WE developed an in vitro organ bath method to measure permeability and
contractility simultaneously in murine intestinal segments, To invest
igate whether permeability and contractility are correlated and influe
nced by mucosal damage owing to inflammation, BALB/c mice were exposed
to a 10% dextran sulphate sodium (DSS) solution for 8 days to induce
colitis. The effect of pharmacologically induced smooth muscle relaxat
ion and contraction on permeability was tested in vitro, Regional perm
eability differences were observed in both control and 10% DSS-treated
cilice, Distal colon segments were less permeable to H-3-mannitol and
C-14-PEG 400 molecules compared with proximal colon and ileum. Intest
inal permeability in control vs. 10% DSS mice was not altered, althoug
h histologic inflammation score and IFN-gamma pro-inflammatory cytokin
e levels were significantly increased in proximal and distal colon. IL
-1 beta levels were enhanced in these proximal and distal segments, bu
t not significantly different from controls. Any effect of pharmacolog
ically induced contractility on intestinal permeability could not be o
bserved. In conclusion, intestinal permeability and contractility are
not correlated in this model of experimentally induced colitis in mice
. Although simultaneous measurement in a physiological set-up is possi
ble, this method has to be further validated.