Literature DB >> 3760592

Suppression of spontaneous insulin-dependent diabetes in BB rats by administration of ciamexone.

U Kiesel, K Maruta, U Treichel, U Bicker, H Kolb.   

Abstract

BB rats spontaneously develop an insulin dependent diabetes which resembles in many features human type I diabetes. We have tested the effect of the immunomodulatory drug Ciamexone, a 2-cyan-aziridine-derivative, on the development of diabetes in BB rats. Ciamexone was given once daily during 6 days per week beginning with the age of 42 or 50 days up to 120 days. For comparison cyclosporin A (10 mg/kg) was applied following the same protocol. At 1 mg/kg ciamexone administration led to complete prevention of diabetes in females but was not beneficial in males. At 10 mg/kg the drug caused significant suppression of diabetes development in males but more pronounced in females. Both, a reduction of the incidence of diabetes and a delay in the onset of hyperglycaemia was observed only in females. After administration of cyclosporin A none of the animals developed diabetes. Ciamexone treatment did not affect granulocyte and lymphocyte counts and subsets in the peripheral blood except for a tendency to suppress eosinophilia. The growth of animals was not retarded. It is concluded that ciamexone seems to influence the autoimmune state of the BB rat resulting in partial suppression of the disease.

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Year:  1986        PMID: 3760592     DOI: 10.3109/08923978609026496

Source DB:  PubMed          Journal:  J Immunopharmacol        ISSN: 0163-0571


  3 in total

1.  Metabolism of ciamexon by human liver microsomes: an investigation into the formation of stable, chemically reactive and cytotoxic metabolites.

Authors:  M D Tingle; B K Park
Journal:  Br J Clin Pharmacol       Date:  1990-05       Impact factor: 4.335

2.  Ciamexone, a highly selective immunomodulator--a tool for autoimmune diseases?

Authors:  U Bicker; K H Usadel
Journal:  Klin Wochenschr       Date:  1986-12-15

3.  The specificity of rejection and the absence of susceptibility of pancreatic islet beta cells to nonspecific immune destruction in mixed strain islets grafted beneath the renal capsule in the rat.

Authors:  R Sutton; D W Gray; P McShane; M J Dallman; P J Morris
Journal:  J Exp Med       Date:  1989-09-01       Impact factor: 14.307

  3 in total

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