Results 91 to 100 of about 5,995 (180)
Rifampicin is a prototypical clinical inducer used in drug–drug interaction (DDI) studies. However, the clinical relevance and predictability of rifampicin‐mediated hepatic transporter induction remain poorly defined. Conventional hepatocyte culture models fail to capture clinically relevant regulation of transporters and drug‐metabolizing enzymes ...
Mattie E. Hartauer +9 more
wiley +1 more source
Hydralazine is widely used to treat hypertension during pregnancy and has epigenetic effects in cancer therapy. Cryoplatable human hepatocytes showed concentration-dependent increase in DNA damage response (linear trend p = 0.0069) following 24 h ...
Mariam R. Habil +7 more
doaj +1 more source
Advances in New Approach Methodologies at FDA's Division of Applied Regulatory Science
New Approach Methodologies (NAMs) represent a paradigm shift in drug development and regulatory science, offering human‐relevant alternatives to traditional preclinical models. This mini‐review highlights recent advances in NAM development, validation, and regulatory application from FDA's Division of Applied Regulatory Science (DARS).
Ksenia Blinova +9 more
wiley +1 more source
CYP1A2 polymorphism does not modulate caffeine's effects on sprint performance or its metabolites during a soccer match simulation [PDF]
The effectiveness of caffeine supplementation on exercise performance varies between individuals. Cytochrome P450 1A2 (CYP1A2) is an important enzyme that controls the primary catabolism of caffeine to paraxanthine, theobromine and theophylline, which ...
C.K. Chan +10 more
core +1 more source
ABSTRACT Epilepsy is the most disabling neurological disease that affects all economic classes, age groups, regions, and races. Although many antiseizure drugs are approved for epilepsy treatment, they fail to work in about 30%–40% of patients. Thus, there is a great need to identify better pharmacological agents to treat epilepsy.
Janakiraman Pillai Udaiyappan +3 more
wiley +1 more source
Effects of tropoxine on activity of isoforms CYP2С9 and CYP2С9 of cytochrome P450 using marker drugs losartane and caffeine were studied. Tropoxine in the effective dose (30 mg/kg) after 4-days intraperitoneal administration (3 times per day) in rats did
V. P. Zherdev +5 more
doaj
Previous reports showed that CYP1A2 and CYP2B4 can affect each other’s activity when present in the same vesicles with subsaturating NADPH‐P450 reductase (CPR). Specifically, systems containing both P450s exhibited increased CYP1A2 and decreased CYP2B4 activities when compared with those containing each P450 alone.
John Connick, James Reed, Wayne Backes
openaire +1 more source
Schematic representation of STE (smokeless tobacco extract) impact on AhR and AhR‐related genes. TSNAs present in STE induce AhR that results in to AhR conformational changes and translocation to the nucleus. Inside the nucleus, AhR heterodimerizes with Arnt and binds to XRE region of genome.
Mohammad Sajid +5 more
wiley +1 more source
Aim: to investigate the potential influence of CYP1A2 polymorphisms on olanzapine plasma concentration of inpatients with schizophrenia in real-life settings.
Yan Zhang, Lisha Sun, Yanli Su, Hui Wang
doaj +1 more source
INDUCTION OF CYP1A2 WITH AROMATIC AMINES
Male F344 rats were treated with a chemical (aniline, nitrobenzene, 2-methoxy-p-phenylenediamine, 2-methoxy-4-nitroaniline or 2-methoxy-4-nitroazobenzene) produced by the azo-reduction and/or N-oxidation of 2-methoxy-4-aminoazobenzene, a selective inducer of CYP1A2, and effects of their chemicals on CYP1A induction in the liver were examined at the ...
DEGAWA, Masakuni +4 more
openaire +2 more sources

