Literature DB >> 1085708

Independance of glucagon and insulin handling by the isolated perfused dog kidney.

P J Lefebvre, A S Luyckx, A H Nizet.   

Abstract

The effect of raising arterial plasma glucagon concentrations on kidney glucagon uptake was investigated using an isolated dog kidney perfused with whole blood. In addition, the effect of insulin on the magnitude of glucagon uptake by the kidney was studied at various glucagon concentrations. Renal vein plasma glucagon (V) has been found to be proportional to renal artery plasma glucagon (A). V and A were highly significantly correlated. In the absence of exogenous insulin infusion, V equalled 0.733 +/- 0.034 A, while in the presence of insulin V equalled 0.747 +/- 0.015 A. When kidney glucagon uptake was measured directly it increased as a function of arterial plasma glucagon. The calculated regression lines were similar in the presence and in the absence of insulin. The mean clearance rate of glucagon by the kidney was similar at low, medium or high concentrations of glucagon and was not affected by the presence of insulin at a mean concentration of 335.7 +/- 15.7 muU/ml. At this concentration of insulin, kidney insulin uptake was not affected by glucagon at concentrations ranging from 32 to 1600 pg/ml. Comparison of kidney glucagon uptake at similar arterial plasma glucagon concentrations, but with different renal plasma flows, indicated that kidney glucagon uptake is more dependant on arterial plasma glucagon concentration than on the quantity of glucagon entering the kidney per minute. It is concluded that: 1) kidney glucagon uptake increases as a function of arterial plasma glucagon concentration; 2) the clearance rate of glucagon is similar at low, medium or high arterial concentrations of glucagon; 3) at concentration of 300-350 muU/ml, insulin does not affect kidney glucagon uptake, and 4) at concentrations of glucagon up to 1600 pg/ml, renal insulin uptake is not affected by glucagon. These studies indicate that insulin and glucagon are handled independantly by the kidney of the dog.

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Year:  1976        PMID: 1085708     DOI: 10.1007/bf00420980

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  15 in total

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Authors:  A S HUGGETT; D A NIXON
Journal:  Lancet       Date:  1957-08-24       Impact factor: 79.321

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Review 3.  The isolated perfused kidney: possibilities, limitations and results.

Authors:  A Nizet
Journal:  Kidney Int       Date:  1975-01       Impact factor: 10.612

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Authors:  W C Duckworth
Journal:  Biochim Biophys Acta       Date:  1976-07-21

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Authors:  W C Duckworth; A E Kitabchi
Journal:  Diabetes       Date:  1974-06       Impact factor: 9.461

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Authors:  H J Quabbe
Journal:  Diabetologia       Date:  1969-04       Impact factor: 10.122

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Authors:  S G George; J Kenny
Journal:  Biochem J       Date:  1973-05       Impact factor: 3.857

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Authors:  Y Cuypers; A Nizet; A Baerten
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Authors:  D S Zaharko; L V Beck; R Blankenbaker
Journal:  Diabetes       Date:  1966-09       Impact factor: 9.461

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  4 in total

1.  From plant physiology to human metabolic investigations.

Authors:  P J Lefèbvre
Journal:  Diabetologia       Date:  1985-05       Impact factor: 10.122

2.  Factors controlling gastric-glucagon release.

Authors:  P J Lefèbvre; A S Luyckx
Journal:  J Clin Invest       Date:  1977-04       Impact factor: 14.808

3.  B-cell response to a standardized breakfast in end-stage renal failure.

Authors:  J C Daubresse; P Henrivaux; F Dehout; J C Meunier; A S Luyckx; P J Lefebvre
Journal:  Acta Diabetol Lat       Date:  1985 Jan-Mar

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Authors:  D S Emmanouel; J B Jaspan; A H Rubenstein; A H Huen; E Fink; A I Katz
Journal:  J Clin Invest       Date:  1978-07       Impact factor: 14.808

  4 in total

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