Sivasankar Mahalakshmi, Nofziger Charity, Blazer-Yost Bonnie
Department of Speech, Language, and Hearing Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Laryngoscope. 2008 Aug;118(8):1511-7. doi: 10.1097/MLG.0b013e3181772d63.
OBJECTIVES/HYPOTHESIS: Cyclic adenosine monophosphate (cAMP) is an important biological molecule that regulates ion transport and inflammatory responses in epithelial tissue. The present study examined whether the adenylyl cyclase activator, forskolin, would increase cAMP concentration in porcine vocal fold mucosa and whether the effects of increased cAMP would be manifested as a functional increase in transepithelial ion transport. Additionally, changes in cAMP concentrations following exposure to an inflammatory mediator, tumor necrosis factor-alpha (TNFalpha) were investigated.
In vitro experimental design with matched treatment and control groups.
Porcine vocal fold mucosae (N = 30) and tracheal mucosae (N = 20) were exposed to forskolin, TNFalpha, or vehicle (dimethyl sulfoxide) treatment. cAMP concentrations were determined with enzyme-linked immunosorbent assay. Ion transport was measured using electrophysiological techniques.
Thirty minute exposure to forskolin significantly increased cAMP concentration and ion transport in porcine vocal fold and tracheal mucosae. However, 30-minute and 2-hour exposure to TNFalpha did not significantly alter cAMP concentration.
We demonstrate that forskolin-sensitive adenylyl cyclase is present in vocal fold mucosa, and further, that the product, cAMP increases vocal fold ion transport. The results presented here contribute to our understanding of the intracellular mechanisms underlying vocal fold ion transport. As ion transport is important for maintaining superficial vocal fold hydration, data demonstrating forskolin-stimulated ion transport in vocal fold mucosa suggest opportunities for developing pharmacological treatments that increase surface hydration.
目的/假设:环磷酸腺苷(cAMP)是一种重要的生物分子,可调节上皮组织中的离子转运和炎症反应。本研究旨在探讨腺苷酸环化酶激活剂福斯高林是否会增加猪声带黏膜中的cAMP浓度,以及cAMP增加的效应是否会表现为跨上皮离子转运功能增强。此外,还研究了暴露于炎症介质肿瘤坏死因子-α(TNFα)后cAMP浓度的变化。
采用配对治疗组和对照组的体外实验设计。
将猪声带黏膜(N = 30)和气管黏膜(N = 20)分别用福斯高林、TNFα或溶剂(二甲基亚砜)处理。用酶联免疫吸附测定法测定cAMP浓度。使用电生理技术测量离子转运。
暴露于福斯高林30分钟可显著增加猪声带和气管黏膜中的cAMP浓度及离子转运。然而,暴露于TNFα 30分钟和2小时并未显著改变cAMP浓度。
我们证明声带黏膜中存在对福斯高林敏感的腺苷酸环化酶,而且其产物cAMP可增加声带离子转运。本文结果有助于我们理解声带离子转运的细胞内机制。由于离子转运对于维持声带表面水合作用很重要,证明福斯高林刺激声带黏膜离子转运的数据提示了开发增加表面水合作用的药物治疗方法的机会。