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. 1979 Jul 15;182(1):17–25. doi: 10.1042/bj1820017

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

K Grankvist, S Marklund, J Sehlin, I B Täljedal
PMCID: PMC1161229  PMID: 40548

Abstract

Experiments with isolated pancreatic islets or dispersed islet cells from non-inbred ob/ob mice were performed to test the hypothesis that free radicals, notably OH., mediate the diabetogenic toxicity of alloxan. Accumulation of 86Rb+ by whole islets and exclusion of Trypan Blue by dispersed cells were used as previously validated criteria of islet-cell viability. Alloxan alone drastically inhibited the Rb+ accumulation and significantly decreased the frequency of cells excluding Trypan Blue. Enzymic scavengers of O2.- and H2O2 or non-enzymic scavengers of OH. or singlet oxygen were added to the incubation medium and tested for their ability to protect against these effects of alloxan. Superoxide dismutase, catalase, dimethyl sulphoxide, benzoate, and mannitol counteracted the effects of alloxan in both cytotoxicity assays. Significant protection of the Rb+-accumulating capacity was also afforded by butanol, caffeine, theophylline, NADH, NADPH and, to a small extent, NAD+. Urea has a poor affinity for OH. and did not protect against alloxan. No effect was obtained with the singlet-oxygen scavenger, histidine. Except for the protection by NADH and NADPH, which may be due to a direct reaction with alloxan in the medium, the results strongly support the hypothesis. beta-Cells may be particularly vulnerable to alloxan because their metabolic specialization facilitates reduction of the drug and perhaps of other substrates for O2.--yielding redox cycles.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ammon H. P. Effect of tolbutamide on aminophylline-, 3,5-AMP-dibutyrate- or glucagon-induced insulin release from pancreatic islets after impairment of pyridine nucleotide metabolism caused by 6-aminonicotinamide (6-AN). Naunyn Schmiedebergs Arch Pharmacol. 1975;290(2-3):251–264. doi: 10.1007/BF00510554. [DOI] [PubMed] [Google Scholar]
  2. Ammon H. P., Patel T. N., Steinke J. The role of the pentose phosphate shunt in glucose induced insulin release: in vitro studies with 6-aminonicotinamide, methylene blue, NAD + , NADH, NADP + , NADPH and nicotinamide on isolated pancreatic rat islets. Biochim Biophys Acta. 1973 Feb 28;297(2):352–367. doi: 10.1016/0304-4165(73)90083-4. [DOI] [PubMed] [Google Scholar]
  3. Berne C. Nicotinamide adenine dinucleotide phosphate-converting enzymes and adenosine triphosphate citrate lyase in some tissues and organs of New Zealand obese mice with special reference to the enzyme pattern of the pancreatic islets. J Histochem Cytochem. 1975 Sep;23(9):660–665. doi: 10.1177/23.9.240882. [DOI] [PubMed] [Google Scholar]
  4. Bray R. C., Cockle S. A., Fielden E. M., Roberts P. B., Rotilio G., Calabrese L. Reduction and inactivation of superoxide dismutase by hydrogen peroxide. Biochem J. 1974 Apr;139(1):43–48. doi: 10.1042/bj1390043. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cohen G., Heikkila R. E. The generation of hydrogen peroxide, superoxide radical, and hydroxyl radical by 6-hydroxydopamine, dialuric acid, and related cytotoxic agents. J Biol Chem. 1974 Apr 25;249(8):2447–2452. [PubMed] [Google Scholar]
  6. Cooperstein S. J., Lazarow A. Uptake of glucose by islet of Langerhans and other tissues of the toadfish Opsanus tau. Am J Physiol. 1969 Dec;217(6):1784–1788. doi: 10.1152/ajplegacy.1969.217.6.1784. [DOI] [PubMed] [Google Scholar]
  7. Cooperstein S. J., Watkins D. Effect of alloxan on islet tissue permeability: protection and reversal by NADPH. Biochem Biophys Res Commun. 1977 Dec 7;79(3):756–762. doi: 10.1016/0006-291x(77)91176-7. [DOI] [PubMed] [Google Scholar]
  8. Grankvist K., Lernmark A., Täljedal I. B. Alloxan cytotoxicity in vitro. Microscope photometric analyses of Trypan Blue uptake by pancreatic islet cells in suspension. Biochem J. 1977 Jan 15;162(1):19–24. doi: 10.1042/bj1620019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gunnarsson R. Inhibition of insulin biosynthesis by alloxan, streptozotocin, and N-nitrosomethylurea. Mol Pharmacol. 1975 Nov;11(6):759–765. [PubMed] [Google Scholar]
