Zhu Jiwen, Liu Qi, Chen Yan, Zhang JiaMing, Xu Qinghua, Wu Zhengwei
Institute of Advanced Technology, University of Science and Technology of China, Hefei, Anhui, 230026, China.
School of Nuclear Science and Technology, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Heliyon. 2024 Aug 11;10(16):e36079. doi: 10.1016/j.heliyon.2024.e36079. eCollection 2024 Aug 30.
Neurodegenerative disorders are chronic conditions that progressively damage and destroy parts of the nervous system, and are currently considered permanent and incurable. Alternative strategies capable of effectively healing neuronal damage have been actively pursued. Here, we report the neuroprotective effects of baicalin (BA) combined with plasma-activated medium (PAM) against glutamate-induced excitotoxicity in SH-SY5Y cells. Through in vitro assays, the cell viability, inflammation, apoptosis, and oxidative stress were evaluated. The co-application of BA and PAM significantly enhanced cell viability, reduced pro-inflammatory markers (TNF-α and NF-κB), decreased apoptotic proteins (Bax and Caspase-3) and boosted antioxidative defenses (increased SOD activity and lowered ROS levels). This study confirms the potential of combining BA with PAM as an effective therapeutic strategy for mitigating the effects of excitotoxicity. PAM is a promising adjunct and potential drug delivery method in neuroprotective therapy, providing a new avenue for developing treatments for diseases characterized by neuronal damage.
神经退行性疾病是一类慢性疾病,会逐渐损害并破坏神经系统的部分结构,目前被认为是永久性且无法治愈的。人们一直在积极探索能够有效修复神经元损伤的替代策略。在此,我们报告了黄芩苷(BA)与血浆激活培养基(PAM)联合使用对SH-SY5Y细胞中谷氨酸诱导的兴奋性毒性的神经保护作用。通过体外试验,评估了细胞活力、炎症、凋亡和氧化应激情况。BA与PAM联合应用显著提高了细胞活力,降低了促炎标志物(TNF-α和NF-κB),减少了凋亡蛋白(Bax和Caspase-3),并增强了抗氧化防御能力(提高了SOD活性,降低了ROS水平)。本研究证实了将BA与PAM联合使用作为减轻兴奋性毒性影响的有效治疗策略的潜力。PAM是神经保护治疗中一种有前景的辅助手段和潜在的药物递送方法,为开发针对以神经元损伤为特征的疾病的治疗方法提供了一条新途径。