Buday Tomas, Brozmanova Mariana, Biringerova Zuzana, Gavliakova Silvia, Poliacek Ivan, Calkovsky Vladimir, Shetthalli Manjunath V, Plevkova Jana
Department of Pathophysiology, Comenius University, Jessenius Faculty of Medicine Martin, Sklabinska Str, 26, Martin, 036 01, Slovak Republic.
Cough. 2012 Dec 3;8(1):11. doi: 10.1186/1745-9974-8-11.
Cough, the most important airways defensive mechanism is modulated by many afferent inputs either from respiratory tussigenic areas, but also by afferent drive from other organs. In animal models, modulation of cough by nasal afferent inputs can either facilitate or inhibit the cough response, depending on the type of trigeminal afferents stimulated.
In this study we addressed the question of possible bidirectional modulation of cough response in human healthy volunteers by nasal challenges with TRPA1 and TRPM8 agonists respectively. After nasal challenges with isocyanate (AITC), cinnamaldehyde, (-) menthol and (+) menthol (all 10-3 M) nasal symptom score, cough threshold (C2), urge to cough (Cu) and cumulative cough response were measured).
Nasal challenges with TRPA1 relevant agonists induced considerable nasal symptoms, significantly enhanced urge to cough (p<0.05) but no statistically significant modulation of the C2 and cumulative cough response. In contrast, both TRPM8 agonists administered to the nose significantly modulated all parameters including C2 (p<0.05), Cu (p<0.01) and cumulative cough response (p <0.01) documenting strong anti irritating potential of menthol isomers.
In addition to trigeminal afferents expressing TRP channels, olfactory nerve endings, trigemino - olfactoric relationships, the smell perception process and other supramedullar influences should be considered as potential modulators of the cough response in humans.
咳嗽是最重要的气道防御机制,受许多传入神经输入的调节,这些传入神经输入既来自呼吸道咳嗽诱发区域,也来自其他器官的传入驱动。在动物模型中,鼻传入神经输入对咳嗽的调节可促进或抑制咳嗽反应,这取决于所刺激的三叉神经传入神经的类型。
在本研究中,我们分别用TRPA1和TRPM8激动剂对健康志愿者进行鼻腔激发试验,探讨咳嗽反应可能的双向调节问题。在用异硫氰酸烯丙酯(AITC)、肉桂醛、(-)薄荷醇和(+)薄荷醇(均为10-3 M)进行鼻腔激发试验后,测量鼻腔症状评分、咳嗽阈值(C2)、咳嗽冲动(Cu)和累积咳嗽反应。
用TRPA1相关激动剂进行鼻腔激发试验可引起明显的鼻腔症状,显著增强咳嗽冲动(p<0.05),但对C2和累积咳嗽反应无统计学显著调节作用。相比之下,向鼻腔施用两种TRPM8激动剂均显著调节了所有参数,包括C2(p<0.05)、Cu(p<0.01)和累积咳嗽反应(p<0.01),证明薄荷醇异构体具有强大的抗刺激潜力。
除了表达TRP通道的三叉神经传入神经外,嗅神经末梢、三叉神经-嗅觉关系、嗅觉感知过程和其他延髓上的影响也应被视为人类咳嗽反应的潜在调节因素。