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DOI 10.1111/j.1440-1746.2008.05771.x

Медицинская библиотека · Journal of gastroenterology and hepatology · 2009

Retinoid metabolism in the small intestine during development of liver cirrhosis.

Natarajan Sathish Kumar, Amirtharaj G Jayakumar, Ramachandran Anup, Pulimood Anna B, Balasubramanian Kunissery A

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND AND AIMS: Retinoids are important mediators of cellular differentiation and proliferation in various epithelia of the body including the small intestine. Though alterations in intestinal epithelial cell proliferation have been noted in liver cirrhosis, mechanisms involved in the process are not well understood. This study examined the levels of various retinoids and retinoid-metabolizing enzymes in the small intestine during development of liver cirrhosis.

METHODS

Four groups of animals were used (control, phenobarbitone control, thioacetamide and carbon tetrachloride treatment). Twice-weekly intragastric or i.p. administration of carbon tetrachloride or thioacetamide, respectively, produced liver cirrhosis after 3 months, which was confirmed through histology and serum markers. Retinoid levels were measured by high-performance liquid chromatography.

RESULTS

A decrease in the levels of retinal, retinoic acid and retinol was evident in the intestine by 3 months, when cirrhosis was evident histologically, and these remained low until 6 months. A decrease in the activities of retinaldehyde oxidase, retinaldehyde reductase and retinol dehydrogenase was also seen in intestine from cirrhotic rats.

CONCLUSION

These results suggest that altered retinoid metabolism in the intestine of cirrhotic rats might have an influence on changes in intestinal epithelial cell differentiation, seen in liver cirrhosis.

Для цитирования: Natarajan Sathish Kumar, Amirtharaj G Jayakumar, Ramachandran Anup, Pulimood Anna B, Balasubramanian Kunissery A. Retinoid metabolism in the small intestine during development of liver cirrhosis.. Journal of gastroenterology and hepatology. 2009. DOI: 10.1111/j.1440-1746.2008.05771.x.

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