TY - JOUR
T1 - Hypersensitivity of airway reflexes induced by hydrogen sulfide
T2 - Role of TRPA1 receptors
AU - Chung, Chi Li
AU - Lin, You Shuei
AU - Chan, Nai Ju
AU - Chen, Yueh Yin
AU - Hsu, Chun Chun
N1 - Funding Information:
Funding: This research was funded in part by Taipei Medical University Hospital (105TMU‐TMUH‐12), Ministry of Science and Technology (MOST108 ‐2320‐B ‐038‐059‐MY3, M OST103 ‐2320‐B ‐038‐014 and MOST104 ‐ 2320‐B ‐038‐029) and Ministry of Education (DP2‐108‐21121‐01‐T‐01‐03, DP2‐109‐21121‐01‐T‐02‐03) from Taiwan.
Funding Information:
This research was funded in part by Taipei Medical University Hospital (105TMU-TMUH-12), Ministry of Science and Technology (MOST108-2320-B-038-059-MY3, M OST103-2320-B-038-014 and MOST104-2320-B-038-029) and Ministry of Education (DP2-108-21121-01-T-01-03, DP2-109-21121-01-T-02-03) from Taiwan.We would like to thank Lu-Yuan Lee (University of Kentucky) for providing intellectual assistance and special equipment. We also thank I-Hsuan Huang and Sheng-Hsuan Lan (Taipei Medical University) for their technical help.
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - The activation of capsaicin-sensitive lung vagal (CSLV) afferents can elicit airway reflexes. Hypersensitivity of these afferents is kn own to contribute to the airway hypersensitivity during airway inflammation. Hydrogen sulfide (H2S) has been suggested as a potential therapeutic agent for airway hypersensitivity diseases, such as asthma, because of its relaxing effect on airway smooth muscle and anti-inflammatory effect. However, it is still unknown whether H2S affects airway reflexes. Our previous study demonstrated that exogenous application of H2S sensitized CSLV afferents and enhanced Ca2+ transients in CSLV neurons. The present study aimed to determine whether the H2S-induced sensitization leads to functional changes in airway reflexes and elevates the electrical excitability of the CSLV neurons. Our results showed that, first and foremost, in anesthetized, spontaneously breathing rats, the inhalation of aerosolized sodium hydrosulfide (NaHS, a donor of H2S; 5 mg/mL, 3 min.) caused an enhancement in apneic response evoked by several stimulants of the CSLV afferents. This enhancement effect was found 5 min. after NaHS inhalation and returned to control 30 min. later. However, NaHS no longer enhanced the apneic response after perineural capsaicin treatment on both cervical vagi that blocked the conduction of CSLV fibers. Furthermore, the enhancing effect of NaHS on apneic response was totally abolished by pretreatment with intravenous HC-030031 (a TRPA1 antagonist; 8 mg/kg), whereas the potentiating effect was not affected by the pretreatment with the vehicle of HC-030031. We also found that intracerebroventricular infusion pretreated with HC-030031 failed to alter the potentiating effect of NaHS on the apneic response. Besides, the cough reflex elicited by cap saicin aerosol was enhanced by inhalation of NaHS in conscious guinea pigs. Nevertheless, this effect was entirely eliminated by pretreatment with HC-030031, not by its vehicle. Last but not least, voltage-clamp electrophysiological analysis of isolated rat CSLV neurons showed a similar pattern of potentiating effects of NaHS on capsaicin-induced inward current, and the involvement of TRPA1 receptors was also distinctly shown. In conclusion, these results suggest that H2S non-specifically enhances the airway reflex responses, at least in part, through action on the TRPA1 receptors expressed on the CSLV afferent s. Therefore, H2S should be used with caution when applying for therapeutic purposes in airway hypersensitivity diseases.
AB - The activation of capsaicin-sensitive lung vagal (CSLV) afferents can elicit airway reflexes. Hypersensitivity of these afferents is kn own to contribute to the airway hypersensitivity during airway inflammation. Hydrogen sulfide (H2S) has been suggested as a potential therapeutic agent for airway hypersensitivity diseases, such as asthma, because of its relaxing effect on airway smooth muscle and anti-inflammatory effect. However, it is still unknown whether H2S affects airway reflexes. Our previous study demonstrated that exogenous application of H2S sensitized CSLV afferents and enhanced Ca2+ transients in CSLV neurons. The present study aimed to determine whether the H2S-induced sensitization leads to functional changes in airway reflexes and elevates the electrical excitability of the CSLV neurons. Our results showed that, first and foremost, in anesthetized, spontaneously breathing rats, the inhalation of aerosolized sodium hydrosulfide (NaHS, a donor of H2S; 5 mg/mL, 3 min.) caused an enhancement in apneic response evoked by several stimulants of the CSLV afferents. This enhancement effect was found 5 min. after NaHS inhalation and returned to control 30 min. later. However, NaHS no longer enhanced the apneic response after perineural capsaicin treatment on both cervical vagi that blocked the conduction of CSLV fibers. Furthermore, the enhancing effect of NaHS on apneic response was totally abolished by pretreatment with intravenous HC-030031 (a TRPA1 antagonist; 8 mg/kg), whereas the potentiating effect was not affected by the pretreatment with the vehicle of HC-030031. We also found that intracerebroventricular infusion pretreated with HC-030031 failed to alter the potentiating effect of NaHS on the apneic response. Besides, the cough reflex elicited by cap saicin aerosol was enhanced by inhalation of NaHS in conscious guinea pigs. Nevertheless, this effect was entirely eliminated by pretreatment with HC-030031, not by its vehicle. Last but not least, voltage-clamp electrophysiological analysis of isolated rat CSLV neurons showed a similar pattern of potentiating effects of NaHS on capsaicin-induced inward current, and the involvement of TRPA1 receptors was also distinctly shown. In conclusion, these results suggest that H2S non-specifically enhances the airway reflex responses, at least in part, through action on the TRPA1 receptors expressed on the CSLV afferent s. Therefore, H2S should be used with caution when applying for therapeutic purposes in airway hypersensitivity diseases.
KW - Airway inflammation
KW - Airway reflex
KW - C -fibers
KW - HS
KW - Sensory neuron
KW - TRPA1
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U2 - 10.3390/ijms21113929
DO - 10.3390/ijms21113929
M3 - Article
C2 - 32486252
AN - SCOPUS:85085891770
SN - 1661-6596
VL - 21
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 11
M1 - 3929
ER -