Cited by 37Aluminum toxicity and tolerance in plants and animalsHeavy Metal Exposure and ToxicityParathyroid Disorders and Treatments

The DOI matches its Crossref record.

Renal Handling of Aluminium

Shirley, D.G., Lote, C.J.·2005·Nephron Physiology

Abstract

Aluminium (Al) is absorbed from a variety of foodstuffs and medications. Its major route of elimination from the body is in the urine. However, current knowledge concerning its glomerular filtration and, more particularly, its reabsorption/secretion is fragmentary. Most (80-90%) of Al in the plasma is normally bound to protein (mainly transferrin) and is therefore unfilterable; the remainder is bound to low molecular mass compounds, of which citrate appears to be the most important. In vitro determinations using artificial membranes indicate that approximately 10% of Al is filtered at normal plasma concentrations. However, when plasma Al is raised experimentally, its filterability falls, unless the excess Al is complexed with citrate; the aluminium citrate complex appears to be freely filtered. Information on tubular Al reabsorption at normal plasma concentrations is inconsistent. Filtered Al appears to be at least partially reabsorbed, although the reabsorptive mechanisms remain speculative. A consensus is emerging that elevated plasma Al concentrations result in a fall in fractional Al reabsorption, and a recent micropuncture study indicates that under these circumstances the only significant site of Al reabsorption is the loop of Henle.

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Research works printed but not linked: 14

  1. 10.1034%2Fj.1600-0773.2001.d01-98.x · DOI
  2. 10.1016%2FS0009-9120%2898%2900028-9 · DOI
  3. 10.1016%2Fj.fct.2003.09.010 · DOI · Paper page
  4. 10.1177%2F096032719501400605 · DOI
  5. 10.1042%2FCS20040052 · DOI
  6. 10.1007%2FBF02917259 · DOI
  7. 10.1016%2F0002-9343%2892%2990742-T · DOI
  8. 10.1620%2Ftjem.196.139 · DOI
  9. 10.1016%2FS0300-483X%2898%2900037-7 · DOI
  10. 10.1074%2Fjbc.270.4.1843 · DOI
  11. 10.1093%2Fndt%2F13.suppl_3.98 · DOI
  12. 10.1038%2Fki.1987.264 · DOI
  13. 10.1016%2F0378-4274%2889%2990006-4 · DOI
  14. 10.1159%2F000185064 · DOI

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Metadata

Authors
Shirley, D. G., & Lote, C. J.
Affiliations
  • University College London (GB)
  • University of Birmingham (GB)
Venue
Nephron Physiology
Publisher
S. Karger AG
Published
2005-11-14
Volume
101
Issue
4
Pages
p99-p103
ISSN
1660-2137 (ISSN-L)
OpenAlex
W2127807040
Cited by
37
References
0
Citations by year
2025: 1 · 2024: 3 · 2023: 1 · 2022: 7 · 2021: 3 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 2
FWCI
1.20
Type
journal article
Language
en
Open access
closed
Locations
  • Nephron Physiology (publishedVersion)
  • PubMed (publishedVersion)
  • UCL Discovery (University College London) (submittedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Funders
  • Wellcome Trust
  • Fonds National de la Recherche Luxembourg
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Aluminum toxicity and tolerance in plants and animals
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
  • Health Sciences › Medicine › Nephrology › Parathyroid Disorders and Treatments
Keywords
aluminum, renal handling, glomerular filtration, tubular reabsorption, transferrin, citrate complexes, aluminum citrate, loop of Henle, micropuncture, aluminum toxicity
MeSH terms
Aluminum, Animals, Humans, Kidney

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