Bell C
Br J Pharmacol. 1985 May;85(1):249-53. doi: 10.1111/j.1476-5381.1985.tb08853.x.
The antagonistic effects of the alpha-adrenoceptor blocking agent phentolamine on vasoconstrictor responses to intraluminal noradrenaline and lumbar sympathetic nerve stimulation were compared in the hindlimb of the anaesthetized dog. Sympathetic stimulation with 1 pulse or trains of 4-10 pulses at 0.4-40 Hz produced graded vasoconstrictor responses that were matched in amplitude by intra-arterial injections of 10(-8) - 10(-6) g noradrenaline. Phentolamine (0.5 mg kg-1 i.v.) attenuated amplitude-matched responses to both types of stimuli to quite similar extents. The extent of the effect of phentolamine on neurogenic responses was greater with 1 pulse stimulation than with trains, and greater with 4 pulse than with 10 pulse trains. The effect was maximal within 2 min of phentolamine administration and wore off in parallel with that on responses to injected noradrenaline. The results are consistent with the view that transmitter released from noradrenergic vasoconstrictor nerves acts primarily on subjunctional alpha-adrenoceptors.
在麻醉犬的后肢中,比较了α-肾上腺素能受体阻断剂酚妥拉明对腔内去甲肾上腺素和腰交感神经刺激引起的血管收缩反应的拮抗作用。以0.4 - 40Hz的频率给予1个脉冲或4 - 10个脉冲的串刺激交感神经,可产生分级的血管收缩反应,其幅度与动脉内注射10(-8) - 10(-6)g去甲肾上腺素相匹配。酚妥拉明(0.5mg kg-1静脉注射)对两种类型刺激的幅度匹配反应的减弱程度相当相似。酚妥拉明对神经源性反应的作用程度,1个脉冲刺激时比串刺激时更大,4个脉冲串刺激时比10个脉冲串刺激时更大。酚妥拉明给药后2分钟内作用最大,并与对注射去甲肾上腺素反应的作用同时消退。这些结果与以下观点一致,即去甲肾上腺素能血管收缩神经释放的递质主要作用于接头后α-肾上腺素能受体。