Neuroprotective Effects of Thymol-Loaded Selenium Nanoparticles Against 6-OHDA-Induced Apoptosis and Oxidative Stress in an In Vitro Parkinson's Disease Model.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Farzaneh Abbasinezhad-Moud, Matin Shirazinia, Raheleh Mirzabeyki, Elham Einafshar, Mohaddeseh Sadat Alavi, Sayeh Shaban, Elaheh Gheibi, Afsane Bahrami
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引用次数: 0

Abstract

Introduction: Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons within the substantia nigra, leading to progressive motor dysfunction. There are still limited diseasemodifying options that counteract the process of disease progression. This study aimed to evaluate the neuroprotective effects of thymol, both in its free form and when loaded onto selenium nanoparticles (SeNPs), in a 6-hydroxydopamine (6-OHDA)-induced PD model using SH-SY5Y cells.

Method: SeNPs were synthesized using a chemical reduction method with ascorbic acid, achieving a 68% entrapment efficiency for thymol. FTIR analysis suggested an interaction between thymol and selenium, which was confirmed by EDX analysis. Nano-Se-thymol particles were observed to be spherical, with a mean size of 135.7 nm and a negative surface charge.

Results: Nano-Se-thymol exhibited low toxicity in normal fibroblast cells and demonstrated greater neuroprotective effects against 6-OHDA-induced cytotoxicity compared to thymol. Nano-Se-thymol significantly reduced ROS generation and increased cell viability compared to 6-OHDA. Furthermore, Nano-Se-thymol decreased the expression of NF-κB inflammatory markers and caspase-3 apoptotic proteins, which were elevated by 6-OHDA, compared to thymol alone.

Discussion: Nano-Se-Thymol significantly attenuates 6-OHDA-induced cytotoxicity in an established in vitro model of PD. The neuroprotective efficacy of Nano-Se-Thymol is attributed to its enhanced antioxidant capacity, as evidenced by a significant reduction in ROS levels, along with its ability to inhibit apoptosis and modulate cell cycle progression.

Conclusions: Nano-Se-thymol is a potential disease-modifying agent for the treatment of PD; however, further studies and long-term safety assessments are essential to confirm these benefits and understand the underlying mechanisms.

胸腺负载硒纳米颗粒对6-羟多巴胺诱导的帕金森病模型的凋亡和氧化应激的神经保护作用
简介:帕金森病(PD)的特点是黑质内多巴胺能神经元变性,导致进行性运动功能障碍。仍然有有限的疾病改善选择,以抵消疾病进展的过程。在SH-SY5Y细胞诱导的6-羟多巴胺(6-OHDA)诱导的PD模型中,本研究旨在评估百里香酚的神经保护作用,无论是游离形式还是负载于硒纳米粒子(SeNPs)上。方法:采用抗坏血酸化学还原法合成SeNPs,百里酚的包封率为68%。FTIR分析表明百里香酚与硒存在相互作用,EDX分析证实了这一点。纳米se -thymol颗粒呈球形,平均尺寸为135.7 nm,表面带负电荷。结果:与百里香酚相比,纳米se -thymol在正常成纤维细胞中表现出低毒性,并且对6- ohda诱导的细胞毒性表现出更大的神经保护作用。与6-OHDA相比,纳米se -thymol显著减少ROS的产生,提高细胞活力。此外,纳米se-百里香酚降低了NF-κB炎症标志物和caspase-3凋亡蛋白的表达,而6-OHDA升高了这些蛋白的表达。讨论:纳米se - thymol显著减弱6- ohda诱导的PD体外模型的细胞毒性。纳米se - thymol的神经保护功效归功于其增强的抗氧化能力,这一点可以通过其显著降低ROS水平以及抑制细胞凋亡和调节细胞周期进程的能力来证明。结论:纳米se-百里香酚是治疗帕金森病的潜在疾病调节剂;然而,进一步的研究和长期的安全性评估是必要的,以确认这些益处和了解潜在的机制。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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