Toda N, Okamura T
Department of Pharmacology, Shiga University of Medical Sciences, Seta, Japan.
J Cardiovasc Pharmacol. 1993 Nov;22(5):744-9. doi: 10.1097/00005344-199311000-00011.
In helical strips of dog distal superficial temporal artery denuded of endothelium and partially contracted with prostaglandin F2 alpha (PGF2 alpha), nicotine produced a moderate relaxation preceded by no contraction or a slight contraction. The contraction was less than that observed in proximal arterial strips obtained from the same dogs and was abolished by alpha-adrenoceptor antagonists. Relaxations under alpha-receptor blockade were greater in the distal than in the proximal arteries. Treatment with NG-nitro-L-arginine (L-NA), a nitric oxide (NO) synthase inhibitor, abolished the relaxation caused by nicotine and transmural electrical stimulation (5 Hz for 40 s), the response being reversed by L- but not by D-arginine. In monkey temporal arteries of the distal and proximal portions treated with alpha-antagonists, nicotine produced similar magnitudes of relaxation, which were abolished by treatment with the NO synthase inhibitor. Vasodilator nerves appear to play an important role in regulation of small arterial tone; noradrenergic vasoconstrictor function is less and vasodilator nerve function is more evident in dog distal arteries than in dog proximal arteries. The neurally induced relaxation in dog and monkey distal temporal arteries is postulated to be mediated by NO derived from nerves.
在去除内皮并部分用前列腺素F2α(PGF2α)收缩的犬颞浅动脉远端螺旋条带中,尼古丁产生适度舒张,之前无收缩或仅有轻微收缩。该收缩小于从同一只犬获取的近端动脉条带中观察到的收缩,且被α-肾上腺素能受体拮抗剂消除。α受体阻断下的舒张在远端动脉大于近端动脉。用一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸(L-NA)处理可消除尼古丁和经壁电刺激(5Hz,持续40秒)引起的舒张,该反应可被L-精氨酸而非D-精氨酸逆转。在用α拮抗剂处理的猴颞动脉远端和近端部分,尼古丁产生相似程度的舒张,用NO合酶抑制剂处理可消除该舒张。血管舒张神经似乎在小动脉张力调节中起重要作用;去甲肾上腺素能血管收缩功能在犬远端动脉中较弱,而血管舒张神经功能在犬远端动脉中比在近端动脉中更明显。犬和猴颞动脉远端神经诱导的舒张被推测由神经源性NO介导。