Bouskela E, Cyrino F Z, Marcelon G
Department of Physiology and Biophysics, University of Lund, Sweden.
J Cardiovasc Pharmacol. 1994 Jul;24(1):165-70. doi: 10.1097/00005344-199407000-00025.
We investigated the influence of alpha-adrenoceptors blockers and calcium blockers on the effects of the venotonic agent Ruscus extract on the diameter of arterioles (ID 10-70 microns) and venules (ID 20-135 microns) of hamster cheek pouch microvasculature in vivo. For microcirculatory measurements, the preparations were placed under an intravital microscope coupled to a closed-circuit TV system. The TV monitor display was used to obtain arteriolar and venular internal diameter recordings (always at the same site) by an image shearing device. All drugs were applied topically. Ruscus extract was tested in different concentrations and in combination with prazosin (alpha 1-adrenoceptor antagonist), rauwolscine (alpha 2-adrenoceptor antagonist), or diltiazem (calcium blocker). Topical application of Ruscus extract elicited concentration-dependent responses in the studied vessels: arterioles remained unchanged in the concentration range tested, whereas venules remained unchanged or constricted depending on the concentration used. The observed venular constriction could be blocked by low concentrations (10(-9) M) of prazosin or diltiazem and by high concentrations (> 10(-6) M) of rauwolscine. Our results suggest that the venular constriction elicited by Ruscus extract in vivo, at the microcirculatory level, is mediated by calcium and by alpha-adrenoceptors and further support data previously reported on larger vessels and on patients with venous insufficiency.
我们研究了α-肾上腺素受体阻滞剂和钙阻滞剂对静脉张力剂鲁斯可提取物对仓鼠颊囊微脉管系统体内小动脉(内径10 - 70微米)和小静脉(内径20 - 135微米)直径影响的作用。对于微循环测量,将标本置于与闭路电视系统相连的活体显微镜下。通过图像剪切装置利用电视监视器显示屏获取小动脉和小静脉内径记录(始终在同一部位)。所有药物均局部应用。对不同浓度的鲁斯可提取物以及与哌唑嗪(α1 - 肾上腺素受体拮抗剂)、育亨宾(α2 - 肾上腺素受体拮抗剂)或地尔硫䓬(钙阻滞剂)联合使用进行了测试。局部应用鲁斯可提取物在所研究的血管中引发浓度依赖性反应:在所测试的浓度范围内小动脉保持不变,而小静脉根据所用浓度保持不变或收缩。观察到的小静脉收缩可被低浓度(10(-9) M)的哌唑嗪或地尔硫䓬以及高浓度(> 10(-6) M)的育亨宾阻断。我们的结果表明,鲁斯可提取物在体内微循环水平引发的小静脉收缩是由钙和α - 肾上腺素受体介导的,进一步支持了先前关于较大血管和静脉功能不全患者的报道数据。