By John L. Wallace
Ailments of the digestive process have the next morbidity fee than the other staff of sickness. there's a becoming physique of proof that the immune approach participates within the pathogenesis of quite a lot of those illnesses, together with peptic ulcer disorder and the gastropathy prompted by way of nonsteroidal anti inflammatory medicines (NSAIDS). For those purposes, efforts to enhance novel remedies for digestive ailments are more and more concerned about the immune method. This quantity studies the immunopharmacology of the gastrointestinal tract at 4 distinctive degrees: Immunomodulation at a mobile point mobile targers for immunomodulating medicines particular sessions of inflammatory mediators application and mechanisms of motion of glucocorticoids within the therapy of ailments of the gastrointestinal tract
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Additional resources for Immunopharmacology of the Gastrointestinal System
1988). , 1991), which may then initiate or compound an existing inflammatory response. However, in this instance the investigators favoured a scenario where the cytokines activated MMCs to release an unidentified neutrophil chemoattractant. , 1991). These researchers propose that IL-1 inhibits the release o f histamine from gastric enterochromaffin-like cells: histamine in turn acts through H2 receptors on parietal cells to stimulate acid secretion. Increased stomach acidity is neutralized by epithelial bicarbonate release and therefore epithelial biochemistry may be indirectly influenced by cytokine activity.
Am. J . Physiol. 2 5 4 , K , Scott, H . , Kett, K. O. (1988). LymG307-G314. phoepithelial interactions in the mucosal immune system. E. and Dharmsathaphorn, K. (1991). In "The TextGut 2 9 , 1 1 1 6 - 1 1 3 0 . book of Gastroenterology" (ed T. Yamada), pp. 2 6 5 - 2 9 4 . , Kvale, Lippincott, Philadelphia. , Scott, H. M. (1989). Barrett, K . E . , Dharmsathaphorn, K. I. (1989). Differing effects of apical and mucosa: humoral immunity and intraepithelial lymphocytes. basolateral adenosine on colonic epithelial cell line T84.
1981). Consequently, VIP has the potential to affect the epithelium directly as well as via neuronal-mediated actions. , 1982). , 1989). Furthermore, VIP is structurally related to PHI, which may also affect epithelial mucus production. NPY is a 36 amino acid residue, C-terminally amidated neuropeptide. , 1988). , 1991a). It has also been reported that NPY and a structural peptide, PYY, inhibits PGE2-induced intestinal water secretion in rat jejunum (Sari and Beubler, 1985). Moreover, in contrast to NPY's neuronal distribution, PYY is confined to enterochromaffin cells, particularly in the lower ileum and colon.