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Abnormal Hepatic Iron Accumulation in LEC Rats
The LEC (Long‐Evans cinnamon) rat is a mutant strain displaying hereditary hepatitis and spontaneous hepatocellular carcinoma, and shows abnormal hepatic copper accumulation similar to that occurring in Wilson's disease. We evaluated the iron metabolism of LEC rats compared to LEA (Long‐Evans a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1993
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919139/ https://www.ncbi.nlm.nih.gov/pubmed/8387476 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02859.x |
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author | Kato, Junji Kohgo, Yutaka Sugawara, Naoki Katsuki, Shinichi Shintani, Naoaki Fujikawa, Kohshi Miyazaki, Etsu Kobune, Masayoshi Takeichi, Noritoshi Niitsu, Yoshiro |
author_facet | Kato, Junji Kohgo, Yutaka Sugawara, Naoki Katsuki, Shinichi Shintani, Naoaki Fujikawa, Kohshi Miyazaki, Etsu Kobune, Masayoshi Takeichi, Noritoshi Niitsu, Yoshiro |
author_sort | Kato, Junji |
collection | PubMed |
description | The LEC (Long‐Evans cinnamon) rat is a mutant strain displaying hereditary hepatitis and spontaneous hepatocellular carcinoma, and shows abnormal hepatic copper accumulation similar to that occurring in Wilson's disease. We evaluated the iron metabolism of LEC rats compared to LEA (Long‐Evans agouti) rats. Hepatic iron and ferritin concentrations were remarkably increased depending on age in LEC rats but not in LEA rats. Increased hepatic iron is normally associated with decreased serum transferrin and total iron binding capacity in hepatic iron overload. In LEC rats, however, both serum transferrin and total iron binding capacity increased with increasing hepatic iron. This increase of serum transferrin and hepatic iron may be an additional important factor contributing to liver injury in LEC rats. |
format | Online Article Text |
id | pubmed-5919139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59191392018-05-11 Abnormal Hepatic Iron Accumulation in LEC Rats Kato, Junji Kohgo, Yutaka Sugawara, Naoki Katsuki, Shinichi Shintani, Naoaki Fujikawa, Kohshi Miyazaki, Etsu Kobune, Masayoshi Takeichi, Noritoshi Niitsu, Yoshiro Jpn J Cancer Res Rapid Communication The LEC (Long‐Evans cinnamon) rat is a mutant strain displaying hereditary hepatitis and spontaneous hepatocellular carcinoma, and shows abnormal hepatic copper accumulation similar to that occurring in Wilson's disease. We evaluated the iron metabolism of LEC rats compared to LEA (Long‐Evans agouti) rats. Hepatic iron and ferritin concentrations were remarkably increased depending on age in LEC rats but not in LEA rats. Increased hepatic iron is normally associated with decreased serum transferrin and total iron binding capacity in hepatic iron overload. In LEC rats, however, both serum transferrin and total iron binding capacity increased with increasing hepatic iron. This increase of serum transferrin and hepatic iron may be an additional important factor contributing to liver injury in LEC rats. Blackwell Publishing Ltd 1993-03 /pmc/articles/PMC5919139/ /pubmed/8387476 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02859.x Text en |
spellingShingle | Rapid Communication Kato, Junji Kohgo, Yutaka Sugawara, Naoki Katsuki, Shinichi Shintani, Naoaki Fujikawa, Kohshi Miyazaki, Etsu Kobune, Masayoshi Takeichi, Noritoshi Niitsu, Yoshiro Abnormal Hepatic Iron Accumulation in LEC Rats |
title | Abnormal Hepatic Iron Accumulation in LEC Rats |
title_full | Abnormal Hepatic Iron Accumulation in LEC Rats |
title_fullStr | Abnormal Hepatic Iron Accumulation in LEC Rats |
title_full_unstemmed | Abnormal Hepatic Iron Accumulation in LEC Rats |
title_short | Abnormal Hepatic Iron Accumulation in LEC Rats |
title_sort | abnormal hepatic iron accumulation in lec rats |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919139/ https://www.ncbi.nlm.nih.gov/pubmed/8387476 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02859.x |
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