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枣仁皂甙提取物的镇静和催眠活性相关的靶点和作用机制。

Targets and underlying mechanisms related to the sedative and hypnotic activities of saponin extracts from semen Ziziphus jujube.

机构信息

College of Food and Bioengineering, South China University of Technology, Guangzhou, 510640, China.

出版信息

Food Funct. 2020 May 1;11(5):3895-3903. doi: 10.1039/d0fo00098a. Epub 2020 May 14.

DOI:10.1039/d0fo00098a
PMID:32407431
Abstract

Semen Ziziphus jujube (SZJ) has been widely consumed because it is recognized as edible in China to treat insomnia disorders. However, the underlying mechanisms and potential therapeutic targets remain obscure. SZJ-I and SZJ-II with a saponin content of 52.10% and 75.20%, respectively, were extracted from SZJ. LC-MS analysis presented quite different chemical profiles of SZJ-I and SZJ-II. Mice with p-chlorophenylalanine (PCPA)-induced insomnia were used to comparatively and systematically test the sedative-hypnotic activities of SZJ-I and SZJ-II. In vivo behavioral tests revealed that SZJ-I and SZJ-II significantly shortened the immobility time and potentiated sodium pentobarbital-induced sleep. SZJ-II with a higher saponin content showed greater potency than SZJ-I. SZJ-I and SZJ-II also protected against PCPA-triggered neuropathological damages in the brain. Concentrations of 5-hydroxytryptamine (5-HT), dopamine (DA), noradrenaline (NE), glutamate (Glu), interleukin-6 (IL-6), interleukin-1β (IL-1β), nitric oxide (NO) and prostaglandin D (PGD) in plasma were significantly affected by SZJ-I and SZJ-II application. SZJ-I and SZJ-II also exhibited differential modulation of 5-hydroxytryptamine 1A (5-HT), 5-hydroxytryptamine 2A (5-HT), GABA receptor α2 (GABARα2), GABA receptor α3 (GABARα3), glutamic acid decarboxylase (GAD) 65/67, IL-6 and IL-1β expression in the hypothalamus and hippocampus. SZJ-I and SZJ-II might exert excellent sedative-hypnotic effects through multiple mechanisms that worked simultaneously. SZJ-I and especially SZJ-II are promising candidates for relieving insomnia.

摘要

酸枣仁(SZJ)在中国被广泛食用,被认为可用于治疗失眠症。然而,其潜在的作用机制和治疗靶点仍不清楚。从 SZJ 中提取出的 SZJ-I 和 SZJ-II 的总皂甙含量分别为 52.10%和 75.20%。LC-MS 分析表明 SZJ-I 和 SZJ-II 的化学组成有很大差异。使用对氯苯丙氨酸(PCPA)诱导的失眠小鼠比较和系统地测试了 SZJ-I 和 SZJ-II 的镇静催眠活性。体内行为测试表明,SZJ-I 和 SZJ-II 可显著缩短不动时间并增强戊巴比妥钠诱导的睡眠。总皂甙含量较高的 SZJ-II 比 SZJ-I 更有效。SZJ-I 和 SZJ-II 还可防止 PCPA 引发的脑内神经病理损伤。SZJ-I 和 SZJ-II 处理后,血浆 5-羟色胺(5-HT)、多巴胺(DA)、去甲肾上腺素(NE)、谷氨酸(Glu)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)、一氧化氮(NO)和前列腺素 D(PGD)的浓度均显著受到影响。SZJ-I 和 SZJ-II 对下丘脑和海马 5-羟色胺 1A(5-HT)、5-羟色胺 2A(5-HT)、GABA 受体 α2(GABARα2)、GABA 受体 α3(GABARα3)、谷氨酸脱羧酶(GAD)65/67、IL-6 和 IL-1β 的表达也有不同的调节作用。SZJ-I 和 SZJ-II 可能通过多种同时作用的机制发挥优异的镇静催眠作用。SZJ-I 尤其是 SZJ-II 是缓解失眠症的有希望的候选药物。

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