Davis C, Kannan M S, Jones T R, Daniel E E
J Appl Physiol Respir Environ Exerc Physiol. 1982 Nov;53(5):1080-7. doi: 10.1152/jappl.1982.53.5.1080.
An in vitro study of neural and myogenic control of human tracheal smooth muscle was undertaken. Over 80% of these had active tension and 13% had phasic contractile activity. Tonic and phasic activities were not reversed by indomethacin, 5,8,11,14-eicosatetraynoic acid, methysergide, mepyramine, atropine, or tetrodotoxin (TTX) but were blocked by the calcium antagonist verapamil. In some quiescent strips, tonic and/or phasic activity was induced by exposure to potassium-conductance blockers such as 4-aminopyridine (4-AP) and tetraethylammonium chloride (TEA). Electrical (field) stimulation resulted in frequency-dependent biphasic responses: an initial atropine-sensitive cholinergic contraction followed by a nonadrenergic relaxation. This biphasic response to low stimulus parameters (less than 0.5 ms, less than 15 Hz) was blocked by TTX and scorpion venom and enhanced by 4-AP and TEA, consistent with a neural mechanism. Relaxation responses to longer pulse durations (0.5-1 ms) were not blocked by TTX despite abolition of contraction nor were they enhanced by 4-AP and TEA, suggesting a nonneural mechanism. ATP, adenosine, arachidonate metabolites, histamine, 5-hydroxytryptamine, neurotensin, or vasoactive intestinal polypeptide were ruled out as possible nonadrenergic mediators. The nature and physiological significance of the nonneural inhibitory response remains unknown.
开展了一项关于人气管平滑肌神经和肌源性控制的体外研究。其中超过80%具有主动张力,13%具有相位性收缩活动。强直和相位性活动不受消炎痛、5,8,11,14 - 二十碳四烯酸、甲基麦角新碱、美吡拉敏、阿托品或河豚毒素(TTX)的影响,但被钙拮抗剂维拉帕米阻断。在一些静止的条带上,通过暴露于钾通道阻滞剂如4 - 氨基吡啶(4 - AP)和氯化四乙铵(TEA)可诱导出强直和/或相位性活动。电(场)刺激导致频率依赖性双相反应:最初是阿托品敏感的胆碱能收缩,随后是非肾上腺素能舒张。这种对低刺激参数(小于0.5毫秒,小于15赫兹)的双相反应被TTX和蝎毒阻断,并被4 - AP和TEA增强,这与神经机制一致。对较长脉冲持续时间(0.5 - 1毫秒)的舒张反应尽管收缩被消除但未被TTX阻断,也未被4 - AP和TEA增强,提示存在非神经机制。ATP、腺苷、花生四烯酸代谢产物、组胺、5 - 羟色胺、神经降压素或血管活性肠肽被排除为可能的非肾上腺素能介质。非神经抑制反应的性质和生理意义仍不清楚。