AJP - GI Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 286: G596-G605, 2004. First published November 6, 2003; doi:10.1152/ajpgi.00390.2002
0193-1857/04 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
286/4/G596    most recent
00390.2002v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hagen, S. J.
Right arrow Articles by Yang, D. X.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hagen, S. J.
Right arrow Articles by Yang, D. X.

MUCOSAL BIOLOGY

Restitution of the bullfrog gastric mucosa is dependent on a DIDS-inhibitable pathway not related to ion transport

Susan J. Hagen, Sarah W. Morrison, Christina S. Law, and David X. Yang

Department of Surgery, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215

Submitted 11 September 2002 ; accepted in final form 3 November 2003

This study was conducted to determine the contribution of ion transport to restitution after injury in the gastric mucosa. For this, intact sheets of stomach from the bullfrog, Rana catesbeiana, were mounted in Ussing chambers. Restitution was evaluated in the presence or absence of ion transport inhibitors amiloride, DIDS, and bumetanide to block Na+/H+ exchange, / exchange and / co-transport, and Na+-K+-2Cl- cotransport, respectively. Ion substitution experiments with Na+-free, Cl--free, and -free solutions were also performed. Injury to the mucosa was produced with 1 M NaCl, and restitution was evaluated by recovery of transepithelial resistance (TER), mannitol flux, and morphology. Amiloride, bumetanide, Cl--free, or -free solutions did not affect restitution. In Na+-free solutions, recovery of TER and mannitol flux did not occur because surface cells did not attach to the underlying basement membrane. In contrast, all aspects of restitution were inhibited by DIDS, a compound that inhibits Na+-dependent transport. Because -free solutions did not inhibit restitution, it was concluded that DIDS must block a yet undefined pathway not involved in ion transport but essential for cell migration after injury and restitution in the gastric mucosa.

Rana catesbeiana; sodium bicarbonate cotransport; injury and repair



Address for reprint requests and other correspondence: S. J. Hagen, Dept. of Surgery, Beth Israel Deaconess Medical Center, Dana 805, 330 Brookline Ave., Boston, MA 02215 (E-mail: shagen{at}bidmc.harvard.edu).




This article has been cited by other articles:


Home page
J. Pharmacol. Exp. Ther.Home page
R. Ragasa, E. Nakamura, L. Marrone, S. Yanaka, S. Hayashi, K. Takeuchi, and S. J. Hagen
Isothiocyanate Inhibits Restitution and Wound Repair after Injury in the Stomach: Ex Vivo and in Vitro Studies
J. Pharmacol. Exp. Ther., October 1, 2007; 323(1): 1 - 9.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A Schwab, H Rossmann, M Klein, P Dieterich, B Gassner, C Neff, C Stock, and U Seidler
Functional role of Na+-HCO3- cotransport in migration of transformed renal epithelial cells
J. Physiol., October 15, 2005; 568(2): 445 - 458.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the American Physiological Society.