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新型氮杂螺烷SK&F 105685的治疗活性,其具有诱导抑制细胞的活性。

Therapeutic activity of SK&F 105685, a novel azaspirane with suppressor-cell inducing activity.

作者信息

Badger A M, Swift B A

机构信息

Department of Cellular Biochemistry, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406.

出版信息

Clin Exp Rheumatol. 1993 Mar-Apr;11 Suppl 8:S107-9.

PMID:8324933
Abstract

SK&F 105685, methotrexate (MTX) and chloroquine (CHL) were examined for their ability to inhibit paw inflammation in the adjuvant arthritic rat (AA) and for their ability to induce non-specific suppressor cells (SC) in the spleens of these animals. Compared to SK&F 105685 (84-90%) inhibition and MTX (91% inhibition) CHL, at the maximally tolerated dose, only inhibited paw lesions by 29%. MTX did not induce splenic SC activity and, despite the structural similarities between CHL and SK&F 105685, only the latter induced suppressor cells.

摘要

对SK&F 105685、甲氨蝶呤(MTX)和氯喹(CHL)进行了研究,观察它们抑制佐剂性关节炎大鼠(AA)爪部炎症的能力,以及诱导这些动物脾脏中非特异性抑制细胞(SC)的能力。与SK&F 105685(抑制率84 - 90%)和MTX(抑制率91%)相比,CHL在最大耐受剂量时仅抑制爪部损伤29%。MTX未诱导脾脏SC活性,尽管CHL与SK&F 105685结构相似,但只有后者诱导出抑制细胞。

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