Nguyen Linh P, Bradfield Christopher A
McArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53706, USA.
Chem Res Toxicol. 2008 Jan;21(1):102-16. doi: 10.1021/tx7001965. Epub 2007 Dec 13.
The primary design of this perspective is to describe the major ligand classes of the aryl hydrocarbon receptor (AHR). A grander objective is to provide models that may help define the physiological activator or "endogenous ligand" of the AHR. We present evidence supporting a developmental role for the AHR and propose mechanisms by which an endogenous ligand and consequent AHR activation might be important during normal physiology and development. From this vista, we survey the known xenobiotic, endogenous, dietary, and "unconventional" activators of the AHR, including, when possible, information about their induction potency, receptor binding affinity, and potential for exposure. In light of the essential function of the AHR in embryonic development, we discuss the candidacy of each of these compounds as physiologically important activators.
本观点的主要设计目的是描述芳烃受体(AHR)的主要配体类别。一个更宏大的目标是提供可能有助于定义AHR的生理激活剂或“内源性配体”的模型。我们提供了支持AHR具有发育作用的证据,并提出了内源性配体以及随之而来的AHR激活在正常生理和发育过程中可能重要的机制。从这个角度出发,我们审视了已知的AHR的外源性、内源性、饮食性和“非常规”激活剂,包括在可能的情况下,关于它们的诱导效力、受体结合亲和力以及暴露可能性的信息。鉴于AHR在胚胎发育中的重要功能,我们讨论了这些化合物作为生理上重要激活剂的可能性。