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尼卡地平治疗对自发性高血压大鼠脑血管微观解剖学变化的保护作用。

Protective effect of nicardipine treatment on cerebrovascular microanatomical changes in spontaneously hypertensive rats.

作者信息

Amenta F, Ferrante F, Ricci A, Sabbatini M

机构信息

Sezione di Anatomia Umana, Istituto di Farmacologia, Universita di Camerino, Roma, Italy.

出版信息

Clin Exp Pharmacol Physiol Suppl. 1995 Dec;22(1):S331-2. doi: 10.1111/j.1440-1681.1995.tb02941.x.

DOI:10.1111/j.1440-1681.1995.tb02941.x
PMID:9072415
Abstract
  1. The effect of long-term treatment with the dihydropyridine Ca2+ antagonist, nicardipine, on the morphology of different sized pial arteries was assessed in spontaneously hypertensive rats (SHR) using histological techniques associated with image analysis. 2. In control 20 week old SHR blood pressure values, the thickness of the tunica media, the media-to-lumen ratio and connective tissue content were significantly increased in comparison with reference normotensive Wistar-Kyoto (WKY) rats. 3. Treatment for 8 weeks with a daily dose of 3 mg/kg of nicardipine decreased blood pressure values in SHR and significantly reduced the area occupied by the tunica media and the media-to-lumen ratio. This effect was observed primarily in small sized pial arteries and to a lesser extent in medium sized pial arteries. Nicardipine administration was without effect on connective tissue content in the wall of cerebral arteries. 4. These results indicate that treatment with nicardipine reduces blood pressure elevation in SHR and exerts a protective effect on arteries controlling cerebrovascular resistance. The activity of the compound primarily on small sized pial arteries may protect the brain from generalized vasodilation which could cause cerebral hypoperfusion.
摘要
  1. 使用与图像分析相关的组织学技术,评估二氢吡啶类钙离子拮抗剂尼卡地平长期治疗对自发性高血压大鼠(SHR)不同大小软脑膜动脉形态的影响。2. 在20周龄的对照SHR血压值中,与正常血压的Wistar-Kyoto(WKY)大鼠相比,中膜厚度、中膜与管腔比值以及结缔组织含量显著增加。3. 每日剂量3 mg/kg的尼卡地平治疗8周可降低SHR的血压值,并显著减少中膜所占面积和中膜与管腔比值。这种作用主要在小尺寸软脑膜动脉中观察到,在中等尺寸软脑膜动脉中程度较轻。给予尼卡地平对脑动脉壁中的结缔组织含量无影响。4. 这些结果表明,尼卡地平治疗可降低SHR的血压升高,并对控制脑血管阻力的动脉发挥保护作用。该化合物主要作用于小尺寸软脑膜动脉的活性可能保护大脑免受可能导致脑灌注不足的全身性血管舒张的影响。

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