Human intestinal specificity toward dietary sterols studied by balance methods

Human intestinal specificity toward sterols was studied by a balance method in 10 hyperlipoproteinemic patients fed plant sterol mixture with chromium sesquioxide as fecal flow marker. The mean fecal recovery of campesterol (C₂₈) was 20% less than that of β-sitosterol (C₂₂). This difference persiste...

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Veröffentlicht in:Nutrition and metabolism (Basel) 1975, Vol.18 (1), p.23-30
Hauptverfasser: Subbiah, M.T.R, Kottke, B.A, Carlo, I.A, Naylor, M.C
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creator Subbiah, M.T.R
Kottke, B.A
Carlo, I.A
Naylor, M.C
description Human intestinal specificity toward sterols was studied by a balance method in 10 hyperlipoproteinemic patients fed plant sterol mixture with chromium sesquioxide as fecal flow marker. The mean fecal recovery of campesterol (C₂₈) was 20% less than that of β-sitosterol (C₂₂). This difference persisted when corrected for fecal flow (by marker recovery), indicating differences in their intestinal uptake (C₂₈ > C₂₂). The ratio of fecal cholesterol to its 5β-reduction products was lower than that of β-sitosterol in all patients; in vitro, 5β-reduction of both sterols was similar. The recovery of sterols from patients was unrelated to their 5β-reduction in the intestine.
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The mean fecal recovery of campesterol (C₂₈) was 20% less than that of β-sitosterol (C₂₂). This difference persisted when corrected for fecal flow (by marker recovery), indicating differences in their intestinal uptake (C₂₈ &gt; C₂₂). The ratio of fecal cholesterol to its 5β-reduction products was lower than that of β-sitosterol in all patients; in vitro, 5β-reduction of both sterols was similar. The recovery of sterols from patients was unrelated to their 5β-reduction in the intestine.</description><identifier>ISSN: 0029-6678</identifier><identifier>EISSN: 2571-6506</identifier><identifier>PMID: 1165855</identifier><language>eng</language><publisher>Switzerland: S. 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The mean fecal recovery of campesterol (C₂₈) was 20% less than that of β-sitosterol (C₂₂). This difference persisted when corrected for fecal flow (by marker recovery), indicating differences in their intestinal uptake (C₂₈ &gt; C₂₂). The ratio of fecal cholesterol to its 5β-reduction products was lower than that of β-sitosterol in all patients; in vitro, 5β-reduction of both sterols was similar. The recovery of sterols from patients was unrelated to their 5β-reduction in the intestine.</abstract><cop>Switzerland</cop><pub>S. Karger</pub><pmid>1165855</pmid><tpages>8</tpages></addata></record>
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subjects Cholesterol - analogs & derivatives
Cholesterol, Dietary - metabolism
Chromium - analysis
Feces - chemistry
human nutrition
Humans
Hyperlipidemias - metabolism
Intestines - metabolism
nutrition education
Original Papers
Phytosterols - metabolism
Sitosterols - metabolism
title Human intestinal specificity toward dietary sterols studied by balance methods
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