Hehuan Anshen decoction inhibits ferroptosis to ameliorate p-Chlorophenylalanine-induced insomnia by activating GPX4 pathway

Qing Deng , Yanan Li , Wenyun Kui , Linting He , Yuxia Wang , Nana Li , Jian Xu , Kaiqiang Wang , Chunchun Xue , Zhongwei Sha
{"title":"Hehuan Anshen decoction inhibits ferroptosis to ameliorate p-Chlorophenylalanine-induced insomnia by activating GPX4 pathway","authors":"Qing Deng ,&nbsp;Yanan Li ,&nbsp;Wenyun Kui ,&nbsp;Linting He ,&nbsp;Yuxia Wang ,&nbsp;Nana Li ,&nbsp;Jian Xu ,&nbsp;Kaiqiang Wang ,&nbsp;Chunchun Xue ,&nbsp;Zhongwei Sha","doi":"10.1016/j.prmcm.2024.100504","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Insomnia is a chronic disease affecting a third of the global adult population. Hehuan Anshen Decoction (HHASD), an innovative formula derived from Traditional Chinese medicine, has demonstrated therapeutic efficacy in treating insomnia, however, the potential pharmacological mechanism underlying its anti-insomnia effects remains incompletely elucidated. This study aimed to explore the underlying mechanism of HHASD treatment in mice with insomnia induced by p-Chlorophenylalanine (PCPA).</p></div><div><h3>Methods</h3><p>The active constituents of HHASD were analysed by means of UPLC<img>HRMS. PCPA mice were administered HHASD orally for 7 days. The anti-insomnia phenotype of HHASD were assessed by behavioral tests, encompassing the open field test and pentobarbital sodium-induced sleep test, alongside the measurement of hypothalamic 5-HT levels. Then, we conducted an in-depth analysis of specific ferroptosis markers, considering biochemistry, genetics and morphology. Additionally, ferroptosis inhibitor RSL3 was used to observe the underlying mechanism of the effects of HHASD.</p></div><div><h3>Results</h3><p>HHASD could effectively improve the insomnia behaviors induced by PCPA, resulting in increased movement trajectories, decreased sleep latency and prolonged sleep duration. Specifically, HHASD exerted a neuroprotective effect by enhancing the integrity of Nissl bodies in the hypothalamus of the PCPA mice. Mechanistic analysis revealed that HHASD could reverse the hypothalamic ferroptosis phenotype of insomnia mice by restoring the lowered levels of glutathione (GSH), inhibiting iron accumulation and elevated malondialdehyde (MDA), and mitigating mitochondrial cristae damage. Furthermore, HHASD enhanced the expression of SLC7A11 and GPX4 and reduced the ASCL4 in the hypothalamus, while the anti-insomnia effect of HHASD in the PCPA mice was eliminated by the GPX4 inhibitor RLS3.</p></div><div><h3>Conclusion</h3><p>HHASD ameliorates insomnia-related behaviors and protects against neuronal damage by suppressing ferroptosis by regulation GPX4 signaling. This study is not only a valuable attempt to explore the potential mechanism of Traditional Chinese formula but also will provide a novel targeted therapy for the treatment strategy of insomnia.</p></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"13 ","pages":"Article 100504"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667142524001465/pdfft?md5=fc851356a17336fcd2a9eaf3831f7f37&pid=1-s2.0-S2667142524001465-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacological Research - Modern Chinese Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667142524001465","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Insomnia is a chronic disease affecting a third of the global adult population. Hehuan Anshen Decoction (HHASD), an innovative formula derived from Traditional Chinese medicine, has demonstrated therapeutic efficacy in treating insomnia, however, the potential pharmacological mechanism underlying its anti-insomnia effects remains incompletely elucidated. This study aimed to explore the underlying mechanism of HHASD treatment in mice with insomnia induced by p-Chlorophenylalanine (PCPA).

Methods

The active constituents of HHASD were analysed by means of UPLCHRMS. PCPA mice were administered HHASD orally for 7 days. The anti-insomnia phenotype of HHASD were assessed by behavioral tests, encompassing the open field test and pentobarbital sodium-induced sleep test, alongside the measurement of hypothalamic 5-HT levels. Then, we conducted an in-depth analysis of specific ferroptosis markers, considering biochemistry, genetics and morphology. Additionally, ferroptosis inhibitor RSL3 was used to observe the underlying mechanism of the effects of HHASD.

Results

HHASD could effectively improve the insomnia behaviors induced by PCPA, resulting in increased movement trajectories, decreased sleep latency and prolonged sleep duration. Specifically, HHASD exerted a neuroprotective effect by enhancing the integrity of Nissl bodies in the hypothalamus of the PCPA mice. Mechanistic analysis revealed that HHASD could reverse the hypothalamic ferroptosis phenotype of insomnia mice by restoring the lowered levels of glutathione (GSH), inhibiting iron accumulation and elevated malondialdehyde (MDA), and mitigating mitochondrial cristae damage. Furthermore, HHASD enhanced the expression of SLC7A11 and GPX4 and reduced the ASCL4 in the hypothalamus, while the anti-insomnia effect of HHASD in the PCPA mice was eliminated by the GPX4 inhibitor RLS3.

Conclusion

HHASD ameliorates insomnia-related behaviors and protects against neuronal damage by suppressing ferroptosis by regulation GPX4 signaling. This study is not only a valuable attempt to explore the potential mechanism of Traditional Chinese formula but also will provide a novel targeted therapy for the treatment strategy of insomnia.

Abstract Image

合欢安神煎丸通过激活 GPX4 通路抑制铁变态反应,从而改善对氯苯丙氨酸诱导的失眠症
导言失眠是一种慢性疾病,影响着全球三分之一的成年人。合欢安神汤(HHASD)是一种源自传统中药的创新配方,在治疗失眠方面具有显著疗效,但其抗失眠作用的潜在药理机制仍未完全阐明。本研究旨在探讨对氯苯丙氨酸(PCPA)诱导的失眠小鼠服用华蟾素治疗失眠的潜在机制。给 PCPA 小鼠口服 HHASD 7 天。通过行为测试,包括开阔地测试和戊巴比妥钠诱导睡眠测试,以及下丘脑5-羟色胺水平的测量,来评估HHASD的抗失眠表型。然后,我们从生物化学、遗传学和形态学等方面对特定的铁变态反应标志物进行了深入分析。结果HHASD能有效改善PCPA诱导的失眠行为,使运动轨迹增加,睡眠潜伏期缩短,睡眠时间延长。具体而言,HHASD通过增强PCPA小鼠下丘脑中Nissl体的完整性而发挥神经保护作用。机理分析表明,HHASD可以通过恢复谷胱甘肽(GSH)的降低水平、抑制铁积累和丙二醛(MDA)的升高以及减轻线粒体嵴的损伤来逆转失眠小鼠下丘脑的铁中毒表型。此外,HHASD 还能增强下丘脑中 SLC7A11 和 GPX4 的表达,减少 ASCL4 的表达,而 GPX4 抑制剂 RLS3 则会消除 HHASD 对 PCPA 小鼠的抗失眠作用。该研究不仅是探索中药配方潜在作用机制的一次有益尝试,也将为失眠症的治疗策略提供一种新的靶向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.60
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信