Literature DB >> 8615814

Glycogen synthesis in amphibian oocytes: evidence for an indirect pathway.

E Kessi1, V Guixé, A Preller, T Ureta.   

Abstract

Glycogen is the main end product of glucose metabolism in amphibian oocytes. However, in the first few minutes after [U-14C]glucose microinjection most of the label is found in lactate. The burst of lactate production and the shape of the time curves for the labelling of glucose 6-phosphate, fructose 6-phosphate, glucose 1-phosphate and glycogen suggest a precursor-product relationship of lactate with respect to glycogen and its intermediates. Expansion (by microinjection) of the pool of glycolytic intermediates, such as dihydroxyacetone phosphate, glyceraldehyde 3-phosphate, 3-phosphoglycerate or phosphoenolpyruvate, results in a marked decrease in [U-14C]glucose incorporation into glycogen. After co-injection of doubly labelled glucoses, extensive detritiation (93%) of the glucosyl units of glycogen was observed with [2-3H, U-14C]glucose and partial detritiation with [3-3H,U-14C]glucose (34%) or [5-3H,U-14C]glucose (46%). After injection of [6-3H,U-14C]glucose, a small but significant and reproducible detritiation (13%) in glycogen was observed. Co-injection of [U-14C]glucose and 3-mercaptopicolinate resulted in marked inhibition of glycogen labelling. Half-maximal inhibition was observed at 0.58 mM 3-mercaptopicolinate, which agrees with the IC50 value (0.47 mM) for the inhibition in vitro of phosphoenolpyruvate carboxykinase activity. We concluded that in frog oocytes most of the glucosyl units are incorporated into glycogen by an indirect pathway involving breakdown of glucose to lactate, which is then converted into glycogen via gluconeogenesis. Both processes, glycolytic degradation of glucose to lactate and subsequent reconversion of the latter into hexose phosphates and glycogen, occur in the same cell.

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Year:  1996        PMID: 8615814      PMCID: PMC1217217          DOI: 10.1042/bj3150455

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  28 in total

1.  Assay of phosphoenolpyruvate carboxykinase in crude yeast extracts.

Authors:  R J Hansen; H Hinze; H Holzer
Journal:  Anal Biochem       Date:  1976-08       Impact factor: 3.365

Review 2.  From dietary glucose to liver glycogen: the full circle round.

Authors:  J D McGarry; M Kuwajima; C B Newgard; D W Foster; J Katz
Journal:  Annu Rev Nutr       Date:  1987       Impact factor: 11.848

3.  The glucose-phosphorylating capacity of liver as measured by three independent assays. Implications for the mechanism of hepatic glycogen synthesis.

Authors:  M Kuwajima; C B Newgard; D W Foster; J D McGarry
Journal:  J Biol Chem       Date:  1986-07-05       Impact factor: 5.157

4.  Effect of mercaptopicolinic acid and of transaminase inhibitors on glycogen synthesis by rat hepatocytes.

Authors:  F Okajima; J Katz
Journal:  Biochem Biophys Res Commun       Date:  1979-03-15       Impact factor: 3.575

Review 5.  Enzyme-enzyme interactions and the regulation of metabolic reaction pathways.

Authors:  D K Srivastava; S A Bernhard
Journal:  Curr Top Cell Regul       Date:  1986

6.  Effect of 3-mercaptopicolinic acid on gluconeogenesis and gluconeogenic metabolite concentrations in the isolated perfused rat liver.

Authors:  M N Goodman
Journal:  Biochem J       Date:  1975-07       Impact factor: 3.857

7.  3-Mercaptopicolinate. A reversible active site inhibitor of avian liver phosphoenolpyruvate carboxykinase.

Authors:  A L Makinen; T Nowak
Journal:  J Biol Chem       Date:  1983-10-10       Impact factor: 5.157

8.  Efficient hepatic glycogen synthesis in refeeding rats requires continued carbon flow through the gluconeogenic pathway.

Authors:  C B Newgard; S V Moore; D W Foster; J D McGarry
Journal:  J Biol Chem       Date:  1984-06-10       Impact factor: 5.157

9.  Studies on the mechanism by which exogenous glucose is converted into liver glycogen in the rat. A direct or an indirect pathway?

Authors:  C B Newgard; L J Hirsch; D W Foster; J D McGarry
Journal:  J Biol Chem       Date:  1983-07-10       Impact factor: 5.157

10.  3-mercaptopicolinic acid, an inhibitor of gluconeogenesis.

Authors:  N W DiTullio; C E Berkoff; B Blank; V Kostos; E J Stack; H L Saunders
Journal:  Biochem J       Date:  1974-03       Impact factor: 3.857

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  1 in total

1.  Thioredoxin-interacting protein regulates glucose metabolism and affects cytoplasmic streaming in mouse oocytes.

Authors:  Su-Yeon Lee; Hyun-Seo Lee; Eun-Young Kim; Jung-Jae Ko; Tae Ki Yoon; Woo-Sik Lee; Kyung-Ah Lee
Journal:  PLoS One       Date:  2013-08-19       Impact factor: 3.240

  1 in total

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