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Positive inotropic action of insulin on piglet heart.

This study was designed to investigate changes in cardiac performance during hypoglycemia produced by the administration of insulin in the newborn piglet. With heart rate, aortic pressure, and aortic flow held constant, the treated group demonstrated a pronounced positive inotropic response manifest...

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Detalles Bibliográficos
Autores principales: Rieker, R. P., Lee, J. C., Downing, S. E.
Formato: Texto
Lenguaje:English
Publicado: Yale Journal of Biology and Medicine 1975
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595248/
https://www.ncbi.nlm.nih.gov/pubmed/1210341
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author Rieker, R. P.
Lee, J. C.
Downing, S. E.
author_facet Rieker, R. P.
Lee, J. C.
Downing, S. E.
author_sort Rieker, R. P.
collection PubMed
description This study was designed to investigate changes in cardiac performance during hypoglycemia produced by the administration of insulin in the newborn piglet. With heart rate, aortic pressure, and aortic flow held constant, the treated group demonstrated a pronounced positive inotropic response manifested by an increase of dP/dt max to 138% of control values. Central nervous system function and beta adrenergic activity were excluded from the preparation by ligation of the brachiocephalic vessels and administration of practolol. For reasons discussed, it is unlikely that the findings can be ascribed to glucagon contamination. Therefore, the increase in contractility presumably resulted from a direct effect of insulin upon the myocardium. Clinical and laboratory data suggest that the resistance of the neonate to hypoxia is modified by glycogen stores. Insulin is known to increase glycogen synthesis, and this effect might be expected to augment myocardial resistance to hypoxia. Under the conditions of these experiments, however, pretreatment with insulin had no demonstrable influence on the rate of deterioration of cardiac function during hypoxia. The mechanism of cardiac stimulation by insulin is unknown but may involve calcium fluxes.
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spelling pubmed-25952482008-12-05 Positive inotropic action of insulin on piglet heart. Rieker, R. P. Lee, J. C. Downing, S. E. Yale J Biol Med Research Article This study was designed to investigate changes in cardiac performance during hypoglycemia produced by the administration of insulin in the newborn piglet. With heart rate, aortic pressure, and aortic flow held constant, the treated group demonstrated a pronounced positive inotropic response manifested by an increase of dP/dt max to 138% of control values. Central nervous system function and beta adrenergic activity were excluded from the preparation by ligation of the brachiocephalic vessels and administration of practolol. For reasons discussed, it is unlikely that the findings can be ascribed to glucagon contamination. Therefore, the increase in contractility presumably resulted from a direct effect of insulin upon the myocardium. Clinical and laboratory data suggest that the resistance of the neonate to hypoxia is modified by glycogen stores. Insulin is known to increase glycogen synthesis, and this effect might be expected to augment myocardial resistance to hypoxia. Under the conditions of these experiments, however, pretreatment with insulin had no demonstrable influence on the rate of deterioration of cardiac function during hypoxia. The mechanism of cardiac stimulation by insulin is unknown but may involve calcium fluxes. Yale Journal of Biology and Medicine 1975-11 /pmc/articles/PMC2595248/ /pubmed/1210341 Text en
spellingShingle Research Article
Rieker, R. P.
Lee, J. C.
Downing, S. E.
Positive inotropic action of insulin on piglet heart.
title Positive inotropic action of insulin on piglet heart.
title_full Positive inotropic action of insulin on piglet heart.
title_fullStr Positive inotropic action of insulin on piglet heart.
title_full_unstemmed Positive inotropic action of insulin on piglet heart.
title_short Positive inotropic action of insulin on piglet heart.
title_sort positive inotropic action of insulin on piglet heart.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2595248/
https://www.ncbi.nlm.nih.gov/pubmed/1210341
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