Nuclear receptors and nonalcoholic fatty liver disease

MC Cave, HB Clair, JE Hardesty, KC Falkner… - … et Biophysica Acta (BBA …, 2016 - Elsevier
Nuclear receptors are transcription factors which sense changing environmental or
hormonal signals and effect transcriptional changes to regulate core life functions including …

Targeting nuclear receptors for the treatment of fatty liver disease

N Tanaka, T Aoyama, S Kimura, FJ Gonzalez - Pharmacology & …, 2017 - Elsevier
Ligand-activated nuclear receptors, including peroxisome proliferator-activated receptor
alpha (PPARα), pregnane X receptor, and constitutive androstane receptor, were first …

Nuclear tau, a key player in neuronal DNA protection

A Sultan, F Nesslany, M Violet, S Bégard… - Journal of Biological …, 2011 - ASBMB
Tau, a neuronal protein involved in neurodegenerative disorders such as Alzheimer
disease, which is primarily described as a microtubule-associated protein, has also been …

Xenobiotic metabolism, disposition, and regulation by receptors: from biochemical phenomenon to predictors of major toxicities

CJ Omiecinski, JP Vanden Heuvel… - Toxicological …, 2011 - academic.oup.com
To commemorate the 50th anniversary of the Society of Toxicology, this special edition
article reviews the history and current scope of xenobiotic metabolism and transport, with …

Novel mechanisms for DHEA action

RA Prough, BJ Clark, CM Klinge - Journal of molecular …, 2016 - jme.bioscientifica.com
Dehydroepiandrosterone (3β-hydroxy-5-androsten-17-one, DHEA), secreted by the adrenal
cortex, gastrointestinal tract, gonads, and brain, and its sulfated metabolite DHEA-S are the …

Mode of action and human relevance analysis for nuclear receptor-mediated liver toxicity: A case study with phenobarbital as a model constitutive androstane receptor …

CR Elcombe, RC Peffer, DC Wolf, J Bailey… - Critical reviews in …, 2014 - Taylor & Francis
The constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are important
nuclear receptors involved in the regulation of cellular responses from exposure to many …

Drug-drug interactions that alter the exposure of glucuronidated drugs: Scope, UDP-glucuronosyltransferase (UGT) enzyme selectivity, mechanisms (inhibition and …

JO Miners, TM Polasek, JA Hulin, A Rowland… - Pharmacology & …, 2023 - Elsevier
Drug-drug interactions (DDIs) arising from the perturbation of drug metabolising enzyme
activities represent both a clinical problem and a potential economic loss for the …

[HTML][HTML] Cellular adaptation to xenobiotics: Interplay between xenosensors, reactive oxygen species and FOXO transcription factors

LO Klotz, H Steinbrenner - Redox biology, 2017 - Elsevier
Cells adapt to an exposure to xenobiotics by upregulating the biosynthesis of proteins
involved in xenobiotic metabolism. This is achieved largely via activation of cellular …

Phenobarbital indirectly activates the constitutive active androstane receptor (CAR) by inhibition of epidermal growth factor receptor signaling

S Mutoh, M Sobhany, R Moore, L Perera… - Science …, 2013 - science.org
Phenobarbital is a central nervous system depressant that also indirectly activates nuclear
receptor constitutive active androstane receptor (CAR), which promotes drug and energy …

Mechanisms of induction of cytosolic and microsomal glutathione transferase (GST) genes by xenobiotics and pro-inflammatory agents

LG Higgins, JD Hayes - Drug metabolism reviews, 2011 - Taylor & Francis
Glutathione transferase (GST) isoezymes are encoded by three separate families of genes
(designated cytosolic, microsomal and mitochondrial transferases), with distinct evolutionary …