Literature DB >> 3130260

Inhibition of secondary bile acid formation in the large intestine by lactulose in healthy subjects of two different age groups.

F M Nagengast1, M P Hectors, W A Buys, J H van Tongeren.   

Abstract

Secondary bile acids have been implicated in colonic carcinogenesis. Transformation of primary into secondary bile acids (7 alpha-dehydroxylation) in the large bowel is a pH-dependent process. Inhibition of this reaction could be achieved by lowering colonic pH. We, therefore, studied the effects of lactulose (a non-absorbable disaccharide), which is capable of acidifying colonic contents, on secondary bile acid metabolism. Because this metabolism is age dependent, lactulose was given (0.3 g kg-1 twice daily for 12 weeks) to nine middle-aged (age 31-54 years; mean 45.7) and ten elderly subjects (age 56-81 years; mean 66.4). Twice before, and after 6 and 12 weeks' lactulose administration, biliary and faecal bile acids, whole gut transit time, faecal weight and dry weight, and faecal pH were recorded. The concentration of (iso)lithocholic and deoxycholic acid in faeces was higher in elderly subjects (P less than 0.05) but the excretion was comparable. After lactulose the concentration and excretion of the major secondary bile acids decreased. The primary bile acid fraction rose from 5% before, to more than 20% after, lactulose (P less than 0.05). Faecal weight increased and faecal dry weight decreased, resulting in a higher faecal water output during lactulose. Whole gut transit time did not change. The faecal pH dropped after 6 (P less than 0.05) and further after 12 weeks' lactulose (P less than 0.05). The percentage deoxycholic acid in bile was higher, and cholic acid lower, in elderly subjects (P less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1988        PMID: 3130260     DOI: 10.1111/j.1365-2362.1988.tb01166.x

Source DB:  PubMed          Journal:  Eur J Clin Invest        ISSN: 0014-2972            Impact factor:   4.686


  5 in total

1.  Bile acid metabolism by fresh human colonic contents: a comparison of caecal versus faecal samples.

Authors:  L A Thomas; M J Veysey; G French; P B Hylemon; G M Murphy; R H Dowling
Journal:  Gut       Date:  2001-12       Impact factor: 23.059

2.  Effect of resistant starch on colonic fermentation, bile acid metabolism, and mucosal proliferation.

Authors:  I P van Munster; A Tangerman; F M Nagengast
Journal:  Dig Dis Sci       Date:  1994-04       Impact factor: 3.199

3.  Calcium, phosphorus, vitamin D, dairy products and colorectal carcinogenesis: a French case--control study.

Authors:  M C Boutron; J Faivre; P Marteau; C Couillault; P Senesse; V Quipourt
Journal:  Br J Cancer       Date:  1996-07       Impact factor: 7.640

4.  Research on Gut Microbiota-Derived Secondary Bile Acids in Cancer Progression.

Authors:  Rong Yang; Li Qian
Journal:  Integr Cancer Ther       Date:  2022 Jan-Dec       Impact factor: 3.077

Review 5.  The potential role of lactulose pharmacotherapy in the treatment and prevention of diabetes.

Authors:  Natural Chu; James Ling; He Jie; Kathy Leung; Emily Poon
Journal:  Front Endocrinol (Lausanne)       Date:  2022-09-15       Impact factor: 6.055

  5 in total

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