Boussery Koen, Delaey Christophe, Van de Voorde Johan
Department of Physiology and Pathophysiology, Ghent University, Ghent, Belgium.
Invest Ophthalmol Vis Sci. 2004 Feb;45(2):552-9. doi: 10.1167/iovs.03-0749.
To assess and characterize the vasorelaxing effect of adrenomedullin (AM) on isolated bovine retinal arteries (BRAs).
Retinal arteries were isolated from bovine eyes and mounted in a wire myograph for isometric tension recording. Concentration-response curves were generated by cumulative addition of AM (1 pM to 0.1 micro M) to the organ bath.
AM caused a concentration-dependent relaxation of the BRAs. Removal of the endothelium of the BRAs, inhibition of nitric oxide synthase with -nitro-L-arginine (L-NA) or inhibition of soluble guanylyl cyclase with 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) significantly reduced the AM response. Cyclooxygenase inhibition with indomethacin or sodium diclofenac did not reduce, but rather increased, vasodilation. The AM-receptor antagonist AM 22-52 slightly, but significantly, reduced the AM response, whereas the CGRP-receptor antagonist CGRP 8-37 caused a more pronounced reduction. The adenosine receptor antagonist 8-(p-sulfophenyl) theophylline (8-SPT) did not affect AM-induced vasorelaxation. Inhibition of several intracellular calcium (Ca(2+))-reducing mechanisms failed to block the relaxation induced by AM. Only inhibition of the plasma membrane Ca(2+)-adenosine triphosphatase (ATPase) with vanadate significantly attenuated the AM response.
AM induces vasodilation in isolated bovine retinal arteries. Endothelium-derived NO and stimulation of CGRP- and AM-receptors appear to be involved in the AM response, whereas prostanoids and activation of adenosine receptors are not involved. Activation of Ca(2+)-extrusion by the plasma membrane Ca(2+)-ATPase may elicit the relaxation of BRAs in response to AM.
评估和表征肾上腺髓质素(AM)对离体牛视网膜动脉(BRA)的血管舒张作用。
从牛眼中分离出视网膜动脉,并安装在钢丝肌动描记器中进行等长张力记录。通过向器官浴中累积添加AM(1皮摩尔至0.1微摩尔)生成浓度-反应曲线。
AM引起BRA的浓度依赖性舒张。去除BRA的内皮、用L-硝基-L-精氨酸(L-NA)抑制一氧化氮合酶或用1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)抑制可溶性鸟苷酸环化酶可显著降低AM反应。用吲哚美辛或双氯芬酸钠抑制环氧化酶并未降低反而增加了血管舒张。AM受体拮抗剂AM 22-52轻微但显著地降低了AM反应,而降钙素基因相关肽(CGRP)受体拮抗剂CGRP 8-37导致更明显的降低。腺苷受体拮抗剂8-(对磺基苯基)茶碱(8-SPT)不影响AM诱导的血管舒张。抑制几种细胞内钙([Ca(2+)]i)降低机制未能阻断AM诱导的舒张。仅用钒酸盐抑制质膜钙(Ca(2+)-三磷酸腺苷酶(ATPase)可显著减弱AM反应。
AM在离体牛视网膜动脉中诱导血管舒张。内皮衍生的一氧化氮以及CGRP和AM受体的刺激似乎参与了AM反应,而前列腺素和腺苷受体的激活不参与。质膜Ca(2+)-ATPase激活Ca(2+)外流可能引发BRA对AM的舒张反应。