Intestinal Consumption of Intravenously Administered Fuels

Abstract

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 μmol/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 μmol/kg·min, respectively. No significant uptake of β-hydroxybutyrate was determined in the basal studies (0.27 ± 0.10 μmol/kg·min). During substrate infusion, gut glucose uptake was unchanged (2.68 ± 1.67 μmol/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 μmol/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)