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Expression of drug transporters in human kidney: impact of sex, age, and ethnicity

BACKGROUND: Differences in expression of drug transporters in human kidney contribute to changes in pharmacokinetics and toxicokinetics of a variety of drug compounds. The basal expression levels of genes involved in drug transport processes in the kidney introduces differences in bioavailability, d...

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Autores principales: Joseph, Stancy, Nicolson, Tamara J, Hammons, George, Word, Beverly, Green-Knox, Bridgett, Lyn-Cook, Beverly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352278/
https://www.ncbi.nlm.nih.gov/pubmed/25750709
http://dx.doi.org/10.1186/s13293-015-0020-3
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author Joseph, Stancy
Nicolson, Tamara J
Hammons, George
Word, Beverly
Green-Knox, Bridgett
Lyn-Cook, Beverly
author_facet Joseph, Stancy
Nicolson, Tamara J
Hammons, George
Word, Beverly
Green-Knox, Bridgett
Lyn-Cook, Beverly
author_sort Joseph, Stancy
collection PubMed
description BACKGROUND: Differences in expression of drug transporters in human kidney contribute to changes in pharmacokinetics and toxicokinetics of a variety of drug compounds. The basal expression levels of genes involved in drug transport processes in the kidney introduces differences in bioavailability, distribution, and clearance of drugs, possibly influencing drug efficacy and adverse reactions. Sex differences in gene expression of transporters are a key cause of differences in sex-dependent pharmacokinetics, which may characterize many drugs and contribute to individual differences in drug efficacy and toxicity. Therefore, evaluating the expression of drug transporters in normal human kidneys is important to better understand differences in drug bioavailability, distribution, and clearance of drugs in humans. Other factors such as age and ethnicity may also contribute to individual differences in gene expression of drug transporters in the human kidney. METHODS: Quantitative real-time PCR (QRT-PCR) was performed to determine the gene expression of 30 drug transporters in 95 age-matched normal human kidney tissues. Multiple Student’s t-tests (Sidak-Bonferroni correction) and two-way ANOVA (Bonferroni correction) analyses were used to determine statistically significant differences. RESULTS: In the 30 transporter genes examined, sex, ethnicity, and age differences in gene expression were exhibited in normal human kidney tissue. These changes in expression were not found to be differentially significant. However, sex-age and sex-ethnicity interactions were found to be statistically significant. For sex-age interactions, SCL22A12 was found to be significantly higher expressed in females <50 years compared to males <50 years. Expression levels of SLC22A2, SLC22A12, SLC6A16, and ABCB6 were significantly higher in females <50 years compared to females ≥50 years. In sex-ethnicity interactions, expression levels of ATP7B and KCNJ8 were found to be significantly higher in African American females compared to European American females. Also, the expression of SLC31A2 was significantly higher in European American males compared to European American females. CONCLUSIONS: Sex, age, and ethnic differences impacted the expression of drug transporters in normal human kidneys, which suggests that the analysis of gene expression of drug transporters will aid in improving the usage/dosage of drug therapies influencing personalized medicine and susceptibility to adverse drug reactions.
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spelling pubmed-43522782015-03-08 Expression of drug transporters in human kidney: impact of sex, age, and ethnicity Joseph, Stancy Nicolson, Tamara J Hammons, George Word, Beverly Green-Knox, Bridgett Lyn-Cook, Beverly Biol Sex Differ Research BACKGROUND: Differences in expression of drug transporters in human kidney contribute to changes in pharmacokinetics and toxicokinetics of a variety of drug compounds. The basal expression levels of genes involved in drug transport processes in the kidney introduces differences in bioavailability, distribution, and clearance of drugs, possibly influencing drug efficacy and adverse reactions. Sex differences in gene expression of transporters are a key cause of differences in sex-dependent pharmacokinetics, which may characterize many drugs and contribute to individual differences in drug efficacy and toxicity. Therefore, evaluating the expression of drug transporters in normal human kidneys is important to better understand differences in drug bioavailability, distribution, and clearance of drugs in humans. Other factors such as age and ethnicity may also contribute to individual differences in gene expression of drug transporters in the human kidney. METHODS: Quantitative real-time PCR (QRT-PCR) was performed to determine the gene expression of 30 drug transporters in 95 age-matched normal human kidney tissues. Multiple Student’s t-tests (Sidak-Bonferroni correction) and two-way ANOVA (Bonferroni correction) analyses were used to determine statistically significant differences. RESULTS: In the 30 transporter genes examined, sex, ethnicity, and age differences in gene expression were exhibited in normal human kidney tissue. These changes in expression were not found to be differentially significant. However, sex-age and sex-ethnicity interactions were found to be statistically significant. For sex-age interactions, SCL22A12 was found to be significantly higher expressed in females <50 years compared to males <50 years. Expression levels of SLC22A2, SLC22A12, SLC6A16, and ABCB6 were significantly higher in females <50 years compared to females ≥50 years. In sex-ethnicity interactions, expression levels of ATP7B and KCNJ8 were found to be significantly higher in African American females compared to European American females. Also, the expression of SLC31A2 was significantly higher in European American males compared to European American females. CONCLUSIONS: Sex, age, and ethnic differences impacted the expression of drug transporters in normal human kidneys, which suggests that the analysis of gene expression of drug transporters will aid in improving the usage/dosage of drug therapies influencing personalized medicine and susceptibility to adverse drug reactions. BioMed Central 2015-03-02 /pmc/articles/PMC4352278/ /pubmed/25750709 http://dx.doi.org/10.1186/s13293-015-0020-3 Text en © Joseph et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Joseph, Stancy
Nicolson, Tamara J
Hammons, George
Word, Beverly
Green-Knox, Bridgett
Lyn-Cook, Beverly
Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title_full Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title_fullStr Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title_full_unstemmed Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title_short Expression of drug transporters in human kidney: impact of sex, age, and ethnicity
title_sort expression of drug transporters in human kidney: impact of sex, age, and ethnicity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352278/
https://www.ncbi.nlm.nih.gov/pubmed/25750709
http://dx.doi.org/10.1186/s13293-015-0020-3
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