Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats

Detalhes bibliográficos
Autor(a) principal: Khalifa, Fares
Data de Publicação: 2016
Outros Autores: El-Halwagy, Manal E., Hussein, Rasha H.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Bioscience journal (Online)
Texto Completo: https://seer.ufu.br/index.php/biosciencejournal/article/view/29952
Resumo: Kidney plays a central role in maintaining the composition of body fluids by regulating water, NaCl, acid base, and solute reabsorption and excretion, respectively. The study was done to investigate the physiological role of thiamine in regulation of renal response to metabolic acidosis induced by NH4Cl in adult male rats. For this experiment, fifty rats were used. They were divided into five groups. Control rats received basal diet; rats fed on basal diet mixed with NH4Cl (4g NH4Cl/100g diet) to induce severe metabolic acidosis, rats fed on basal supplemented diet with thiamine (600 mg/kg diet), and rats fed on basal supplemented diet with thiamine before and after induction of metabolic acidosis by NH4Cl for 14 days. The results showed that the plasma levels of chloride, urea, and creatinine were significantly elevated in metabolic acidosis induced by NH4Cl. Thiamine supplementation at high dose before or after induction improved the chloride values. Feeding diets supplemented with thiamine modulated the plasma sodium and bicarbonate values. Supplementation with vitamin B1 as preventive agent significantly restored these changes to near control value and when used as curative agent improved plasma creatinine and urea levels. Urinary pH and potassium levels were decreased significantly in metabolic acidotic rats when compared to all experimental groups. Urinary ammonia and aldosterone levels were decreased by thiamine supplementation as protective agent. Supplementation with vitamin B1 as preventive and curative agents, restored the affected parameters and regulate the response of kidney to metabolic acidosis induced by ammonium chloride. 
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spelling Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats Renal ResponseThiamine SupplementationAmmonium ChlorideMetabolic AcidosisAnion GapHealth SciencesKidney plays a central role in maintaining the composition of body fluids by regulating water, NaCl, acid base, and solute reabsorption and excretion, respectively. The study was done to investigate the physiological role of thiamine in regulation of renal response to metabolic acidosis induced by NH4Cl in adult male rats. For this experiment, fifty rats were used. They were divided into five groups. Control rats received basal diet; rats fed on basal diet mixed with NH4Cl (4g NH4Cl/100g diet) to induce severe metabolic acidosis, rats fed on basal supplemented diet with thiamine (600 mg/kg diet), and rats fed on basal supplemented diet with thiamine before and after induction of metabolic acidosis by NH4Cl for 14 days. The results showed that the plasma levels of chloride, urea, and creatinine were significantly elevated in metabolic acidosis induced by NH4Cl. Thiamine supplementation at high dose before or after induction improved the chloride values. Feeding diets supplemented with thiamine modulated the plasma sodium and bicarbonate values. Supplementation with vitamin B1 as preventive agent significantly restored these changes to near control value and when used as curative agent improved plasma creatinine and urea levels. Urinary pH and potassium levels were decreased significantly in metabolic acidotic rats when compared to all experimental groups. Urinary ammonia and aldosterone levels were decreased by thiamine supplementation as protective agent. Supplementation with vitamin B1 as preventive and curative agents, restored the affected parameters and regulate the response of kidney to metabolic acidosis induced by ammonium chloride. EDUFU2016-04-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://seer.ufu.br/index.php/biosciencejournal/article/view/2995210.14393/BJ-v32n2a2016-29952Bioscience Journal ; Vol. 32 No. 2 (2016): Mar./Apr.; 543-549Bioscience Journal ; v. 32 n. 2 (2016): Mar./Apr.; 543-5491981-3163reponame:Bioscience journal (Online)instname:Universidade Federal de Uberlândia (UFU)instacron:UFUenghttps://seer.ufu.br/index.php/biosciencejournal/article/view/29952/18152Brazil; ContemporaryCopyright (c) 2016 Fares Khalifa, Manal E. El-Halwagy, Rasha H. Husseinhttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessKhalifa, FaresEl-Halwagy, Manal E.Hussein, Rasha H.2022-05-19T01:12:36Zoai:ojs.www.seer.ufu.br:article/29952Revistahttps://seer.ufu.br/index.php/biosciencejournalPUBhttps://seer.ufu.br/index.php/biosciencejournal/oaibiosciencej@ufu.br||1981-31631516-3725opendoar:2022-05-19T01:12:36Bioscience journal (Online) - Universidade Federal de Uberlândia (UFU)false
dc.title.none.fl_str_mv Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
title Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
spellingShingle Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
Khalifa, Fares
Renal Response
Thiamine Supplementation
Ammonium Chloride
Metabolic Acidosis
Anion Gap
Health Sciences
title_short Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
title_full Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
title_fullStr Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
title_full_unstemmed Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
title_sort Clinical role of dietary thiamine on regulation of renal response to metabolic acidosis in adult rats
author Khalifa, Fares
author_facet Khalifa, Fares
El-Halwagy, Manal E.
