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Paeoniflorin Alleviates Abnormalities in Rats with Functional Dyspepsia by Stimulating the Release of Acetylcholine.

Authors :
Zou X
Wang Y
Wang Y
Yang J
Guo H
Cai Z
Source :
Drug design, development and therapy [Drug Des Devel Ther] 2020 Dec 22; Vol. 14, pp. 5623-5632. Date of Electronic Publication: 2020 Dec 22 (Print Publication: 2020).
Publication Year :
2020

Abstract

Introduction: Paeoniflorin is a main active component in traditional Chinese medicine. Paeoniae alba radix is widely used as a spasmolytic and pain-relieving agent for abdominal spasmodic pain. Functional dyspepsia (FD) is characterized by pain or burning in the epigastrium, fullness, bloating and nausea. However, limited information is available about the effect of paeoniflorin on FD.<br />Materials and Methods: In this study, iodoacetamide or clonidine-induced FD rat models were established to investigate the impacts of paeoniflorin on FD induced by different pathophysiologic disturbances.<br />Results: We found the therapeutic effect of paeoniflorin through assessing the gastric emptying, gastric accommodation and visceral hypersensitivity. This function of paeoniflorin was related to the release of acetylcholine (ACh), which was accompanied by reduced acetylcholinesterase (AchE) activity in stomach and hypothalamus. Paeoniflorin administration inhibited the cyclo-oxygenase-2 (COX-2) expression and increased the level of ghrelin in the stomach. Besides, the levels of occludin and ZO-1 were elevated in the duodenum from paeoniflorin-treated rats, suggesting the impaired duodenal barrier was ameliorated.<br />Discussion: These results indicate that paeoniflorin possesses the ability to alleviate functional dyspepsia.<br />Competing Interests: The authors report no conflicts of interest in this work.<br /> (© 2020 Zou et al.)

Details

Language :
English
ISSN :
1177-8881
Volume :
14
Database :
MEDLINE
Journal :
Drug design, development and therapy
Publication Type :
Academic Journal
Accession number :
33376306
Full Text :
https://doi.org/10.2147/DDDT.S260703