Literature DB >> 5097572

The glycogenolytic activity of immunoreactive pancreatic glucagon in plasma.

J Marco, G R Faloona, R H Unger.   

Abstract

Conclusions concerning the physiologic role of pancreatic glucagon in health and its contribution to disorders of carbohydrate metabolism, such as diabetes mellitus, are based entirely on measurements of plasma glucagon by radioimmunoassay. The changes in plasma immunoreactive glucagon can have the metabolic and clinical significance which has been implied, only if the glucagon detected by immunoassay has biological activity. The present study was designed to determine if a relationship between the immunoassayable glucagon and glycogenolytic activity of plasma could be demonstrated. Plasma specimens obtained from normal and diabetic subjects under widely varying circumstances of alpha cell activity were extracted by a modification of the Kenny technique and the recovery of immunoreactive glucagon was calculated. Glycogenolytic activity of each extract was determined by perfusion in the Mortimore rat liver system, modified so as to detect as little as 1 ng of crystalline glucagon.A significant correlation between the calculated quantity of immunoreactive glucagon and the glycogenolytic activity of plasma extracts was observed for both normal and diabetic subjects. Most of the glycogenolytic activity was abolished by incubating the extract with antiglucagon serum. It was concluded that the glycogenolytic activity of extractable glucagon is proportional to its immunoreactivity as calculated from its original concentration in plasma. This would tend to support the view that all or most of the immunoreactive glucagon of plasma is biologically active.

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Year:  1971        PMID: 5097572      PMCID: PMC442065          DOI: 10.1172/JCI106654

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  9 in total

1.  Extractable glucagon of the human pancreas.

Authors:  A J KENNY
Journal:  J Clin Endocrinol Metab       Date:  1955-09       Impact factor: 5.958

2.  The role of cyclic AMP in the control of liver metabolism.

Authors:  J H Exton; C R Park
Journal:  Adv Enzyme Regul       Date:  1968

3.  Abnormal alpha-cell function in diabetes. Response to carbohydrate and protein ingestion.

Authors:  W A Müller; G R Faloona; E Aguilar-Parada; R H Unger
Journal:  N Engl J Med       Date:  1970-07-16       Impact factor: 91.245

4.  Control of gluconeogenesis in liver. II. Effects of glucagon, catecholamines, and adenosine 3',5'-monophosphate on gluconeogenesis in the perfused rat liver.

Authors:  J H Exton; C R Park
Journal:  J Biol Chem       Date:  1968-08-25       Impact factor: 5.157

5.  Large glucagon immunoreactivity in extracts of pancreas.

Authors:  D Rigopoulou; I Valverde; J Marco; G Faloona; R H Unger
Journal:  J Biol Chem       Date:  1970-02-10       Impact factor: 5.157

6.  Bioassay of glucagon using the isolated perfused rat liver.

Authors:  J E Sokal
Journal:  Endocrinology       Date:  1970-12       Impact factor: 4.736

7.  Molecular size of extractable glucagon and glucagon-like immunoreactivity (GLI) in plasma.

Authors:  I Valverde; D Rigopoulou; J Marco; G R Faloona; R H Unger
Journal:  Diabetes       Date:  1970-09       Impact factor: 9.461

8.  [Evolution of hormonal parameters (glucagon, cortisol, growth hormone) and energetic parameters (glucose, fatty acids, free glycerol) in 10 severe cases of diabetic acido-ketosis under treatment].

Authors:  R Assan; G Hautecouverture; S Guillemant; F Dauchy; P Protin; M Derot
Journal:  Pathol Biol (Paris)       Date:  1969-12

9.  Studies of pancreatic alpha cell function in normal and diabetic subjects.

Authors:  R H Unger; E Aguilar-Parada; W A Müller; A M Eisentraut
Journal:  J Clin Invest       Date:  1970-04       Impact factor: 14.808

  9 in total
  2 in total

1.  Neonatal secretion of gastrin and glucagon.

Authors:  I M Rogers; D C Davidson; J Lawrence; J Ardill; K D Buchanan
Journal:  Arch Dis Child       Date:  1974-10       Impact factor: 3.791

2.  Suppressive effect of secretin upon pancreatic alpha cell function.

Authors:  F Santeusanio; G R Faloona; R H Unger
Journal:  J Clin Invest       Date:  1972-07       Impact factor: 14.808

  2 in total

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