Cahn J, Borzeix M G
Sem Hop. 1983 Jul 7;59(27-28):2031-4.
Cerebral microvessel permeability disturbances following rapid injection of autologous blood into the carotid artery are evidenced in cross sections of the rat brain by extravascular dye leakage. Here, Evans blue was injected intravenously 2 hours after the blood injection and 30 minutes before sacrificing the animals. Five groups of 10 rats each were given Procyanidolic Oligomers (PCO) in respective doses of 10, 30 and 300 mg/kg by oral route and 10 and 30 mg/kg by intraperitoneal route. Three PCO doses were administered prior to blood injection, on D-2, D-1 and DO. At oral doses of 10 and 30 mg/kg, the blue color in the injected hemisphere was significantly less intense than in the untreated group. When administered intraperitoneally, PCO showed a preventive effect on both the degree and extent of lesions. The following mechanism of action of PCO has been put forward in this experimental model: these compounds may increase the resistance of the tight junctions of arteriolar capillaries, thus interfering with the sudden rise in pressure at the time of blood injection.
通过血管外染料渗漏在大鼠脑横断面中证实了向颈动脉快速注射自体血后出现的脑微血管通透性紊乱。在此,在注射血液后2小时且在处死动物前30分钟静脉注射伊文思蓝。每组10只大鼠,共五组,分别通过口服途径给予原花青素低聚物(PCO),剂量为10、30和300mg/kg,通过腹腔途径给予10和30mg/kg。在注射血液前,即第-2天、第-1天和第0天给予三种PCO剂量。口服剂量为10和30mg/kg时,注射侧半球的蓝色强度明显低于未治疗组。当腹腔注射时,PCO对损伤的程度和范围均显示出预防作用。在该实验模型中提出了PCO的以下作用机制:这些化合物可能会增加小动脉毛细血管紧密连接的阻力,从而干扰注射血液时压力的突然升高。