吸入莪术挥发油可通过激活 Nrf2 途径减轻氧化应激和改善线粒体功能障碍,从而减轻抑郁样行为。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Meixizi Lai, Dan Su, Zhifu Ai, Ming Yang, Zhentao Zhang, Qi Zhang, Wenxiang Shao, Tao Luo, Genhua Zhu, Yonggui Song
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引用次数: 0

摘要

目的:莪术(Curcumae Rhizoma,CR)是一种临床常用的传统中药,其挥发性成分具有多种活性作用。本研究探讨了莪术挥发油(CRVO)对抑郁小鼠的影响及其可能的作用机制:方法:采用 GC-MS 分析莪术挥发油的化学成分。采用 DPPH 和 ABTS 自由基清除试验评估 CRVO 的体外抗氧化能力。慢性不可预知轻度应激(CUMS)模型用于评估 CRVO 的抗抑郁作用。使用 Nissl 染色、ELISA 和透射电子显微镜研究了 CRVO 对体内氧化应激的影响。免疫印迹法和免疫荧光法检测了 Nrf2/HO-1/NQO1 信号通路。使用 Nrf2 抑制剂 ML385 验证了 Nrf2 对接受 CRVO 治疗的 CUMS 小鼠的影响:植物化学分析显示,CRVO含有丰富的特征成分,包括莪术烯(31.1%)、莪术二酮(30.56%)和莪术酮(12.44%)。在体内,施用 CRVO 能明显改善 CUMS 引起的类似抑郁的行为。此外,吸入 CRVO 还能明显减轻 CUMS 引起的氧化应激,改善神经元损伤和线粒体功能障碍。机理研究结果表明,CRVO的作用机制与Nrf2/HO-1/NQO1通路有关,使用ML385时,CRVO的抗氧化和抗抑郁作用减弱:总之,通过调节Nrf2通路,吸入CRVO可以降低抑郁小鼠的氧化应激,从而减少神经元损伤和线粒体功能障碍,缓解抑郁样行为。我们的研究为满足临床用药的多样性提供了前瞻性研究基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhalation of Curcumae Rhizoma volatile oil attenuates depression-like behaviours via activating the Nrf2 pathway to alleviate oxidative stress and improve mitochondrial dysfunction.

Objectives: Curcumae Rhizoma (CR) is a traditional Chinese medicine used frequently in clinics, which contains volatile components that exhibit various active effects. This study explores the effect of Curcumae Rhizoma volatile oil (CRVO) on depressive mice and its possible mechanism of action.

Methods: Chemical composition of CRVO was analysed by GC-MS. DPPH and ABTS free radical scavenging assays were used to evaluate the in vitro antioxidant capacity of CRVO. A chronic unpredictable mild stress (CUMS) model was used to evaluate the antidepressant effect of CRVO. The effects of CRVO on oxidative stress in vivo were investigated using Nissl staining, ELISA and transmission electron microscopy. The Nrf2/HO-1/NQO1 signalling pathway was detected by western blotting and immunofluorescence. ML385, a Nrf2 inhibitor was used to validate the effect of Nrf2 on CUMS mice with CRVO treatment.

Key findings: Phytochemical analysis showed that CRVO is rich in its characteristic components, including curzerene (31.1%), curdione (30.56%), and germacrone (12.44%). In vivo, the administration of CRVO significantly ameliorated CUMS-induced depressive-like behaviours. In addition, inhalation of CRVO significantly alleviated the oxidative stress caused by CUMS and improved neuronal damage and mitochondrial dysfunction. The results of mechanistic studies showed that the mechanism of action is related to the Nrf2/HO-1/NQO1 pathway and the antioxidant and antidepressant effects of CRVO were weakened when ML385 was used.

Conclusions: In summary, by regulating the Nrf2 pathway, inhalation of CRVO can reduce oxidative stress in depressed mice, thereby reducing neuronal damage and mitochondrial dysfunction to alleviate depression-like behaviours. Our study offers a prospective research foundation to meet the diversity of clinical medication.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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