Differential interactions of antiretroviral agents with LXR, ER and GR nuclear receptors: potential contributing factors to adverse events

@article{Svrd2014DifferentialIO,
  title={Differential interactions of antiretroviral agents with LXR, ER and GR nuclear receptors: potential contributing factors to adverse events},
  author={Jenny Sv{\"a}rd and Fernando Blanco and D. Nevin and Darren Fayne and Fiona Mulcahy and Martina Hennessy and J Paul Spiers},
  journal={British Journal of Pharmacology},
  year={2014},
  volume={171}
}
Antiretroviral (ARV) drugs activate pregnane X receptors and constitutive androstane receptors, increasing the risk of drug interactions due to altered drug metabolism and disposition. The closely related liver X receptors (LXRα/β), oestrogen receptors (ERα/β) and glucocorticoid receptor (GR) regulate many endogenous processes such as lipid/cholesterol homeostasis, cellular differentiation and inflammation. However, ARV drug activation of these nuclear receptors has not been thoroughly… 
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