Effects of oral aspirin and oxaprozin on the development of lupus-like disease in MRL/1 mice.

R P Carlson, S C Gilman, T G Hodge, L O'Neill-Davis, E M Blazek, A J Lewis
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引用次数: 5

Abstract

We examined the effects of two prostaglandin synthetase inhibitors, aspirin and oxaprozin, on the development of lupus-like disease in MRL/1 mice. Daily oral administration of 100 mg/kg of these compounds over a period of 3 months significantly reduced thymic lymphoid hyperplasia. In addition, aspirin but not oxaprozin significantly lowered total lymphocyte counts in the peripheral blood. Other drug-related changes, including reduced hyperplasia in the spleen and lymph nodes and an improvement in kidney vasculitis by aspirin, did not reach statistical significance. Neither aspirin nor oxaprozin influenced the circulating levels of anti-ds DNA antibodies or the severity of kidney glomerulonephritis. While the overall effects of these cyclooxygenase inhibitors were not dramatic, the results do indicate that further studies are warranted to determine the precise therapeutic role, if any, for PG-synthetase inhibitors in lupus-like disease.

口服阿司匹林和奥沙普嗪对MRL/1小鼠狼疮样疾病发展的影响
我们研究了两种前列腺素合成酶抑制剂阿司匹林和奥沙普嗪对MRL/1小鼠狼疮样疾病发展的影响。每天口服100毫克/公斤这些化合物,持续3个月,可显著减少胸腺淋巴样增生。此外,阿司匹林能显著降低外周血淋巴细胞总数,而奥沙普嗪不能。其他药物相关的变化,包括脾脏和淋巴结增生减少以及阿司匹林对肾血管炎的改善,没有达到统计学意义。阿司匹林和奥沙丙嗪均不影响血液中抗ds DNA抗体的水平或肾小球肾炎的严重程度。虽然这些环氧化酶抑制剂的总体效果并不显著,但结果确实表明,需要进一步的研究来确定pg合成酶抑制剂在狼疮样疾病中的确切治疗作用,如果有的话。
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