Literature DB >> 1275075

Circadian distribution of bile acids in the enterohepatic circulatory system in rats.

K J Ho.   

Abstract

The bile acid pool was first determined in six adult male rats to be 12.8 +/- 0.7 mg/100 g by comparing the total radioactivity of tritiated bile acid drained through the bile fistula and the initial bile acid specific activity. The distribution of bile acids in the enterohepatic circulatory system at various times of the day was then studied in 24 additional rats, each received a single dose of tritiated taurocholate intraperitoneally and was sacrificed 24 h later. The nearly complete recovery of the administered radioactivity from the serum, liver intestinal wall and content, and 24-h feces indicated the confinement of bile acids to the enterohepatic circulation. A remarkable circadian fluctuation of the bile acid content was observed in serum, liver, and intestinal contents. The patterns of such rhythmic change varied from each other in various segments of the intestinal tract but seemed to correlate with the time sequence of movement of bowel content and absorption of bile acids. The circadian rhythm of hepatic synthesis of bile acids but not cholesterol observed by others might be, in part, directly related to the circadian fluctuation of the amount of bile acids in the liver.

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Year:  1976        PMID: 1275075     DOI: 10.1152/ajplegacy.1976.230.5.1331

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  8 in total

1.  Distribution of bile acids in rats.

Authors:  K Uchida; I Okuno; H Takase; Y Nomura; M Kadowaki; N Takeuchi
Journal:  Lipids       Date:  1978-01       Impact factor: 1.880

2.  Time-dependent absorption of phenprobamate following multiple dosing in rats.

Authors:  J X Sun; K Embil; C S Lee
Journal:  Pharm Res       Date:  1988-06       Impact factor: 4.200

3.  Distribution of 13N in rat tissues following intravenous administration of nitroso-labeled BCNU.

Authors:  B R Freed; R L McQuinn; R S Tilbury; G A Digenis
Journal:  Cancer Chemother Pharmacol       Date:  1982-12       Impact factor: 3.333

4.  Hepatocyte FRS2α is essential for the endocrine fibroblast growth factor to limit the amplitude of bile acid production induced by prandial activity.

Authors:  Cong Wang; Chaofeng Yang; Julia Yf Chang; Pan You; Yue Li; Chengliu Jin; Yongde Luo; Xiaokun Li; Wallace L McKeehan; Fen Wang
Journal:  Curr Mol Med       Date:  2014       Impact factor: 2.222

5.  Diurnal variations of mouse plasma and hepatic bile acid concentrations as well as expression of biosynthetic enzymes and transporters.

Authors:  Yu-Kun Jennifer Zhang; Grace L Guo; Curtis D Klaassen
Journal:  PLoS One       Date:  2011-02-08       Impact factor: 3.240

Review 6.  Lipids around the Clock: Focus on Circadian Rhythms and Lipid Metabolism.

Authors:  Davide Gnocchi; Matteo Pedrelli; Eva Hurt-Camejo; Paolo Parini
Journal:  Biology (Basel)       Date:  2015-02-05

Review 7.  Bile Acid Signaling Pathways from the Enterohepatic Circulation to the Central Nervous System.

Authors:  Kim L Mertens; Andries Kalsbeek; Maarten R Soeters; Hannah M Eggink
Journal:  Front Neurosci       Date:  2017-11-07       Impact factor: 4.677

8.  Network Modeling of Liver Metabolism to Predict Plasma Metabolite Changes During Short-Term Fasting in the Laboratory Rat.

Authors:  Kalyan C Vinnakota; Venkat R Pannala; Martha L Wall; Mohsin Rahim; Shanea K Estes; Irina Trenary; Tracy P O'Brien; Richard L Printz; Jaques Reifman; Masakazu Shiota; Jamey D Young; Anders Wallqvist
Journal:  Front Physiol       Date:  2019-03-01       Impact factor: 4.566

  8 in total

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