Differential Regulation of ASICs and TRPV1 by Zinc in Rat Bronchopulmonary Sensory Neurons
| Autor: | Charles R. Moss, Qihai Gu, Zhanna V. Vysotskaya |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Male
Pulmonary and Respiratory Medicine Sensory Receptor Cells TRPV1 TRPV Cation Channels chemistry.chemical_element Bronchi Zinc Sensitivity and Specificity Rats Sprague-Dawley chemistry.chemical_compound Transient receptor potential channel Reference Values Animals Lung Acid-sensing ion channel Ion channel Analysis of Variance Vagus Nerve Long-term potentiation Rats Acid Sensing Ion Channels nervous system chemistry Biochemistry Models Animal Biophysics Capsazepine Intracellular Signal Transduction |
| Zdroj: | Lung. 192:927-934 |
| ISSN: | 1432-1750 0341-2040 |
| DOI: | 10.1007/s00408-014-9634-1 |
| Popis: | Zinc has been known to act as a signaling molecule that regulates a variety of neuronal functions. In this study, we aimed to study the effect of zinc on two populations of acid-sensitive ion channels, acid-sensing ion channels (ASICs), and transient receptor potential vanilloid receptor-1 (TRPV1), in vagal bronchopulmonary sensory neurons. Rat vagal sensory neurons innervating lungs and airways were retrogradely labeled with a fluorescent tracer. Whole-cell perforated patch-clamp recordings were carried out in primarily cultured bronchopulmonary sensory neurons. The acid-evoked ASIC and TRPV1 currents were measured and compared between before and after the zinc pretreatment. ASIC currents were induced by a pH drop from 7.4 to 6.8 or 6.5 in the presence of capsazepine (10 µM), a specific TRPV1 antagonist. Pretreatment with zinc (50 or 300 µM, 2 min) displayed different effects on the two distinct phenotypes of ASIC currents: a marked potentiation on ASIC channels with fast kinetics of activation and inactivation or no significant effect on ASIC currents with slow activation and inactivation. On the other hand, pretreatment with zinc significantly inhibited the acid (pH 5.5 or 5.3)-induced TRPV1 currents. The inhibition was abolished by intracellular chelation of zinc by TPEN (25 µM), indicating that intracellular accumulation of zinc was likely required for its inhibitory effect on TRPV1 channels. Our study showed that zinc differentially regulates the activities of ASICs and TRPV1 channels in rat vagal bronchopulmonary sensory neurons. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink