TY - JOUR
T1 - Endotoxin-induced increases in regional glucose utilization by small intestine
T2 - A TNF-independent effect
AU - Lang, C. H.
AU - Obih, J. C A
AU - Bagby, G. J.
AU - Bagwell, J. N.
AU - Spitzer, J. J.
PY - 1991/1/1
Y1 - 1991/1/1
N2 - The purpose of the present study was to determine whether the lipopolysaccharide (LPS)-induced increase in glucose uptake was a generalized response along the length of the entire gastrointestinal (GI) tract and to assess the relative contributions of the mucosa and muscularis. The putative roles of tumor necrosis factor (TNF) and blood flow in the metabolic response of the intestine to LPS were also examined. In vivo glucose uptake (R(g)) was determined for various segments of the GI tract under basal postabsorptive conditions and 3 h after intravenous injection of Escherichia coli LPS using 2-[14C]deoxyglucose. At this time, LPS-treated rats were euglycemic, and R(g) was elevated in all sections of the GI tract (52-96%). In control animals, mucosal R(g) accounted for 79% of the glucose uptake by the entire small intestine; LPS increased R(g) in both the mucosa and muscularis and did not alter this relationship. The LPS-induced increase in intestinal R(g) was not attenuated by pretreatment with TNF antibody. Cardiac output (CO) and intestinal blood flow, assessed using radiolabeled microspheres, were not different from control values 3 h after LPS. Blood flow to the muscularis was increased (120%) in all sections of the small intestine from LPS-treated rats. These results indicate that 3 h after a low dose of LPS, glucose uptake by the entire length of the GI tract was elevated, and the majority of increase was due to enhanced uptake by the mucosa, which was blood flow independent. Furthermore, the increased R(g) was not dependent on elevations in plasma glucose, insulin, or TNF levels. However, an increased blood flow to the muscularis was associated with an elevated R(g) in that region.
AB - The purpose of the present study was to determine whether the lipopolysaccharide (LPS)-induced increase in glucose uptake was a generalized response along the length of the entire gastrointestinal (GI) tract and to assess the relative contributions of the mucosa and muscularis. The putative roles of tumor necrosis factor (TNF) and blood flow in the metabolic response of the intestine to LPS were also examined. In vivo glucose uptake (R(g)) was determined for various segments of the GI tract under basal postabsorptive conditions and 3 h after intravenous injection of Escherichia coli LPS using 2-[14C]deoxyglucose. At this time, LPS-treated rats were euglycemic, and R(g) was elevated in all sections of the GI tract (52-96%). In control animals, mucosal R(g) accounted for 79% of the glucose uptake by the entire small intestine; LPS increased R(g) in both the mucosa and muscularis and did not alter this relationship. The LPS-induced increase in intestinal R(g) was not attenuated by pretreatment with TNF antibody. Cardiac output (CO) and intestinal blood flow, assessed using radiolabeled microspheres, were not different from control values 3 h after LPS. Blood flow to the muscularis was increased (120%) in all sections of the small intestine from LPS-treated rats. These results indicate that 3 h after a low dose of LPS, glucose uptake by the entire length of the GI tract was elevated, and the majority of increase was due to enhanced uptake by the mucosa, which was blood flow independent. Furthermore, the increased R(g) was not dependent on elevations in plasma glucose, insulin, or TNF levels. However, an increased blood flow to the muscularis was associated with an elevated R(g) in that region.
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U2 - 10.1152/ajpgi.1991.260.4.g548
DO - 10.1152/ajpgi.1991.260.4.g548
M3 - Article
C2 - 2018131
AN - SCOPUS:0025882650
SN - 0002-9513
VL - 260
SP - G548-G555
JO - American Journal of Physiology - Gastrointestinal and Liver Physiology
JF - American Journal of Physiology - Gastrointestinal and Liver Physiology
IS - 4 23-4
ER -