Literature DB >> 1911145

Redistribution of cellular energy following renal ischemia.

K M Gaudio1, G Thulin, T Ardito, M Kashgarian, N J Siegel.   

Abstract

In order to elucidate the pattern of redistribution of cellular energy and the restoration of basic cellular metabolism following an ischemic renal insult, suspensions enriched in proximal tubule segments were studied after 45 min of bilateral artery occlusion and 15 min and 2 h of reflow from rats given either normal saline (control), ATP-MgCl2 (which enhances postischemic recovery of ATP), or alpha, beta-methyl adenosine diphosphate (AMPCP), which inhibits nucleotide degradation during ischemia. In non-ischemic control animals, approximately half of the energy is distributed to functional pump activity and half directed for non-transport purposes. When cellular ATP is reduced to 56% of control values, functional pump activity is significantly reduced to 61% of control, while energy delegated for non-transport purposes is decreased by a significantly smaller increment to only 78% of control at 15 min of reflow. In animals given ATP-MgCl2, the cellular and metabolic profile at 15 min of reflow was no different from ischemic control animals with cellular ATP levels similar at 58%. However, by 2 h, cellular ATP levels had increased significantly to 74%, and this was associated with a redistribution of cellular energy to functional pump activity (119% of control) with little change in non-transport function (76%). In animals treated with AMPCP, the cellular ATP levels were 74% of controls, similar to ATP-MgCl2-treated rats after 2 h of reflow. Despite the differences in reflow interval, the distribution of cellular energy was similar (functional pump activity 120% and non-transport activity 79%). By 2 h, cellular ATP was at 95% and both functional pump activity and non-transport activity were 100%.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1911145     DOI: 10.1007/bf00856647

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  11 in total

1.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
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2.  Mechanisms whereby exogenous adenine nucleotides improve rabbit renal proximal function during and after anoxia.

Authors:  L J Mandel; T Takano; S P Soltoff; S Murdaugh
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3.  Metabolic alterations in proximal tubule suspensions obtained from ischemic kidneys.

Authors:  K M Gaudio; G Thulin; T Ardito; M Kashgarian; N J Siegel
Journal:  Am J Physiol       Date:  1989-09

4.  Oxygen deprivation-induced injury to isolated rabbit kidney tubules.

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5.  Improved renal cortical tubule suspension: spectrophotometric study of O2 delivery.

Authors:  R S Balaban; S P Soltoff; J M Storey; L J Mandel
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6.  Chemical and functional correlates of postischemic renal ATP levels.

Authors:  M E Stromski; K Cooper; G Thulin; K M Gaudio; N J Siegel; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

7.  Role of oxygen free radical species in in vitro models of proximal tubular ischemia.

Authors:  S C Borkan; J H Schwartz
Journal:  Am J Physiol       Date:  1989-07

8.  Accelerated recovery of single nephron function by the postischemic infusion of ATP-MgCl2.

Authors:  K M Gaudio; M R Taylor; I H Chaudry; M Kashgarian; N J Siegel
Journal:  Kidney Int       Date:  1982-07       Impact factor: 10.612

9.  Increases of cell ATP produced by exogenous adenine nucleotides in isolated rabbit kidney tubules.

Authors:  J M Weinberg; H D Humes
Journal:  Am J Physiol       Date:  1986-04

10.  Intracellular respiratory dysfunction and cell injury in short-term anoxia of rabbit renal proximal tubules.

Authors:  T Takano; S P Soltoff; S Murdaugh; L J Mandel
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

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