1994
DOI: 10.1006/bbrc.1994.1962
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Interleukin-1 Receptor Antagonist Prevents Low-Dose Streptozotocin-Induced Diabetes in Mice

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Cited by 65 publications
(50 citation statements)
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“…The clinical and histological protection afforded by IL-18 bp:Fc prophylaxis was accompanied by a tendency to normalize immunoinflammatory functions considered to be important in the pathogenesis of murine STZ induced diabetes [4,5,19]. Hence, both T lymphocyte and macrophage functions were affected as judged by the reduced numbers of IFN-+ secreting spleen MNC and the release of lower amounts of NO and IL-1 g by peritoneal macrophages from the IL-18 bp:Fc-treated mice as compared to controls.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The clinical and histological protection afforded by IL-18 bp:Fc prophylaxis was accompanied by a tendency to normalize immunoinflammatory functions considered to be important in the pathogenesis of murine STZ induced diabetes [4,5,19]. Hence, both T lymphocyte and macrophage functions were affected as judged by the reduced numbers of IFN-+ secreting spleen MNC and the release of lower amounts of NO and IL-1 g by peritoneal macrophages from the IL-18 bp:Fc-treated mice as compared to controls.…”
Section: Discussionmentioning
confidence: 99%
“…In particular, the central role of IL-1 and IFN-+ in the pathogenesis of STZ-induced diabetes is proven by the possibility to prevent hyperglycemia in this model by negating the action of endogenous IL-1 or IFN-+ with specific inhibitors such as neutralizing monoclonal antibody, soluble receptors or the IL-1 receptor antagonist [4][5]. In addition, exogenously-administered IFN-+ exacerbates the course of STZ-induced diabetes [3] and expression of IFN-+ in intrapancreatic lymphocytes has been reported in the early stages of STZ-induced diabetes [2].…”
Section: Introductionmentioning
confidence: 99%
“…IL1RN overproduction prevented the deleterious effects of IL-1β on beta cell function and apoptosis in cultured human islets [20]. In vivo, IL1RN administration prevented low-dose streptozotocin (STZ)-induced diabetes [21], and protected transplanted islets from allogeneic rejection [22] and autoimmune attack [23]. However, the potential effects of IL1RN on the initial non-specific beta cell damage after transplantation have not been determined.…”
Section: Introductionmentioning
confidence: 99%
“…ІЛ-1 також гальмує секре-цію інсуліну, що викликає при-гнічення утилізації глюкози тка-нинами і депресію глікогеноутво-рення. Таким чином, інсуліноре-зистентність, посилення глюко-неогенезу і пригнічення утилі-зації глюкози, зрештою, призво-дять до розвитку гіперглікемії та до порушення толерантності до глюкози [2,6,11,13,15,16].…”
Section: Diabetes Mellitus (Dm) Is One Of Global Medical and Social Punclassified