Gozalov A, Petersen K A, Mortensen C, Jansen-Olesen I, Klaerke D, Olesen J
Danish Headache Center and Department of Neurology, Glostrup University Hospital, DK-2600 Glostrup, Denmark.
Cephalalgia. 2005 Apr;25(4):249-60. doi: 10.1111/j.1468-2982.2004.00848.x.
The aim of the present study was to examine the effect of K(ATP) channel openers pinacidil and levcromakalim on rat dural and pial arteries as well as their inhibition by glibenclamide. We used an in-vivo genuine closed cranial window model and an in-vitro organ bath. Glibenclamide alone reduced the dural but not the pial artery diameter compared with controls. Intravenous pinacidil and levcromakalim induced dural and pial artery dilation that was significantly attenuated by glibenclamide. In the organ bath pinacidil and levcromakalim induced dural and middle cerebral artery relaxation that was significantly attenuated by glibenclamide. In conclusion, K(ATP) channel openers induce increasing diameter/relaxation of dural and pial arteries after intravenous infusion in vivo and on isolated arteries in vitro. Furthermore, dural arteries were more sensitive to K(ATP) channel openers than pial arteries.
本研究的目的是考察钾离子通道开放剂吡那地尔和左旋克罗卡林对大鼠硬脑膜动脉和软脑膜动脉的作用以及它们被格列本脲抑制的情况。我们使用了一种体内真实闭合颅骨窗模型和一个体外器官浴槽。与对照组相比,单独使用格列本脲可使硬脑膜动脉直径减小,但对软脑膜动脉直径无影响。静脉注射吡那地尔和左旋克罗卡林可引起硬脑膜动脉和软脑膜动脉扩张,而格列本脲可显著减弱这种扩张。在器官浴槽中,吡那地尔和左旋克罗卡林可引起硬脑膜动脉和大脑中动脉舒张,而格列本脲可显著减弱这种舒张。总之,钾离子通道开放剂在体内静脉输注后以及在体外对分离的动脉可引起硬脑膜动脉和软脑膜动脉直径增加/舒张。此外,硬脑膜动脉对钾离子通道开放剂比软脑膜动脉更敏感。