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3β-Acetyloxy-oleanolic Acid Attenuates Pristane-Induced Lupus Nephritis by Regulating Th17 Differentiation

机译:3β-乙酰氧基-油醇酸通过调节Th17分化减轻rist烷诱导的狼疮性肾炎。

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摘要

Th17 activity has been implicated in systemic lupus erythematosus (SLE), which is a systemic autoimmune disease with a typical clinical manifestation of lupus nephritis (LN). Retinoic acid receptor-related orphan receptor gamma t (RORγt) has been shown to be important for Th17 differentiation. In this study, we evaluated the inhibition of RORγt activity by 3β-acetyloxy-oleanolic acid (AOA), a small molecule isolated from the root of Symplocos laurina, a traditional herb belonging to South China. We demonstrated that AOA can inhibit RORγt activity and prevent SLE pathogenesis in a pristane-induced LN model. The results showed that AOA decreased RORγt transcription activity in a reporter assay and prevented Th17 differentiation in vitro. In vivo studies showed that AOA treatment decreased serum anti-dsDNA antibody and alleviated renal pathologic damage as well as antibody complex accumulation in the pristane-induced LN model. These results demonstrated that AOA can improve the clinical manifestation of LN, indicating potential application in SLE therapy.
机译:Th17活性与系统性红斑狼疮(SLE)有关,系统性红斑狼疮是一种系统性自身免疫疾病,具有典型的狼疮性肾炎(LN)临床表现。视黄酸受体相关的孤儿受体γt(RORγt)已被证明对Th17分化很重要。在这项研究中,我们评估了3β-乙酰氧基-油酸(AOA)对RORγt活性的抑制作用,这是一种小分子,它是从属于中国南方传统草药Syplocos laurina的根中分离出来的。我们证明了AOA可以抑制RORγt活性,并防止在rist烷诱导的LN模型中的SLE发病机理。结果表明,在报告基因分析中,AOA降低了RORγt转录活性,并在体外阻止了Th17的分化。体内研究表明,AOA处理可降低血清抗dsDNA抗体,减轻肾脏病理损伤以及在rist烷诱导的LN模型中抗体复合物的积累。这些结果表明,AOA可以改善LN的临床表现,表明其在SLE治疗中的潜在应用。

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