Aluminium accumulation in chronic renal failure affects erythropoises

Aluminium (Al) toxicity has been associated with anaemia in exposed patients with chronic renal failure (CRF). The present study was undertaken to determine whether the ingestion of Al citrate was able to affect erythropoiesis in rats with normal or impaired renal function. The renal insufficiency w...

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Autores principales: Nesse, Alcira Beatriz, Garbosa, Graciela, Stripeikis, Jorge Daniel, Gálvez, Gladys Alicia, Lauricella, Ana María
Publicado: 1997
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13205358_v3_n4_p347_Nesse
http://hdl.handle.net/20.500.12110/paper_13205358_v3_n4_p347_Nesse
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spelling paper:paper_13205358_v3_n4_p347_Nesse2023-06-08T16:10:22Z Aluminium accumulation in chronic renal failure affects erythropoises Nesse, Alcira Beatriz Garbosa, Graciela Stripeikis, Jorge Daniel Gálvez, Gladys Alicia Lauricella, Ana María Aluminium and erythropoiesis Aluminum Aluminum toxicity Chronic renal failure aluminum citrate animal experiment animal model animal tissue article bone brain chronic kidney failure controlled study erythropoiesis kidney liver male nonhuman priority journal rat serum tissue distribution toxicity testing Aluminium (Al) toxicity has been associated with anaemia in exposed patients with chronic renal failure (CRF). The present study was undertaken to determine whether the ingestion of Al citrate was able to affect erythropoiesis in rats with normal or impaired renal function. The renal insufficiency was induced by surgical procedures and control rats were sham operated. Twenty-four rats were allocated to four groups of six rats each: (A) Sham; (B) Sham+Al; (C) CRF; and (D) CRF+Al. The groups B and D received daily doses of Al citrate (0.5 μmol/g bodyweight) and the groups A and C, deionized water, via the intragastric route. At the end of the experimental period (15 weeks) cultures of late erythroid progenitor cells (CFU-E) stimulated with erythropoietin were performed and haematological parameters determined. The liver, kidney, brain, bone and serum Al amounts were quantified. The results are expressed as median and interquartile range. The CFU-E growth was found inhibited in B and D groups (A: 100; B: 74/54-83; C: 86/54-98; D: 46/39-53 %). The haematocrit values were significantly diminished in rats with renal insufficiency when compared to controls (A: 42/40-43; B: 45/42-46; C: 37/32-40 and D: 37/24-39 %). Serum Al accumulation was observed in B and D groups receiving Al (A: 8/5-12; B: 36/36-44; C: 5/5- 6; D: 45126-132 μg Al]l). No differences among groups were found in the liver and kidney Al contents, but uraemic state favoured Al accumulation in brain (A: 6/5.0-9.0; B: 4/3.8-4.3; C: 2/2.0-3.0; D: 15/12.0-21.0 μg Al/g tissue) and bone (A: 29/27-31; B: 30/29-39; C: 42/33-48; D: 68/56-79 μg Al/g tissue). We suggest that the heavy accumulation of Al in the bone compartment may result in a protracted endogenous exposure of bone marrow cells, affecting the erythropoiesis in vive. Fil:Nesse, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Garbossa, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Stripeikis, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gálvez, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Lauricella, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13205358_v3_n4_p347_Nesse http://hdl.handle.net/20.500.12110/paper_13205358_v3_n4_p347_Nesse
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Aluminium and erythropoiesis
Aluminum
Aluminum toxicity
Chronic renal failure
aluminum citrate
animal experiment
animal model
animal tissue
article
bone
brain
chronic kidney failure
controlled study
erythropoiesis
kidney
liver
male
nonhuman
priority journal
rat
serum
tissue distribution
toxicity testing
spellingShingle Aluminium and erythropoiesis
