Literature DB >> 7131132

Necrosis of the pars recta (S3 segment) of the rat kidney produced by hexachloro 1:3 butadiene.

J Ishmael, I Pratt, E A Lock.   

Abstract

Administration of hexachloro 1:3 butadiene (HCBD) intraperitoneally at a dose of 200 mg/kg body weight caused necrosis of the parts recta of the proximal tubules situated in the outer stripe of the outer medulla of the rat kidney. The earliest morphological changes detectable by light microscopy were observed after eight hours, with several proximal tubules showing necrosis. By sixteen hours a distinct band of tubular necrosis was seen in the outer stripe of the outer medulla. One and two days after dosing proximal tubular necrosis was still evident whereas distal tubules were unaffected. By three days, vacuolation was observed in the pars convoluta of some proximal tubules. Active tubular regeneration was apparent by day five, which was accompanied by a marked increase in renal water and nonprotein sulphydryl content (NP-SH). By day fourteen substantial recovery had occurred. Ultrastructural changes were seen as early as one hour after HCBD (300 mg/kg, ip) although necrosis was not marked until 8 hr. Mitochondrial swelling was seen 1-4 hr after dosing in the S1 and S2 segments of the proximal tubule. By 8 hr the major pathological changes were largely confined to the S2 segment and consisted of loss of brush border, mitochondrial swelling and cellular necrosis. In conclusion HCBD produces a site-specific nephrotoxic effect on the proximal tubule in the rat. The pattern of injury was similar to that associated with some other nephrotoxic and ischaemic models of acute renal failure.

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Year:  1982        PMID: 7131132     DOI: 10.1002/path.1711380202

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  5 in total

1.  Mapping Adverse Outcome Pathways for Kidney Injury as a Basis for the Development of Mechanism-Based Animal-Sparing Approaches to Assessment of Nephrotoxicity.

Authors:  Angela Mally; Sebastian Jarzina
Journal:  Front Toxicol       Date:  2022-06-15

2.  Deacetylation and further metabolism of the mercapturic acid of hexachloro-1,3-butadiene by rat kidney cytosol in vitro.

Authors:  I S Pratt; E A Lock
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

3.  Studies on the comparative toxicity of S-(1,2-dichlorovinyl)-L-cysteine, S-(1,2-dichlorovinyl)-L-homocysteine and 1,1,2-trichloro-3,3,3-trifluoro-1-propene in the Fischer 344 rat.

Authors:  M L Anthony; C R Beddell; J C Lindon; J K Nicholson
Journal:  Arch Toxicol       Date:  1994       Impact factor: 5.153

4.  Transport of N-acetyl-S-pentachloro-1,3-butadienylcysteine by rat renal cortex.

Authors:  E A Lock; J Odum; P Ormond
Journal:  Arch Toxicol       Date:  1986-05       Impact factor: 5.153

5.  A Systematic Review of Clinical Characteristics and Histologic Descriptions of Acute Tubular Injury.

Authors:  Yumeng Wen; Chen Yang; Steven P Menez; Avi Z Rosenberg; Chirag R Parikh
Journal:  Kidney Int Rep       Date:  2020-08-31
  5 in total

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