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甲氨蝶呤和甲基泼尼松龙未能改变模型免疫复合物的清除率。

Failure of methotrexate and methylprednisolone to alter the clearance of model immune complexes.

作者信息

Schrieber L, Mullins W W, Plotz P H

出版信息

J Rheumatol. 1985 Dec;12(6):1044-7.

PMID:4093911
Abstract

We evaluated the effect of methotrexate (MTX) and methylprednisolone (MP) on reticuloendothelial system (RES) clearance of soluble model immune complexes (IC) in BALB/C mice. MTX was administered by intraperitoneal route either as a single dose (0.5 mg/kg) or as 10 alternate day doses (0.1 or 0.5 mg/kg), MP as a single intravenous (IV) bolus (50 mg/kg) with normal saline used as a control. Mice were then injected IV with radiolabelled IgG anti-DNP covalently crosslinked IC. Blood radioactivity was measured over a 3 h period at which time organ uptake, corrected for blood contamination, was determined. Clearance curves for each mouse were derived using the Marquardt-Levenberg curve fitting method. No significant differences in IC clearance or organ uptake were found between drug and control groups at any drug dose or time period. Our findings argue against an influence of MP and MTX on immunospecific clearance of soluble IC.

摘要

我们评估了甲氨蝶呤(MTX)和甲基泼尼松龙(MP)对BALB/C小鼠网状内皮系统(RES)清除可溶性模型免疫复合物(IC)的影响。MTX通过腹腔注射给药,单次剂量为(0.5mg/kg)或分10次隔日给药(0.1或0.5mg/kg),MP通过静脉推注单次给药(50mg/kg),以生理盐水作为对照。然后给小鼠静脉注射放射性标记的IgG抗DNP共价交联IC。在3小时内测量血液放射性,此时测定校正血液污染后的器官摄取量。使用Marquardt-Levenberg曲线拟合方法得出每只小鼠的清除曲线。在任何药物剂量或时间段,药物组和对照组之间在IC清除或器官摄取方面均未发现显著差异。我们的研究结果表明MP和MTX对可溶性IC的免疫特异性清除没有影响。

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