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1.
Br Poult Sci ; 45(3): 367-79, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15327123

RESUMO

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.


Assuntos
Carne , Mitocôndrias Musculares/fisiologia , Músculo Esquelético/ultraestrutura , Perus , Acidose , Envelhecimento , Animais , Composição Corporal , Glicólise , Histocitoquímica , Concentração de Íons de Hidrogênio , Ácido Láctico/sangue , Microscopia Eletrônica , Mitocôndrias Musculares/enzimologia , Músculo Esquelético/crescimento & desenvolvimento , Oxirredução , Fosforilação Oxidativa , Consumo de Oxigênio , Mudanças Depois da Morte , Complexo Piruvato Desidrogenase/metabolismo , Ácido Pirúvico/metabolismo , Controle de Qualidade , Retículo Sarcoplasmático/fisiologia
2.
Mol Genet Metab ; 74(4): 489-91, 2001 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11749054

RESUMO

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.


Assuntos
Códon sem Sentido , Glicogênio Fosforilase Muscular/genética , Doença de Depósito de Glicogênio Tipo V/genética , Adulto , Feminino , Heterogeneidade Genética , Doença de Depósito de Glicogênio Tipo V/enzimologia , Humanos
4.
Eur J Biochem ; 268(5): 1422-9, 2001 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11231295

RESUMO

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.


Assuntos
Carnitina/análogos & derivados , Coração/efeitos dos fármacos , Lipopolissacarídeos/farmacologia , Mitocôndrias Musculares/efeitos dos fármacos , Músculo Esquelético/efeitos dos fármacos , Miocárdio/metabolismo , Animais , Carnitina/metabolismo , Respiração Celular/efeitos dos fármacos , Transporte de Elétrons/efeitos dos fármacos , Feminino , Coração/fisiologia , Técnicas In Vitro , Masculino , Mitocôndrias Musculares/metabolismo , Fibras Musculares Esqueléticas/citologia , Fibras Musculares Esqueléticas/efeitos dos fármacos , Fibras Musculares Esqueléticas/metabolismo , Músculo Esquelético/citologia , Músculo Esquelético/metabolismo , Miocárdio/citologia , Especificidade de Órgãos , Perfusão , Ácido Pirúvico/metabolismo , Coelhos , Saponinas/metabolismo , Sepse/induzido quimicamente , Manejo de Espécimes , Ácido Succínico/metabolismo , Fatores de Tempo , Resistência Vascular/efeitos dos fármacos
5.
Clin Chem Lab Med ; 38(7): 629-32, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11028769

RESUMO

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.


Assuntos
Envelhecimento/sangue , Separação Celular/métodos , Centrifugação/métodos , Índices de Eritrócitos , Eritrócitos/citologia , Eletroforese , Humanos , Proteínas de Membrana/análise
6.
Biochem Soc Trans ; 28(2): 164-9, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10816120

RESUMO

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.


Assuntos
Difosfato de Adenosina/metabolismo , Membranas Intracelulares/fisiologia , Mitocôndrias/ultraestrutura , Animais , Apoptose , Compartimento Celular , Grupo dos Citocromos c/metabolismo , Citosol/metabolismo , Difusão , Mitocôndrias Cardíacas/metabolismo , Mitocôndrias Hepáticas/metabolismo , Oxigênio/metabolismo , Coelhos , Ratos , Traumatismo por Reperfusão , Saponinas/metabolismo
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