Aluminum
Aluminum toxicity
Chronic renal failure
aluminum citrate
animal experiment
animal model
animal tissue
article
bone
brain
chronic kidney failure
controlled study
erythropoiesis
kidney
liver
male
nonhuman
priority journal
rat
serum
tissue distribution
toxicity testing
Nesse, Alcira Beatriz
Garbosa, Graciela
Stripeikis, Jorge Daniel
Gálvez, Gladys Alicia
Lauricella, Ana María
Aluminium accumulation in chronic renal failure affects erythropoises
topic_facet Aluminium and erythropoiesis
Aluminum
Aluminum toxicity
Chronic renal failure
aluminum citrate
animal experiment
animal model
animal tissue
article
bone
brain
chronic kidney failure
controlled study
erythropoiesis
kidney
liver
male
nonhuman
priority journal
rat
serum
tissue distribution
toxicity testing
description Aluminium (Al) toxicity has been associated with anaemia in exposed patients with chronic renal failure (CRF). The present study was undertaken to determine whether the ingestion of Al citrate was able to affect erythropoiesis in rats with normal or impaired renal function. The renal insufficiency was induced by surgical procedures and control rats were sham operated. Twenty-four rats were allocated to four groups of six rats each: (A) Sham; (B) Sham+Al; (C) CRF; and (D) CRF+Al. The groups B and D received daily doses of Al citrate (0.5 μmol/g bodyweight) and the groups A and C, deionized water, via the intragastric route. At the end of the experimental period (15 weeks) cultures of late erythroid progenitor cells (CFU-E) stimulated with erythropoietin were performed and haematological parameters determined. The liver, kidney, brain, bone and serum Al amounts were quantified. The results are expressed as median and interquartile range. The CFU-E growth was found inhibited in B and D groups (A: 100; B: 74/54-83; C: 86/54-98; D: 46/39-53 %). The haematocrit values were significantly diminished in rats with renal insufficiency when compared to controls (A: 42/40-43; B: 45/42-46; C: 37/32-40 and D: 37/24-39 %). Serum Al accumulation was observed in B and D groups receiving Al (A: 8/5-12; B: 36/36-44; C: 5/5- 6; D: 45126-132 μg Al]l). No differences among groups were found in the liver and kidney Al contents, but uraemic state favoured Al accumulation in brain (A: 6/5.0-9.0; B: 4/3.8-4.3; C: 2/2.0-3.0; D: 15/12.0-21.0 μg Al/g tissue) and bone (A: 29/27-31; B: 30/29-39; C: 42/33-48; D: 68/56-79 μg Al/g tissue). We suggest that the heavy accumulation of Al in the bone compartment may result in a protracted endogenous exposure of bone marrow cells, affecting the erythropoiesis in vive.
author Nesse, Alcira Beatriz
Garbosa, Graciela
Stripeikis, Jorge Daniel
Gálvez, Gladys Alicia
Lauricella, Ana María
author_facet Nesse, Alcira Beatriz
Garbosa, Graciela
Stripeikis, Jorge Daniel
Gálvez, Gladys Alicia
Lauricella, Ana María
author_sort Nesse, Alcira Beatriz
title Aluminium accumulation in chronic renal failure affects erythropoises
title_short Aluminium accumulation in chronic renal failure affects erythropoises
title_full Aluminium accumulation in chronic renal failure affects erythropoises
title_fullStr Aluminium accumulation in chronic renal failure affects erythropoises
title_full_unstemmed Aluminium accumulation in chronic renal failure affects erythropoises
title_sort aluminium accumulation in chronic renal failure affects erythropoises
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13205358_v3_n4_p347_Nesse
http://hdl.handle.net/20.500.12110/paper_13205358_v3_n4_p347_Nesse
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AT garbosagraciela aluminiumaccumulationinchronicrenalfailureaffectserythropoises
AT stripeikisjorgedaniel aluminiumaccumulationinchronicrenalfailureaffectserythropoises
AT galvezgladysalicia aluminiumaccumulationinchronicrenalfailureaffectserythropoises
AT lauricellaanamaria aluminiumaccumulationinchronicrenalfailureaffectserythropoises
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