Literature DB >> 772185

Antiarthritic properties and unique pharmacologic profile of a potential chrysotherapeutic agent: S K & F D-30162.

D T Walz, M J DiMartino, L W Chakrin, B M Sutton, A MISHER.   

Abstract

SK&F D-39162, a potential chrysotherapeutic agent, on oral administration was effective in suppressing the development of inflammatory lesions and 7S anti-sheep red blood cell antibody formation in adjuvant arthritic rats. Oral absorption of SK&F D-39162 was indicated by the presence of serum gold levels. In contrast to orally administered SK&F D-39162, gold sodium thiomalate administered intramuscularly at equivalent gold doses, appeared to be less effective in suppressing the primary and secondary lesions of adjuvant arthritis, produced relatively higher levels of gold in both serum and kidneys and produced marked toxicity. Other pharmacologic properties of SK&F D-39162 distinguishing it from gold sodium thiomalate which may have clinical significance include potent inhibitory activity on antibody-forming cells, immediate hypersensitivity reactions and extracellular release of lysosomal enzymes. In further contrast to gold sodium thiomalate, SK&F D-39162 is not a potent inhibitor of sulfhydryl group reactivity. In pharmacokinetic studies, the daily oral administration of SK&F D-39162 to normal rats produced greater stability of blood gold levels and less kidney gold accumulation than parenterally administered gold sodium thiomalate.

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Year:  1976        PMID: 772185

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  24 in total

1.  A comparison of tissue gold levels in guinea-pigs after treatment with myocrisin injected intramuscularly and triethylphosphine gold chloride and myocrisin administered orally.

Authors:  H Kamel; D H Brown; J M Ottaway; W E Smith; J Cottney; A J Lewis
Journal:  Agents Actions       Date:  1978-10

2.  Modulation of the release of histamine and arachidonic acid metabolites from human basophils and mast cells by auranofin.

Authors:  G Marone; M Columbo; D Galeone; G Guidi; A Kagey-Sobotka; L M Lichtenstein
Journal:  Agents Actions       Date:  1986-04

Review 3.  Clinical pharmacokinetics of oral and injectable gold compounds.

Authors:  K L Blocka; H E Paulus; D E Furst
Journal:  Clin Pharmacokinet       Date:  1986 Mar-Apr       Impact factor: 6.447

Review 4.  Auranofin. A preliminary review of its pharmacological properties and therapeutic use in rheumatoid arthritis.

Authors:  M Chaffman; R N Brogden; R C Heel; T M Speight; G S Avery
Journal:  Drugs       Date:  1984-05       Impact factor: 9.546

5.  Oral gold: a comparison with placebo and with intramuscular sodium aurothiomalate.

Authors:  D Lewis; H A Capell
Journal:  Clin Rheumatol       Date:  1984-03       Impact factor: 2.980

6.  Longterm experience with oral gold in rheumatoid arthritis and psoriatic arthritis.

Authors:  J Dequeker; W Verdickt; G Gevers; K Vanschoubroek
Journal:  Clin Rheumatol       Date:  1984-03       Impact factor: 2.980

7.  Changes in mononuclear cell function in patients with rheumatoid arthritis following treatment with auranofin.

Authors:  R J Coughlan; M B Richter; G S Panayi
Journal:  Clin Rheumatol       Date:  1984-03       Impact factor: 2.980

8.  Immunomodulatory effects of therapeutic gold compounds. Gold sodium thiomalate inhibits the activity of T cell protein kinase C.

Authors:  K Hashimoto; C E Whitehurst; T Matsubara; K Hirohata; P E Lipsky
Journal:  J Clin Invest       Date:  1992-06       Impact factor: 14.808

9.  Auranofin. New oral gold compound for treatment of rheumatoid arthritis.

Authors:  A E Finkelstein; D T Walz; V Batista; M Mizraji; F Roisman; A Misher
Journal:  Ann Rheum Dis       Date:  1976-06       Impact factor: 19.103

10.  Chronic immune synovitis in rabbits. II. Modulation by anti-inflammatory and anti-rheumatic agents.

Authors:  M B Goldlust; L C Rich
Journal:  Agents Actions       Date:  1981-12
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