Wahl M, Kuschinsky W
Circ Res. 1979 Feb;44(2):161-5. doi: 10.1161/01.res.44.2.161.
We studied the effect of histamine and H1 or H2 blockers on the diameter of pial arteries (39-227 micron) using microapplication into the perivascular space. Concentration-response curves for histamine showed dilations which started at 10(-7) M and were maximal at 10(-5) and 10(-4) M. The H2 blocker, cimetidine, induced no vascular reaction over the whole concentration range tested (10(-7) to 10(-3) M). The H1 blocker, mepyramine, was not vasoactive in the concentration range from 10(-7) to 5 X 10(-5) M and evoked dilations at higher concentrations. The concentration-response curve for histamine was only slightly displaced by 10(-5) M mepyramine but was significantly shifted to the right by 10(-5) M cimetidine. The dilating effect of histamine could be reduced in a stepwise manner by increasing concentrations of cimetidine. These findings are in accordance with a selective antagonism between histamine and cimetidine at the H2 receptors of smooth muscle cells of pial arteries. The insignificant role of H1 receptors in histamine-induced dilations is supported by the finding that a combination of H1 and H2 blockers resulted in the same reduction of histamine-induced dilation as did the application of the H2 blocker.
我们通过向血管周围间隙微量注射组胺、H1或H2受体阻滞剂,研究了它们对软脑膜动脉(直径39 - 227微米)直径的影响。组胺的浓度 - 反应曲线显示,从10^(-7) M开始出现扩张,在10^(-5) M和10^(-4) M时达到最大。H2受体阻滞剂西咪替丁在整个测试浓度范围(10^(-7)至10^(-3) M)内未引起血管反应。H1受体阻滞剂甲氧苄胺在10^(-7)至5×10^(-5) M浓度范围内无血管活性,在更高浓度时引起血管扩张。组胺的浓度 - 反应曲线仅被10^(-5) M甲氧苄胺轻微移位,但被10^(-5) M西咪替丁显著右移。通过增加西咪替丁的浓度,组胺的扩张作用可逐步降低。这些发现与组胺和西咪替丁在软脑膜动脉平滑肌细胞H2受体处的选择性拮抗作用一致。H1受体在组胺诱导的扩张中作用不显著这一观点得到了以下发现的支持:H1和H2受体阻滞剂联合使用导致的组胺诱导扩张的降低程度与单独使用H2受体阻滞剂相同。