|
|
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Vol. 305, Issue 2, 549-556, May 2003
Division of Clinical Pharmacology and Section of
Gastroenterology, Medizinische Klinik Innenstadt, University of Munich,
Germany (F.L., P.F., N.L., R.H., K.S., C.B., B.S., F.R., M.D., S.E.,
A.E); Institute of Pathology, University of Mainz, Germany (H.-A.L.);
and Schering AG Berlin, Germany (J.F.K.)
Mesopram, a specific inhibitor of type-4 phosphodiesterase, decreases
the synthesis of tumor necrosis factor-
(TNF-
) and interferon-
(IFN-
). In the present study, we investigated the effect of mesopram
in dextran sulfate sodium (DSS)-induced murine colitis. In the
preventive model, colitis was induced by DSS simultaneously with the
application of mesopram in BALB/c mice. In the therapeutic model,
colitis was induced in BALB/c mice by DSS over 7 days. At day 8, DSS
was discontinued, and treatment was started. Mesopram was applied
intraperitoneally or orally. The clinical score was calculated daily
during the course of each study. Post mortem, colon length, histologic
score, and expression of TNF-
and IFN-
in colons were determined.
In the preventive model, mesopram significantly reduced the maximal
clinical score, decreased colon shortening, and the histologic score. A
dose finding study, using the preventive model, showed that most
clinical and post mortem benefit was achieved with 50 mg/kg mesopram
compared with 2 and 10 mg/kg. In the therapeutic model, i.p. mesopram
treatment led to a significant reduction of clinical score. Both, i.p.
and p.o. mesopram significantly reversed DSS-induced colon shortening
and reduced the ex vivo colonic production of IFN-
. We conclude that
the specific type-4 phosphodiesterase inhibitor mesopram
ameliorates murine colitis both in a preventive and a therapeutic setting.
This article has been cited by other articles:
![]() |
M. Sanchez-Alavez and T. Bartfai It all happens between Toll receptors and Caspase 1 PNAS, May 8, 2007; 104(19): 7733 - 7734. [Full Text] [PDF] |
||||
![]() |
S. Videla, J. Vilaseca, C. Medina, M. Mourelle, F. Guarner, A. Salas, and J.-R. Malagelada Selective Inhibition of Phosphodiesterase-4 Ameliorates Chronic Colitis and Prevents Intestinal Fibrosis J. Pharmacol. Exp. Ther., February 1, 2006; 316(2): 940 - 945. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-C. Chen, S. Louie, B. A. McCormick, W. A. Walker, and H. N. Shi Helminth-Primed Dendritic Cells Alter the Host Response to Enteric Bacterial Infection J. Immunol., January 1, 2006; 176(1): 472 - 483. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-C. Chen, S. Louie, B. McCormick, W. A. Walker, and H. N. Shi Concurrent Infection with an Intestinal Helminth Parasite Impairs Host Resistance to Enteric Citrobacter rodentium and Enhances Citrobacter-Induced Colitis in Mice Infect. Immun., September 1, 2005; 73(9): 5468 - 5481. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Loher, C. Bauer, N. Landauer, K. Schmall, B. Siegmund, H. A. Lehr, M. Dauer, M. Schoenharting, S. Endres, and A. Eigler The Interleukin-1{beta}-Converting Enzyme Inhibitor Pralnacasan Reduces Dextran Sulfate Sodium-Induced Murine Colitis and T Helper 1 T-Cell Activation J. Pharmacol. Exp. Ther., February 1, 2004; 308(2): 583 - 590. [Abstract] [Full Text] [PDF] |
||||