Results 101 to 110 of about 6,716 (130)
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The Journal of Pharmacology and Experimental Therapeutics, 2009
Pharmacotherapy of central nervous system (CNS) disorders is impaired by the drug efflux transporter, P-glycoprotein, which limits drug penetration across the blood-brain barrier into the CNS. One strategy to increase brain drug levels is to modulate P-glycoprotein regulation.
Melanie, Ott +2 more
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Pharmacotherapy of central nervous system (CNS) disorders is impaired by the drug efflux transporter, P-glycoprotein, which limits drug penetration across the blood-brain barrier into the CNS. One strategy to increase brain drug levels is to modulate P-glycoprotein regulation.
Melanie, Ott +2 more
openaire +2 more sources
[Role of pregnane X receptor (PXR) in endobiotic metabolism].
Sheng li xue bao : [Acta physiologica Sinica], 2019As a member of the nuclear receptor superfamily, the pregnane X receptor (PXR) is a ligand-activated transcription factor. PXR is highly expressed in liver and intestinal tissues, and also found in other tissues and organs, such as stomach and kidney. After heterodimerization with retinoid X receptor (RXR), PXR recruits numerous co-activating factors ...
Zhi-Lin, Luan +3 more
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Interleukin (IL)‐6 downregulates expression of the pregnane X receptor (PXR) in mice
Clinical Pharmacology & Therapeutics, 2003Clinical Pharmacology & Therapeutics (2003) 73, P60–P60; doi:
G. Hartmann +2 more
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Drug Metabolism Reviews, 2006
Constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are members of the nuclear receptor superfamily. These transcription factors are predominantly expressed in the liver, where they are activated by structurally diverse compounds, including many drugs and endogenous substances.
Thomas K H, Chang, David J, Waxman
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Constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are members of the nuclear receptor superfamily. These transcription factors are predominantly expressed in the liver, where they are activated by structurally diverse compounds, including many drugs and endogenous substances.
Thomas K H, Chang, David J, Waxman
openaire +2 more sources
Species differences in the induction and activation of the pregnane X receptor (PXR)
Toxicology, 2006The pregnane X receptor (PXR) is regarded as the master regulator of the mammalian xenobiotic response. It has evolved the ability to respond to a variety of chemically unrelated endogenous and exogenous compounds, and regulate a large repertoire of genes involved in their uptake, metabolism and excretion, such as the cytochrome P450 (CYP) 3A gene ...
Anthony J. Zucker +4 more
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Evaluation of pregnane X receptor (PXR)-mediated CYP3A4 drug-drug interactions in drug development
Drug Metabolism Reviews, 2013The increased capacity to rapidly eliminate drugs can have a profound effect on the efficacious exposure of coadministered drugs, especially in today's medical world of polypharmacy. There are numerous drug-drug interactions (DDIs) related to a loss of therapeutic efficacy and many of these are caused by pregnane X receptor (PXR)-mediated ...
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Current treatment and recent progress in gastric cancer
Ca-A Cancer Journal for Clinicians, 2021Smita S Joshi, Brian D Badgwell
exaly

