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Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease

Chronic kidney disease (CKD) is a major public health problem, since 300,000,000 people in the world display a glomerular filtration rate (GFR) below 60 mL/min/1.73m(2). Patients with CKD have high rates of complications and comorbidities. Thus, they require the prescription of numerous medications,...

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Autores principales: Santana Machado, Tacy, Cerini, Claire, Burtey, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521271/
https://www.ncbi.nlm.nih.gov/pubmed/30959953
http://dx.doi.org/10.3390/toxins11040209
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author Santana Machado, Tacy
Cerini, Claire
Burtey, Stéphane
author_facet Santana Machado, Tacy
Cerini, Claire
Burtey, Stéphane
author_sort Santana Machado, Tacy
collection PubMed
description Chronic kidney disease (CKD) is a major public health problem, since 300,000,000 people in the world display a glomerular filtration rate (GFR) below 60 mL/min/1.73m(2). Patients with CKD have high rates of complications and comorbidities. Thus, they require the prescription of numerous medications, making the management of patients very complex. The prescription of numerous drugs associated with an altered renal- and non-renal clearance makes dose adjustment challenging in these patients, with frequent drug-related adverse events. However, the mechanisms involved in this abnormal drug clearance during CKD are not still well identified. We propose here that the transcription factor, aryl hydrocarbon receptor, which is the cellular receptor for indolic uremic toxins, could worsen the metabolism and the excretion of drugs in CKD patients.
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spelling pubmed-65212712019-05-31 Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease Santana Machado, Tacy Cerini, Claire Burtey, Stéphane Toxins (Basel) Review Chronic kidney disease (CKD) is a major public health problem, since 300,000,000 people in the world display a glomerular filtration rate (GFR) below 60 mL/min/1.73m(2). Patients with CKD have high rates of complications and comorbidities. Thus, they require the prescription of numerous medications, making the management of patients very complex. The prescription of numerous drugs associated with an altered renal- and non-renal clearance makes dose adjustment challenging in these patients, with frequent drug-related adverse events. However, the mechanisms involved in this abnormal drug clearance during CKD are not still well identified. We propose here that the transcription factor, aryl hydrocarbon receptor, which is the cellular receptor for indolic uremic toxins, could worsen the metabolism and the excretion of drugs in CKD patients. MDPI 2019-04-07 /pmc/articles/PMC6521271/ /pubmed/30959953 http://dx.doi.org/10.3390/toxins11040209 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Santana Machado, Tacy
Cerini, Claire
Burtey, Stéphane
Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title_full Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title_fullStr Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title_full_unstemmed Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title_short Emerging Roles of Aryl Hydrocarbon Receptors in the Altered Clearance of Drugs during Chronic Kidney Disease
title_sort emerging roles of aryl hydrocarbon receptors in the altered clearance of drugs during chronic kidney disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521271/
https://www.ncbi.nlm.nih.gov/pubmed/30959953
http://dx.doi.org/10.3390/toxins11040209
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