Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
1.
Br Poult Sci ; 45(3): 367-79, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15327123

ABSTRACT

1. M. iliotibialis (MIT) and M. pectoralis (MP) of the BUT Big 6 and Kelly BBB turkey were characterised with respect to physical properties, mitochondrial function, metabolic state, morphology and meat quality. 2. Mitochondrial enzyme activity and respiration rates in MP declined with increasing age while glycolytic enzyme activity remained nearly constant. 3. There were no major differences between BUT Big 6 and Kelly BBB with respect to histological, histochemical or biochemical variables. In spite of the greater adult weight of BUT Big 6, body proportion was equal in both strains. 4. In agreement with the histochemical findings MIT showed higher oxidative capacities, while glycolytic enzyme activity was higher in MP. 5. Pyruvate was the best substrate for oxidative phosphorylation in MIT, but not in MP. Pyruvate dehydrogenase (PDH) activity was up to 15 times less in MP and blood lactate was correlated with intramuscular pH. 6. Turkey breast muscle was restricted in its ability to oxidise pyruvate, especially in those animals that tended to develop intramuscular acidosis post mortem. 7. It is concluded that the in vivo metabolic environment results in acidosis and impaired meat quality, at least in turkey M. pectoralis.


Subject(s)
Meat , Mitochondria, Muscle/physiology , Muscle, Skeletal/ultrastructure , Turkeys , Acidosis , Aging , Animals , Body Composition , Glycolysis , Histocytochemistry , Hydrogen-Ion Concentration , Lactic Acid/blood , Microscopy, Electron , Mitochondria, Muscle/enzymology , Muscle, Skeletal/growth & development , Oxidation-Reduction , Oxidative Phosphorylation , Oxygen Consumption , Postmortem Changes , Pyruvate Dehydrogenase Complex/metabolism , Pyruvic Acid/metabolism , Quality Control , Sarcoplasmic Reticulum/physiology
2.
Mol Genet Metab ; 74(4): 489-91, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11749054

ABSTRACT

We identified a novel nonsense mutation in the myophoshorylase gene in a patient of Italian origin with McArdle disease. This homozygous C-to-T transition (805C > T) results in the replacement of a arginine at amino acid position 269 with a stop codon (R269X). Our data further expand the genetic heterogeneity in patients with McArdle disease.


Subject(s)
Codon, Nonsense , Glycogen Phosphorylase, Muscle Form/genetics , Glycogen Storage Disease Type V/genetics , Adult , Female , Genetic Heterogeneity , Glycogen Storage Disease Type V/enzymology , Humans
4.
Eur J Biochem ; 268(5): 1422-9, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11231295

ABSTRACT

The involvement of mitochondrial dysfunction in septic disturbances of tissues is controversial. The aim of this study was to investigate the effects of endotoxin-induced sepsis on the function of heart and skeletal muscle mitochondria. Rabbits were made septic by subcutaneous injection of endotoxin (lipopolysaccharide, LPS) from Escherichia coli at concentrations of 100 or 150 microg LPS.kg(-1) 24 h prior to the experiments. Mitochondrial respiration was measured in saponin-skinned muscle fibers and compared with photometrically detected activities of respiratory chain enzymes as well as with function of perfused hearts. In heart fibers a dosage of 100 microg LPS.kg(-1) caused a significant decrease of state 3-respiration for the substrates pyruvate (-38%), octanoyl-carnitine (-38%) and succinate (-30%) with correspondingly decreased respiratory control indexes (RCI). In addition, endotoxin caused a decreased temporal stability of the rate of state 3-respiration. At least in part these changes can be attributed to a reduced activity of complex I + III (-50%) of the respiratory chain. State 4-respiration rates were not significantly altered. The lowered state 3-respiration in heart mitochondria seems to contribute to the impairment of heart muscle function as detected by an increase of coronary vascular resistance (CVR) in endotoxin-treated hearts. Functional properties of mitochondria from M. Vastus lasteralis were not affected by 100 microg LPS.kg(-1) but a higher dosage of 150 microg LPS.kg(-1) caused decreased RCI for the substrates pyruvate (-29%) and octanoyl-carnitine (-32%). Also the activity of complex I + III was not significantly affected at lower dose of endotoxin but decreased (-42%) after treatment with 150 microg LPS.kg(-1). Results demonstrate the involvement of impaired mitochondria in the pathophysiology of septic organ failure and a tissue specificity of endotoxaemia.


