Literature DB >> 3953769

Topography of focal proximal tubular necrosis after ischemia with reflow in the rat kidney.

P F Shanley, M D Rosen, M Brezis, P Silva, F H Epstein, S Rosen.   

Abstract

The topography of renal injury after ischemia-reflow was studied in intact rats by clamping the right renal artery for variable periods of time and examining the histologic appearance of the kidney in large 1-mu plastic sections. As reported by others, the straight portion of the proximal tubule (S3) was especially susceptible to ischemia-reflow injury. The pattern of focal necrosis produced in S3 by short (15-30-minute) and longer (45-60-minute) periods of arterial occlusion appeared related to gradients to oxygenation during reflow, in that more extensive injury was seen in areas remote from blood vessels, while perivascular tubules were protected. A similar pattern was seen in S1 and S2 after a longer period (45-60-minutes) of ischemia, which produced extensive but incomplete necrosis in these convoluted segments, with protected tubules lying within zones surrounding arcuate and interlobular arteries. The immediate postglomerular portion of S1, a tubular segment normally well supplied with oxygen, was an exception to this rule. Selective necrosis limited to this portion of the nephron appeared after only 15-30 minutes of ischemia, recalling the special sensitivity of S1 cells to inhibition of mitochondrial respiration. These results suggest that in different segments of the proximal tubule, injury after ischemia-reflow is determined not only by changes that occur during complete ischemia but also by the adequacy of oxygenation during the reflow period.

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Year:  1986        PMID: 3953769      PMCID: PMC1888206     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  11 in total

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Authors:  R D STEWART; S E SADEK; J D SWANK; H C DODD
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2.  Alterations in renal cortex following ischemic injury. 3. Ultrastructure of proximal tubules after ischemia or autolysis.

Authors:  K A Reimer; C E Ganote; R B Jennings
Journal:  Lab Invest       Date:  1972-04       Impact factor: 5.662

3.  On the molecular pathology of ischemic renal cell death. Reversible and irreversible cellular and mitochondrial metabolic alterations.

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Authors:  H P Leichtweiss; D W Lübbers; C Weiss; H Baumgärtl; W Reschke
Journal:  Pflugers Arch       Date:  1969-06-19       Impact factor: 3.657

Review 5.  Enzyme distribution along the nephron.

Authors:  W G Guder; B D Ross
Journal:  Kidney Int       Date:  1984-08       Impact factor: 10.612

6.  Selective distal nephron damage during isolated kidney perfusion.

Authors:  D Alcorn; K R Emslie; B D Ross; G B Ryan; J D Tange
Journal:  Kidney Int       Date:  1981-05       Impact factor: 10.612

7.  Pathogenesis of acute renal failure following temporary renal ischemia in the rat.

Authors:  W J Arendshorst; W F Finn; C W Gottschalk
Journal:  Circ Res       Date:  1975-11       Impact factor: 17.367

8.  Studies on the pathogenesis of ischemic cell injury. II. Morphological changes of the pars convoluta (P1 and P2) of the proximal tubule of the rat kidney made ischemic in vivo.

Authors:  B Glaumann; H Glaumann; I K Berezesky; B F Trump
Journal:  Virchows Arch B Cell Pathol       Date:  1975-12-19

9.  Selective vulnerability of the medullary thick ascending limb to anoxia in the isolated perfused rat kidney.

Authors:  M Brezis; S Rosen; P Silva; F H Epstein
Journal:  J Clin Invest       Date:  1984-01       Impact factor: 14.808

10.  Ischemic damage and repair in the rat proximal tubule: differences among the S1, S2, and S3 segments.

Authors:  M A Venkatachalam; D B Bernard; J F Donohoe; N G Levinsky
Journal:  Kidney Int       Date:  1978-07       Impact factor: 10.612

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  28 in total

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3.  Combination therapy of N-acetylcysteine, sodium nitroprusside and phosphoramidon attenuates ischemia-reperfusion injury in rat kidney.

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Journal:  Mol Cell Biochem       Date:  2002-11       Impact factor: 3.396

4.  Evaluation and management of acute kidney injury in the intensive care unit.

Authors:  Timothy M Saettele; Jason Mohr; Gary A Salzman
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5.  PARP-1 inhibits glycolysis in ischemic kidneys.

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6.  Albumin uptake in OK cells exposed to rotenone: a model for studying the effects of mitochondrial dysfunction on endocytosis in the proximal tubule?

Authors:  A M Hall; M Campanella; A Loesch; M R Duchen; R J Unwin
Journal:  Nephron Physiol       Date:  2010-05-13

7.  Adult stem cell-like tubular cells reside in the corticomedullary junction of the kidney.

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Journal:  Int J Clin Exp Pathol       Date:  2008-01-01

8.  Ischemia-reperfusion model of acute kidney injury and post injury fibrosis in mice.

Authors:  Nataliya I Skrypnyk; Raymond C Harris; Mark P de Caestecker
Journal:  J Vis Exp       Date:  2013-08-09       Impact factor: 1.355

9.  NLRP3 inflammasome mediates albumin-induced renal tubular injury through impaired mitochondrial function.

Authors:  Yibo Zhuang; Guixia Ding; Min Zhao; Mi Bai; Lingyun Yang; Jiajia Ni; Rong Wang; Zhanjun Jia; Songming Huang; Aihua Zhang
Journal:  J Biol Chem       Date:  2014-07-24       Impact factor: 5.157

10.  In vivo MR imaging of magnetically labeled mesenchymal stem cells in a rat model of renal ischemia.

Authors:  Sung Il Jung; Seung Hyup Kim; Hyo-Cheol Kim; Kyu Ri Son; Se Young Chung; Woo Kyung Moon; Hoe Suk Kim; Jong-Sun Choi; Min Hoan Moon; Chang-Kyu Sung
Journal:  Korean J Radiol       Date:  2009-04-22       Impact factor: 3.500

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