低pH溶液对豚鼠肺中辣椒素敏感神经激活的调节。

Pharmacology & toxicology Pub Date : 2000-01-01
S Auberson, J S Lacroix, J M Lundberg
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引用次数: 0

摘要

我们研究了低pH溶液对气道感觉神经的刺激及其引起的支气管收缩。比较了低pH缓冲液和相同pH(5和6)下乳酸溶液的效果,记录了低pH对辣椒素效果的影响。我们采用离体豚鼠灌注肺模型,以充气压力作为支气管平滑肌张力的指标,肺灌注液中降钙素基因相关肽样免疫反应性表征感觉神经激活。低pH缓冲液和相同pH为5和6的乳酸溶液(3和4.1 mM)诱导pH依赖性支气管收缩和肽释放,经辣椒素系统预处理后完全消除。在无Ca2+输注后,这两种反应都被显著抑制。选择性辣椒素拮抗剂Capsazepine (10(-6) M)可显著降低所有溶液引起的降钙素基因相关肽样免疫反应性溢出。环合酶阻断剂双氯芬酸(10(-5)M)对pH 5、pH 6和乳酸3 mM (pH 6)诱导的肽释放有抑制作用,但对乳酸4.1 mM (pH 5)的肽释放无抑制作用。双氯芬酸对乳酸3 mM的肽释放无显著影响,而辣椒平对乳酸3 mM的肽释放有显著影响。辣椒素与低pH缓冲液对降钙素基因相关肽样免疫反应性释放有协同作用,对支气管收缩有加性作用。由此可见,在离体豚鼠肺中,乳酸和低pH缓冲液通过刺激辣椒素敏感的C纤维,通过部分依赖于细胞外Ca2+的途径,诱导降钙素基因相关肽样免疫反应性释放和支气管收缩。pH值为6时,降钙素基因相关肽样免疫反应性释放的机制似乎相同,而pH值为5时,低pH缓冲液与乳酸之间存在明显差异。我们的研究结果还表明,质子活性可能对辣椒素敏感的感觉神经发挥调节作用,其机制尚不清楚。
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Modulation of capsaicin-sensitive nerve activation by low pH solutions in guinea-pig lung.

We have studied the stimulation of airways sensory nerves by low pH solutions and concomitantly induced bronchoconstriction. The effect of low pH buffer and lactic acid solutions at the same pH (5 and 6) were compared and the influence of low pH on the capsaicin effect was recorded. We have used the isolated guinea-pig perfused lung model taking the insufflation pressure as an indicator of bronchial smooth muscle tone while the calcitonin gene-related peptide-like immunoreactivity measured in the lung perfusate represented sensory nerves activation. Low pH buffer and lactic acid solution (3 and 4.1 mM) at the same pH of 5 and 6 induced pH-dependent bronchoconstriction and peptides release which were completely abolished after systemic pretreatment with capsaicin. Both responses were significantly inhibited after Ca2+-free infusion. Capsazepine (10(-6) M), a selective capsaicin antagonist, significantly reduced the calcitonin gene-related peptide-like immunoreactivity overflow evoked by all the solutions studied. Diclofenac (10(-5) M), a cyclooxygenase blocker, inhibited pH 5, pH 6 and lactic acid 3 mM (pH 6)-evoked peptide release, but not lactic acid 4.1 mM (pH 5). The functional response was not significantly modified after diclofenac while only the lactic acid 3 mM response was significantly reduced by capsazepine. There was a synergistic interaction between capsaicin and low pH buffer on calcitonin gene-related peptide-like immunoreactivity release and an additive effect on bronchoconstriction. It is concluded that in the isolated perfused guinea-pig lung, lactic acid and low pH buffer induced calcitonin gene-related peptide-like immunoreactivity release and bronchoconstriction by stimulation of capsaicin-sensitive C fibres via a pathway partly dependent of extracellular Ca2+. The mechanism of calcitonin gene-related peptide-like immunoreactivity release seems to be the same at pH 6, while differences are evident at pH 5 between low pH buffer and lactic acid. Our results also suggest that proton activity could exert a modulatory role on the capsaicin-sensitive sensory nerves by a mechanism which remains to be clarified.

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