[HTML][HTML] CYP2E1 and oxidant stress in alcoholic and non-alcoholic fatty liver disease
TM Leung, N Nieto - Journal of hepatology, 2013 - Elsevier
Alcoholic (ALD) and non-alcoholic fatty liver diseases (NAFLD) are clinical conditions
leading to hepatocellular injury and inflammation resulting from alcohol consumption, high …
leading to hepatocellular injury and inflammation resulting from alcohol consumption, high …
Increased expression of cytochrome P450 2E1 in nonalcoholic fatty liver disease: mechanisms and pathophysiological role
J Aubert, K Begriche, L Knockaert, MA Robin… - Clinics and research in …, 2011 - Elsevier
Due to the worldwide surge in obesity and type 2 diabetes, the increased incidence of
nonalcoholic fatty liver disease (NAFLD) is a major concern for the public health. Indeed …
nonalcoholic fatty liver disease (NAFLD) is a major concern for the public health. Indeed …
Drug-drug interactions that alter the exposure of glucuronidated drugs: Scope, UDP-glucuronosyltransferase (UGT) enzyme selectivity, mechanisms (inhibition and …
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 …
activities represent both a clinical problem and a potential economic loss for the …
Age‐and genotype‐dependent variability in the protein abundance and activity of six major uridine diphosphate‐glucuronosyltransferases in human liver
DK Bhatt, A Mehrotra, A Gaedigk… - Clinical …, 2019 - Wiley Online Library
The ontogeny of hepatic uridine diphosphate‐glucuronosyltransferases (UGTs) was
investigated by determining their protein abundance in human liver microsomes isolated …
investigated by determining their protein abundance in human liver microsomes isolated …
Drug metabolism alterations in nonalcoholic fatty liver disease
MD Merrell, NJ Cherrington - Drug metabolism reviews, 2011 - Taylor & Francis
Drug-metabolizing enzymes play a vital role in the elimination of the majority of therapeutic
drugs. The major organ involved in drug metabolism is the liver. Chronic liver diseases have …
drugs. The major organ involved in drug metabolism is the liver. Chronic liver diseases have …
UDP-glucuronosyltransferases (UGTs) and their related metabolic cross-talk with internal homeostasis: A systematic review of UGT isoforms for precision medicine
N Yang, R Sun, X Liao, J Aa, G Wang - Pharmacological research, 2017 - Elsevier
UDP-glucuronosyltransferases (UGTs) are the primary phase II enzymes catalyzing the
conjugation of glucuronic acid to the xenobiotics with polar groups for facilitating their …
conjugation of glucuronic acid to the xenobiotics with polar groups for facilitating their …
Effects of perfluorooctane sulfonate on rat thyroid hormone biosynthesis and metabolism
WG Yu, W Liu, YH Jin - Environmental Toxicology and …, 2009 - Wiley Online Library
The potential toxicity of perfluorooctane sulfonate (PFOS), an environmentally persistent
organic pollutant, is of great concern. The present study examines the ability of PFOS to …
organic pollutant, is of great concern. The present study examines the ability of PFOS to …
A comprehensive untargeted metabonomic analysis of human steatotic liver tissue by RP and HILIC chromatography coupled to mass spectrometry reveals important …
JC García-Canaveras, MT Donato… - Journal of proteome …, 2011 - ACS Publications
Steatosis, or excessive accumulation of lipids in the liver, is a generally accepted previous
step to the development of more severe conditions like nonalcoholic steatohepatitis, fibrosis …
step to the development of more severe conditions like nonalcoholic steatohepatitis, fibrosis …
Signaling control of the constitutive androstane receptor (CAR)
H Yang, H Wang - Protein & cell, 2014 - academic.oup.com
The constitutive androstane receptor (CAR, NR1I3) plays a crucial role in the regulation of
drug metabolism, energy homeostasis, and cancer development through modulating the …
drug metabolism, energy homeostasis, and cancer development through modulating the …
Endocrine effects of hexabromocyclododecane (HBCD) in a one-generation reproduction study in Wistar rats
LTM van der Ven, T van de Kuil, PEG Leonards… - Toxicology letters, 2009 - Elsevier
The brominated flame retardant (BFR) hexabromocyclododecane was tested in a one-
generation reproduction assay in Wistar rats, enhanced for endocrine parameters. A solution …
generation reproduction assay in Wistar rats, enhanced for endocrine parameters. A solution …