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Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.

To investigate the pathologic change of gallbladder mucosa related to gallstone formation, 52 mice were fed a lithogenic diet containing 1% cholesterol and 0.5% cholic acid and we evaluated the sequential morphologic changes in the gallbladder from two days to 40 weeks. Cholesterol gallstones began...

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Detalles Bibliográficos
Autores principales: Chang, H. J., Suh, J. I., Kwon, S. Y.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054388/
https://www.ncbi.nlm.nih.gov/pubmed/10402171
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author Chang, H. J.
Suh, J. I.
Kwon, S. Y.
author_facet Chang, H. J.
Suh, J. I.
Kwon, S. Y.
author_sort Chang, H. J.
collection PubMed
description To investigate the pathologic change of gallbladder mucosa related to gallstone formation, 52 mice were fed a lithogenic diet containing 1% cholesterol and 0.5% cholic acid and we evaluated the sequential morphologic changes in the gallbladder from two days to 40 weeks. Cholesterol gallstones began to appear after two weeks and all the mice had gallstones after eight weeks. At two days, the mitotic index was at its highest. The gallbladder mucosa showed progressive hyperplastic change with earlier papillary projection of the folds and later inward proliferation. At the same time of stone formation, mucous cells forming glands appeared. Their histochemical profile of mucin was different from that of normal epithelium. Numbers of mucous cells increased gradually until 24 weeks but slightly decreased afterward. These results suggest hyperplasia and metaplasia are closely related to the gallstone formation. Hyperplasia is probably reactive to irritating effect of lithogenic bile or stone. Metaplasia and cholesterol gallstone may develop simultaneously, and act synergistically.
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spelling pubmed-30543882011-03-15 Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet. Chang, H. J. Suh, J. I. Kwon, S. Y. J Korean Med Sci Research Article To investigate the pathologic change of gallbladder mucosa related to gallstone formation, 52 mice were fed a lithogenic diet containing 1% cholesterol and 0.5% cholic acid and we evaluated the sequential morphologic changes in the gallbladder from two days to 40 weeks. Cholesterol gallstones began to appear after two weeks and all the mice had gallstones after eight weeks. At two days, the mitotic index was at its highest. The gallbladder mucosa showed progressive hyperplastic change with earlier papillary projection of the folds and later inward proliferation. At the same time of stone formation, mucous cells forming glands appeared. Their histochemical profile of mucin was different from that of normal epithelium. Numbers of mucous cells increased gradually until 24 weeks but slightly decreased afterward. These results suggest hyperplasia and metaplasia are closely related to the gallstone formation. Hyperplasia is probably reactive to irritating effect of lithogenic bile or stone. Metaplasia and cholesterol gallstone may develop simultaneously, and act synergistically. Korean Academy of Medical Sciences 1999-06 /pmc/articles/PMC3054388/ /pubmed/10402171 Text en
spellingShingle Research Article
Chang, H. J.
Suh, J. I.
Kwon, S. Y.
Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title_full Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title_fullStr Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title_full_unstemmed Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title_short Gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
title_sort gallstone formation and gallbladder mucosal changes in mice fed a lithogenic diet.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054388/
https://www.ncbi.nlm.nih.gov/pubmed/10402171
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