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Intestinal Consumption of Intravenously Administered Fuels
Author(s) -
Souba Wiley W.,
Scott Thomas E.,
Wilmore Douglas W.
Publication year - 1985
Publication title -
journal of parenteral and enteral nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.935
H-Index - 98
eISSN - 1941-2444
pISSN - 0148-6071
DOI - 10.1177/014860718500900118
Subject(s) - consumption (sociology) , medicine , intensive care medicine , chemistry , environmental science , anesthesia , sociology , social science
Total parenteral nutrition has been extensively used to feed patients with a variety of gastrointestinal diseases, but little attention has focused on the nutritional requirements of the gut. To investigate intestinal consumption of intravenously administered nutrients, uptake of three principal fuels determined from in vitro studies was quantitated in seven awake, unrestrained dogs. Portal blood flow was measured by a dye dilution technique and, simultaneously, substrate samples were obtained from chronic indwelling arterial and portal venous catheters. Studies were performed during a postabsorptive basal period and during separate infusions of glutamine (0.10 mmol/kg. min), glucose (0.10 mmol/kg·min), and β‐hydroxybutyrate, (0.40 mmol/kg·min). During the basal period there was a significant arterial‐portal vein gradient for glucose (144 ± 26 μ mol/liter) and glutamine (49 ± 11 μmol/liter). These substances were taken up by the gut at rates of 4.11 ± 1.23 and 1.43 ± 0.19 μ mol/kg·min, respectively. No significant uptake of β‐hydroxybutyrate was determined in the basal studies (0.27 ± 0.10 μ mol/kg·min). During substrate infusion, gut glucose uptake was unchanged (2.68 ± 1.67 μ mol/kg·min, NS), but consumption of glutamine (4.60 ± 0.66 μ mol/kg·min, p < 0.001) and β‐hydroxybutyrate (4.33 ± 0.71 μ mol/kg·min, p < 0.001) increased significantly. During parenteral feedings in patients with gastrointestinal disorders, circulating levels of β‐hydroxybutyrate and glutamine are often low, and glutamine is absent from standard amino acid solutions. Current parenteral formulation may not provide appropriate fuels for the gastrointestinal tract. (Journal of Parenteral and Enteral Nutrition 9 :18–22, 1985)

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