Tanaka K, Koga T, Konishi F, Nakamura M, Mitsuyama M, Himeno K, Nomoto K
Infect Immun. 1986 Aug;53(2):267-71. doi: 10.1128/iai.53.2.267-271.1986.
Protection against Escherichia coli inoculated intraperitoneally into mice was enhanced by intraperitoneal, intravenous, or subcutaneous administration of a water-soluble, high-molecular-weight fraction extracted from a dialyzed hot-water extract from a strain of Chlorella vulgaris (CVE-A). The enhancing effect was detected with doses over 2.0 mg/kg and when doses were administered 1, 4, or 7 days before the infection. The elimination of bacteria from the spleen of CVE-A-treated mice was increased, and this enhanced elimination may have been related to the acceleration of superoxide generation and chemokinesis in polymorphonuclear leucocytes by CVE-A treatment. A cyclophosphamide-induced decrease in protection against E. coli could be prevented by subcutaneous administration of CVE-A.
腹腔内、静脉内或皮下注射从普通小球藻(CVE-A)菌株的透析热水提取物中提取的水溶性高分子量级分,可增强对腹腔注射大肠杆菌的小鼠的保护作用。当剂量超过2.0mg/kg以及在感染前1、4或7天给药时,可检测到增强效果。CVE-A处理的小鼠脾脏中细菌的清除增加,这种增强的清除可能与CVE-A处理使多形核白细胞中超氧化物生成和趋化作用加速有关。皮下注射CVE-A可预防环磷酰胺诱导的对大肠杆菌保护作用的降低。