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J Keul  E Doll  D Keppler 《Experientia》1967,23(11):974-979
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Skeletal muscle is a highly oxygen-consuming tissue that ensures body support and movement, as well as nutrient and temperature regulation. DNA damage induced by reactive oxygen species is present in muscles and tends to accumulate with age. Here, we present a summary of data obtained on DNA damage and its implication in muscle homeostasis, myogenic differentiation and neuromuscular disorders. Controlled and transient DNA damage appears to be essential for muscular homeostasis and differentiation while uncontrolled and chronic DNA damage negatively affects muscle health.  相似文献   

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Summary Resting oxygen consumption of the vascularly isolated gracilis anticus muscle of the rat perfused by natural circulation via the femoral artery with diluted or undiluted blood depends on oxygen delivery (the product of flow rate and arterial oxygen concentration-DO2) only when DO2 falls below 16 l/min/g.  相似文献   

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The turnover of adenosine triphosphate (ATP) in vertebrate skeletal muscle can increase more than a hundredfold during high-intensity exercise while the content of ATP in muscle may remain virtually unchanged. This requires that the rates of ATP hydrolysis and ATP synthesis are exactly balanced despite large fluctuations in reaction rates. ATP is regenerated initially at the expense of phosphocreatine (PCr) and then mainly through glycolysis from muscle glycogen. The increased ATP turnover in contracting muscle will cause an increase in the contents of adenosine diphosphate (ADP), adenosine monophosphate (AMP) and inorganic phosphate (Pi), metabolites that are substrates and activators of regulatory enzymes such as glycogen phosphorylase and phosphofructokinase. An intracellular metabolic feedback mechanism is thus activated by muscle contraction. How muscle metabolism is integrated in the intact body under physiological conditions is not fully understood. Common frogs are suitable experimental animals for the study of this problem because they can readily be induced to change from rest to high-intensity exercise, in the form of swimming. The changes in metabolites and effectors in gastrocnemius muscle were followed during exercise, post-exercise recovery and repeated exercise. The results suggest that glycolytic flux in muscle is modulated by signals from outside the muscle and that fructose 2,6-bisphosphate is a key signal in this process.  相似文献   

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Summary Autoradiographic, stereological and histological studies have been carried out to determine the origin of muscle fibre splitting which supposedly occurs during muscle hypertrophy. The results obtained clearly indicate that the supposedly split fibres are a transient response probably derived from satellite cells and are not derived from pre-existing fibres by true splitting. Similarly, increases in muscle fibre size are not achieved by recruitment of satellite structures as indicated by lack of myonuclear recruitment.Acknowledgment. This work was carried out with the aid of a grant from the Medical Research Council of Great Britain. The authors are grateful for the excellent technical assistance of Miss H. Caulton, M.J. Wild and M. Fenner.  相似文献   

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Studies of the last two decades have demonstrated that sphingolipids are important signalling molecules exerting key roles in the control of fundamental biological processes including proliferation, differentiation, motility and survival. Here we review the role of bioactive sphingolipids such as ceramide, sphingosine, sphingosine 1-phosphate, ganglioside GM3, in the regulation of skeletal muscle biology. The emerging picture is in favour of a complex role of these molecules, which appear implicated in the activation of muscle resident stem cells, their proliferation and differentiation, finalized at skeletal muscle regeneration. Moreover, they are involved in the regulation of contractile properties, tissue responsiveness to insulin and muscle fiber trophism. Hopefully, this article will provide a framework for future investigation into the field, aimed at establishing whether altered sphingolipid metabolism is implicated in the onset of skeletal muscle diseases and identifying new pharmacological targets for the therapy of multiple illnesses, including muscular dystrophies and diabetes. Received 30 April 2008; received after revision 19 June 2008; accepted 14 July 2008  相似文献   

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Summary Isolated rat skeletal muscle mitochondria took up about 40-ng-atoms O per min per mg protein, with glutamine as the only respiratory substrate. The mitochondria incubated in the presence of glutamine and KCN formed both ammonia and glutamate in equivalent amounts. The experiments reported here provide suggestive evidence that rat skeletal muscle mitochondria contain glutaminase (L-glutamine amidohydrolase EC 3.5.1.2.) activity.This work was supported by the Polish Academy of Sciences within the project II. 1, 2, 6.  相似文献   

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Isolated rat skeletal muscle mitochondria took up about 40-ng-atoms O per mg protein, with glutamine as the only respiratory substrate. The mitochondria incubated in the presence of glutamine and KCN formed both ammonia and glutamate in equivalent amounts. The experiments reported here provide suggestive evidence that rat skeletal muscle mitochondria contain glutaminase (L-glutamine amidohydrolase EC 3.5.1.2.) activity.  相似文献   

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Résumé Nous avons étudié in vitro la réaction des fibres musculaires, à l'action de l'acétylcholine, de la tubocurarine et du décaméthonium. L'acétylcholine a provoqué une contraction un peu après la fusion des myoblastes, avant que les fibres ne deviennent striées. La sensibilité des fibres à l'acétylcholine a augmenté avec le développement morphologique. Elle s'est manifestée le long des fibres et les drogues de blocage neuromusculaire ont agi comme prévu.  相似文献   

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Development of acetylcholine sensitivity in cultured skeletal muscle   总被引:3,自引:0,他引:3  
W F Dryden 《Experientia》1970,26(9):984-986
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Summary The common digital extensor (lateral head) is one of the few porcine muscles of convenient dimensions for in vitro studies of intact cells. Its removal and use in physiological studies are described.Acknowledgments. The pigs used in this investigation were provided by Drs D. G. Topel, L. L. Christian and G. A. Gronert whose cooperation is appreciated. Gratitude is also expressed to Dr N. G. Ghoshal for assistance with anatomical identifications.  相似文献   

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Résumé Ces expériences ont montré quantitativement que la méphénésine affecte la structure des muscles du squelette en empèchant le sarcomère de se contracter normalement. Par l'affaiblissement de la contraction du muscle, l'hétérogénéité de la longueur des sarcomères se trouve fortement réduite.  相似文献   

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