Hussein, Rasha H.
author_role author
author2 El-Halwagy, Manal E.
Hussein, Rasha H.
author2_role author
author
dc.contributor.author.fl_str_mv Khalifa, Fares
El-Halwagy, Manal E.
Hussein, Rasha H.
dc.subject.por.fl_str_mv Renal Response
Thiamine Supplementation
Ammonium Chloride
Metabolic Acidosis
Anion Gap
Health Sciences
topic Renal Response
Thiamine Supplementation
Ammonium Chloride
Metabolic Acidosis
Anion Gap
Health Sciences
description Kidney plays a central role in maintaining the composition of body fluids by regulating water, NaCl, acid base, and solute reabsorption and excretion, respectively. The study was done to investigate the physiological role of thiamine in regulation of renal response to metabolic acidosis induced by NH4Cl in adult male rats. For this experiment, fifty rats were used. They were divided into five groups. Control rats received basal diet; rats fed on basal diet mixed with NH4Cl (4g NH4Cl/100g diet) to induce severe metabolic acidosis, rats fed on basal supplemented diet with thiamine (600 mg/kg diet), and rats fed on basal supplemented diet with thiamine before and after induction of metabolic acidosis by NH4Cl for 14 days. The results showed that the plasma levels of chloride, urea, and creatinine were significantly elevated in metabolic acidosis induced by NH4Cl. Thiamine supplementation at high dose before or after induction improved the chloride values. Feeding diets supplemented with thiamine modulated the plasma sodium and bicarbonate values. Supplementation with vitamin B1 as preventive agent significantly restored these changes to near control value and when used as curative agent improved plasma creatinine and urea levels. Urinary pH and potassium levels were decreased significantly in metabolic acidotic rats when compared to all experimental groups. Urinary ammonia and aldosterone levels were decreased by thiamine supplementation as protective agent. Supplementation with vitamin B1 as preventive and curative agents, restored the affected parameters and regulate the response of kidney to metabolic acidosis induced by ammonium chloride. 
publishDate 2016
dc.date.none.fl_str_mv 2016-04-04
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://seer.ufu.br/index.php/biosciencejournal/article/view/29952
10.14393/BJ-v32n2a2016-29952
url https://seer.ufu.br/index.php/biosciencejournal/article/view/29952
identifier_str_mv 10.14393/BJ-v32n2a2016-29952
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://seer.ufu.br/index.php/biosciencejournal/article/view/29952/18152
dc.rights.driver.fl_str_mv Copyright (c) 2016 Fares Khalifa, Manal E. El-Halwagy, Rasha H. Hussein
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2016 Fares Khalifa, Manal E. El-Halwagy, Rasha H. Hussein
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv Brazil; Contemporary
dc.publisher.none.fl_str_mv EDUFU
publisher.none.fl_str_mv EDUFU
dc.source.none.fl_str_mv Bioscience Journal ; Vol. 32 No. 2 (2016): Mar./Apr.; 543-549
Bioscience Journal ; v. 32 n. 2 (2016): Mar./Apr.; 543-549
1981-3163
reponame:Bioscience journal (Online)
instname:Universidade Federal de Uberlândia (UFU)
instacron:UFU
instname_str Universidade Federal de Uberlândia (UFU)
instacron_str UFU
institution UFU
reponame_str Bioscience journal (Online)
collection Bioscience journal (Online)
repository.name.fl_str_mv Bioscience journal (Online) - Universidade Federal de Uberlândia (UFU)
repository.mail.fl_str_mv biosciencej@ufu.br||
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