Antiarthritic properties and unique pharmacologic profile of a potential chrysotherapeutic agent: S K & F D-30162
- PMID: 772185
Antiarthritic properties and unique pharmacologic profile of a potential chrysotherapeutic agent: S K & F D-30162
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.
Similar articles
-
Distribution of gold in blood following administration of auranofin (SK&F D-39162).J Rheumatol Suppl. 1979;5:56-60. J Rheumatol Suppl. 1979. PMID: 114638
-
Immunopharmacology of auranofin and gold sodium thiomalate: effects on humoral immunity.J Rheumatol Suppl. 1979;5:74-81. J Rheumatol Suppl. 1979. PMID: 114651
-
Pharmacokinetics of gold following administration of auranofin (SK+FD-39162) and myochrysine to rats.J Rheumatol. 1980 Nov-Dec;7(6):820-4. J Rheumatol. 1980. PMID: 6782245
-
Biologic actions and pharmacokinetic studies of auranofin.Am J Med. 1983 Dec 30;75(6A):90-108. doi: 10.1016/0002-9343(83)90481-3. Am J Med. 1983. PMID: 6318557 Review.
-
The pharmacological profile of auranofin, an orally active gold compound.Scand J Rheumatol Suppl. 1983;51:16-25. doi: 10.3109/03009748309095339. Scand J Rheumatol Suppl. 1983. PMID: 6426049 Review.
Cited by
-
Changes in mononuclear cell function in patients with rheumatoid arthritis following treatment with auranofin.Clin Rheumatol. 1984 Mar;3 Suppl 1:25-32. doi: 10.1007/BF03342619. Clin Rheumatol. 1984. PMID: 6432410 Clinical Trial.
-
Longterm experience with oral gold in rheumatoid arthritis and psoriatic arthritis.Clin Rheumatol. 1984 Mar;3 Suppl 1:67-74. doi: 10.1007/BF03342624. Clin Rheumatol. 1984. PMID: 6432416 Clinical Trial.
-
Pharmacokinetics of gold sodium thiomalate in rabbits.Pharm Res. 1987 Aug;4(4):332-6. doi: 10.1023/a:1016453421958. Pharm Res. 1987. PMID: 3150043
-
Comparison of auranofin and aurothioglucose in the treatment of rheumatoid arthritis: a single blind study.Clin Rheumatol. 1984 Mar;3 Suppl 1:51-6. doi: 10.1007/BF03342622. Clin Rheumatol. 1984. PMID: 6432414 Clinical Trial.
-
Oral gold: a comparison with placebo and with intramuscular sodium aurothiomalate.Clin Rheumatol. 1984 Mar;3 Suppl 1:83-96. doi: 10.1007/BF03342626. Clin Rheumatol. 1984. PMID: 6432418