Research Cluster Molecular & Cognitive Neuroscience, Neurobiology Laboratory for Brain Aging and Mental Health, University of Basel, Basel, Switzerland; Psychiatric University Clinics, Basel, Switzerland.
Laboratoire Boiron, Messimy, France.
J Ethnopharmacol. 2025 Jan 10;336:118714. doi: 10.1016/j.jep.2024.118714. Epub 2024 Aug 22.
Gelsemium dynamized dilutions (GDD) are known as a remedy for a wide range of behavioral and psychological symptoms of depression and anxiety at ultra-low doses, yet the underlying mechanisms of the mode of action of G. sempervirens itself are not well understood.
The present study was designed to examine the neuroprotective effects of Gelsemium preparations in counteracting stress-related mitochondrial dysfunctions in neuronal cells.
We started by studying how serum deprivation affects the mitochondrial functions of human neuroblastoma (SH-SY5Y) cells. Next, we looked into the potential of various Gelsemium dilutions to improve cell survival and ATP levels. After identifying the most effective dilutions, 3C and 5C, we tested their ability to protect SH-SY5Y cells from stress-induced mitochondrial deficits. We measured total and mitochondrial superoxide anion radicals using fluorescent dyes dihydroethidium (DHE) and the red mitochondrial superoxide indicator (MitoSOX). Additionally, we assessed total nitric oxide levels with 4,5-diaminofluorescein diacetate (DAF-2DA), examined the redox state using pRA305 cells stably transfected with a plasmid encoding a redox-sensitive green fluorescent protein, and analyzed mitochondrial network morphology using an automated high-content analysis device, Cytation3. Furthermore, we investigated bioenergetics by measuring ATP production with a bioluminescence assay (ViaLighTM HT) and evaluated mitochondrial respiration (OCR) and glycolysis (ECAR) using the Seahorse Bioscience XF24 Analyzer. Finally, we determined cell survival using an MTT reduction assay.
Our research indicates that Gelsemium dilutions (3C and 5C) exhibited neuroprotective effects by: - Normalizing total and mitochondrial superoxide anion radicals and total nitric oxide levels. - Regulating the mitochondrial redox environment and mitochondrial networks morphology. - Increasing ATP generation as well as OCR and ECAR levels, thereby reducing the viability loss induced by serum withdrawal stress.
These findings highlight that dynamized Gelsemium preparations may have neuroprotective effects against stress-induced cellular changes in the brain by regulating mitochondrial functions, essential for the survival, plasticity, and function of neurons in depression.
已证实,极低剂量的筋骨草动力稀释剂(GDD)可有效缓解抑郁和焦虑的多种行为和心理症状,但其作用机制尚不清楚。
本研究旨在研究筋骨草制剂在对抗应激相关神经元细胞线粒体功能障碍方面的神经保护作用。
我们首先研究了血清剥夺如何影响人神经母细胞瘤(SH-SY5Y)细胞的线粒体功能。接下来,我们研究了各种筋骨草稀释剂提高细胞存活率和 ATP 水平的潜力。在确定最有效的 3C 和 5C 稀释剂后,我们测试了它们保护 SH-SY5Y 细胞免受应激诱导的线粒体缺陷的能力。我们使用荧光染料二氢乙啶(DHE)和红色线粒体超氧阴离子指示剂(MitoSOX)测量总超氧阴离子自由基和线粒体超氧阴离子自由基。此外,我们使用 4,5-二氨基荧光素二乙酸酯(DAF-2DA)评估总一氧化氮水平,使用稳定转染编码氧化还原敏感绿色荧光蛋白质粒的 pRA305 细胞评估氧化还原状态,并使用自动高内涵分析设备 Cytation3 分析线粒体网络形态。此外,我们通过生物发光测定法(ViaLighTM HT)测量 ATP 产生来研究生物能,使用 Seahorse Bioscience XF24 分析仪评估线粒体呼吸(OCR)和糖酵解(ECAR)。最后,我们使用 MTT 还原测定法测定细胞存活率。
我们的研究表明,筋骨草稀释剂(3C 和 5C)通过以下方式发挥神经保护作用:- 使总超氧阴离子自由基、线粒体超氧阴离子自由基和总一氧化氮水平正常化。- 调节线粒体氧化还原环境和线粒体网络形态。- 增加 ATP 生成以及 OCR 和 ECAR 水平,从而减少血清剥夺应激引起的细胞活力丧失。
这些发现强调了动力化筋骨草制剂可能通过调节线粒体功能对大脑应激诱导的细胞变化具有神经保护作用,线粒体功能对神经元的存活、可塑性和功能至关重要。