sodium and water rose 12 and five times, respectively. Morphological changes developed in parallel with the functional changes. They were widespread, varied in intensity from cell to cell, were more severe in the distal third of the proximal convoluted tubule and consisted of cytoplasmic swelling, reduced organelle concentration, reduction or loss of basal infoldings, widening of lateral intercellular spaces, extrusion of bubbles of cell sap into the tubular lumen; brush borders were preserved. No casts were present up to 90 min. Similar results were seen when p-aminophenol was added to the perfusate of the isolated perfused kidney. It is proposed that metabolic and morphological damage leads rapidly to both impairment of proximal tubular sodium reabsorption and increased flow resistance in the cortical collecting system. Both effects contribute to a rise in tubular pressures which oppose glomerular filtration.

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Year:  1983        PMID: 6674670     DOI: 10.1038/ki.1983.221

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  10 in total

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Authors:  Liudmila L Mazaleuskaya; Katrin Sangkuhl; Caroline F Thorn; Garret A FitzGerald; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2015-08       Impact factor: 2.089

2.  Urinalysis for detection of chemically induced renal damage (3)--Establishment and application of radioimmunoassay for lysozyme of rat urine.

Authors:  H Ohata; T Hashimoto; K Monose; A Takahashi; T Terao
Journal:  Arch Toxicol       Date:  1988-08       Impact factor: 5.153

3.  Biochemical characterisation of para-aminophenol-induced nephrotoxic lesions in the F344 rat.

Authors:  K P Gartland; F W Bonner; J A Timbrell; J K Nicholson
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

4.  2-Bromoethanamine nephrotoxicity in the nude mouse: an atypical targetting for the renal cortex.

Authors:  N J Gregg; P H Bach
Journal:  Int J Exp Pathol       Date:  1990-10       Impact factor: 1.925

5.  Effects of biliary cannulation and buthionine sulphoximine pretreatment on the nephrotoxicity of para-aminophenol in the Fischer 344 rat.

Authors:  K P Gartland; C T Eason; F W Bonner; J K Nicholson
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

6.  Effect of ascorbic acid, acivicin and probenecid on the nephrotoxicity of 4-aminophenol in the Fischer 344 rat.

Authors:  L M Fowler; J R Foster; E A Lock
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

7.  Tubular ultrastructure in acute renal failure in man: epithelial necrosis and regeneration.

Authors:  T S Olsen; H S Olsen; H E Hansen
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

8.  Tubular ultrastructure in acute renal failure: alterations of cellular surfaces (brush-border and basolateral infoldings).

Authors:  T S Olsen; H E Hansen; H S Olsen
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

9.  Studies on the effects of L(alpha S,5S)-alpha-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125) on 4-aminophenol-induced nephrotoxicity in the Fischer 344 rat.

Authors:  M L Anthony; C R Beddell; J C Lindon; J K Nicholson
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

10.  Nephrotoxicity of 4-amino-3-S-glutathionylphenol and its modulation by metabolism or transport inhibitors.

Authors:  L M Fowler; J R Foster; E A Lock
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

  10 in total

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