Soporific Effect of Modified Suanzaoren Decoction and Its Effects on the Expression of CCK-8 and Orexin-A

• Published in: Evidence-based complementary and alternative medicine Vol. 2020; no. 2020; pp. 1 - 17
• Main Authors: Jin, Hai-Ying, Lv, Gui-Yuan, Chen, Su-Hong, Luo, Rong, Zhou, Cong, Teng, Xi, Li, Bo, Lei, Shan-Shan, Yang, Ke, Dong, Ying-Jie, Zhan, Liang-Hui, Yu, Qiao-Xian
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 2020; Hindawi; John Wiley & Sons, Inc; Hindawi Limited
• Subjects: Acids; Animal models; Body weight; Cholecystokinin; Drug dosages; Esophagus; Exploratory behavior; GABA; Gastric juice; Gastrin; Gastrointestinal diseases; Herbal medicine; Insomnia; Latency; Open-field behavior; Orexins; Pentobarbital; Pepsin; Peptides; Sleep; Sleep deprivation; Sleep disorders; Stomach; γ-Aminobutyric acid; China; United States > US
• ISSN: 1741-427X; 1741-4288
• DOI: 10.1155/2020/6984087

Suanzaoren decoction (SZRT), a classic Chinese herbal prescription, has been used as a treatment for insomnia for more than a thousand years. However, recent studies have found no significant effects of SZRT as a treatment for insomnia caused by gastric discomfort. Herein, we studied the effects of modified Suanzaoren decoction (MSZRD) on gastrointestinal disorder-related insomnia. The main constituents of MSZRD were spinosin (2.21 mg/g) and 6-feruloylspinosin (0.78 mg/g). A pentobarbital-induced animal model of insomnia showed that MSZRD shortened sleep latency and prolonged sleep time of the male Institute of Cancer Research (ICR) mice treated for 7 days with oral MSZRD. Sprague-Dawley male rats were treated daily with oral MSZRD or placebo for 11 days and then deprived of sleep for the last 4 days to establish a model of insomnia. Of note, MSZRD-treated animals had significantly improved body weight, organ index scores, and fecal moisture relative to placebo-treated animals, as well as reduced temperature. Sleep-deprived rats exhibited more exploratory behaviors in an open-field anxiety test; however, this effect was significantly reduced in MSZRD-treated animals. We found that MSZRD treatment decreased gastric acid pH, decreased the production of gastrin, pepsin, and Orexin-A, and increased the expression of MTL and CCK-8. Importantly, serum GABA concentration was increased by treatment with MSZRD, as reflected by a decreased Glu/GABA ratio. Treated animals had increased the expression of GAD1, GABARA1, and CCKBR but decreased the expression of Orexin R1. In summary, these results suggest that MSZRD has soporific and gastroprotective effects that may be mediated by differential expression of CCK-8 and Orexin-A.