  10. Halliwell B. Superoxide-dependent formation of hydroxyl radicals in the presence of iron chelates: is it a mechanism for hydroxyl radical production in biochemical systems? FEBS Lett. 1978 Aug 15;92(2):321–326. doi: 10.1016/0014-5793(78)80779-0. [DOI] [PubMed] [Google Scholar]
  11. Heikkila R. E., Barden H., Cohen G. Prevention of alloxan-induced diabetes by ethanol administration. J Pharmacol Exp Ther. 1974 Sep;190(3):501–506. [PubMed] [Google Scholar]
  12. Heikkila R. E. The prevention of alloxan-induced diabetes in mice by dimethyl sulfoxide. Eur J Pharmacol. 1977 Jul 15;44(2):191–193. doi: 10.1016/0014-2999(77)90106-6. [DOI] [PubMed] [Google Scholar]
  13. Heikkila R. E., Winston B., Cohen G. Alloxan-induced diabetes-evidence for hydroxyl radical as a cytotoxic intermediate. Biochem Pharmacol. 1976 May 1;25(9):1085–1092. doi: 10.1016/0006-2952(76)90502-5. [DOI] [PubMed] [Google Scholar]
  14. Hellerström C., Gunnarsson R. [Bioenergetics of islet function: oxygen utilization and oxidative metabolism in the beta-cells]. Acta Diabetol Lat. 1970 Sep;7 (Suppl 1):127–158. [PubMed] [Google Scholar]
  15. Hellman B., Idahl L. A., Lernmark A., Sehlin J., Täljedal I. B. Role of thiol groups in insulin release: studies with poorly permeating disulphides. Mol Pharmacol. 1973 Nov;9(6):792–801. [PubMed] [Google Scholar]
  16. Hellman B., Idahl L. A., Lernmark A., Sehlin J., Täljedal I. B. Stimulation of insulin release by thiols. Biochim Biophys Acta. 1975 May 5;392(1):101–109. doi: 10.1016/0304-4165(75)90170-1. [DOI] [PubMed] [Google Scholar]
  17. Hellman B., Sehlin J., Täljedal I. B. Transport of -aminoisobutyric acid in mammalian pancretic -cells. Diabetologia. 1971 Aug;7(4):256–265. doi: 10.1007/BF01211878. [DOI] [PubMed] [Google Scholar]
  18. Hellman B., Sehlin J., Täljedal I. B. Transport of 3-O-methyl-D-glucose into mammalian pancreatic -cells. Pflugers Arch. 1973;340(1):51–58. doi: 10.1007/BF00592196. [DOI] [PubMed] [Google Scholar]
  19. Idahl L. A., Lernmark A., Sehlin J., Täljedal I. B. Alloxan cytotoxicity in vitro. Inhibition of rubidium ion pumping in pancreatic beta-cells. Biochem J. 1977 Jan 15;162(1):9–18. doi: 10.1042/bj1620009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Idahl L. A., Lernmark A., Sehlin J., Täljedal I. B. The dynamics of insulin release from mouse pancreatic islet cells in suspension. Pflugers Arch. 1976 Nov 5;366(2-3):185–188. doi: 10.1007/BF00585876. [DOI] [PubMed] [Google Scholar]
  21. Kellogg E. W., 3rd, Fridovich I. Liposome oxidation and erythrocyte lysis by enzymically generated superoxide and hydrogen peroxide. J Biol Chem. 1977 Oct 10;252(19):6721–6728. [PubMed] [Google Scholar]
  22. Kellogg E. W., 3rd, Fridovich I. Superoxide, hydrogen peroxide, and singlet oxygen in lipid peroxidation by a xanthine oxidase system. J Biol Chem. 1975 Nov 25;250(22):8812–8817. [PubMed] [Google Scholar]
  23. Lacy P. E., McDaniel M. L., Fink C. J., Roth C. Effect of methylxanthines on alloxan inhibition of insulin release. Diabetologia. 1975 Dec;11(6):501–507. doi: 10.1007/BF01222099. [DOI] [PubMed] [Google Scholar]
  24. Lernmark A. The preparation of, and studies on, free cell suspensions from mouse pancreatic islets. Diabetologia. 1974 Oct;10(5):431–438. doi: 10.1007/BF01221634. [DOI] [PubMed] [Google Scholar]
  25. Lynch R. E., Fridovich I. Effects of superoxide on the erythrocyte membrane. J Biol Chem. 1978 Mar 25;253(6):1838–1845. [PubMed] [Google Scholar]
  26. Malaisse W. J., Hutton J. C., Kawazu S., Sener A. The stimulus-secretion coupling of glucose-induced insulin release. Metabolic effects of menadione in isolated islets. Eur J Biochem. 1978 Jun 1;87(1):121–130. doi: 10.1111/j.1432-1033.1978.tb12357.x. [DOI] [PubMed] [Google Scholar]
  27. Marklund S., Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974 Sep 16;47(3):469–474. doi: 10.1111/j.1432-1033.1974.tb03714.x. [DOI] [PubMed] [Google Scholar]
