Decreased Motility of the Lower Esophageal Sphincter in a Rat Model of Gastroesophageal Reflux Disease May Be Mediated by Reductions of Serotonin and Acetylcholine Signaling
-
- Saegusa Yayoi
- Department of Pathophysiology and Therapeutics, Division of Pharmasciences, Faculty of Pharmaceutical Sciences, Hokkaido University Tsumura Research Laboratories, Tsumura & Co.
-
- Takeda Hiroshi
- Department of Pathophysiology and Therapeutics, Division of Pharmasciences, Faculty of Pharmaceutical Sciences, Hokkaido University Department of Gastroenterology and Hematology, Hokkaido University Graduate School of Medicine
-
- Muto Shuichi
- Department of Gastroenterology and Hematology, Hokkaido University Graduate School of Medicine Department of Otolaryngology-Head & Neck Surgery, Hokkaido University Graduate School of Medicine
-
- Oridate Nobuhiko
- Gastroenterology, Tomakomai City General Hospital
-
- Nakagawa Koji
- Department of Pathophysiology and Therapeutics, Division of Pharmasciences, Faculty of Pharmaceutical Sciences, Hokkaido University
-
- Sadakane Chiharu
- Department of Pathophysiology and Therapeutics, Division of Pharmasciences, Faculty of Pharmaceutical Sciences, Hokkaido University Tsumura Research Laboratories, Tsumura & Co.
-
- Nahata Miwa
- Tsumura Research Laboratories, Tsumura & Co.
-
- Harada Yumi
- Tsumura Research Laboratories, Tsumura & Co.
-
- Iizuka Mizuki
- Tsumura Research Laboratories, Tsumura & Co.
-
- Hattori Tomohisa
- Tsumura Research Laboratories, Tsumura & Co.
-
- Asaka Masahiro
- Department of Gastroenterology and Hematology, Hokkaido University Graduate School of Medicine
この論文をさがす
抄録
To elucidate the altered function of the lower esophageal sphincter (LES) in gastroesophageal reflux disease (GERD), we evaluated the motility proximal to LES using force transducers, contraction and relaxation responses to neurotransmitters in LES strips, and gene expression of neurotransmitter receptors in GERD rats. Force transducers were applied to the proximal LES, and contraction of the LES was monitored during free moving. In addition, LES was isolated from sham-operated and GERD rats to investigate the LES function in an organ bath, and to determine gene expression. The in vivo motility proximal to LES (% motility index) in conscious rats was decreased by atropine treatment and increased by cisapride (5-HT4 receptor agonist) treatment. Acetylcholine- and serotonin (5-HT)-induced LES contraction and sodium nitroprusside-induced relaxation in LES strips of GERD rats markedly decreased compared to sham-operated rats. The mRNA expressions of 5-HT4 and muscarinic acetylcholine 3 receptors were significantly reduced in esophageal LES strips of GERD rats compared with sham-operated rats. Intraperitoneal administration of cisapride improves the erosive damage in the esophagus in GERD rats. It is suggested that the reduction of 5-HT-induced contraction in LES strips in GERD rats may be partly due to the decrease in 5-HT4-receptor activation. The reduction of LES function may be due to the decrease in neurotransmitters signal transduction, leading to the deterioration of histopathological damage in GERD.
収録刊行物
-
- Biological & Pharmaceutical Bulletin
-
Biological & Pharmaceutical Bulletin 34 (5), 704-711, 2011
公益社団法人 日本薬学会
- Tweet
キーワード
詳細情報 詳細情報について
-
- CRID
- 1390282679601891456
-
- NII論文ID
- 130000657784
-
- NII書誌ID
- AA10885497
-
- ISSN
- 13475215
- 09186158
-
- HANDLE
- 2115/45485
-
- NDL書誌ID
- 11057942
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- IRDB
- NDL
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可