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细胞因子作为芳烃受体配体的分子靶点:对毒性和外源性化合物解毒的影响。

Cytokines as molecular targets for aryl hydrocarbon receptor ligands: implications for toxicity and xenobiotic detoxification.

机构信息

Institut de Recherche en Environnement, Santé et Travail (IRSET)/INSERM U 1085, Faculté de Pharmacie, 2 Avenue du Pr Léon Bernard, 35043 Rennes, France.

出版信息

Expert Opin Drug Metab Toxicol. 2013 Feb;9(2):141-52. doi: 10.1517/17425255.2013.738194. Epub 2012 Dec 12.

Abstract

INTRODUCTION

The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor historically known for regulating expression of several important drug-detoxifying proteins. Besides drug metabolism pathways, cytokines have been recently recognized as targeted by the AhR signaling cascade, which may contribute to toxicity and changes in xenobiotic detoxification caused by AhR agonists.

AREAS COVERED

This article summarizes the nature of the main cytokines regulated by AhR ligands and reviews their involvement in toxic effects of AhR ligands, especially in relation with inflammation. The article also discusses the potential implications for drug detoxification pathways.

EXPERT OPINION

Even if various cytokines, including inflammatory ones, have already been demonstrated to constitute robust targets for AhR, the exact role played by AhR with respect to inflammation remains to be determined. Further studies are also required to better characterize the molecular mechanisms implicated in regulation of cytokines by AhR ligands and to determine the role that may play AhR-targeted cytokines in alteration of xenobiotic detoxification. Finally, changes in cytokine receptor expression triggered by AhR ligands have additionally to be taken into account to better and more extensively comprehend the role played by AhR in the cytokine/inflammation area.

摘要

简介

芳香烃受体(AhR)是一种配体激活的转录因子,历史上以调节几种重要药物解毒蛋白的表达而闻名。除了药物代谢途径外,细胞因子最近也被认为是 AhR 信号级联的靶向目标,这可能导致 AhR 激动剂引起的毒性和对外源化合物解毒的改变。

涵盖领域

本文总结了 AhR 配体调节的主要细胞因子的性质,并回顾了它们在 AhR 配体的毒性作用中的作用,特别是与炎症的关系。本文还讨论了对药物解毒途径的潜在影响。

专家意见

尽管已经证明各种细胞因子,包括炎症细胞因子,是 AhR 的强有力靶标,但 AhR 与炎症的确切关系仍有待确定。还需要进一步的研究来更好地描述 AhR 配体调节细胞因子所涉及的分子机制,并确定 AhR 靶向细胞因子在外源化合物解毒改变中的作用。最后,还需要考虑 AhR 配体引发的细胞因子受体表达的变化,以更好、更广泛地理解 AhR 在细胞因子/炎症领域的作用。

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