Kimoto Y, Ito Y
Br J Urol. 1987 May;59(5):463-72. doi: 10.1111/j.1464-410x.1987.tb04847.x.
Neural control of the penile artery and vein of dogs was investigated using isometric tension recording and microelectrode methods. Field stimulation evoked twitch-like contractions of these two vessels and these contractions were blocked by guanethidine. In the artery, twitch-like contractions were more effectively blocked by yohimbine than by prazosin. During high tone of arterial and venous tissues evoked by noradrenaline (NA) in the presence of guanethidine, field stimulation evoked muscle relaxation that was not affected by atropine but was abolished by tetrodotoxin. In parallel to the mechanical responses, field stimulation evoked excitatory junction potentials (EJPs) in both arterial and venous smooth muscle cells. In the case of the artery, an action potential was superimposed on the EJP. The NA-induced contraction was suppressed by vasoactive intestinal polypeptide (VIP), dose-dependently. On the other hand, alpha, beta-methylene-ATP did not affect the muscle relaxation induced by field stimulation. These results indicate that the penile artery and vein of the dog are innervated by adrenergic excitatory nerves and non-adrenergic, non-cholinergic inhibitory nerves. The transmitter possibly involved in the latter is discussed.
采用等长张力记录法和微电极法研究了犬阴茎动脉和静脉的神经控制。场刺激可诱发这两种血管出现类似抽搐的收缩,且这些收缩可被胍乙啶阻断。在动脉中,育亨宾比哌唑嗪更有效地阻断类似抽搐的收缩。在胍乙啶存在的情况下,去甲肾上腺素(NA)诱发动脉和静脉组织产生高张力时,场刺激可诱发肌肉松弛,该松弛不受阿托品影响,但可被河豚毒素消除。与机械反应平行,场刺激在动脉和静脉平滑肌细胞中均诱发兴奋性接头电位(EJP)。在动脉中,动作电位叠加在EJP上。血管活性肠肽(VIP)剂量依赖性地抑制NA诱导的收缩。另一方面,α,β-亚甲基三磷酸腺苷不影响场刺激诱导的肌肉松弛。这些结果表明,犬阴茎动脉和静脉受肾上腺素能兴奋性神经和非肾上腺素能、非胆碱能抑制性神经支配。文中讨论了可能参与后者的递质。