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Morphologic and functional alterations of erythroid cells induced by long-term ingestion of aluminium
Abstract
Anaemia has been associated with aluminium (Al) accumulation in plasma and/or bone tissue in patients with chronic renal insufficiency. Nevertheless, in previous works, we have found shortened red-cell life span, increased osmotic resistance and inhibition of colony-forming units-erythroid (CFU-E) development in Al-overloaded rats with normal renal function. To elucidate further the action of Al on in vivo erythropoiesis, aluminium citrate was provided to Sprague Dawley rats (n = 18) in the drinking water for 8 months. Significant decreases in haematocrit (38.8 +/- 4.29 versus 43.1 +/- 3.58%, p < 0.05) and blood haemoglobin concentration (137 +/- 10.1 versus 148 +/- 8.5 g/l, p < 0.05), reticulocytosis (1.8/1.3-4.2 versus 1.2/0.4-3.7%, p < 0.05), and severe inhibition of CFU-E growth (670/120-950 versus 1530/810-2440 CFU-E/2 x 10(5) cells, p < 0.005) were found. Anysocytosis, poikilocytosis and schistocytosis were detected in peripheral blood stained films. Scanning electron microscopy revealed the presence of erythrocytes with abnormal shape, including crenated and target cells. Aluminium was localised specially inside the schistocytes by EDAX analysis. Decreased haptoglobin concentration (107/83-127 versus 139/89-169 mg/l, p < 0.05) supports the assumption of haemolytic nature of the anaemia. Rats were not iron depleted, as plasma iron concentration and total iron binding capacity were found in the range of control values, and sideroblasts and haemosiderin deposits were observed in bone marrow smears. Total 59Fe uptake and 59Fe incorporated to haem by the bone marrow cells were found decreased. In conclusion, the erythropoiesis impairment induced by Al may be a combined effect of direct action on circulating erythrocytes and interference with the cellular iron metabolism in erythroid progenitors.
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After long-term oral intake of Al, schistocytes and target cells were observed in stained peripheral blood of rats.
“After long-term oral intake of Al, schistocytes and target cells were observed in stained peripheral blood of rats (Vittori et al., 1999).”
From Aluminium toxicosis: a review of toxic actions and effects (2019) · cites this paper as Vittori et al., 1999
Al exposure has been associated with significant inhibition of colony forming units-erythroid (CFU-E) development in the bone marrow of mice and rats exposed to Al.
“Al exposure has been associated with significant inhibition of colony forming units-erythroid (CFU-E) development in the bone marrow of mice exposed to 13 mg Al/kg as Al citrate or chloride administered via gavage for 5 days/week for 22 weeks (Garbossa et al., 1996), rats exposed to 27 mg Al/kg as Al citrate administered via gavage 5 days/week for 15 weeks (Garbossa et al., 1998), and rats exposed”
From Aluminium toxicosis: a review of toxic actions and effects (2019) · cites this paper as Vittori et al., 1999
Significant decreases in hemoglobin, hematocrit and erythrocyte osmotic fragility were reported after Al exposure.
“Significant decreases in hemoglobin, hematocrit (packed cell volume) and erythrocyte osmotic fragility were reported after Al exposure (Garbossa et al., 1996; Garbossa et al., 1998; Vittori et al., 1999; Farina et al., 2005).”
From Aluminium toxicosis: a review of toxic actions and effects (2019) · cites this paper as Vittori et al., 1999
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Metadata
- Authors
- Vittori, D., Nesse, A., Pérez, G., & Garbossa, G.
- Affiliations
- Universidad de Buenos Aires (AR)
- Corresponding author
- Garbossa, Graciela
- ORCID
- Vittori, Daniela
- Venue
- Journal of Inorganic Biochemistry
- Publisher
- Elsevier BV
- Published
- 1999-08
- Volume
- 76
- Issue
- 2
- Pages
- 113-120
- ISSN
- 0162-0134 (ISSN-L)
- OpenAlex
- W2026890404
- Cited by
- 66
- References
- 26
- Citations by year
- 2024: 1 · 2022: 1 · 2020: 2 · 2019: 3 · 2017: 2 · 2016: 1 · 2015: 2 · 2014: 1 · 2013: 9 · 2012: 6
- FWCI
- 3.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Inorganic Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Manchester
- Universidad de Buenos Aires
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Aluminum toxicity and tolerance in plants and animals
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
- Keywords
- aluminum toxicity, erythropoiesis, erythroid progenitor cells, CFU-E, anemia, hemolysis, reticulocytosis, schistocytes, haptoglobin, iron metabolism, sideroblasts, hemosiderin, erythrocyte morphology, aluminum citrate, chronic renal insufficiency, bone marrow
- MeSH terms
- Aluminum, Animals, Biological Availability, Bone Marrow Cells, Erythrocyte Deformability, Erythrocytes, Female, Hemolysis, Iron, Microscopy, Electron, Scanning, Rats, Sprague-Dawley, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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