In keeping with the effects on angiogenesis induced by contact hypersensitivity reactions in mouse ears, VS-I-treated mice revealed significantly reduced oedema formation, resulting from lower plasma leakage and inhibition of inflammation-associated vascular remodelling [66]. Intravital microscopy studies of inflamed ears showed a decrease
in the fraction of rolling leucocytes in VS-I-treated mice [66]. In addition to anti-microbial activity [67] Cgs may play important role in the neuroimmune interaction in relation to inflammatory function. This review will remain focused upon the function of Cgs in inflammatory responses in the gut. Circulating CgA levels, a marker for neuroendocrine tumours including carcinoids, have Protease Inhibitor Library recently been found elevated in some patients with IBD [68]. In this context the disease activity and TNF-α levels influence the CgA pattern, which could reflect the neuroendocrine system activation in
response to inflammation [69]. In a recent letter addressed to the aforementioned study, Sidhu and collaborators [70,71] confirmed the observation of Sciolia et al.[69] of an elevated level of CgA see more serum in both IBD and diarrhoea-predominant IBS patients. The unifying hypothesis proposed could be the EC cell hyperplasia producing an elevated serum CgA levels, as reported previously [72]. The differential replication of EC cells in IBS patients could also explain why elevated levels are found only in a proportion of patients, and levels decline with time. Further studies of serial serum CgA measurements in both these conditions would strengthen our understanding of the plausible mechanisms behind these observations. In the context of experimental colitis, intrarectal injection of CAT can decrease the inflammatory markers [73]. Disease activity index, macroscopic and histological scores, as well Erlotinib price as myeloperoxidase
(MPO) activity, were decreased significantly in mice treated with CAT compared to mice that received DSS only. Treatment decreased the onset of clinical disease as assessed by loose stools, weight loss and rectal bleeding. In addition, colonic tissue levels of IL-1β, IL-6 and TNF-α were decreased significantly in mice treated with CAT. Conversely, the biochemically modified fragment had no effect on the severity of colitis. These results support the hypothesis that Cgs-derived peptides modulate intestinal inflammation in a murine model of colitis by acting directly or indirectly on the microbiota and the immune system. Identification of the molecular and cellular mechanisms underlying the protective role of this peptide may lead to a novel therapeutic option in IBD.