PROXIMAL DUODENAL ENTEROCYTE TRANSPORT - EVIDENCE FOR NA-H+ AND CL--HCO3- EXCHANGE AND NAHCO3 COTRANSPORT()

Citation
Ji. Isenberg et al., PROXIMAL DUODENAL ENTEROCYTE TRANSPORT - EVIDENCE FOR NA-H+ AND CL--HCO3- EXCHANGE AND NAHCO3 COTRANSPORT(), The American journal of physiology, 265(4), 1993, pp. 70000677-70000685
Citations number
43
Categorie Soggetti
Physiology
ISSN journal
00029513
Volume
265
Issue
4
Year of publication
1993
Part
1
Pages
70000677 - 70000685
Database
ISI
SICI code
0002-9513(1993)265:4<70000677:PDET-E>2.0.ZU;2-4
Abstract
The duodenum, in contrast to the jejunum, actively secretes HCO3- at a high rate, a process that protects the mucosa from acid/peptic injury . Our purpose was to define the mechanisms involved in HCO3- transport by studying the acid-base transport processes in isolated duodenal en terocytes. Individual rat duodenocytes, isolated by a combination of C a2+ chelation and collagenase, attached to a collagen matrix were load ed with the pH-sensitive fluoroprobe 2',7'-bis(2-carboxyethyl)-5(6)-ca rboxyfluorescein acetoxymethyl ester (BCECF-AM), and intracellular pH was monitored by microfluorospectrophotometry. To identify Na+-H+ tran sport, cells in N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid 1) were pulsed with NH4Cl (40 mM) in the absence and presence of amilori de and 2) were removed of Na+. To examine Cl-, HCO3- exchange, Cl- was removed from Ringer-HCO superfusate in the presence and absence of hy dro-4,4'-diisothio-cyanostilbene-2,2'-disulfonic acid (H-2DIDS). The N aHCO3, cotransporter was studied by addition and subtraction of Na+ to amiloride-treated and Cl--depleted enterocytes perfused with Na+- and Cl--free Ringer-HCO- buffer with and without H2DIDS. Mammalian duoden ocytes contain at least three acidbase transporters: an amiloride-sens itive Na+-H+ exchanger that extrudes acid, a DIDS-sensitive Cl--HCO3- exchanger that extrudes base, and a NaHCO:, cotransporter. also DIDS s ensitive, that functions as a base loader. These acid-base transporter s likely play a key role in duodenal mucosal HCO3- secretion.