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Cytokine and Adhesion Molecule Expression Induced by Different Strains of Staphylococcus aureus in Type 1 Diabetic Rats: Role of Insulin

机译:1型糖尿病大鼠中不同菌株金黄色葡萄球菌诱导的细胞因子和粘附分子表达:胰岛素的作用

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>Introduction: Staphylococcus aureus may provoke peritonitis and death, especially in immunocompromized individuals such as diabetic patients. We evaluated the role of insulin in S. aureus-induced peritoneal infection in diabetic and non-diabetic rats.>Materials/Methods: Alloxan-diabetic male Wistar rats and their respective controls received intraperitoneal injections of different strains of S. aureus or sterile phosphate-buffered saline. After 3 days of infection, the first set of diabetic and non-diabetic rats received 4 and 1 IU, respectively, of neutral protamine Hagedorn insulin and were analyzed 8 h later. The second set of diabetic and non-diabetic rats received 4 and 1 IU, respectively, of insulin 2 h before intraperitoneal infection and a half dose of insulin at 5 p.m. for the next 2 days and were analyzed 16 h later. The following measurements were performed: (a) number of cells in the peritoneal lavage fluid (PeLF), white blood cell count, and blood glucose; (b) serum insulin and corticosterone; (c) cytokine levels in the PeLF; (d) expression of adhesion molecules in the vascular endothelium; and (e) microbicidal activity.>Results: Diabetic rats showed an increased number of polymorphonuclear leukocytes (PMNs) and increased concentrations of CINC-1, IL-4, and IFN-γ in the PeLF after infection with the ATCC 25923 or N315 αHL+ strain. The mesenteric expression of PECAM-1 was increased after infection with the N315 HLA+ strain. ICAM-1 expression was increased with ATCC infection. Treatment of diabetic rats with a single dose of insulin restored CINC-1 levels in the PeLF for both strains; however, PMN migration, IL-4, and IFN-γ were restored in rats infected with the ATCC strain, whereas the PeLF concentrations of CINC-2, IL-1β, and IL-4 were increased in N315-infected animals. Insulin restored PMN migration and CINC-2 levels in the PeLF in ATCC-infected rats. After multiple treatments with insulin, the levels of IL-1β, IL-6, and IFN-γ were increased in the PeLF of diabetic rats after infection with either strain, and CINC-2 levels were restored in N315-infected animals.>Conclusion: These results suggest that insulin distinctively modulates cytokine production or release, PMN leukocyte migration, and adhesion molecule expression during the course of peritonitis induced by different strains of S. aureus.
机译:>简介:金黄色葡萄球菌可能引起腹膜炎和死亡,尤其是在免疫功能低下的个体(如糖尿病患者)中。我们评估了胰岛素在糖尿病和非糖尿病大鼠中金黄色葡萄球菌引起的腹膜感染中的作用。>材料/方法:四氧嘧啶糖尿病雄性Wistar大鼠及其各自的对照组接受不同菌株的腹膜内注射金黄色葡萄球菌或无菌磷酸盐缓冲盐水。感染3天后,第一组糖尿病和非糖尿病大鼠分别接受了4 IU和1 IU中性鱼精蛋白Hagedorn胰岛素,并在8小时后进行了分析。第二组糖尿病和非糖尿病大鼠在腹膜内感染前2 h分别接受4和1 IU胰岛素,并在下午5点接受一半剂量的胰岛素。接下来的2天,并在16小时后进行了分析。进行以下测量:(a)腹腔灌洗液(PeLF)中的细胞数量,白细胞计数和血糖; (b)血清胰岛素和皮质酮; (c)PeLF中的细胞因子水平; (d)粘附分子在血管内皮中的表达; >结果:糖尿病大鼠感染后,PeLF中多形核白细胞(PMN)数量增加,CILF-1,IL-4和IFN-γ浓度增加。 ATCC 25923或N315αHL + 菌株。 N315 HLA + 株感染后,PECAM-1的肠系膜表达增加。随着ATCC感染,ICAM-1表达增加。用单剂量胰岛素治疗糖尿病大鼠,两种品系在PeLF中恢复CINC-1水平;然而,在ATCC株感染的大鼠中,PMN迁移,IL-4和IFN-γ得以恢复,而在N315感染的动物中,CINC-2,IL-1β和IL-4的PeLF浓度升高。胰岛素可恢复ATCC感染大鼠的PeLF中PMN迁移和CINC-2水平。胰岛素多次治疗后,任一株感染的糖尿病大鼠的PeLF中IL-1β,IL-6和IFN-γ的水平均升高,并且在N315感染的动物中CINC-2的水平得以恢复。 >结论:这些结果表明,在由金黄色葡萄球菌不同菌株引起的腹膜炎过程中,胰岛素可显着调节细胞因子的产生或释放,PMN白细胞迁移以及粘附分子表达。

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