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Adult renal function is modified by perinatal taurine status in conscious male rats

Perinatal taurine exposure influences renal function in adult female offspring. This study tests the hypothesis that prenatal rather than postnatal taurine exposure alters renal function in adult conscious male rats. Female Sprague Dawley rats were fed normal rat chow and tap water alone (Control),...

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Autores principales: Roysommuti, Sanya, Malila, Pisamai, Jirakulsomchok, Dusit, Wyss, J Michael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994393/
https://www.ncbi.nlm.nih.gov/pubmed/20804607
http://dx.doi.org/10.1186/1423-0127-17-S1-S31
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author Roysommuti, Sanya
Malila, Pisamai
Jirakulsomchok, Dusit
Wyss, J Michael
author_facet Roysommuti, Sanya
Malila, Pisamai
Jirakulsomchok, Dusit
Wyss, J Michael
author_sort Roysommuti, Sanya
collection PubMed
description Perinatal taurine exposure influences renal function in adult female offspring. This study tests the hypothesis that prenatal rather than postnatal taurine exposure alters renal function in adult conscious male rats. Female Sprague Dawley rats were fed normal rat chow and tap water alone (Control), tap water containing 3% β-alanine (taurine depletion, TD) or tap water containing 3% taurine (taurine supplementation, TS) either from conception until delivery (fetal period; TDF or TSF) or from delivery until weaning (lactation period; TDL or TSL). After weaning, male offspring were fed with the normal rat chow and tap water ad libitum. At 7-8 weeks of age, renal function was studied in conscious, restrained rats. Mean arterial pressures were slightly higher in rats receiving taurine supplementation during either the fetal or lactation periods (compared to Control and TD groups), but heart rates were not significantly different among groups. Effective renal blood flows were lower in TDF, TDL, and TSF rats (TDF 4.6±0.8 ml/min/g kidney weight (KW), TDL 3.0±0.9 ml/min/g KW, and TSF 2.8±0.7 ml/min/g KW) than in TSL (7.7±0.9 ml/min/g KW) or Control rats (7.3±1.6 ml/min/g KW). These differences were correlated with significant increases in renal vascular resistance in TDF, TDL, and TSF groups compared to TSL and Control rats. In contrast, glomerular filtration rates were not significantly different among groups. Although basal water and sodium excretion were slightly lower in TDL and TSF rats compared to other groups, their diuretic and natriuretic responses to an acute saline load were not different from Control. The present data indicate that in adult male rats, both perinatal supplementation and depletion of taurine can alter renal hemodynamics, and these effects are differentially time-dependent.
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spelling pubmed-29943932010-12-01 Adult renal function is modified by perinatal taurine status in conscious male rats Roysommuti, Sanya Malila, Pisamai Jirakulsomchok, Dusit Wyss, J Michael J Biomed Sci Review Perinatal taurine exposure influences renal function in adult female offspring. This study tests the hypothesis that prenatal rather than postnatal taurine exposure alters renal function in adult conscious male rats. Female Sprague Dawley rats were fed normal rat chow and tap water alone (Control), tap water containing 3% β-alanine (taurine depletion, TD) or tap water containing 3% taurine (taurine supplementation, TS) either from conception until delivery (fetal period; TDF or TSF) or from delivery until weaning (lactation period; TDL or TSL). After weaning, male offspring were fed with the normal rat chow and tap water ad libitum. At 7-8 weeks of age, renal function was studied in conscious, restrained rats. Mean arterial pressures were slightly higher in rats receiving taurine supplementation during either the fetal or lactation periods (compared to Control and TD groups), but heart rates were not significantly different among groups. Effective renal blood flows were lower in TDF, TDL, and TSF rats (TDF 4.6±0.8 ml/min/g kidney weight (KW), TDL 3.0±0.9 ml/min/g KW, and TSF 2.8±0.7 ml/min/g KW) than in TSL (7.7±0.9 ml/min/g KW) or Control rats (7.3±1.6 ml/min/g KW). These differences were correlated with significant increases in renal vascular resistance in TDF, TDL, and TSF groups compared to TSL and Control rats. In contrast, glomerular filtration rates were not significantly different among groups. Although basal water and sodium excretion were slightly lower in TDL and TSF rats compared to other groups, their diuretic and natriuretic responses to an acute saline load were not different from Control. The present data indicate that in adult male rats, both perinatal supplementation and depletion of taurine can alter renal hemodynamics, and these effects are differentially time-dependent. BioMed Central 2010-08-24 /pmc/articles/PMC2994393/ /pubmed/20804607 http://dx.doi.org/10.1186/1423-0127-17-S1-S31 Text en Copyright ©2010 Roysommuti et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Roysommuti, Sanya
Malila, Pisamai
Jirakulsomchok, Dusit
Wyss, J Michael
Adult renal function is modified by perinatal taurine status in conscious male rats
title Adult renal function is modified by perinatal taurine status in conscious male rats
title_full Adult renal function is modified by perinatal taurine status in conscious male rats
title_fullStr Adult renal function is modified by perinatal taurine status in conscious male rats
title_full_unstemmed Adult renal function is modified by perinatal taurine status in conscious male rats
title_short Adult renal function is modified by perinatal taurine status in conscious male rats
title_sort adult renal function is modified by perinatal taurine status in conscious male rats
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994393/
https://www.ncbi.nlm.nih.gov/pubmed/20804607
http://dx.doi.org/10.1186/1423-0127-17-S1-S31
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