González C, Barroso C, Martín C, Gulbenkian S, Estrada C
Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma de Madrid, Spain.
J Cereb Blood Flow Metab. 1997 Sep;17(9):977-84. doi: 10.1097/00004647-199709000-00007.
The participation of nitric oxide and vasoactive intestinal peptide (VIP) in the neurogenic regulation of bovine cerebral arteries was investigated. Nitrergic nerve fibers and ganglion-like groups of neurons were revealed by NADPH-diaphorase staining in the adventitial layer of bovine cerebral arteries. NADPH diaphorase also was present in endothelial cells but not in the smooth muscle layer. Double immunolabeling for neuronal nitric oxide synthase and VIP indicated that both molecules co-localized in the same nerve fibers in these vessels. Transmural nerve stimulation (200 mA, 0.2 milliseconds, 1 to 8 Hz) of endothelium-denuded bovine cerebral artery rings precontracted with prostaglandin F2 alpha, produced tetrodotoxin-sensitive relaxations that were completely suppressed by NG-nitro-L-arginine methyl ester (L-NAME) and by the guanylyl cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxaline (ODQ), but were not affected by the adenylyl cyclase inhibitor 9-(tetrahydro-2-furanyl)-9H-purin-6-amine (SQ 22,536), nor by VIP tachyphylaxis induced by pretreatment with 1 mumol/L VIP. Transmural nerve stimulation also elicited increases in intracellular cyclic GMP concentration, which were prevented by L-NAME, and small decreases in intracellular cyclic AMP concentration. Addition of VIP to bovine cerebral artery rings without endothelium produced a concentration-dependent relaxation that was partially inhibited by L-NAME, ODQ, and SQ 22,536. The effects of L-NAME and SQ 22,536 were additive. VIP induced a transient increase in intracellular cyclic GMP concentration, which was maximal 1 minute after VIP addition, when the highest relaxation rate was observed, and which was blocked by L-NAME. It is concluded that nitric oxide produced by perivascular neurons and nerve fibers fully accounts for the experimental neurogenic relaxation of bovine cerebral arteries and that VIP, which also is present in the same perivascular fibers, acts as a neuromodulator by activating neuronal nitric oxide synthase.
研究了一氧化氮和血管活性肠肽(VIP)在牛脑动脉神经源性调节中的作用。通过NADPH-黄递酶染色在牛脑动脉外膜层发现了含氮能神经纤维和神经元样神经节群。NADPH黄递酶也存在于内皮细胞中,但不存在于平滑肌层。神经元型一氧化氮合酶和VIP的双重免疫标记表明,这两种分子共定位于这些血管的同一神经纤维中。对用前列腺素F2α预收缩的去内皮牛脑动脉环进行跨壁神经刺激(200 mA,0.2毫秒,1至8 Hz),产生了对河豚毒素敏感的舒张反应,该反应被NG-硝基-L-精氨酸甲酯(L-NAME)和鸟苷酸环化酶抑制剂1H-[1,2,4]恶二唑并[4,3-a]喹喔啉(ODQ)完全抑制,但不受腺苷酸环化酶抑制剂9-(四氢-2-呋喃基)-9H-嘌呤-6-胺(SQ 22,536)的影响,也不受1 μmol/L VIP预处理诱导的VIP快速耐受的影响。跨壁神经刺激还引起细胞内环鸟苷酸浓度升高,这被L-NAME阻止,同时细胞内环腺苷酸浓度略有下降。向无内皮的牛脑动脉环中加入VIP产生浓度依赖性舒张,该舒张被L-NAME、ODQ和SQ 22,536部分抑制。L-NAME和SQ 22,536的作用是相加的。VIP诱导细胞内环鸟苷酸浓度短暂升高,在加入VIP后1分钟达到最大值,此时观察到最高的舒张速率,并且该升高被L-NAME阻断。结论是,血管周围神经元和神经纤维产生的一氧化氮完全解释了牛脑动脉的实验性神经源性舒张,并且同样存在于同一血管周围纤维中的VIP通过激活神经元型一氧化氮合酶发挥神经调节剂的作用。