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Experimental rat model for alcohol-induced osteonecrosis of the femoral head

Alcohol-induced osteonecrosis of the femoral head (ONFH) is observed in alcohol abusers and patients with alcoholic fatty liver disease. It has been reported that Toll-like receptor 4 (TLR4) signalling plays a crucial role in the pathogenesis of alcoholic fatty liver disease. We previously reported...

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Autores principales: Okazaki, Shunichiro, Nagoya, Satoshi, Tateda, Kenji, Katada, Ryuichi, Mizuo, Keisuke, Watanabe, Satoshi, Yamashita, Toshihiko, Matsumoto, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781777/
https://www.ncbi.nlm.nih.gov/pubmed/24020403
http://dx.doi.org/10.1111/iep.12035
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author Okazaki, Shunichiro
Nagoya, Satoshi
Tateda, Kenji
Katada, Ryuichi
Mizuo, Keisuke
Watanabe, Satoshi
Yamashita, Toshihiko
Matsumoto, Hiroshi
author_facet Okazaki, Shunichiro
Nagoya, Satoshi
Tateda, Kenji
Katada, Ryuichi
Mizuo, Keisuke
Watanabe, Satoshi
Yamashita, Toshihiko
Matsumoto, Hiroshi
author_sort Okazaki, Shunichiro
collection PubMed
description Alcohol-induced osteonecrosis of the femoral head (ONFH) is observed in alcohol abusers and patients with alcoholic fatty liver disease. It has been reported that Toll-like receptor 4 (TLR4) signalling plays a crucial role in the pathogenesis of alcoholic fatty liver disease. We previously reported a corticosteroid-induced ONFH rat model, and suggested that TLR4 signalling contributes to the pathogenesis of ONFH. Thus, it is thought that the pathogenesis of alcohol-induced ONFH is probably similar to that of corticosteroid-induced ONFH. The aim of this study was to develop a new animal model for alcohol-induced ONFH and to evaluate the relationship between the pro-inflammatory response via TLRs and the development of ONFH in rats. Male Wistar rats were fed a Lieber–DeCarli liquid diet containing 5% ethanol (experimental group) or dextran (control group) for 1–24 weeks. Histopathological and biochemical analyses were performed. Feeding the ethanol-containing liquid diet resulted in the development of ONFH with hepatic steatosis, hepatic dysfunction and hyperlipidaemia, whereas feeding the dextran-containing diet did not cause ONFH. However, we could not recognize any relationship between the pro-inflammatory response via TLR4 and the development of alcohol-induced ONFH. Thus in this study we have developed a new rat model for alcohol-induced ONFH based on the feeding of an ethanol liquid diet. ONFH was observed within seven days from the start of feeding with 5% ethanol-containing liquid diet. Although this was linked to hepatic steatosis, a TLR4 association was not a feature of this model.
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spelling pubmed-37817772013-10-04 Experimental rat model for alcohol-induced osteonecrosis of the femoral head Okazaki, Shunichiro Nagoya, Satoshi Tateda, Kenji Katada, Ryuichi Mizuo, Keisuke Watanabe, Satoshi Yamashita, Toshihiko Matsumoto, Hiroshi Int J Exp Pathol Original Articles Alcohol-induced osteonecrosis of the femoral head (ONFH) is observed in alcohol abusers and patients with alcoholic fatty liver disease. It has been reported that Toll-like receptor 4 (TLR4) signalling plays a crucial role in the pathogenesis of alcoholic fatty liver disease. We previously reported a corticosteroid-induced ONFH rat model, and suggested that TLR4 signalling contributes to the pathogenesis of ONFH. Thus, it is thought that the pathogenesis of alcohol-induced ONFH is probably similar to that of corticosteroid-induced ONFH. The aim of this study was to develop a new animal model for alcohol-induced ONFH and to evaluate the relationship between the pro-inflammatory response via TLRs and the development of ONFH in rats. Male Wistar rats were fed a Lieber–DeCarli liquid diet containing 5% ethanol (experimental group) or dextran (control group) for 1–24 weeks. Histopathological and biochemical analyses were performed. Feeding the ethanol-containing liquid diet resulted in the development of ONFH with hepatic steatosis, hepatic dysfunction and hyperlipidaemia, whereas feeding the dextran-containing diet did not cause ONFH. However, we could not recognize any relationship between the pro-inflammatory response via TLR4 and the development of alcohol-induced ONFH. Thus in this study we have developed a new rat model for alcohol-induced ONFH based on the feeding of an ethanol liquid diet. ONFH was observed within seven days from the start of feeding with 5% ethanol-containing liquid diet. Although this was linked to hepatic steatosis, a TLR4 association was not a feature of this model. Blackwell Publishing Ltd 2013-10 2013-09-10 /pmc/articles/PMC3781777/ /pubmed/24020403 http://dx.doi.org/10.1111/iep.12035 Text en © 2013 The Authors. International Journal of Experimental Pathology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Okazaki, Shunichiro
Nagoya, Satoshi
Tateda, Kenji
Katada, Ryuichi
Mizuo, Keisuke
Watanabe, Satoshi
Yamashita, Toshihiko
Matsumoto, Hiroshi
Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title_full Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title_fullStr Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title_full_unstemmed Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title_short Experimental rat model for alcohol-induced osteonecrosis of the femoral head
title_sort experimental rat model for alcohol-induced osteonecrosis of the femoral head
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781777/
https://www.ncbi.nlm.nih.gov/pubmed/24020403
http://dx.doi.org/10.1111/iep.12035
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