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西氯他宁对易卒中型自发性高血压大鼠血管壁的保护作用

[Protective action of cicletanine on the vascular walls in stroke-prone spontaneously hypertensive rats].

作者信息

Ruchoux M M, Droy-Lefaix M T, Bakri F, Berthet P, Bosquet D, Lhuintre Y

机构信息

Laboratoire d'anatomie pathologique, CHU Bretonneau, Tours, France.

出版信息

Arch Mal Coeur Vaiss. 1989 Jul;82(7):1163-8.

PMID:2510643
Abstract

UNLABELLED

In previous works, cicletanine has proven a protective effect on tissues in stroke-prone spontaneously hypertensive rats. The mechanism by which cicletanine lessens the tissue lesion incidence may be explained by the direct vascular effect of increased prostacyclin synthesis and by interaction with various agents mobilizing intracellular. Ca2+ ions. Histological so as to ultrastructural studies of the capillaries and small arteries were performed, specially on those of brain, kidney, heart, and choroid. Method : 36 SHR-SP/A 3N Iffa Credo rats aged 11 weeks were divided into 3 groups. Their drinking water was added with 1 p. 100 NaCl in. Group I was a control group, groups II and III were orally treated with cicletanine, respectively 100 and 150 mg/Kg. Systolic blood pressure, body weight, survival were reported. After 7 weeks of treatment the surviving rats were sacrificed.

RESULTS

the control group arterioles showed endoluminal debris with intimal proliferation and a large disorganisation of the media with adventitial fibrosis. The treated groups only showed a slight oedema of the subendothelial space in ultrastructure with no intimal proliferation and no muscle coat disorganisation or proliferation.

CONCLUSION

even though the decrease in blood pressure turned out to be very unimportant, the amount of lesions in vessels was striking even when treatment had been started on a already high blood pressure. The vessel walls only presented the impairments usually observed in early arterial response to hypertension. This study shows that cicletanine, due to its properties to increase PG12 synthesis and counterbalance the increase of cytosolic free Ca2+, improves the normal course of hypertensive vascular lesions in the SHR-SP.

摘要

未标注

在先前的研究中,西氯他宁已被证明对易患中风的自发性高血压大鼠的组织具有保护作用。西氯他宁可通过增加前列环素合成的直接血管效应以及与各种动员细胞内钙离子的物质相互作用来解释其降低组织损伤发生率的机制。对毛细血管和小动脉进行了组织学乃至超微结构研究,特别是对脑、肾、心和脉络膜的血管。方法:将36只11周龄的SHR-SP/A 3N Iffa Credo大鼠分为3组。在它们的饮用水中添加1‰的氯化钠。第一组为对照组,第二组和第三组分别口服100和150mg/kg的西氯他宁。记录收缩压、体重和存活率。治疗7周后,处死存活的大鼠。

结果

对照组小动脉显示腔内有碎屑,内膜增生,中膜严重紊乱并伴有外膜纤维化。治疗组在超微结构上仅显示内皮下间隙有轻微水肿,无内膜增生,无肌层紊乱或增生。

结论

尽管血压下降幅度很小,但即使在高血压已经很高时开始治疗,血管病变的数量仍很惊人。血管壁仅出现了通常在高血压早期动脉反应中观察到的损伤。本研究表明,西氯他宁由于其增加PGI2合成和平衡胞质游离钙增加的特性,改善了SHR-SP中高血压血管病变的正常进程。

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