Literature DB >> 7417422

Asymmetric binding of steroids to internal and external sites in the glucose carrier of erythrocytes.

R M Krupka, R Devés.   

Abstract

Steroids inhibit glucose transport in erythrocytes by binding to sites in the carrier which are exposed on both the outer and inner surfaces of the cell membrane. Some steroids are bound almost exclusively at inner sites (androstendione and androstandione), while others are bound about as firmly on one side as the other (corticosterone). Still others exhibit a moderate preference for the internal site (deoxycorticosterone). The inhibition is in all cases competitive with respect to a substrate which is bound at the same surface of the membrane as the inhibitor. However, in experiments on substrate entry, internally bound inhibitors act in an apparently non-competitive fashion, as expected if the carrier model is valid. This behaviour explains the appearance of competitive, non-competitive and mixed inhibitions with different steroids (Lacko, L., Wittke, B. and Geck, P. (1975) J. Cell Physiol. 86, 673--680).

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Year:  1980        PMID: 7417422     DOI: 10.1016/0005-2736(80)90271-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  8 in total

1.  Asymmetrical binding of phloretin to the glucose transport system of human erythrocytes.

Authors:  R M Krupka
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2.  Contribution of glucose transport to the control of the glycolytic flux in Trypanosoma brucei.

Authors:  B M Bakker; M C Walsh; B H ter Kuile; F I Mensonides; P A Michels; F R Opperdoes; H V Westerhoff
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3.  Effect of glucose transport inhibitors on vincristine efflux in multidrug-resistant murine erythroleukaemia cells overexpressing the multidrug resistance-associated protein (MRP) and two glucose transport proteins, GLUT1 and GLUT3.

Authors:  R L Martell; C A Slapak; S B Levy
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

4.  Interactions of androgens, green tea catechins and the antiandrogen flutamide with the external glucose-binding site of the human erythrocyte glucose transporter GLUT1.

Authors:  Richard J Naftalin; Iram Afzal; Philip Cunningham; Mansur Halai; Clare Ross; Naguib Salleh; Stuart R Milligan
Journal:  Br J Pharmacol       Date:  2003-08-26       Impact factor: 8.739

5.  Glycation of the human erythrocyte glucose transporter in vitro and its functional consequences.

Authors:  P J Bilan; A Klip
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

6.  Interactions of ATP, oestradiol, genistein and the anti-oestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1.

Authors:  Iram Afzal; Philip Cunningham; Richard J Naftalin
Journal:  Biochem J       Date:  2002-08-01       Impact factor: 3.857

7.  Inhibition of glucose transport in human erythrocytes by 2,3-dioxoindole (isatin).

Authors:  M L Gargari; R C Bansal; K Singh; A Mahmood
Journal:  Experientia       Date:  1994-09-15

8.  Reaction of the glucose carrier of erythrocytes with sodium tetrathionate: evidence for inward-facing and outward-facing carrier conformations.

Authors:  R M Krupka
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

  8 in total

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