Abstract
Background
When studied in enterocyte-like cell lines (Caco-2 and RIE cells), agonists and antagonists
of the sweet taste receptor (STR) augment and decrease glucose uptake, respectively.
We hypothesize that exposure to STR agonists and antagonists in vivo will augment glucose absorption in the rat.
Materials and methods
About 30-cm segments of jejunum in anesthetized rats were perfused with iso-osmolar
solutions containing 10, 35, and 100 mM glucose solutions (n = 6 rats, each group) with and without the STR agonist 2 mM acesulfame potassium
and the STR inhibitor 10 μM U-73122 (inhibitor of the phospholipase C pathway). Carrier-mediated
absorption of glucose was calculated by using stereospecific and nonstereospecific
14C-d-glucose and 3H-l-glucose, respectively.
Results
Addition of the STR agonist acesulfame potassium to the 10, 35, and 100 mM glucose
solutions had no substantive effects on glucose absorption from 2.1 ± 0.2 to 2.0 ±
0.3, 5.8 ± 0.2 to 4.8 ± 0.2, and 15.5 ± 2.3 to 15.7 ± 2.7 μmoL/min/30-cm intestinal
segment (P > 0.05), respectively. Addition of the STR inhibitor (U-73122) also had no effect
on absorption in the 10, 35, and 100 mM solutions from 2.3 ± 0.1 to 2.1 ± 0.2, 7.7
± 0.5 to 7.2 ± 0.5, and 15.7 ± 0.9 to 15.2 ± 1.1 μmoL/min/30-cm intestinal segment,
respectively.
Conclusions
Provision of glucose directly into rat jejunum does not augment glucose absorption
via STR-mediated mechanisms within the jejunum in the rat. Our experiments show either
no major role of STRs in mediating postprandial augmentation of glucose absorption
or that proximal gastrointestinal tract stimulation of STR or other luminal factors
may be required for absorption of glucose to be augmented by STR.
Keywords
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Article info
Publication history
Published online: March 13, 2013
Accepted:
February 19,
2013
Received in revised form:
February 15,
2013
Received:
October 11,
2012
Identification
Copyright
© 2013 Elsevier Inc. Published by Elsevier Inc. All rights reserved.