Detre Z, Jellinek H
Pathol Res Pract. 1986 Mar;181(1):60-70. doi: 10.1016/S0344-0338(86)80189-3.
Malignant renal hypertension was induced in male Wistar rats. In the early phase of the disease, ie. the 1st week, a transient and generalized activation of arterial cellular functions was observed, while later, on day 21 widespread intimal proliferations developed in the arteries. This early activation included an increase in transmural permeability, DNA-, protein, collagen, elastin and ground substance synthesis, a rise in mural PGI2 content and an increase in number of Weibel-Palade bodies. An activation of platelets and monocytes could also be detected during the 1st week. In a group of rats the development of malignant hypertension was interrupted following the early activation of arteries and the incidence of intimal proliferations was compared with that of rats with maintained hypertension. No intimal proliferation was observed on day 21 in the rats with interrupted hypertension. It is concluded that the early activation of the artery does not furnish enough stimulus for triggering intimal proliferations and intimal plaques are not direct sequelae of the early arterial reaction. Furthermore the entrance of plasma materials during transmural permeability increase can not induce smooth muscle proliferation if the hypertension is interrupted.
在雄性Wistar大鼠中诱发恶性肾性高血压。在疾病的早期阶段,即第1周,观察到动脉细胞功能出现短暂的全身性激活,而在后期,即第21天,动脉中出现广泛的内膜增生。这种早期激活包括跨壁通透性增加、DNA、蛋白质、胶原蛋白、弹性蛋白和基质合成增加、壁内前列环素(PGI2)含量升高以及魏-帕小体数量增加。在第1周期间还可检测到血小板和单核细胞的激活。在一组大鼠中,动脉早期激活后恶性高血压的发展被阻断,并将内膜增生的发生率与持续高血压的大鼠进行比较。在高血压被阻断的大鼠中,第21天时未观察到内膜增生。得出的结论是,动脉的早期激活没有提供足够的刺激来引发内膜增生,内膜斑块不是早期动脉反应的直接后遗症。此外,如果高血压被阻断,跨壁通透性增加期间血浆物质的进入不会诱导平滑肌增殖。