Upregulation of acid sensing ion channels is associated with esophageal hypersensitivity in GERD

• Published in: The FASEB journal Vol. 36; no. 1; pp. e22083 - n/a
• Main Authors: Han, Xu, Zhang, Yawen, Lee, Allen, Li, Zhaoshen, Gao, Jun, Wu, Xiaoyin, Zhao, Jiulong, Wang, Hui, Chen, Di, Zou, Duowu, Owyang, Chung
• Format: Journal Article
• Language: English
• Published: United States 01.01.2022
• Subjects: acid sensing ion channel 1 and 3 (ASIC1 and 3); Acid Sensing Ion Channels - biosynthesis; Acid Sensing Ion Channels - genetics; Animals; Esophagus - metabolism; Gastroesophageal Reflux - genetics; Gastroesophageal Reflux - metabolism; gastroesophageal reflux disease (GERD); Heartburn - genetics; Heartburn - metabolism; Humans; Male; neuronal hyperexcitability; Rats; Rats, Sprague-Dawley; Up-Regulation; visceral hypersensitivity; acid sensing ion channel 1 and 3 (ASIC1 and 3); gastroesophageal reflux disease (GERD); neuronal hyperexcitability; visceral hypersensitivity
• ISSN: 0892-6638; 1530-6860
• DOI: 10.1096/fj.202100606R

Proton pump inhibitors (PPIs) are the mainstay of therapy for gastroesophageal reflux disease (GERD) but up to 60% of patients have inadequate response to therapy. Acid sensing ion channels (ASICs) play important roles in nociception. This study aimed to investigate whether the increased expression of ASICs results in neuronal hyperexcitability in GERD. Esophageal biopsies were taken from GERD patients and healthy subjects to compare expression of ASIC1 and 3. Next, gene and protein expression of ASIC1 and 3 from esophageal mucosa and dorsal root ganglia (DRG) neurons were measured by qPCR, Western‐blot and immunofluorescence in rodent models of reflux esophagitis (RE), non‐erosive reflux disease (NERD), and sham operated groups. Excitability of DRG neurons in the GERD and sham groups were also tested by whole‐cell patch‐clamp recordings. We demonstrated that ASIC1 and 3 expression were significantly increased in patients with RE compared with healthy controls. This correlated positively with symptom severity of heartburn and regurgitation (p < .001). Next, ASIC1 and 3 gene and protein expression in rodent models of RE and NERD were similarly increased in esophageal mucosa as well as T3–T5 DRG neurons compared with sham operation. DRG neurons from RE animals showed hyperexcitability compared with sham group. However, intrathecal injection of ASIC specific inhibitors, PcTx1 and APTEx‐2, as well as silencing ASIC1 and 3 genes with specific siRNAs prevented visceral hypersensitivity. Overall, upregulation of ASIC1 and 3 may lead to visceral hypersensitivity in RE and NERD and may be a potential therapeutic target for PPI non‐responsive patients.