Literature DB >> 864000

The effects of anoxia on the morphology and composite metabolism of the intact aortic intima-media preparation.

A D Morrison, L Orci, L Berwick, A Perrelet, A I Winegrad.   

Abstract

Paired samples of an intact rabbit aortic intima-media preparation were incubated for short periods under aerobic or anoxic conditions in Krebsbicarbonate buffer containing 6% albumin and 5 mM glucose. During aerobic incubation for as long as 1 h the preparation retained an electron microscopic (EM) appearance similar to that of tissue fixed in situ, and scanning EM confirmed the presence of an uninterrupted endothelial surface. After 2.5 min of anoxia there was widespread endothelial swelling, but the alterations in the EM appearance of these cells were not striking and did not progress during a subsequent 30 min aerobic incubation in fresh medium. After 10 min of anoxia there were marked and widespread alterations in endothelial cell structure, including loss of cell integrity, and numerous discrete interruptions in the endothelium were consistently observed on both transmission and scanning EM. After a subsequent 30 min aerobic incubation in fresh buffer, a major fraction of the luminal surface was denuded of endothelium. The aortic vascular smooth muscle cells did not exhibit evidence of irreversible anoxic injury after 2.5 or 10 min of anoxia or after subsequent aerobic incubation for 30 min. Exposure to anoxia for 10 min induced persistent alterations in the composite metabolism of the preparation during subsequent aerobic incubation in fresh medium; O(2) uptake was reduced, and the fraction of the glucose uptake that was accounted for by lactate production increased approximately 100%. The observations suggest that aortic endothelial cells are dependent upon respiration for the preservation of normal ultrastructure and cell integrity, and probably derive the major fraction of their energy requirements from reactions linked to respiration. Under the conditions employed in these experiments, short periods of anoxia did not induce EM evidence of irreversible anoxic injury in aortic vascular smooth muscle cells; this negative result is not incompatible with other data suggesting that these cells normally derive the major fraction of their energy requirements from respiration. Aortic intima-media does not exhibit a high rate of aerobic glycolysis under aerobic conditions which preserve a normal EM appearance of the preparation, but this pattern of metabolism can be induced by prior anoxic exposure.

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Year:  1977        PMID: 864000      PMCID: PMC372314          DOI: 10.1172/JCI108725

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  13 in total

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2.  Metabolism of glucose-U-C-14 in rat aorta in vitro.

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Review 5.  The Pasteur effect and the relations between respiration and fermentation.

Authors:  H A Krebs
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Review 6.  Vascular smooth muscle. I. Normal structure, pathology, biochemistry, and biophysics.

Authors:  A P Somlyo; A V Somlyo
Journal:  Pharmacol Rev       Date:  1968-12       Impact factor: 25.468

7.  Effects of elevated glucose concentrations on the metabolism of the aortic wall.

Authors:  A D Morrison; R S Clements; A I Winegrad
Journal:  J Clin Invest       Date:  1972-12       Impact factor: 14.808

8.  Ultrastructural intimal changes in the rabbit aorta after a moderate carbon monoxide exposure.

Authors:  K Kjeldsen; P Astrup; J Wanstrup
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9.  Morphology and metabolism of an aortic intima-media preparation in which an intact endothelium is preserved.

Authors:  A D Morrison; L Berwick; L Orci; A I Winegrad
Journal:  J Clin Invest       Date:  1976-03       Impact factor: 14.808

10.  Practical stereological methods for morphometric cytology.

Authors:  E R Weibel; G S Kistler; W F Scherle
Journal:  J Cell Biol       Date:  1966-07       Impact factor: 10.539

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  9 in total

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2.  Hypoxia- and endothelium-mediated changes in the pharmacological responsiveness of circumflex coronary artery rings from the sheep.

Authors:  Y W Kwan; R M Wadsworth; K A Kane
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3.  Basal phosphatidylinositol turnover controls aortic Na+/K+ ATPase activity.

Authors:  D A Simmons; E F Kern; A I Winegrad; D B Martin
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4.  Mechanism of glucose-induced (Na+, K+)-ATPase inhibition in aortic wall of rabbits.

Authors:  D A Simmons; A I Winegrad
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5.  Injury to primary cultures of rat heart endothelial cells by hypoxia and glucose deprivation.

Authors:  D Acosta; C P Li
Journal:  In Vitro       Date:  1979-11

6.  Elevated extracellular glucose inhibits an adenosine-(Na+,K+)-ATPase regulatory system in rabbit aortic wall.

Authors:  D A Simmons; A I Winegrad
Journal:  Diabetologia       Date:  1991-03       Impact factor: 10.122

7.  Mechanisms in rabbit aorta for hyperglycaemia-induced alterations in angiotensin II and norepinephrine effects.

Authors:  D A Simmons; A I Winegrad
Journal:  Diabetologia       Date:  1992-08       Impact factor: 10.122

8.  Insulin does not regulate vascular smooth muscle Na+, K(+)-ATPase activity in rabbit aorta.

Authors:  D A Simmons; A I Winegrad
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9.  Prostacyclin production by the deendothelialized rabbit aorta.

Authors:  J M Boeynaems; N Galand; P Ketelbant
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  9 in total

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