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Vol. 304, Issue 1, 272-276, January 2003
Departments of Medicine-Laboratory of Epithelial Cell Biology
(L.A.B., S.K.) and Pharmacology (L.A.B., W.C.d.G.), University of
Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; and Department
of Pharmacology (A.L.,C.A.M.), Research Laboratories, Florence, Italy
Tachykinins have been implicated in inflammatory responses such as
those occurring in inflammatory bowel disease. Accordingly, we
investigated the effect of a selective neurokinin (NK) 2 receptor antagonist, nepadutant, on proto-oncogene expression in the
L6-S1 spinal cord as well as in dorsal root
ganglion (DRG) neurons after either non-noxious colorectal distension
(CRD) or trinitrobenzenesulfonic acid (TNBS)-induced colitis in the
adult rat. In both preparations, c-fos was expressed in
similar spinal cord regions, including medial and lateral dorsal
horn, dorsal commissure (DCM; laminae X above the central
canal), and the sacral parasympathetic nucleus (SPN, laminae V-VII).
However, TNBS-induced colitis produced significantly larger numbers
(8-10-fold increase over control) of Fos-positive spinal cord neurons.
In addition, there was also a significant increase (3-4-fold) in the
number of Jun-positive colon DRG neurons after colitis compared with
CRD. Nepadutant had no significant effect on proto-oncogene expression
induced by CRD in either spinal cord neurons or DRG neurons. In
contrast, nepadutant significantly decreased (70%) the number of
Fos-positive neurons in dorsal horn, DCM, and SPN spinal cord regions
and significantly decreased (75%) the number of Jun-positive DRG
neurons after TNBS-induced irritation of the colon. These findings
indicate that nepadutant suppresses the responses of colonic afferent
neurons to nociceptive stimuli and that NK2 receptor antagonists may be
beneficial in the treatment of sensory symptoms of colitis.