Bemana I, Takahashi E, Nakamura T, Kuyama H, Nagao S
Department of Neurological Surgery, Kagawa Medical University, Japan.
Acta Neurochir Suppl. 1997;70:194-7. doi: 10.1007/978-3-7091-6837-0_60.
We examined the effect of orally administered OPC-21268, a nonpeptide Arginine Vasopressin V1 receptor antagonist, on cold induced vasogenic brain edema in rat. Cold brain injury was induced by applying a copper rode cooled with liquid nitrogen for one minute. To mimic clinical use, one hour after induction of the cold lesion, rats were treated with orally administered OPC-21268 at doses of 100 mg, 200 mg, and 300 mg/kg every 8 hr for 24 hours. Two percent Evans blue in saline, in a volume of 1 ml/kg was given intravenously prior to cold injury. Twenty four hours after induction the cold lesion, brain water, brain tissue electrolytes, and plasma osmolality and electrolytes were measured. Quantitative evaluation of BBB permeability was performed using the Evans blue fluorescence method. The injury resulted in significant increases in the brain water and brain tissue sodium, and Evans blue concentration in both the lesioned and contralateral hemispheres (p < 0.01). OPC-21268 at doses of 200 mg and 300 mg/kg significantly decreased brain water and Evans blue concentrations in both the lesioned and contralateral hemispheres (p < 0.01). Brain tissue sodium content was significantly reduced at a dose of 300 mg/kg in the lesioned side (p < 0.05). There were no significant changes in other parameters throughout the experiments. Our results indicate that OPC-21268 exerts a protective effect in areas where the maximal amount of BBB breakdown occurs.
我们研究了口服给予非肽类精氨酸加压素V1受体拮抗剂OPC - 21268对大鼠冷诱导血管源性脑水肿的影响。通过用液氮冷却的铜棒接触一分钟来诱导脑冷损伤。为模拟临床应用,在冷损伤诱导后1小时,给大鼠口服OPC - 21268,剂量分别为100 mg、200 mg和300 mg/kg,每8小时给药一次,共给药24小时。在冷损伤前静脉注射1 ml/kg含2%伊文思蓝的生理盐水。冷损伤诱导24小时后,测量脑含水量、脑组织电解质、血浆渗透压和电解质。采用伊文思蓝荧光法对血脑屏障通透性进行定量评估。损伤导致损伤侧和对侧半球的脑含水量、脑组织钠含量以及伊文思蓝浓度显著增加(p < 0.01)。200 mg和300 mg/kg剂量的OPC - 21268显著降低了损伤侧和对侧半球的脑含水量和伊文思蓝浓度(p < 0.01)。损伤侧300 mg/kg剂量时脑组织钠含量显著降低(p < 0.05)。在整个实验过程中,其他参数无显著变化。我们的结果表明,OPC - 21268在血脑屏障破坏最严重的区域发挥保护作用。