Johnson H G, McNee M L, Johnson M A, Miller M D
Int Arch Allergy Appl Immunol. 1983;71(3):214-8. doi: 10.1159/000233392.
Leukotrienes have been implicated as putative mediators in several air way diseases. In previous canine studies it was shown that leukotriene C4 (LTC4) enhanced fluid secretion over baseline values and this enhancement could be blocked by hexamethonium. This indicates that leukotrienes have as one of their actions, stimulation of ganglionic motor neurons. In the present study, we determined that LTC4 acts at a similar site as the specific nicotinic receptor agonist dimethylphenylpiperazinium (DMPP). Both LTC4 and DMPP when given alone enhanced mucus secretion and induced tracheal muscle contraction over control baseline (p less than 0.05). When added to DMPP, LTC4 enhanced the DMPP effect of muscle contraction at 5 and 8 micrograms by a synergistic amount, while the secretion was only additive. The slopes of the dose-response curves for DMPP + LTC4 did not differ by a statistically significant amount. LTC4 and DMPP act on a similar, if not the same, ganglionic receptor.
白三烯被认为是几种气道疾病中的假定介质。在先前的犬类研究中表明,白三烯C4(LTC4)使液体分泌量超过基线值,且这种增加可被六甲铵阻断。这表明白三烯的作用之一是刺激神经节运动神经元。在本研究中,我们确定LTC4与特异性烟碱受体激动剂二甲基苯基哌嗪(DMPP)作用于相似位点。单独给予LTC4和DMPP均能使黏液分泌增加,并诱导气管肌肉收缩超过对照基线(p<0.05)。当加入DMPP时,LTC4在5微克和8微克时通过协同作用增强了DMPP的肌肉收缩效应,而分泌仅为相加作用。DMPP + LTC4剂量反应曲线的斜率在统计学上无显著差异。LTC4和DMPP作用于相似(即便不是相同)的神经节受体。