  28. Matheson I. B., Etheridge R. D., Kratowich N. R., Lee J. The quenching of singlet oxygen by amino acids and proteins. Photochem Photobiol. 1975 Mar;21(3):165–171. doi: 10.1111/j.1751-1097.1975.tb06647.x. [DOI] [PubMed] [Google Scholar]
  29. McCord J. M., Day E. D., Jr Superoxide-dependent production of hydroxyl radical catalyzed by iron-EDTA complex. FEBS Lett. 1978 Feb 1;86(1):139–142. doi: 10.1016/0014-5793(78)80116-1. [DOI] [PubMed] [Google Scholar]
  30. McCord J. M., Fridovich I. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J Biol Chem. 1969 Nov 25;244(22):6049–6055. [PubMed] [Google Scholar]
  31. McDaniel M. L., Weaver D. C., Roth C. E., Fink C. J., Swanson J. A., Lacy P. E. Characterization of the uptake of the methylxanthines theophylline and caffeine in isolated pancreatic islets and their effect on D-glucose transport. Endocrinology. 1977 Dec;101(6):1701–1708. doi: 10.1210/endo-101-6-1701. [DOI] [PubMed] [Google Scholar]
  32. Pagliara A. S., Stillings S. N., Zawalich W. S., Williams A. D., Matchinsky F. M. Glucose and 3-O-methylglucose protection against alloxan poisoning of pancreatic alpha and beta cells. Diabetes. 1977 Oct;26(10):973–979. doi: 10.2337/diab.26.10.973. [DOI] [PubMed] [Google Scholar]
  33. Panten U., Christians J. Effect of 2-endo-aminonorbornane-2-carboxylic acid upon insulin secretion and fluorescence of reduced pyridine nucleotides of isolated perifused pancreatic islets. Naunyn Schmiedebergs Arch Pharmacol. 1973;276(1):55–62. doi: 10.1007/BF00500778. [DOI] [PubMed] [Google Scholar]
  34. Rossini A. A., Arcangeli M. A., Cahill G. F., Jr Studies of alloxan toxicity on the beta cell. Diabetes. 1975 May;24(5):516–522. doi: 10.2337/diab.24.5.516. [DOI] [PubMed] [Google Scholar]
  35. SALK J. E., YOUNGNER J. S., WARD E. N. Use of color change of phenol red as the indicator in titrating poliomyelitis virus or its antibody in a tissue-culture system. Am J Hyg. 1954 Sep;60(2):214–230. doi: 10.1093/oxfordjournals.aje.a119714. [DOI] [PubMed] [Google Scholar]
  36. SAMEJIMA T., YANG J. T. RECONSTITUTION OF ACID-DENATURED CATALASE. J Biol Chem. 1963 Oct;238:3256–3261. [PubMed] [Google Scholar]
  37. Scheynius A., Täljedal I. B. On the mechanism of glucose protection against alloxan toxicity. Diabetologia. 1971 Aug;7(4):252–255. doi: 10.1007/BF01211877. [DOI] [PubMed] [Google Scholar]
  38. Schroeder W. A., Shelton J. R., Shelton J. B., Robberson B., Apell G. The amino acid sequence of bovine liver catalase: a preliminary report. Arch Biochem Biophys. 1969 May;131(2):653–655. doi: 10.1016/0003-9861(69)90441-x. [DOI] [PubMed] [Google Scholar]
  39. Sehlin J., Taljedal I. B. Glucose-induced decrease in Rb+ permeability in pancreatic beta cells. Nature. 1975 Feb 20;253(5493):635–636. doi: 10.1038/253635a0. [DOI] [PubMed] [Google Scholar]
  40. Sehlin J., Täljedal I. B. Transport of rubidium and sodium in pancreatic islets. J Physiol. 1974 Oct;242(2):505–515. doi: 10.1113/jphysiol.1974.sp010720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Tomita T., Lacy P. E., Natschinsky F. M., McDaniel M. L. Effect of alloxan on insulin secretion in isolated rat islets perifused in vitro. Diabetes. 1974 Jun;23(6):517–524. doi: 10.2337/diab.23.6.517. [DOI] [PubMed] [Google Scholar]
  42. Watkins D., Cooperstein S. J., Dixit P. K., Lazarow A. Insulin secretion from toadfish islet tissue stimulated by pyridine nucleotides. Science. 1968 Oct 11;162(3850):283–284. doi: 10.1126/science.162.3850.283. [DOI] [PubMed] [Google Scholar]
  43. Watkins D., Cooperstein S. J., Lazarow A. Stimulation of insulin secretion by pyridine nucleotides. Endocrinology. 1971 Jun;88(6):1380–1384. doi: 10.1210/endo-88-6-1380. [DOI] [PubMed] [Google Scholar]
  44. Weaver D. C., McDaniel M. L., Lacy P. E. Alloxan uptake by isolated rat islets of Langerhans. Endocrinology. 1978 Jun;102(6):1847–1855. doi: 10.1210/endo-102-6-1847. [DOI] [PubMed] [Google Scholar]
  45. van Hemmen J. J., Meuling W. J. Inactivation of Escherichia coli by superoxide radicals and their dismutation products. Arch Biochem Biophys. 1977 Aug;182(2):743–748. doi: 10.1016/0003-9861(77)90556-2. [DOI] [PubMed] [Google Scholar]

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