Yeni Yesim, Cicek Betul, Yildirim Serkan, Bolat İsmail, Hacimuftuoglu Ahmet
Faculty of Medicine, Department of Medical Pharmacology, Malatya Turgut Ozal University, Malatya, Turkey.
Faculty of Medicine, Department of Physiology, Erzincan Binali Yildirim University, Erzincan, Turkey.
Toxicol Rep. 2024 Oct 9;13:101762. doi: 10.1016/j.toxrep.2024.101762. eCollection 2024 Dec.
Therapeutic approaches based on isolated compounds derived from natural products are more common in preventing diseases involving inflammation and oxidative stress at present. S-allyl cysteine (SAC) is a promising garlic-derived organosulfur compound with many positive effects in cell models and living systems. SAC has biological activity in various fields, enclosing healing in learning and memory disorders, neurotrophic effects, and antioxidant activity. In this study, we purposed to identify the neuroprotective activity of SAC toward 6-OHDA-induced cell demise in the SH-SY5Ycell line. For this purpose, 6-OHDA-induced cytotoxicity, and biochemical, and gene expression changes were evaluated in SH-SY5Y cells. SH-SY5Y cells grown in cell culture were treated with SAC 24 h before and after 6-OHDA application. Then, cell viability, antioxidant parameters, and gene expressions were measured. Finally, immunofluorescence staining analysis was performed. Our results showed that SAC increased cell viability by 144 % at 80 µg/mL with pre-incubation (2 h). It was observed that antioxidant levels were significantly increased and oxidative stress marker levels were decreased in cells exposed to 6-OHDA after pre-treatment with SAC (). SAC supplementation also suppressed the increase in pro-inflammation levels (TNF-α/IL1/IL8) caused by 6-OHDA While 8-OHdG and Nop10 expressions were observed at a mild level in SAC pretreatment depending on the dose, 8-OHdG, and Nop10 expressions were observed at a moderate level in SAC treatment after 6-OHDA application . Our findings demonstrate the positive effect of pretreatment with SAC on SH-SY5Y cells injured by 6-OHDA, suggesting that SAC may be beneficial for neuroprotection in regulating oxidative stress and neuronal survival in an in vitro model of Parkinson's disease.
目前,基于天然产物中分离出的化合物的治疗方法在预防涉及炎症和氧化应激的疾病方面更为常见。S-烯丙基半胱氨酸(SAC)是一种有前景的源自大蒜的有机硫化合物,在细胞模型和生物系统中有许多积极作用。SAC在各个领域都具有生物活性,包括对学习和记忆障碍的修复、神经营养作用以及抗氧化活性。在本研究中,我们旨在确定SAC对6-羟基多巴胺(6-OHDA)诱导的SH-SY5Y细胞系细胞死亡的神经保护活性。为此,评估了6-OHDA诱导的SH-SY5Y细胞的细胞毒性、生化和基因表达变化。在细胞培养中生长的SH-SY5Y细胞在6-OHDA应用前后24小时用SAC处理。然后,测量细胞活力、抗氧化参数和基因表达。最后,进行免疫荧光染色分析。我们的结果表明,预孵育(2小时)时,80μg/mL的SAC可使细胞活力提高144%。观察到,用SAC预处理后,暴露于6-OHDA的细胞中抗氧化水平显著升高,氧化应激标志物水平降低。补充SAC还抑制了6-OHDA引起的促炎水平(TNF-α/IL1/IL8)的升高。虽然根据剂量在SAC预处理中观察到8-羟基脱氧鸟苷(8-OHdG)和核仁蛋白10(Nop10)表达处于轻度水平,但在6-OHDA应用后SAC处理中观察到8-OHdG和Nop10表达处于中度水平。我们的研究结果证明了SAC预处理对6-OHDA损伤的SH-SY5Y细胞的积极作用,表明SAC在帕金森病体外模型中调节氧化应激和神经元存活方面可能对神经保护有益。