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培哚普利治疗易卒中型自发性高血压大鼠预防卒中及保护脑动脉功能的研究

Prevention of stroke and preservation of the functions of cerebral arteries by treatment with perindopril in stroke-prone spontaneously hypertensive rats.

作者信息

Wang H, Smeda J S, Lee R M

机构信息

Smooth Muscle Research Programme, McMaster University, Hamilton, ON, Canada.

出版信息

Can J Physiol Pharmacol. 1998 Jan;76(1):26-34.

PMID:9564546
Abstract

The aim of this study was to determine whether the prevention of stroke with perindopril treatment in stroke-prone spontaneously hypertensive rats (SHRSP) is associated with the preservation of the myogenic properties of the cerebral arteries. After weaning at 4 weeks of age, male SHRSP were fed a Japanese-style rat diet with high salt to induce stroke development. Treatment with perindopril was given by gavage every morning beginning at 6 weeks of age. There were three experimental groups: two groups treated with 4 mg.kg-1.day-1 perindopril for different durations (8 or 12 weeks) and one control group consisting of littermates given distilled water. All the control animals developed stroke and died within 14 weeks of age, and myogenic response of the middle cerebral arteries (MCA) to pressure increase was lost in these animals. In contrast, all the treated SHRSP survived during the treatment period, and myogenic response of the MCA was preserved. After withdrawal of the treatment, SHRSP treated for a longer period (12 weeks) also survived longer than those treated for a shorter period (8 weeks). The subsequent development of stroke and death following treatment withdrawal after 8 or 12 weeks of treatment was associated with the loss of pressure-dependent constriction in MCA. A longer treatment duration also increased the stiffness of the MCA, MCA from SHRSP after 12 weeks of treatment had smaller external and lumen diameters, and thicker walls than those from the 8-week treatment group. In a separate study, we found that treatment of SHRSP with 1 or 4 mg.kg-1.day-1 of perindopril for 24 weeks beginning at 6 weeks of age also protected them against death related to stroke, because these rats survived up to 43 weeks of age, when the experiment was terminated. We conclude that there is an association between the absence of myogenic response in cerebral arteries and stroke development in SHRSP. Perindopril treatment preserves the myogenic response of MCA in SHRSP and prevents the stroke development in these animals. A prolonged treatment could increase the survival of SHRSP through a remodelling of the MCA and increasing the stiffness of the cerebral arteries.

摘要

本研究的目的是确定培哚普利治疗对易患中风的自发性高血压大鼠(SHRSP)预防中风的作用是否与脑动脉肌源性特性的保留有关。4周龄断奶后,雄性SHRSP喂食高盐的日式大鼠饮食以诱发中风。从6周龄开始,每天早晨通过灌胃给予培哚普利治疗。有三个实验组:两组分别用4mg·kg-1·天-1的培哚普利治疗不同持续时间(8周或12周),一组对照组由给予蒸馏水的同窝仔组成。所有对照动物在14周龄内发生中风并死亡,这些动物大脑中动脉(MCA)对压力升高的肌源性反应丧失。相比之下,所有接受治疗的SHRSP在治疗期间存活,并且MCA的肌源性反应得以保留。停止治疗后,治疗时间较长(12周)的SHRSP比治疗时间较短(8周)的存活时间更长。在8周或12周治疗后停止治疗后中风和死亡的后续发展与MCA中压力依赖性收缩的丧失有关。较长的治疗时间也增加了MCA的硬度,治疗12周后的SHRSP的MCA比8周治疗组的MCA外径和管腔直径更小,壁更厚。在另一项研究中,我们发现从6周龄开始用1或4mg·kg-1·天-1的培哚普利治疗SHRSP 24周也能保护它们免于与中风相关的死亡,因为这些大鼠存活至43周龄,此时实验终止。我们得出结论,脑动脉中肌源性反应的缺失与SHRSP中风的发生之间存在关联。培哚普利治疗可保留SHRSP中MCA的肌源性反应并预防这些动物中风的发生。延长治疗时间可通过MCA重塑和增加脑动脉硬度来提高SHRSP的存活率。

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