Literature DB >> 1206578

Influence of the insulin sensitive central nervous system glucoregulator receptor on hepatic glucose metabolism.

A J Szabo, O Szabo.   

Abstract

Excitation of the insulin sensitive glucoregulator receptor in the central nervous system (C.N.S.) causes an immediate decrease in the systemic blood sugar level in rats. 2. A study was made in animals that were subjected either to evisceration or to evisceration and functional-hepatectomy, in order to assess the role of the liver and pancreatic hormones in the blood sugar decrease following insulin injection into the carotid artery. 3. The results indicate that the change in the systemic blood sugar level, induced by exposing the C.N.S. to insulin, was effected through a direct influence of the receptor centre on glucose metabolism of the liver. 4. Excitation of the insulin-sensitive receptor in the C.N.S. regulates carbohydrate metabolism of the liver, both by inhibiting hepatic glucose output and by facilitating hepatic glucose uptake. 5. The data derived from these animal models reveal that the mode of transmission of the impulse from the C.N.S. region is through efferent neural pathways that directly influence the hepatic carbocydrate metabolism, and not through a modification of pancreatic hormone secretion.

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Year:  1975        PMID: 1206578      PMCID: PMC1348536          DOI: 10.1113/jphysiol.1975.sp011183

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  22 in total

1.  Insulin action upon insulin-insensitive tissue following impaired degradation of the hormone.

Authors:  R J Mahler; O Szabo
Journal:  Proc Soc Exp Biol Med       Date:  1967-07

2.  Neuropharmacological characterization of insulin-sensitive CNS glucoregulator.

Authors:  O Szabo; A J Szabo
Journal:  Am J Physiol       Date:  1975-09

Review 3.  Neural control of the endocrine pancreas.

Authors:  S C Woods; D Porte
Journal:  Physiol Rev       Date:  1974-07       Impact factor: 37.312

4.  Regulation of glycogen metabolism in liver by the autonomic nervous system. II. Neural control of glycogenolytic enzymes.

Authors:  T Shimazu; A Amakawa
Journal:  Biochim Biophys Acta       Date:  1968-10-15

5.  Dynamics of glucose autoregulation in the isolated, blood-perfused canine liver.

Authors:  R J Bucolo; R N Bergman; D J Marsh; F E Yates
Journal:  Am J Physiol       Date:  1974-07

6.  Effect of acetylcholine on glycogen formation and the activity of glycogen synthetase in isolated, perfused rat liver.

Authors:  C Ottolenghi; A Cania; O Barnabei
Journal:  Nature       Date:  1971-02-05       Impact factor: 49.962

7.  Glucose uptake and production during the oral glucose tolerance test.

Authors:  R Steele; C Bjerknes; I Rathgeb; N Altszuler
Journal:  Diabetes       Date:  1968-07       Impact factor: 9.461

8.  Evidence for an insulin-sensitive receptor in the central nervous system.

Authors:  O Szabo; A J Szabo
Journal:  Am J Physiol       Date:  1972-12

9.  Effect of hypothalamic stimulation on plasma glucose, insulin, and glucagon levels.

Authors:  L A Frohman; L L Bernardis
Journal:  Am J Physiol       Date:  1971-12

10.  Glucose kinetics during oral glucose tolerance test in normal, methylprednisolone-treated and alloxan diabetic dogs.

Authors:  B Issekutz; T B Issekutz; D Elahi
Journal:  Diabetes       Date:  1974-08       Impact factor: 9.461

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  3 in total

Review 1.  The neuroendocrine response to multiple trauma.

Authors:  D S Gann; M P Lilly
Journal:  World J Surg       Date:  1983-01       Impact factor: 3.352

Review 2.  Interactions between the central nervous system and pancreatic islet secretions: a historical perspective.

Authors:  Denovan P Begg; Stephen C Woods
Journal:  Adv Physiol Educ       Date:  2013-03       Impact factor: 2.288

3.  Identification of insulin in rat brain.

Authors:  J Havrankova; D Schmechel; J Roth; M Brownstein
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

  3 in total

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