Literature DB >> 1092583

Studies of alloxan toxicity on the beta cell.

A A Rossini, M A Arcangeli, G F Cahill.   

Abstract

The ability of sugars to protect the beta cell from alloxan diabetes is highly stereospecific. The alpha anomer, which is present in equilibrium in both glucose and 3-O-methyl glucose (3-OMG) at approximately 34 per cent, provides greater protection than the beta anomer. The greater protection of the alpha anomer of glucose is present fifteen seconds between its administration and alloxan, but there is no difference in protection following a thirty-second interval. The nonmetabolized analogue, 3-OMG, provides even greater protection than glucose, and this higher affinity is expressed both by the lower dose necessary to provide protection, as well as by the higher dose of mannoheptulose needed to remove thr protection. Mannoheptulose not only removes the protection provided by exogenous glucose but sensitizes the beta cell to the toxic effects of alloxan in the fasting state, probably by inhibiting the protection provided by endogenous glucose. Mannoheptulose is able to remove glucose protection before, with, or after the administration of glucose prior to alloxan injection. Finally, the protective effect of both glucose and 3-OMG is time-related, and the protection not only is due to absolute concentration but also appears to be affected by a changing concentration.

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Year:  1975        PMID: 1092583     DOI: 10.2337/diab.24.5.516

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  7 in total

Review 1.  Alloxan: history and mechanism of action.

Authors:  S Lenzen; U Panten
Journal:  Diabetologia       Date:  1988-06       Impact factor: 10.122

2.  Alloxan-induced alteration of insulin release, rubidium efflux and glucose metabolism in rat islets stimulated by various secretagogues.

Authors:  J C Henquin; P Malvaux; A E Lambert
Journal:  Diabetologia       Date:  1979-04       Impact factor: 10.122

3.  Alloxan cytotoxicity in vitro. Inhibition of rubidium ion pumping in pancreatic beta-cells.

Authors:  L A Idahl; A Lernmark; J Sehlin; I B Täljedal
Journal:  Biochem J       Date:  1977-01-15       Impact factor: 3.857

4.  Ninhydrin inhibition of glucose-induced insulin release.

Authors:  M L McDaniel; C E Roth; C J Fink; J A Swanson; P E Lacy
Journal:  Diabetologia       Date:  1977-12       Impact factor: 10.122

5.  Alloxan-glucose interaction: effect on incorporation of 14C-leucine into pancreatic islets of rat.

Authors:  R Bansal; N Ahmad; J R Kidwai
Journal:  Acta Diabetol Lat       Date:  1980 Apr-Jun

6.  Superoxide dismutase, catalase and scavengers of hydroxyl radical protect against the toxic action of alloxan on pancreatic islet cells in vitro.

Authors:  K Grankvist; S Marklund; J Sehlin; I B Täljedal
Journal:  Biochem J       Date:  1979-07-15       Impact factor: 3.857

7.  p-Hydroxymercuribenzoate-induced hyperglycemia: influence of pre- and post-treatment with L-leucine, tolbutamide, D-mannoheptulose, insulin and alloxan.

Authors:  L Boquist
Journal:  J Endocrinol Invest       Date:  1979 Oct-Dec       Impact factor: 4.256

  7 in total

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