OBJECTIVE: To study the alteration of prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) synthesis and intracellular Ca2+ concentration in chronic inflammatory bowel disease, and to ascertain the effect of anti-inflammatory drugs and other mediators on eicosanoid synthesis and Ca2+ concentration. METHODS: Biopsies taken from the descending colon were isolated biochemically. The suspension of isolated mucosal cells was incubated for 15 min in the presence and absence of arachidonic acid and the Ca2+ ionophore A23187. PGE2 and LTB4 concentrations in the incubation medium were measured by radioimmunoassay, and the intracellular Ca2+ concentration was determined using fura-2. We studied 107 subjects. In addition, the effects of bradykinin, endothelin, cyclosporin A and PGE2 on intracellular Ca2+ concentration were determined in 25 individuals. RESULTS: Untreated patients with active inflammatory bowel disease showed a significant increase in LTB4 synthesis compared with healthy controls. However, in patients receiving steroids, sulphasalazine or 5-aminosalicylic acid, both LTB4 and PGE2 synthesis were markedly decreased. When arachidonic acid was added to the cell suspension, it significantly stimulated LTB4 synthesis, especially in patients with active disease. Patients with active Crohn's disease or ulcerative colitis had moderately higher Ca2+ levels than healthy controls. However, there was a significant decrease in intracellular Ca2+ concentration in patients with quiescent disease who were receiving maintenance therapy. CONCLUSION: We suggest that increased LTB4 synthesis and elevated intracellular Ca2+ concentrations contribute to the pathophysiology of inflammatory bowel disease. Drugs effective in the treatment of these diseases may exert their pharmacological action by normalizing these pathological findings.
OBJECTIVE: To study the alteration of prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) synthesis and intracellular Ca2+ concentration in chronic inflammatory bowel disease, and to ascertain the effect of anti-inflammatory drugs and other mediators on eicosanoid synthesis and Ca2+ concentration. METHODS: Biopsies taken from the descending colon were isolated biochemically. The suspension of isolated mucosal cells was incubated for 15 min in the presence and absence of arachidonic acid and the Ca2+ ionophore A23187. PGE2 and LTB4 concentrations in the incubation medium were measured by radioimmunoassay, and the intracellular Ca2+ concentration was determined using fura-2. We studied 107 subjects. In addition, the effects of bradykinin, endothelin, cyclosporin A and PGE2 on intracellular Ca2+ concentration were determined in 25 individuals. RESULTS: Untreated patients with active inflammatory bowel disease showed a significant increase in LTB4 synthesis compared with healthy controls. However, in patients receiving steroids, sulphasalazine or 5-aminosalicylic acid, both LTB4 and PGE2 synthesis were markedly decreased. When arachidonic acid was added to the cell suspension, it significantly stimulated LTB4 synthesis, especially in patients with active disease. Patients with active Crohn's disease or ulcerative colitis had moderately higher Ca2+ levels than healthy controls. However, there was a significant decrease in intracellular Ca2+ concentration in patients with quiescent disease who were receiving maintenance therapy. CONCLUSION: We suggest that increased LTB4 synthesis and elevated intracellular Ca2+ concentrations contribute to the pathophysiology of inflammatory bowel disease. Drugs effective in the treatment of these diseases may exert their pharmacological action by normalizing these pathological findings.
Authors: N S Nanda Kumar; Satish K Singh; Vazhaikkurichi M Rajendran Journal: Am J Physiol Gastrointest Liver Physiol Date: 2010-07-08 Impact factor: 4.052
Authors: Bu'Hussain Hayee; Farooq Z Rahman; Jane Tempero; Sara McCartney; Stuart L Bloom; Anthony W Segal; Andrew M Smith Journal: Dig Dis Sci Date: 2010-10-09 Impact factor: 3.199