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The effect of thalidomide and supidimide on endotoxin-induced uveitis in rats

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Abstract

• Background: Endotoxin-induced uveitis (EIU) is an animal model of ocular inflammation, produced by footpad injection of endotoxin (lipopolysaccharide, LPS) to mimic the human disease of acute anterior uveitis, that is useful for testing new anti-inflammatory therapy. The purpose of this study was to test the anti-inflammatory effect on EIU of thalidomide and one of its derivatives, supidimide.

• Methods: EIU was produced in rats by hind footpad injection of LPS (100 μg/animal). Animals were killed 20 h after LPS injection. Inflammation was evaluated by anterior chamber determination of proteins and cells.

• Results: A dosage of 400 mg/kg per day of thalidomide was efficient in reducing inflammation whether given in three doses (at − 24 h, − 4 h and + 4 h relative to LPS challenge = THAL-1; p < 0.001 for proteins and cells), in two doses (−4 h and +4 h = THAL-2; p < 0.001 for proteins, p < 0.012 for cells) or in one dose (at +4 h=late THAL; p < 0.001 for proteins, p≤0.02 for cells). A dosage of 300 mg/kg per day of thalidomide was still efficient (p≤0.023 for proteins, p≤0.06 for cells), but 150 mg/kg per day had no effect on inflammation. Supidimide (400 mg/kg per day) had some anti-inflammatory effect (p ≤ 0.053 for proteins, p < 0.06 for cells).

• Conclusion: High-dose thalidomide had a potent anti-inflammatory effect in EIU, but lower doses were not sufficient to reduce inflammation. At similar high doses, supidimide had some effect on EIU but was less effective than thalidomide.

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References

  1. Helm F-C, Frankus E, Friderichs E, Graudums I, Flohé L (1981) Comparative teratological investigation of compounds structurally and pharmacologically related to thalidomide. Arzneimittelforsch/Drug Res 31:941–949

    Google Scholar 

  2. Herbort CP, Okumura A, Mochizuki M (1988) Endotoxin-induced uveitis in the rat: a study of the role of inflammation mediators. Graefe's Arch Clin Exp Ophthalmol 226:553–558

    Google Scholar 

  3. Lenz W (1962) Thalidomide and congenital abnormalities. Lancet 11: 45–46

    Google Scholar 

  4. McBride WG (1961) Thalidomide and congenital abnormalities. Lancet ii: 1358

    Google Scholar 

  5. Moreira AL, Sampaio EP, Zmuidzinas A, Frindt P, Smith KA, Kaplan G (1993) Thalidomide exerts its inhibitory action on tumor necrosis factor α by enhancing mRNA degradation. J Exp Med 177:1675–1680

    Article  CAS  PubMed  Google Scholar 

  6. Neubert R, Nogueira AC, Neubert D (1993) Thalidomide derivatives and the immune system. I. Changes in the pattern of integrin receptors and other surface markers on T lymphocyte subpopulations of marmoset blood. Arch Toxicol 67:1–17

    Google Scholar 

  7. Ochonisky S, Verroust J, Bastujii-Garin S, Gehrardi R, Revuz J (1993) Thalidomide neuropathy: incidence and clinico-electrophysiological features in 42 patients. Rev Med Intern 14 [Suppl 1]: 108

    Google Scholar 

  8. Ramselaar CG, Boone RM, Kluin-Nelemans HC (1986) Thalidomide in the treatment of necro-Behçet's syndrome. Br J Dermatol 115:367–370

    Google Scholar 

  9. Sampaio EP, Sarno EN, Galilly R, Cohn ZA, Kaplan G (1991) Thalidomide selectively inhibits tumor necrosis factor production by stimulated human monocytes. J Exp Med 173:699–703

    Article  CAS  PubMed  Google Scholar 

  10. Saylan T, Saltik I (1982) Thalidomide in the treatment of Behçet's syndrome. Arch Dermatol 118:536

    Google Scholar 

  11. Sheskin J (1965) Thalidomide in the treatment of lepra reaction. Clin Pharmacol Ther 6:303–306

    Google Scholar 

  12. Tamura F, Vogelsang GB, Reitz BA, Baumgartner WA, Herskowitz A (1990) Combination thalidomide and cyclosporine for cardiac allograft rejection. Comparison with methylprednisolone and cyclosporine. Transplantation 49:20–25

    Google Scholar 

  13. Vogelsang GB, Taylor S, Gordon G, Hess AD (1986) Thalidomide, a potent agent for treatment of graft-versus-host disease. Transplant Proc 18:904–906

    Google Scholar 

  14. Vogelsang GB, Farmer ER, Hess AD, Altamonte V, Beschorner WE, Jabs DA, Corio RL, Levin LS, Colvin OM, Wingard JR, Santos GW (1992) Thalidomide for the treatment of chronic graft-versus-host disease. N Engl J Med 326:1055–1058

    Google Scholar 

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These data were presented in part at the first annual ECORA meeting, 4–6 October, 1993, Bonn, Germany

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Guex-Crosier, Y., Pittet, N. & Herbort, C.P. The effect of thalidomide and supidimide on endotoxin-induced uveitis in rats. Graefe's Arch Clin Exp Ophthalmol 233, 90–93 (1995). https://doi.org/10.1007/BF00241478

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  • DOI: https://doi.org/10.1007/BF00241478

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