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肼屈嗪可诱导多核苷酸形成Z-DNA构象,并在接受治疗的患者中引发抗(Z-DNA)抗体。

Hydralazine induces Z-DNA conformation in a polynucleotide and elicits anti(Z-DNA) antibodies in treated patients.

作者信息

Thomas T J, Seibold J R, Adams L E, Hess E V

机构信息

Clinical Research Center, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick 08903.

出版信息

Biochem J. 1993 Sep 1;294 ( Pt 2)(Pt 2):419-25. doi: 10.1042/bj2940419.

Abstract

We studied the effect of hydralazine, an antihypertensive drug with lupus-inducing side effects, on the conformation of poly(dG-m5dC).poly(dG-m5dC) and a plasmid with a 23 bp insert of (dG-dC)n.(dG-dC)n sequences. Using an e.l.i.s.a. with a monoclonal anti-(Z-DNA) antibody Z22, we found that hydralazine provoked the Z-DNA conformation in poly(dG-m5dC).poly(dG-m5dC) at 250-500 microM concentration. The supercoiled form of hydralazine-treated plasmid bound to Z22 in a gel-retardation assay. To examine further whether Z-DNA could act as an inciting agent in anti-nuclear antibody production in patients, we analysed 65 sera from 25 hypertensive patients taking hydralazine and found anti-(Z-DNA) antibodies in 82% of these sera. Sera from age-matched normal controls showed no binding to Z-DNA. Data on sera drawn sequentially from four hypertensive patients showed that antibodies were present after the drug treatment. These data demonstrate the presence of a high incidence of anti-(Z-DNA) antibodies in patients treated with hydralazine and suggest that a possible mechanism for the production of autoantibodies in drug-related lupus might involve the induction and stabilization of Z-DNA by drugs.

摘要

我们研究了具有诱发狼疮副作用的抗高血压药物肼屈嗪对聚(dG-m5dC)·聚(dG-m5dC)以及带有23 bp(dG-dC)n·(dG-dC)n序列插入片段的质粒构象的影响。使用一种带有抗(Z-DNA)单克隆抗体Z22的酶联免疫吸附测定法,我们发现肼屈嗪在浓度为250 - 500 microM时能在聚(dG-m5dC)·聚(dG-m5dC)中引发Z-DNA构象。在凝胶阻滞试验中,经肼屈嗪处理的质粒超螺旋形式与Z22结合。为了进一步研究Z-DNA是否可能是患者抗核抗体产生的诱因,我们分析了25名服用肼屈嗪的高血压患者的65份血清,发现其中82%的血清含有抗(Z-DNA)抗体。年龄匹配的正常对照者的血清与Z-DNA无结合。对4名高血压患者连续采集的血清数据显示,药物治疗后出现了抗体。这些数据表明服用肼屈嗪的患者中抗(Z-DNA)抗体的发生率很高,并提示药物相关性狼疮中自身抗体产生的一种可能机制可能涉及药物对Z-DNA的诱导和稳定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c876/1134470/7e5554897d70/biochemj00104-0119-a.jpg

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