Literature DB >> 6661164

Relationship between regional myocardial blood flow and mitochondrial function.

T Matsubara, K Itoh, M Nanki, K Nishimura, T Kambe, S Sugiyama, T Ozawa, N Sakamoto.   

Abstract

The purpose of this study was to clarify the relationship between myocardial mitochondrial dysfunction and the degree plus duration of restricted coronary blood flow. 135 anesthetized and open-chest dogs were divided into 3 groups according to coronary occlusion time: 10, 20, and 60 min. Regional myocardial blood flow (MBF) was determined in both ischemic and nonischemic areas before and during coronary occlusion using the hydrogen gas clearance method. Myocardial mitochondria were prepared from each area in which MBF was determined after 10, 20, or 60 min of coronary ligation, and their respiratory control index (RCI), ADP/O, and rate of oxygen consumption in state III O2 (St. III O2) were measured. The MBF measured in 135 dogs before coronary ligation was 103 +/- 25 ml/min/100 g (mean +/- SD) for the area to be rendered ischemic and 101 +/- 24 ml/min/100 g for the control area. The MBF in the ischemic area did not cease completely following coronary ligation, and the distribution of MBF showed variations which seemed attributable to individual differences. In the 10-min group, no index of mitochondrial function of the ischemic area differed from that of the nonischemic area at any level of MBF. When MBF was less than 20 ml/min/100 g, RCI of mitochondria from the ischemic area was significantly lower than that from the nonischemic area, in the 20- and 60-min groups. When MBF was less than 20 ml/min/100 g, St. III O2 of mitochondria from the ischemic area significantly decreased compared with that from the nonischemic area, in the 20-min group. In the 60-min group, MBF less than 30 ml/min/100 g, St. III O2 of mitochondria from the ischemic area was likewise significantly decreased. Moreover, with MBF below 20 ml/min/100 g, both RCI and St. III O2 of mitochondria from the ischemic area were significantly lower in the 60-min group than in the 20-min group. These results indicate that ischemia-induced mitochondrial dysfunction depends on the degree of decrease in the blood flow of the area involved as well as on the duration of ischemia, and the blood flow that is critical for survival, based on mitochondrial function, is approximately 20 ml/min/100 g, i.e., a reduction to 20% of normal value.

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Year:  1983        PMID: 6661164     DOI: 10.1007/bf01907218

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  19 in total

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Authors:  J Lekven; A Ilebekk; E Fonstelien; F Kiil
Journal:  Cardiovasc Res       Date:  1975-09       Impact factor: 10.787

2.  Ischemic tissue injury.

Authors:  R B Jennings; C E Ganote; K A Reimer
Journal:  Am J Pathol       Date:  1975-10       Impact factor: 4.307

3.  Studies on the electron transport system. 32. Respiratory control in beef heart mitochondria.

Authors:  Y HATEFI; P JURTSHUK; A G HAAVIK
Journal:  Arch Biochem Biophys       Date:  1961-07       Impact factor: 4.013

4.  Functional behaviour of isolated heart muscle mitochondria after in situ ischemia. Polarographic analysis of mitochondrial oxidative phosphorylation.

Authors:  H Kahles; G G Göring; H Nordbeck; C J Preusse; P G Spieckermann
Journal:  Basic Res Cardiol       Date:  1977 Nov-Dec       Impact factor: 17.165

5.  ST segment deviation and regional myocardial blood flow during experimental partial coronary artery occlusion.

Authors:  G Timogiannakis; I Amende; E Martinez; M Thomas
Journal:  Cardiovasc Res       Date:  1974-07       Impact factor: 10.787

6.  Mapping of left ventricular blood flow with radioactive microspheres in experimental coronary artery occlusion.

Authors:  L C Becker; R Ferreira; M Thomas
Journal:  Cardiovasc Res       Date:  1973-05       Impact factor: 10.787

7.  Recovery time course of ventricular vulnerability after coronary reperfusion in relation to mitochondrial function in ischemic myocardium.

Authors:  S Sugiyama; T Ozawa; T Kato; S Suzuki
Journal:  Am Heart J       Date:  1980-12       Impact factor: 4.749

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Authors:  T Koyama
Journal:  Recent Adv Stud Cardiac Struct Metab       Date:  1975

9.  Biochemical and morphological correlates of acute experimental myocardial ischemia in the dog. IV. Energy mechanisms during very early ischemia.

Authors:  J M Wood; H G Hanley; M L Entman; C J Hartley; J A Swain; U Busch; C H Chang; R M Lewis; W J Morgan; A Schwartz
Journal:  Circ Res       Date:  1979-01       Impact factor: 17.367

10.  Time-dependent changes in canine cardiac mitochondrial function and ultrastructure resulting from coronary occlusion and reperfusion.

Authors:  L R Bush; M Shlafer; D W Haack; B R Lucchesi
Journal:  Basic Res Cardiol       Date:  1980 Jul-Aug       Impact factor: 17.165

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  3 in total

1.  The effects of a high dose of ascorbate on ischemia-reperfusion-induced mitochondrial dysfunction in canine hearts.

Authors:  Y Nishinaka; S Sugiyama; M Yokota; H Saito; T Ozawa
Journal:  Heart Vessels       Date:  1992       Impact factor: 2.037

2.  Hydrogen peroxide generation by mitochondria isolated from regionally ischemic and nonischemic dog myocardium.

Authors:  M Shlafer; K P Gallagher; S Adkins
Journal:  Basic Res Cardiol       Date:  1990 Jul-Aug       Impact factor: 17.165

3.  Effects of acute pressure overload on prostacyclin release and myocardial blood flow in canine hearts: inhibition of prostacyclin synthesis with 15-hydroperoxy-eicosatetraenoic acid.

Authors:  M Imaizumi; Y Ito; T Ito; K Ogawa; T Satake
Journal:  Heart Vessels       Date:  1987       Impact factor: 2.037

  3 in total

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