Literature DB >> 1319952

Isoenzymes of carbohydrate metabolism in primary cultures of hepatocytes from thioacetamide-induced rat liver necrosis: responses to growth factors.

M Cascales1, P Martin-Sanz, A Alvarez, M Sanchez-Pérez, C Diez Fernández, L Boscá.   

Abstract

Hepatocytes isolated from the liver of rats after a necrotizing dose of thioacetamide (6.6 mmol/kg) were used to study the postnecrotic process of liver regeneration. Flow cytometry analysis revealed populations of dedifferentiated hepatocytes exhibiting physical properties (size and fluorescence emission at 530 nm) similar to those found in fetal (22 days old) liver cells. The percentage of these cells increased progressively from 24 to 48 and 72 hr after thioacetamide administration. In primary cultures of hepatocytes the effects of phorbol 12-myristate 13-acetate, bombesin and insulin were investigated on the 6-phosphofructo 2-kinase/fructose 2,6 bisphosphate system. Bombesin and insulin stimulated 6-phosphofructo 2-kinase activity and fructose 2,6-bisphosphate content both in control and in thioacetamide-treated hepatocytes. However, phorbol 12-myristate 13-acetate stimulated 6-phosphofructo 2-kinase activity and increased fructose 2,6-bisphosphate concentration in thioacetamide-treated liver cells, whereas no similar response was found in hepatocytes from control rats. The response of postnecrotic thioacetamide-treated hepatocytes to phorbol 12-myristate 13-acetate was similar to that obtained from 22-day-old fetal liver cells, which reveals that different methods might control fructose 2,6-bisphosphate content and therefore the mechanisms of glycolysis and gluconeogenesis at this regulatory step. The lack of response to glucagon of glycogen phosphorylase a and 6-phosphofructo 2-kinase from thioacetamide-treated hepatocytes may indicate that the expression of specific enzymes of carbohydrate metabolism undergoes transitions to less-differentiated isoenzymatic forms. Moreover, the isoenzyme pattern of hexokinases elicits a complete disturbance in glucokinase and hexokinases activities.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1319952     DOI: 10.1002/hep.1840160134

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  5 in total

1.  Hepatocyte growth factor and transforming growth factor beta regulate 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase gene expression in rat hepatocyte primary cultures.

Authors:  M Joaquin; J L Rosa; C Salvadó; S López; T Nakamura; R Bartrons; J Gil; A Tauler
Journal:  Biochem J       Date:  1996-02-15       Impact factor: 3.857

2.  Effect of dichloromethylene diphosphonate on liver regeneration following thioacetamide-induced necrosis in rats.

Authors:  Mirandeli Bautista; María Ángeles Gómez Del Rio; Juana Benedí; María Isabel Sánchez-Reus; José A Morales-González; Ana María Téllez-López; Maricela López-Orozco
Journal:  World J Hepatol       Date:  2013-07-27

3.  Effect of gadolinium chloride on liver regeneration following thioacetamide-induced necrosis in rats.

Authors:  Mirandeli Bautista; David Andres; María Cascales; José A Morales-González; María Isabel Sánchez-Reus
Journal:  Int J Mol Sci       Date:  2010-11-04       Impact factor: 5.923

4.  Malic enzyme and glucose 6-phosphate dehydrogenase gene expression increases in rat liver cirrhogenesis.

Authors:  N Sanz; C Díez-Fernández; A M Valverde; M Lorenzo; M Benito; M Cascales
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

5.  Role of Kupffer cells in thioacetamide-induced cell cycle dysfunction.

Authors:  Mirandeli Bautista; David Andres; María Cascales; José A Morales-González; María Isabel Sánchez-Reus; Eduardo Madrigal-Santillán; Carmen Valadez-Vega; Tomas Fregoso-Aguilar; Jorge Alberto Mendoza-Pérez; José Gutiérrez-Salinas; Jaime Esquivel-Soto
Journal:  Molecules       Date:  2011-09-29       Impact factor: 4.411

  5 in total

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