Altura B M, Altura B T, Gebrewold A
Br J Pharmacol. 1980 Nov;70(3):351-3. doi: 10.1111/j.1476-5381.1980.tb08709.x.
The actions of the local perivascular application of verapamil to rat mesenteric, pial and cremaster muscle arterioles and muscular venules (15 to 35 micrometers i.d.), was examined in situ, at the microcirculatory level, by use of a high-resolution closed circuit television microscope recording system. Local application of verapamil (1 to 100 micrograms) to cremaster muscle arterioles and venules of the rat induces dose-dependent vasodilatation and increased perfusion of capillaries. However, neither arteriolar nor muscular venular lumen sizes and capillary blood flow of the rat mesenteric or pial vasculatures were altered by even high doses of verapamil. Although these direct in situ microvascular findings do indicate that verapamil can induced dilatation of microscopic resistance and capacitance vessels in skeletal muscle, our data do not support the concept that verapamil induces non-specific peripheral vasodilatation.
利用高分辨率闭路电视显微镜记录系统,在微循环水平原位研究了维拉帕米局部血管周围应用于大鼠肠系膜、软脑膜和提睾肌小动脉及肌性微静脉(内径15至35微米)的作用。将维拉帕米(1至100微克)局部应用于大鼠提睾肌小动脉和微静脉可引起剂量依赖性血管舒张并增加毛细血管灌注。然而,即使高剂量的维拉帕米也不会改变大鼠肠系膜或软脑膜血管系统的小动脉或肌性微静脉管腔大小以及毛细血管血流。虽然这些直接的原位微血管研究结果确实表明维拉帕米可诱导骨骼肌中微小阻力血管和容量血管舒张,但我们的数据并不支持维拉帕米诱导非特异性外周血管舒张这一概念。