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大鼠佐剂性关节炎作为一种测试潜在抗风湿药物的模型。

Rat adjuvant arthritis as a model to test potential antirheumatic agents.

作者信息

Toivonen M L, Tokola O, Vapaatalo H

出版信息

Methods Find Exp Clin Pharmacol. 1982 Aug-Sep;4(6):359-63.

PMID:7144330
Abstract

Adjuvant arthritis was induced in male Sprague-Dawley rats by a subcutaneous injection of Mycobacterium tuberculosis in sterile paraffine oil into the base of the tail. The effects of the immunomodulating drugs N-(2-carboxyphenyl)-4-chloroanthranilic acid disodium (CCA), d-penicillamine and thiabendazole were compared to those of the anti-inflammatory drugs indomethacin, tolfenamic acid and prednisolone. All the anti-inflammatory drugs were highly protective. Of the immunomodulating drugs thiabendazole also showed dose-related inhibitory effect. CCA had only a negligible effect and d-penicillamine enhanced the activity of the arthritic syndrome. An aggravation of the arthritis also occurred after pretreatment with d-penicillamine for 30 days before the induction of arthritis. The complement inhibiting agents epsilon aminocaproic acid and heparin enhanced the symptoms of the adjuvant arthritis as did d-penicillamine. We suggest that the effects of the immunomodulating drugs are dependent on the dose used and the stage of the disease at the beginning of treatment.

摘要

通过在雄性斯普拉格-道利大鼠尾部基部皮下注射无菌石蜡油中的结核分枝杆菌来诱导佐剂性关节炎。将免疫调节药物N-(2-羧苯基)-4-氯邻氨基苯甲酸二钠(CCA)、d-青霉胺和噻苯达唑的效果与抗炎药物吲哚美辛、托芬那酸和泼尼松龙的效果进行比较。所有抗炎药物都具有高度保护作用。在免疫调节药物中,噻苯达唑也显示出剂量相关的抑制作用。CCA只有微不足道的作用,而d-青霉胺增强了关节炎综合征的活性。在诱导关节炎前用d-青霉胺预处理30天也会导致关节炎加重。补体抑制剂ε-氨基己酸和肝素与d-青霉胺一样增强了佐剂性关节炎的症状。我们认为免疫调节药物的效果取决于所用剂量和治疗开始时疾病的阶段。

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