Literature DB >> 7240973

Origins of fecal neutral steroids in rats.

T A Miettinen, A Proia, D J McNamara.   

Abstract

The origins of rat fecal neutral steroids were studied in male and female animals fed a sterol-free diet and maintained in an isotopic steady state. The specific activity of fecal cholesterol was found to be consistently lower than that of plasma cholesterol and of the fecal bile acids, indicating that a considerable portion of the fecal neutral steroids was derived from cholesterol not in equilibrium with the rapidly exchangeable pool of body cholesterol. This non-exchanging fraction of neutral steroids was larger in male than in female rats; it appeared to have at least two origins: skin surface lipids licked off fur, and sterols newly synthesized by the intestinal mucosa and secreted into the gut lumen. When the ingestion of skin sterols rich in cholesterol precursors was minimized, the proportion of the non-exchanging fraction of fecal neutral sterols fell somewhat, but the output of cholesterol precursors dropped markedly. This suggests that a significant portion of the non-exchanging fecal cholesterol fraction originated in the intestinal wall by secretion. It can be concluded that the fecal neutral steroids of rats originate primarily from three sources: 1) de novo cholesterol synthesis by the intestinal mucosa, 2) ingested dietary, skin, and fecal sterols, and 3) a rapidly exchangeable cholesterol pool excreted through bile, the intestinal wall, or both.

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Year:  1981        PMID: 7240973

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  5 in total

Review 1.  From blood to gut: direct secretion of cholesterol via transintestinal cholesterol efflux.

Authors:  Carlos L J Vrins
Journal:  World J Gastroenterol       Date:  2010-12-21       Impact factor: 5.742

Review 2.  Rethinking reverse cholesterol transport and dysfunctional high-density lipoproteins.

Authors:  Baiba K Gillard; Corina Rosales; Bingqing Xu; Antonio M Gotto; Henry J Pownall
Journal:  J Clin Lipidol       Date:  2018-04-12       Impact factor: 4.766

3.  Sterol synthesis from biliary squalene in the jejunal mucosa of the rat in vivo.

Authors:  T E Strandberg
Journal:  Lipids       Date:  1983-08       Impact factor: 1.880

4.  Cholesterol metabolism by Treponema hyodysenteriae.

Authors:  T B Stanton
Journal:  Infect Immun       Date:  1987-02       Impact factor: 3.441

5.  Frozen Autoclaved Sorghum Enhanced Colonic Fermentation and Lower Visceral Fat Accumulation in Rats.

Authors:  Samanthi W Pelpolage; Atsushi Yoshida; Ryuji Nagata; Kenichiro Shimada; Naoki Fukuma; Hiroki Bochimoto; Tetsuo Hamamoto; Michiyo Hoshizawa; Koichi Nakano; Kyu-Ho Han; Michihiro Fukushima
Journal:  Nutrients       Date:  2020-08-12       Impact factor: 5.717

  5 in total

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