Gyoda Y, Tsukada Y, Saito A, Goto K
Institute of Anesthesiology, Nihon University School of Medicine, Tokyo, Japan.
Eur J Pharmacol. 1995 Jun 6;279(1):83-92. doi: 10.1016/0014-2999(95)00142-8.
Although dense networks of adrenergic nerves are present and noradrenaline causes vasoconstriction, electrical field stimulation failed to elicit any constriction of the isolated ring preparation of the guinea pig mesenteric artery. In the presence of an active tone, a vasodilator response was elicited by electrical field stimulation in endothelium-removed tissues. Nonadrenergic, noncholinergic nerves mediate the electrical field stimulation-induced vasodilator response, since guanethidine and atropine did not affect while tetrodotoxin abolished it. Multiple mediators seem to participate in this vasodilatation. NADPH-diaphorase-positive nerves, calcitonin gene-related peptide (CGRP)- and vasoactive intestinal peptide (VIP)-immunoreactive nerves were present in the mesenteric artery. Nitro-L-arginine but not nitro-D-arginine suppressed the electrical field stimulation-induced vasodilator response with rapid onset and L-arginine restored it. VIP and CGRP relaxed the tissue in a dose-dependent manner. Pretreatment of the animals with capsaicin partly reduced the electrical field stimulation-induced vasodilator response. CGRP-(8-37), a CGRP antagonist, slightly attenuated the vasodilator response induced by both electrical field stimulation and CGRP. Glibenclamide, an inhibitor of ATP-sensitive K+ channels, decreased the nitro-L-arginine- and capsaicin-insensitive component of the electrical field stimulation-induced vasodilator response. Zinc protoporphyrin IX, an inhibitor of CO formation, did not affect the electrical field stimulation-induced response. In the presence of nitro-L-arginine without an active tone, electrical field stimulation induced a vasoconstrictor response that was sensitive to bunazosin and guanethidine. The results show that the electrical field stimulation-induced vasodilator response of the mesenteric artery of guinea pigs is mediated by nitric oxide (NO), CGRP and some yet unidentified substance(s). Elimination of the vasodilator response unmasked the adrenergic vasoconstrictor response to electrical field stimulation.
尽管存在密集的肾上腺素能神经网络且去甲肾上腺素可引起血管收缩,但电场刺激未能引起豚鼠肠系膜动脉离体环标本的任何收缩。在有主动张力的情况下,电场刺激在去除内皮的组织中引发了血管舒张反应。非肾上腺素能、非胆碱能神经介导电场刺激诱导的血管舒张反应,因为胍乙啶和阿托品不影响该反应,而河豚毒素可消除该反应。多种介质似乎参与了这种血管舒张。肠系膜动脉中存在NADPH-黄递酶阳性神经、降钙素基因相关肽(CGRP)和血管活性肠肽(VIP)免疫反应性神经。硝基-L-精氨酸而非硝基-D-精氨酸能快速抑制电场刺激诱导的血管舒张反应,L-精氨酸可使其恢复。VIP和CGRP以剂量依赖方式使组织松弛。用辣椒素预处理动物可部分降低电场刺激诱导的血管舒张反应。CGRP拮抗剂CGRP-(8-37)可轻微减弱电场刺激和CGRP诱导的血管舒张反应。格列本脲是一种ATP敏感性钾通道抑制剂,可降低电场刺激诱导的血管舒张反应中对硝基-L-精氨酸和辣椒素不敏感的成分。锌原卟啉IX是一种CO形成抑制剂,不影响电场刺激诱导的反应。在没有主动张力且存在硝基-L-精氨酸的情况下,电场刺激诱导了对布那唑嗪和胍乙啶敏感的血管收缩反应。结果表明,豚鼠肠系膜动脉电场刺激诱导的血管舒张反应由一氧化氮(NO)、CGRP和一些尚未确定的物质介导。血管舒张反应的消除揭示了电场刺激的肾上腺素能血管收缩反应。