Goldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia; National Research Tomsk State University, Tomsk, Russia.
Goldberg Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia.
Microvasc Res. 2018 Sep;119:91-97. doi: 10.1016/j.mvr.2018.04.005. Epub 2018 May 6.
Many pathological mechanisms are involved in the development of arterial hypertension; disturbance of the rheological properties of blood and microvascular rarefaction are among those mechanisms.
The effect of p-tyrosol (Tyr) on hemorheological parameters and microvascularization in the cerebral cortex of spontaneously hypertensive rats (SHRs) at the stage of blood pressure rising (5-11 weeks) was studied.
Blood viscosity (BV), plasma viscosity (PV), hematocrit, erythrocyte aggregation and deformability, the oxygen transport capacity index (OTCI), and the capillary network in the cerebral cortex after the course of treatment of Tyr (50 mg/kg daily i.g. for 6 weeks) were studied. Control normotensive Wistar-Kyoto (WKY) rats and control SHRs received an equivalent amount of 1% starch mucilage.
In comparison with WKY rats, disturbances of rheological blood parameters and a decrease in OTCI were revealed in control SHRs at the 11 weeks of life. By the end of the experiment, brain microvascular rarefaction was observed in the control SHRs (the average density of the capillary bed was reduced due to a decrease in the number of capillaries with a diameter of 3-7 μm). In SHRs rats treated with Tyr, BV and PV, the indices of erythrocyte aggregation were lower, and OTCI was higher in comparison with control SHRs. The density of the capillary network and the number of capillaries of 3-7 μm in the cerebral cortex of SHRs rats receiving Tyr were significantly higher than the corresponding values in control SHRs.
When Tyr is administered to young SHRs during the development of hypertension, it limits the development of hyperviscosity syndrome, improves the oxygen transport capacity and eliminates microvascular rarefaction in the cerebral cortex.
许多病理机制参与了动脉高血压的发展;血液流变学特性的紊乱和微血管稀疏是其中的机制之一。
研究对苯丙氨酸(Tyr)对血压升高阶段(5-11 周)自发性高血压大鼠(SHR)大脑皮质血流动力学参数和微血管化的影响。
研究了 Tyr(每天 50mg/kg 灌胃 6 周)治疗后血液粘度(BV)、血浆粘度(PV)、红细胞压积、红细胞聚集和变形性、氧传输能力指数(OTCI)以及大脑皮质毛细血管网络的变化。用等量 1%淀粉糊给 WKY 正常血压大鼠和 SHR 对照组进行处理。
与 WKY 大鼠相比,11 周龄的对照组 SHR 出现了血液流变学参数紊乱和 OTCI 降低。实验结束时,对照组 SHR 出现了脑微血管稀疏(毛细血管床的平均密度因 3-7μm 直径的毛细血管数量减少而降低)。与对照组 SHR 相比,Tyr 治疗的 SHR 大鼠的 BV 和 PV、红细胞聚集指数降低,OTCI 升高。Tyr 治疗的 SHR 大鼠大脑皮质毛细血管网络的密度和 3-7μm 直径的毛细血管数量明显高于对照组 SHR。
在高血压发展过程中,当 Tyr 被给予年轻的 SHR 时,它限制了高粘度综合征的发展,提高了氧传输能力,并消除了大脑皮质的微血管稀疏。