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PMID: 6241574 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mechanisms of streptozotocin- and alloxan-induced damage in rat B cells.

Diabetologia ·Vol. 27 ·No. 6 ·1984-12-00 ·Pages 587-91

Wilson GL, Patton NJ, McCord JM, Mullins DW, Mossman BT

Abstract

In studies to evaluate possible inhibitors of the B-cell toxin, streptozotocin, the superoxide scavenger, superoxide dismutase, did not prevent or reduce the toxic effects of streptozotocin as determined by loss of insulin secretion from rat pancreatic B cells in monolayer culture. However, 1,1-dimethyl urea, a scavenger of the hydroxyl radical, did afford significant protection. Both scavengers diminished the cytotoxic effects of alloxan. The inhibitors of poly (ADP-ribose) synthetase, 3-aminobenzamide and nicotinamide, also were effective in attenuating alloxan- and streptozotocin-induced B-cell toxicity. Tests of the hydroxyl-scavenging ability of the three streptozotocin antagonists revealed that 3-aminobenzamide, nicotinamide and 1,1-dimethyl urea were effective scavengers of this free radical. Conversely, 1,1-dimethyl urea, although not as potent as 3-aminobenzamide or nicotinamide, was found to inhibit poly (ADP-ribose) synthetase. These data indicate that these chemicals most likely attenuate alloxan-induced toxicity by scavenging the hydroxyl radical and diminish streptozotocin-induced toxicity by inactivation of the poly (ADP-ribose) system.

MeSH Terms
Alloxan/pharmacology Animals Animals, Newborn Benzamides/pharmacology Cells, Cultured Insulin/metabolism Insulin Secretion Islets of Langerhans/drug effects,metabolism,pathology Kinetics Methylurea Compounds/pharmacology Niacinamide/pharmacology Poly(ADP-ribose) Polymerase Inhibitors Rats Streptozocin/pharmacology Superoxide Dismutase/pharmacology
Chemicals
Benzamides Insulin Methylurea Compounds Poly(ADP-ribose) Polymerase Inhibitors Niacinamide Streptozocin Alloxan 3-aminobenzamide Superoxide Dismutase 1,1-dimethylurea
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wilson G L
Patton N J
McCord J M
Mullins D W
Mossman B T
References (19)
19 references, click to expand
  1. Characteristics of nicotinamide and N1-methylnicotinamide protection from alloxan diabetes in mice.
    Toxicol Appl Pharmacol. 1983 Aug;70(1):148-55 PMID: 6225223
  2. Superoxide-dependent production of hydroxyl radical catalyzed by iron-EDTA complex.
    FEBS Lett. 1978 Feb 1;86(1):139-42 PMID: 202505
  3. The interaction of hydroxyl radicals with dimethylsulfoxide produces formaldehyde.
    FEBS Lett. 1980 Jul 28;116(2):220-2 PMID: 6893306
  4. Use of pancreatic beta cells in culture to identify diabetogenic N-nitroso compounds.
    In Vitro. 1983 Jan;19(1):25-30 PMID: 6218070
  5. Protection against streptozotocin-induced diabetes by superoxide dismutase.
    Diabetologia. 1980 Jan;18(1):55-8 PMID: 6444904
  6. Inhibition of alloxan action in isolated pancreatic islets by superoxide dismutase, catalase, and a metal chelator.
    Diabetes. 1980 Mar;29(3):213-6 PMID: 6991324
  7. Insulin immunoassay by back-titration; some characteristics of the technic and the insulin precipitant action of alcohol.
    Diabetes. 1971 Jan;20(1):33-45 PMID: 4322616
  8. Streptozotocin, but not alloxan, induces DNA repair synthesis in mouse pancreatic islets in vitro.
    Diabetologia. 1983 Nov;25(5):444-7 PMID: 6228481
  9. The partial protective effect of the hydroxyl radical scavenger dimethyl urea on streptozotocin-induced diabetes in the mouse in vivo and in vitro.
    Diabetologia. 1982 Oct;23(4):374-8 PMID: 6292033
  10. Protection against alloxan-induced diabetes in mice by the hydroxyl radical scavenger dimethylurea.
    Eur J Pharmacol. 1978 Nov 1;52(1):57-60 PMID: 720388
  11. Studies on the diabetogenic action of streptozotocin (NSC-37917).
    Cancer Chemother Rep. 1963 May;29:91-8 PMID: 13990585
  12. Protection by superoxide dismutase, catalase, and poly(ADP-ribose) synthetase inhibitors against alloxan- and streptozotocin-induced islet DNA strand breaks and against the inhibition of proinsulin synthesis.
    J Biol Chem. 1982 Jun 10;257(11):6084-8 PMID: 6281256
  13. On the mechanism of paraquat action on microsomal oxygen reduction and its relation to lipid peroxidation.
    Toxicol Appl Pharmacol. 1979 Mar 15;47(3):593-602 PMID: 35855
  14. Superoxide dismutase, catalase and scavengers of hydroxyl radical protect against the toxic action of alloxan on pancreatic islet cells in vitro.
    Biochem J. 1979 Jul 15;182(1):17-25 PMID: 40548
  15. Dimethylurea: a radical scavenger that protects isolated pancreatic islets from the effects of alloxan and dihydroxyfumarate exposure.
    Life Sci. 1980 Apr 28;26(17):1405-9 PMID: 6991844
  16. Diabetes induced with multiple subdiabetogenic doses of streptozotocin: lack of protection by exogenous superoxide dismutase.
    Diabetes. 1981 Aug;30(8):634-8 PMID: 6454601
  17. Protection against alloxan-induced diabetes by various urea derivatives: relationship between protective effects and reactivity with the hydroxyl radical.
    J Pharmacol Exp Ther. 1979 Nov;211(2):415-8 PMID: 501570
  18. ADP-ribosylation in mammalian cell ghosts. Dependence of poly(ADP-ribose) synthesis on strand breakage in DNA.
    J Biol Chem. 1980 Nov 10;255(21):10493-501 PMID: 7430132
  19. Chemiluminescence as an index of drug-induced free radical production in pancreatic islets.
    Diabetes. 1984 Feb;33(2):160-3 PMID: 6229439
Article Info
Journal
Diabetologia
Abbr.
Diabetologia
ISSN
0012-186X
Published
1984-12-00
Pages
587-91
Language
English
Region
Germany
NLM ID
0006777
Subset
IM
Grants
NIADDK NIH HHS · AM20527 · United States
NIEHS NIH HHS · ES03066 · United States
NIEHS NIH HHS · ES03113 · United States
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