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首页> 外文期刊>Infection and immunity >Protective Effects of a Human 18-Kilodalton Cationic Antimicrobial Protein (CAP18)-Derived Peptide against Murine Endotoxemia
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Protective Effects of a Human 18-Kilodalton Cationic Antimicrobial Protein (CAP18)-Derived Peptide against Murine Endotoxemia

机译:人类的18 Kilodalton阳离子抗菌蛋白(CAP18)衍生肽对小鼠内毒素血症的保护作用。

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CAP18 (an 18-kDa cationic antimicrobial protein) is a granulocyte-derived protein that can bind lipopolysaccharide (LPS) and inhibit various activities of LPS in vitro. The present study examined the protective effect of a synthetic 27-amino-acid peptide (CAP18109–135) from the LPS-binding domain of CAP18 against antibiotic-induced endotoxin shock, using highly LPS-sensitived-(+)-galactosamine (d-GalN)-sensitized C3H/HeN mice. The antibiotic-induced endotoxin (CAZ-endotoxin) was prepared from the culture filtrate of Pseudomonas aeruginosa PAO1 exposed to ceftazidime (CAZ). Injection of CAP18109–135protected the mice injected with LPS or CAZ-endotoxin from death and lowered their tumor necrosis factor (TNF) levels in serum in a dose-dependent manner. Treatment with CAZ caused death of thed-GalN-sensitized P. aeruginosa PAO-infected mice within 48 h, while injection with CAP18109–135rescued the mice from death. In the mice rescued from death by injection with CAP18109–135, endotoxin levels in plasma and TNF production by liver tissues were decreased but the numbers of viable infecting bacteria in their blood were not decreased significantly and remained at the levels in CAZ-treated mice. These results indicate that CAP18109–135 is capable of preventing antibiotic-induced endotoxic shock in mice with septicemia and that the effect is due to its LPS-neutralizing activity rather than to its antibacterial activity.
机译:CAP18(一种18 kDa的阳离子抗菌蛋白)是粒细胞衍生的蛋白,可以结合脂多糖(LPS)并在体外抑制LPS的各种活性。本研究使用高度LPS敏感的方法,研究了CAP18的LPS结合域中合成的27个氨基酸的肽(CAP18 109–135 )对抗生素诱导的内毒素休克的保护作用。 (+)-半乳糖胺(d-GalN)致敏的C3H / HeN小鼠。抗生素诱导的内毒素(CAZ-内毒素)是由暴露于头孢他啶(CAZ)的铜绿假单胞菌PAO1的培养滤液制备的。注射CAP18 109–135 可以保护注射LPS或CAZ-内毒素的小鼠免于死亡,并以剂量​​依赖性方式降低血清中的肿瘤坏死因子(TNF)水平。 CAZ处理导致d-GalN致敏的 P死亡。铜绿假单胞菌感染PAO的小鼠在48 h内注射CAP18 109–135 可以使小鼠死亡。在通过注射CAP18 109-135 获救的小鼠中,血浆中的内毒素水平和肝脏组织产生的TNF降低,但血液中活感染细菌的数量并未显着减少,并保持在CAZ处理的小鼠体内的水平。这些结果表明,CAP18 109-135 能够预防败血病小鼠的抗生素诱导的内毒素休克,其作用是由于其LPS中和活性而不是其抗菌活性。

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