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体外和体内巨噬细胞中熊果酸对抗炎和抗氧化基因的转录调控。

Bryonolic acid transcriptional control of anti-inflammatory and antioxidant genes in macrophages in vitro and in vivo.

机构信息

Department of Pharmacology, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

J Nat Prod. 2012 Apr 27;75(4):591-8. doi: 10.1021/np200823p. Epub 2012 Feb 16.

Abstract

Bryonolic acid (BA) (1) is a naturally occurring triterpenoid with pleiotropic properties. This study characterizes the mechanisms mediating the anti-inflammatory and antioxidant activities of BA and validates the utility of BA as a tool to explore the relationships between triterpenoid structure and activity. BA reduces the inflammatory mediator NO by suppressing the expression of the inflammatory enzyme inducible nitric oxide synthase (iNOS) in LPS-activated RAW 264.7 macrophage cells. In addition, BA robustly induces the antioxidant protein heme oxygenase-1 (HO-1) in vitro and in vivo in an Nrf2-dependent manner. Further analyses of Nrf2 target genes reveal selectivity for the timing and level of gene induction by BA in treated macrophages with distinct patterns for Nrf2-regulated antioxidant genes. Additionally, the distinct expression profile of BA on Nrf2 target genes relative to oleanolic acid suggests the importance of the triterpenoid scaffold in dictating the pleiotropic effects exerted by these molecules.

摘要

熊果酸(BA)(1)是一种具有多种生物学活性的天然三萜类化合物。本研究旨在探讨 BA 介导抗炎和抗氧化活性的作用机制,并验证 BA 作为一种研究三萜类化合物结构与活性关系的工具的实用性。BA 通过抑制 LPS 激活的 RAW264.7 巨噬细胞中诱导型一氧化氮合酶(iNOS)的表达来降低炎症介质 NO。此外,BA 以 Nrf2 依赖的方式在体外和体内强烈诱导抗氧化蛋白血红素加氧酶-1(HO-1)。对 Nrf2 靶基因的进一步分析表明,BA 对经处理的巨噬细胞中基因诱导的时间和水平具有选择性,并且 Nrf2 调节的抗氧化基因具有不同的模式。此外,与齐墩果酸相比,BA 对 Nrf2 靶基因的表达谱表明三萜类化合物骨架在决定这些分子发挥的多效性作用方面的重要性。

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