Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2011; Volume 203, Supplement 687
First Benelux Congress on Physiology and Pharmacology
3/18/2011-3/19/2011
Liège, Belgium


ROLES OF SGLT1, GLUT1 AND GLUT4 IN THE SECRETION OF GLUCOSE BY ACINAR PAROTID CELLS
Abstract number: O-31

Jurysta1 C., Nicaise2 C., Belkacemi1 L., Louchami1 K., Cetik1 S., Malaisse1 WJ., Sener1 A.

1Laboratories of Experimental Hormonology
2General Histology, Neuroanatomy and Neuropathology, Universit Libre de Bruxelles, Brussels, Belgium

Salivary glucose concentration ranges between 25 to 100 mM in human subjects. A higher salivary glucose concentration prevails in diabetic patients than in non-diabetics. When an oral glucose tolerance test was conducted in normal subjects and diabetic patients, we observed a similar time course for salivary glucose and glycemia: the glucose concentration in unstimulated saliva progressively increased during the first 30 min and decreased thereafter. Salivary glucose is excreted by salivary glands. This study aims at investigating mechanisms for glucose secretion by salivary glands. In the literature, only the presence of SGLT1 has been so far shown at the baso-lateral membrane of parotid acinar cells in rats. We investigated the expression and localization of different glucose transporters in parotid gland from healthy rats and from streptozotocin-induced diabetic rats. Immunochemistry was used to localize SGLT1, GLUT1, GLUT2 and GLUT4. SGLT1, as well as GLUT1 and GLUT4, were observed in acinar cells of rat parotid glands. Their mRNA expression was confirmed by quantitative-PCR. GLUT4 mRNA level was significantly lower in the parotid cells of streptozotocin-induced diabetic as compared to normal rats. However, such a difference was not observed for SGLT1 and GLUT1 mRNA. By analogy with the kidney, we postulate the presence of SGLT1 in the baso-lateral membrane of acinar cells and the presence of GLUT4 and/or GLUT1 in the apical membrane. Further experiments are required to assess the validity of this proposal by co-localization immunohistochemistry.

To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 203, Supplement 687 :O-31

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE