Literature DB >> 27312874

Pathophysiological implications of neurovascular P450 in brain disorders.

Chaitali Ghosh1, Mohammed Hossain2, Jesal Solanki3, Aaron Dadas3, Nicola Marchi4, Damir Janigro5.   

Abstract

Over the past decades, the significance of cytochrome P450 (CYP) enzymes has expanded beyond their role as peripheral drug metabolizers in the liver and gut. CYP enzymes are also functionally active at the neurovascular interface. CYP expression is modulated by disease states, impacting cellular functions, detoxification, and reactivity to toxic stimuli and brain drug biotransformation. Unveiling the physiological and molecular complexity of brain P450 enzymes will improve our understanding of the mechanisms underlying brain drug availability, pharmacological efficacy, and neurotoxic adverse effects from pharmacotherapy targeting brain disorders.
Copyright © 2016 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Year:  2016        PMID: 27312874      PMCID: PMC5067181          DOI: 10.1016/j.drudis.2016.06.004

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  121 in total

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Journal:  Biochem Pharmacol       Date:  1999-08-01       Impact factor: 5.858

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Journal:  Pharmacol Rev       Date:  2014-10       Impact factor: 25.468

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4.  Overexpression of pregnane X and glucocorticoid receptors and the regulation of cytochrome P450 in human epileptic brain endothelial cells.

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5.  Oxidative Stress and Apoptosis in Benzo[a]pyrene-Induced Neural Tube Defects.

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6.  Modulation of glucocorticoid receptor in human epileptic endothelial cells impacts drug biotransformation in an in vitro blood-brain barrier model.

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10.  Development of a human in vitro blood-brain tumor barrier model of diffuse intrinsic pontine glioma to better understand the chemoresistance.

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