Araki S, Kagaya K, Kitoh K, Kimura M, Fukazawa Y
Infect Immun. 1987 Sep;55(9):2164-70. doi: 10.1128/iai.55.9.2164-2170.1987.
The effect of a chemically synthesized polyprenol derivative, dihydroheptaprenol (DHP), on the nonspecific resistance of mice to infection with Escherichia coli was investigated. Mice that had been injected intramuscularly with 100 mg of DHP per kg of body weight, prepared as a microemulsion with lecithin, 1 to 4 days before infection showed enhanced resistance to subcutaneous (s.c.) infection with E. coli. When DHP-injected mice were inoculated s.c. with 3 X 10(8) E. coli, which induces fatal acute systemic infection in normal mice, propagation of bacteria in the blood, liver, and spleen was significantly inhibited. Enhanced resistance of athymic (nude) mice to E. coli infection was also induced by DHP. DHP markedly stimulated the generation of peripheral blood neutrophils, significantly enhanced clearance of E. coli from the bloodstream, and activated neutrophils and peritoneal macrophages for H2O2 generation. DHP restored the resistance to E. coli infection in cyclophosphamide-treated mice over the normal level. Furthermore, DHP shortened the period of the recovery of neutrophils and also enhanced clearance of E. coli from the bloodstream in cyclophosphamide-treated mice. DHP was nontoxic for mice and rats (400 mg/kg intramuscularly and 800 mg/kg s.c.) and nonpyrogenic at a dose of 30 mg/kg when administered intravenously to rabbits. These results suggest that the mechanism of action of DHP for enhancing resistance in mice may be, at least in part, its ability to stimulate the generation of potent neutrophils and to activate macrophages in the reticuloendothelial system.
研究了化学合成的聚戊烯醇衍生物二氢庚戊烯醇(DHP)对小鼠抵抗大肠杆菌感染的非特异性抵抗力的影响。在感染前1至4天,将每千克体重100毫克的DHP与卵磷脂制成微乳剂,通过肌肉注射给小鼠,结果显示这些小鼠对皮下感染大肠杆菌的抵抗力增强。当给注射了DHP的小鼠皮下接种3×10⁸个大肠杆菌(这会在正常小鼠中引发致命的急性全身感染)时,细菌在血液、肝脏和脾脏中的繁殖受到显著抑制。DHP还诱导了无胸腺(裸)小鼠对大肠杆菌感染的抵抗力增强。DHP显著刺激外周血中性粒细胞的生成,显著增强从血液中清除大肠杆菌的能力,并激活中性粒细胞和腹腔巨噬细胞以产生过氧化氢。DHP使环磷酰胺处理的小鼠对大肠杆菌感染的抵抗力恢复到正常水平以上。此外,DHP缩短了环磷酰胺处理的小鼠中性粒细胞恢复的时间,还增强了从血液中清除大肠杆菌的能力。DHP对小鼠和大鼠无毒(肌肉注射400毫克/千克,皮下注射800毫克/千克),静脉注射给兔子时,剂量为30毫克/千克时无致热原性。这些结果表明,DHP增强小鼠抵抗力的作用机制可能至少部分是其刺激产生强效中性粒细胞以及激活网状内皮系统中巨噬细胞的能力。