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用改善病情抗风湿药治疗的佐剂性关节炎大鼠白细胞介素-1活性及急性期反应的改变

Alteration of interleukin-1 activity and the acute phase response in adjuvant arthritic rats treated with disease modifying antirheumatic drugs.

作者信息

Connolly K M, Stecher V J, Danis E, Pruden D J, LaBrie T

机构信息

Department of Pharmacology, Sterling-Winthrop Research Institute, Rensselaer, New York 12144.

出版信息

Agents Actions. 1988 Aug;25(1-2):94-105. doi: 10.1007/BF01969100.

Abstract

Interleukin-1 (IL-1) activity and the acute phase response, as measured by plasma CRP and iron, were used to determine if the standard disease modifying antirheumatic drugs (DMARDs), gold, chloroquine and D-penicillamine had a common profile of activity in the adjuvant arthritic (AA) rat. All drugs were tested at a dose which significantly reduced noninjected paw swelling in AA rats. Inhibition of paw edema ranged from 37% for D-penicillamine (100 mg/kg) to 69% for auranofin (10 mg/kg). Two week medication of AA rats with gold sodium thiomalate (GST, 10 mg/kg, i.m.) or auranofin (10 mg/kg, p.o.) resulted in a significant decrease in splenic IL-1 activity, as measured in the standard lymphocyte activating factor (LAF) assay. The acute phase response, often associated with elevated IL-1 activity, was also significantly reduced following treatment of AA rats with 10 mg/kg of GST or auranofin (oral gold). Inhibition of the acute phase response by gold was determined by a significant reduction of plasma CRP levels (56-71% reduction) and enhancement of plasma iron levels (27-52% enhancement). In contrast to the effect of GST and auranofin on IL-1, CRP and iron, treatment with chloroquine (20, 30 and 35 mg/kg) and D-penicillamine (55 and 100 mg/kg) failed to reduce the acute phase response (as measured by plasma CRP and iron) or alter LAF activity from AA rat spleen cell supernatants. Based on its ability to reduce LAF activity in spleen cell supernatants and reduce the acute phase response, it is possible that the activity of gold in the AA rat may in part be due to its ability to inhibit IL-1 production in vivo. The inability of chloroquine and D-penicillamine to alter LAF activity and the acute phase response in AA rats does not preclude their possession of an immunoregulatory mechanism of action, but it does indicate that their mechanism of action in the AA rat probably differs from that of GST and auranofin.

摘要

通过血浆CRP和铁水平来衡量白细胞介素-1(IL-1)活性及急性期反应,以此确定标准抗风湿药物(DMARDs)、金制剂、氯喹和青霉胺在佐剂性关节炎(AA)大鼠中是否具有共同的活性特征。所有药物均以能显著减轻AA大鼠未注射足爪肿胀的剂量进行测试。足爪水肿的抑制率范围为:青霉胺(100毫克/千克)为37%,金诺芬(10毫克/千克)为69%。用硫代苹果酸金钠(GST,10毫克/千克,肌肉注射)或金诺芬(10毫克/千克,口服)对AA大鼠进行两周用药后,在标准淋巴细胞激活因子(LAF)检测中,脾脏IL-1活性显著降低。急性期反应通常与IL-1活性升高相关,在用10毫克/千克的GST或金诺芬(口服金)治疗AA大鼠后,急性期反应也显著降低。金制剂对急性期反应的抑制作用通过血浆CRP水平显著降低(降低56 - 71%)和血浆铁水平升高(升高27 - 52%)来确定。与GST和金诺芬对IL-1、CRP和铁的影响相反,用氯喹(20、30和35毫克/千克)和青霉胺(55和100毫克/千克)治疗未能降低急性期反应(通过血浆CRP和铁水平衡量),也未改变AA大鼠脾细胞上清液中的LAF活性。基于其降低脾细胞上清液中LAF活性和降低急性期反应的能力,金制剂在AA大鼠中的活性可能部分归因于其在体内抑制IL-1产生的能力。氯喹和青霉胺不能改变AA大鼠的LAF活性和急性期反应,这并不排除它们具有免疫调节作用机制,但确实表明它们在AA大鼠中的作用机制可能与GST和金诺芬不同。

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