Literature DB >> 7040535

Changes in circulating fuels, pancreatic hormones and liver glycogen concentration in fasting or suckling newborn pigs.

J P Pégorier, P H Duée, R Assan, J Peret, J Girard.   

Abstract

The effect of fasting or suckling on blood glucose, circulating fuels, pancreatic hormones and liver glycogen concentration have been measured in newborn pigs during the first 48 h of life. Blood glucose concentrations fell to hypoglycaemic values after 48 h of fasting whereas for the same period of time, suckling piglets maintain a normal blood glucose. These differences are not due to hepatic glycogen mobilization, since liver is totally depleted from its high glycogen stores 24 h after birth, both in fasting and suckling piglets. Blood lactate is present at a high concentration during the first 48 h, both in fasting and suckling piglets. In contrast, blood pyruvate concentration is lower in suckling than in fasting newborn pigs. Colostrum intake leads to an increase in blood amino acid concentrations in the suckling piglets in comparison with the fasting newborn. Plasma non-esterified fatty acid levels and blood glycerol concentrations are lower in fasting piglets than in the suckling ones. In suckling newborn pigs, circulating ketone bodies are very low despite the increase in non-esterified fatty acids levels. The decrease in plasma insulin/glucagon molar ratio at birth, is due to a decrease in plasma insulin and an increase in plasma glucagon, both in fasting and suckling piglets. Plasma insulin and glucagon concentrations are higher during suckling than during fasting. The data suggest that gluconeogenesis could be impaired, in fasting newborn pigs, by a low plasma glucagon level and/or a limiting availability of non-esterified fatty acids.

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Year:  1981        PMID: 7040535

Source DB:  PubMed          Journal:  J Dev Physiol        ISSN: 0141-9846


  7 in total

1.  Acetate represents a major product of heptanoate and octanoate beta-oxidation in hepatocytes isolated from neonatal piglets.

Authors:  X Lin; S H Adams; J Odle
Journal:  Biochem J       Date:  1996-08-15       Impact factor: 3.857

2.  Gene expression of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase in a poorly ketogenic mammal: effect of starvation during the neonatal period of the piglet.

Authors:  S H Adams; C S Alho; G Asins; F G Hegardt; P F Marrero
Journal:  Biochem J       Date:  1997-05-15       Impact factor: 3.857

3.  Isolation of pig mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase gene promoter: characterization of a peroxisome proliferator-responsive element.

Authors:  J A Ortiz; J Mallolas; C Nicot; J Bofarull; J C Rodríguez; F G Hegardt; D Haro; P F Marrero
Journal:  Biochem J       Date:  1999-01-15       Impact factor: 3.857

4.  Dexamethasone selectively increases sodium-dependent alanine transport across neonatal piglet intestine.

Authors:  P S James; M W Smith; D R Tivey; T J Wilson
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

5.  Hepatic ketogenesis in newborn pigs is limited by low mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase activity.

Authors:  P H Duée; J P Pégorier; P A Quant; C Herbin; C Kohl; J Girard
Journal:  Biochem J       Date:  1994-02-15       Impact factor: 3.857

6.  Pharmacologic activation of peroxisome proliferator-activating receptor-α accelerates hepatic fatty acid oxidation in neonatal pigs.

Authors:  Kwanseob Shim; Sheila Jacobi; Jack Odle; Xi Lin
Journal:  Oncotarget       Date:  2018-05-08

7.  Serum protein electrophoretic pattern in piglets during the early postnatal period.

Authors:  Csilla Tóthová; Robert Link; Petronela Kyzeková; Oskar Nagy
Journal:  Sci Rep       Date:  2021-09-02       Impact factor: 4.379

  7 in total

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