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首页> 外文期刊>Journal of International Medical Research >Impact of Combined C1 Esterase Inhibitor/Coagulation Factor XIII or N-Acetylcysteine/Tirilazad Mesylate Administration on Leucocyte Adherence and Cytokine Release in Experimental Endotoxaemia
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Impact of Combined C1 Esterase Inhibitor/Coagulation Factor XIII or N-Acetylcysteine/Tirilazad Mesylate Administration on Leucocyte Adherence and Cytokine Release in Experimental Endotoxaemia

机译:C1酯酶抑制剂/凝血因子XIII或N-乙酰半胱氨酸/甲磺酸Tirilazad联合给药对实验性内毒素血症中白细胞粘附和细胞因子释放的影响

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摘要

We determined the effects of combinations of C1 esterase inhibitor (C1-INH) with factor XIII and of N-acetylcysteine (NAC) with tirilazad mesylate (TM) during lipopolysaccharide (LPS)-induced endotoxaemia in rats. Forty Wistar rats were divided into four groups: the control (CON) group received no LPS; the LPS, C1-INH + factor XIII and NAC + TM groups received endotoxin infusions (5 mg/kg per h). After 30 min of endotoxaemia, 100 U/kg C1-INH + 50 U/kg factor XIII was administered to the C1-INH + factor XIII group, and 150 mg/kg NAC + 10 mg/kg TM was administered in the NAC + TM group. Administration of C1-INH + factor XIII and NAC + TM both resulted in reduced leucocyte adherence and reduced levels of interleukin-1β (IL-1β). The LPS-induced increase in IL-6 levels was amplified by both drug combinations. There was no significant effect on mesenteric plasma extravasation. In conclusion, the administration of C1-INH + factor XIII and NAC + TM reduced endothelial leucocyte adherence and IL-1β plasma levels, but increased IL-6 levels.
机译:我们确定了C1酯酶抑制剂(C1-INH)与XIII因子的组合以及N-乙酰半胱氨酸(NAC)与替拉扎德甲磺酸盐(TM)的组合在脂多糖(LPS)诱导的大鼠内毒素血症期间的作用。 40只Wistar大鼠分为四组:对照组(CON)组不接受LPS;对照组(LPS)不接受LPS。 LPS,C1-INH +因子XIII和NAC + TM组接受内毒素输注(每小时5 mg / kg)。内毒素血症30分钟后,向C1-INH +因子XIII组施用100 U / kg C1-INH + 50 U / kg因子XIII,在NAC +中施用150 mg / kg NAC + 10 mg / kg TM TM组。施用C1-INH +因子XIII和NAC + TM均可导致白细胞粘附减少和白介素1β(IL-1β)水平降低。两种药物组合均放大了LPS诱导的IL-6水平的升高。对肠系膜血浆外渗没有显着影响。总之,C1-INH +因子XIII和NAC + TM的给药降低了内皮白细胞粘附和IL-1β血浆水平,但增加了IL-6水平。

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