首页> 外文期刊>Peptides: An International Journal >Tachyplesin III and granulocyte-colony stimulating factor enhance the efficacy of tazobactam/piperacillin in a neutropenic mouse model of polymicrobial peritonitis.
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Tachyplesin III and granulocyte-colony stimulating factor enhance the efficacy of tazobactam/piperacillin in a neutropenic mouse model of polymicrobial peritonitis.

机译:速激肽III和粒细胞集落刺激因子增强了他唑巴坦/哌拉西林在中性粒细胞减少性腹膜炎小鼠模型中的功效。

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We investigated the efficacy of tazobactam/piperacillin (TZP), tachyplesin III and granulocyte-colony stimulating factor (G-CSF) in an experimental murine neutropenic intraabdominal infection. BALB/c male mice were rendered neutropenic by intraperitoneal administration of cyclophosphamide on days -4 and -2 pre-infection. Septic shock was induced by cecal ligation and puncture. Animals received intravenously isotonic sodium chloride solution (control group C1), 1mg/kg of tachyplesin III, 120 mg/kg of TZP, 0.1mg/kg of G-CSF, tachyplesin III plus TZP, G-CSF plus TZP and finally tachyplesin III plus G-CSF plus TZP, respectively. Lethality, bacterial growth in blood, peritoneum, spleen, liver, and mesenteric lymph nodes, endotoxin, IL-6 and TNF-alpha concentrations in plasma were evaluated. All compounds reduced the lethality when compared to controls. Endotoxin and cytokine plasma levels were significantly higher in TZP-treated animals compared to tachyplesin III-treated animals. Finally, all drug combinations showed to be the most effective treatment in reducing all variables measured. Interestingly, the strongest results concerning the bacterial growth inhibition, lethality and endotoxemia were obtained when the three compounds were contemporaneously administered. The presence of their positive interaction makes tachyplesin III and G-CSF potentially valuable as an adjuvant for antimicrobial chemotherapy of sepsis.
机译:我们调查了他唑巴坦/哌拉西林(TZP),速激肽III和粒细胞集落刺激因子(G-CSF)在实验性鼠中性粒细胞减少性腹腔感染中的功效。在感染前第-4天和第-2天,通过腹膜内给予环磷酰胺使BALB / c雄性小鼠嗜中性白血球减少。盲肠结扎和穿刺引起败血性休克。动物接受静脉等渗氯化钠溶液(对照组C1),1mg / kg速激肽III,120 mg / kg TZP,0.1mg / kg的G-CSF,速激肽III加TZP,G-CSF加TZP和最后的速激肽III加G-CSF加TZP。评估致命性,血液,腹膜,脾脏,肝脏和肠系膜淋巴结中的细菌生长,血浆中的内毒素,IL-6和TNF-α浓度。与对照相比,所有化合物均降低了杀伤力。与经速激肽III治疗的动物相比,经TZP治疗的动物的内毒素和细胞因子血浆水平显着更高。最后,所有药物组合被证明是减少所有测量变量的最有效方法。有趣的是,当同时施用这三种化合物时,获得了关于细菌生长抑制,致死性和内毒素血症的最强结果。它们的积极相互作用的存在使速激肽III和G-CSF可能作为脓毒症抗微生物化疗的佐剂有价值。

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