Duodenal mucosal bicarbonate secretion (DMBS) prevents acid-peptic damage a
nd facilitates nutrient absorption. DMBS is diminished in patients with duo
denal ulcers and is normalized after Helicobacter pylori eradication. The m
easurement of DMBS in human patients in vivo requires intubation with a mul
ti-lumen balloon tube and permits limited testing with putative agonists an
d antagonists. Our purpose was to develop a means to investigate transport
events in human duodenal biopsy samples in vitro. After validation studies
in a modified mini-Ussing chamber were performed, duodenal transport events
were examined in proximal endoscopic biopsy samples from normal volunteers
(n = 17), Tissues were mounted in modified mini-Ussing chambers (volume 2.
5 ml, surface area 3.8 mm(2)). Short circuit current (I-sc), potential diff
erence (PD), and bicarbonate secretion were determined under basal conditio
ns and after stimulation with graded doses of prostaglandin E-2 (PGE(2))(10
(-8) to 10(-4) mol/L) and dibutyryl cAMP (db-cAMP)(10(-4) to 10(-2) mol/L).
Duodenal tissues remained viable for at least 2 hours and exhibited stable
basal HCO3- secretion and electrical parameters. Stimulation with PGE(2) a
nd db-cAMP resulted in dose-related increases in both I-sc and HCO3- secret
ion (P <.05) that were abolished by ouabain and anoxia. It is concluded (1)
that human duodenal bulb biopsy samples maintain their inherent transport
function in mini-Ussing chambers and (2) that by using this novel method it
will be possible to define the transport events that modulate human duoden
al secretion, in particular bicarbonate secretion, in both health and disea
se.