Ruchoux M M, Huguet F, Droy-Lefaix M T, Gelot A, Ruchoux P, Autret A
Neuropathology Department, Hospitalo-Universitary Center of Bretonneau, Tours, France.
Am J Hypertens. 1989 Sep;2(9):683-9. doi: 10.1093/ajh/2.9.683.
The stroke-prone spontaneously hypertensive rat (SHR-SP) is one of the most suitable models for stroke study. The present trial work was undertaken so as to obtain further information concerning the action of a new furopyridine, cicletanine. Forty-six males--SHR-SP/Iffa Credo rats--aged 7 weeks, were divided into three groups. Group 1 was a control group, groups 2 and 3 were orally treated with cicletanine at 30 and 100 mg/kg. Their drinking water contained 1% NaCl. Systolic blood pressure, body weight, and survival were recorded. After 6 weeks, all the rats were sacrificed. Samples of heart, brain, and kidney were fixed for light and ultrastructural examination. We found that cicletanine treatment (30 and 100 mg/kg) had significantly inhibited the incidence of hypertensive cerebral damages as characterized by cerebral infarction and vascular alterations with fibrinoid necrosis. Compared with the control group, the rats treated with the cicletanine had a significantly increased survival rate (P less than .001); the cicletanine also had an important protective effect on tissue. Cicletanine administration prevented the development of hypertensive cerebral vascular damage, probably through direct action on the vascular walls.
易中风自发性高血压大鼠(SHR-SP)是中风研究最合适的模型之一。开展本试验工作是为了获取有关新型呋吡啶环克尿噻作用的更多信息。46只7周龄的雄性SHR-SP/Iffa Credo大鼠被分为三组。第1组为对照组,第2组和第3组分别以30和100mg/kg的剂量口服环克尿噻。它们的饮用水中含有1%的氯化钠。记录收缩压、体重和存活率。6周后,处死所有大鼠。取心脏、脑和肾组织样本进行固定,用于光镜和超微结构检查。我们发现,环克尿噻治疗(30和100mg/kg)显著抑制了以脑梗死和伴有纤维蛋白样坏死的血管改变为特征的高血压性脑损伤的发生率。与对照组相比,接受环克尿噻治疗的大鼠存活率显著提高(P<0.001);环克尿噻对组织也有重要的保护作用。环克尿噻给药可预防高血压性脑血管损伤的发展,可能是通过直接作用于血管壁实现的。