Subject(s)
Carnitine/analogs & derivatives , Heart/drug effects , Lipopolysaccharides/pharmacology , Mitochondria, Muscle/drug effects , Muscle, Skeletal/drug effects , Myocardium/metabolism , Animals , Carnitine/metabolism , Cell Respiration/drug effects , Electron Transport/drug effects , Female , Heart/physiology , In Vitro Techniques , Male , Mitochondria, Muscle/metabolism , Muscle Fibers, Skeletal/cytology , Muscle Fibers, Skeletal/drug effects , Muscle Fibers, Skeletal/metabolism , Muscle, Skeletal/cytology , Muscle, Skeletal/metabolism , Myocardium/cytology , Organ Specificity , Perfusion , Pyruvic Acid/metabolism , Rabbits , Saponins/metabolism , Sepsis/chemically induced , Specimen Handling , Succinic Acid/metabolism , Time Factors , Vascular Resistance/drug effects
5.
Clin Chem Lab Med ; 38(7): 629-32, 2000 Jul.
Article in English | MEDLINE | ID: mdl-11028769

ABSTRACT

During the process of aging red blood cells become denser and smaller. Counterflow centrifugation separates particles of lower density and smaller diameter from those of higher density and bigger diameter. Thus, the question arises: which property of the red cells, density or size, governs the age-related separation by counterflow centrifugation? It is shown that it is the size which dominates the balance between sedimentation and streaming. Age-related separation of human red blood cells by counterflow centrifugation (elutriation) was analysed by the standard hematological parameters (hemoglobin, mean corpuscular volume, mean corpuscular hemoglobin and mean corpuscular hemoglobin concentration), hemoglobin A1c and the membrane protein ratio 4.1a/(4.1a+4.1b). Red blood cells with a high hemoglobin A1c content and a high 4.1a/(4.1a+4.1b) ratio were found in the early fractions of the elutriation. This proves that old cells make up early fractions, while the "youngsters" constitute later ones. The elutriation technique used (yielding human red blood cells in a "healthy state") and the age parameters studied show that the membrane protein ratio 4.1a/(4.1a+4.1b) is another reliable age parameter for the assessment of red blood cell age.


Subject(s)
Aging/blood , Cell Separation/methods , Centrifugation/methods , Erythrocyte Indices , Erythrocytes/cytology , Electrophoresis , Humans , Membrane Proteins/analysis
6.
Biochem Soc Trans ; 28(2): 164-9, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10816120

ABSTRACT

The mitochondrial outer membrane separates the intermembrane space from the cytosol. The whole exchange of metabolites, cations and information between mitochondria and the cell occurs through the outer membrane. Experimental evidence is reviewed supporting the hypothesis of dynamic ADP compartmentation within the intermembrane space. The outer membrane creates a diffusion barrier for small molecules (adenine nucleotides, creatine phosphate, creatine etc.) causing rate-dependent concentration gradients as a prerequisite for the action of ADP shuttles via creatine kinases or adenylate kinases. If the outer membrane becomes leaky, cytochrome c and apoptosis-inducing factor can be released, leading to apoptosis, and as a bioenergetic consequence the cytosolic phosphorylation potential decreases. Leaky outer membranes can be detected in saponin-skinned fibres with spectrophotometric and oxygraphic methods. This is of special interest in respect to acute impairment of mitochondria during ischaemia/reperfusion.


Subject(s)
Adenosine Diphosphate/metabolism , Intracellular Membranes/physiology , Mitochondria/ultrastructure , Animals , Apoptosis , Cell Compartmentation , Cytochrome c Group/metabolism , Cytosol/metabolism , Diffusion , Mitochondria, Heart/metabolism , Mitochondria, Liver/metabolism , Oxygen/metabolism , Rabbits , Rats , Reperfusion Injury , Saponins/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...