TY - JOUR
T1 - Carrier-mediated transport systems for glucose in mucosal cells of the human oral cavity
AU - Oyama, Yujiro
AU - Yamano, Hitoshi
AU - Ohkuma, Akiko
AU - Ogawara, Ken-ichi
AU - Higaki, Kazutaka
AU - Kimura, Toshikiro
N1 - Funding Information:
The authors are grateful to Professor T. Tsuchiya and Dr. T. Kuroda, Gene Research Center, Okayama University, for their helpful guidance with respect to the Western blot analysis. This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture in Japan.
PY - 1999/8
Y1 - 1999/8
N2 - The in vitro uptake study was performed using the isolated cells of human oral mucosa, buccal and the dorsum of the tongue, to investigate the mechanisms of glucose uptake. The uptake of D-glucose was much larger in cells of the dorsum of the tongue than in buccal cells and was inhibited more extensively by 2-deoxy-o-glucose, a substrate of facilitative glucose transporters, than by α-methyl-D-glucoside, a specific substrate of SGLT1, suggesting the larger contribution of a facilitative transporter than Na+/glucose cotransporter. Furthermore, from the results of inhibition studies by several sugar analogue, including maltose and o-mannose, GLUT1 and/or GLUT3 were suggested to take part in the glucose uptake by oral mucosa. Therefore we have attempted to confirm the expression of glucose transporters on the oral mucosa by employing Western blotting. As a result, it was suggested that SGLT1, GLUT1, GLUT2, and GLUT3 are expressed in the epithelial cells of human oral mucosa.
AB - The in vitro uptake study was performed using the isolated cells of human oral mucosa, buccal and the dorsum of the tongue, to investigate the mechanisms of glucose uptake. The uptake of D-glucose was much larger in cells of the dorsum of the tongue than in buccal cells and was inhibited more extensively by 2-deoxy-o-glucose, a substrate of facilitative glucose transporters, than by α-methyl-D-glucoside, a specific substrate of SGLT1, suggesting the larger contribution of a facilitative transporter than Na+/glucose cotransporter. Furthermore, from the results of inhibition studies by several sugar analogue, including maltose and o-mannose, GLUT1 and/or GLUT3 were suggested to take part in the glucose uptake by oral mucosa. Therefore we have attempted to confirm the expression of glucose transporters on the oral mucosa by employing Western blotting. As a result, it was suggested that SGLT1, GLUT1, GLUT2, and GLUT3 are expressed in the epithelial cells of human oral mucosa.
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U2 - 10.1021/js980298f
DO - 10.1021/js980298f
M3 - Article
C2 - 10430550
AN - SCOPUS:0032783827
SN - 0022-3549
VL - 88
SP - 830
EP - 834
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 8
ER -