Laboratory of Pathophysiology Experimental, Postgraduate Program in Health Sciences, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brazil.
Laboratory of Pathophysiology Experimental, Postgraduate Program in Health Sciences, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brazil.
Pharmacol Biochem Behav. 2023 Dec;233:173661. doi: 10.1016/j.pbb.2023.173661. Epub 2023 Oct 23.
This study aimed to evaluate the effects of sertraline associated with gold nanoparticles (AuNPs) in vitro cell viability and in vivo behavior and inflammatory biomarkers in a mouse model of anxiety. Sertraline associated with AuNPs were synthesized and characterized. For the in vitro study, NIH3T3 and HT-22 cells were treated with different doses of sertraline, AuNPs, and sertraline + AuNPs and their viability was evaluated using the MTT assay. For the in vivo study, pregnant Swiss mice were administered a single dose of lipopolysaccharide (LPS) on the ninth day of gestation. The female and male offspring were divided into five treatment groups on PND 60 and administered chronic treatment for 28 days. The animals were subjected to behavioral testing and were subsequently euthanized. Their brains were collected and analyzed for inflammatory biomarkers. Sertraline associated with AuNPs exhibited significant changes in surface characteristics and increased diameters. Different doses of sertraline + AuNPs showed higher cell viability in NIH3T3 and HT-22 cells compared with sertraline alone. The offspring of LPS-treated dams exhibited anxiety-like behavior and neuroinflammatory biomarker changes during adulthood, which were ameliorated via sertraline + AuNPs treatment. The treatment response was sex-dependent and brain region-specific. These results suggest that AuNPs, which demonstrate potential to bind to other molecules, low toxicity, and reduced inflammation, can be synergistically used with sertraline to improve drug efficacy and safety by decreasing neuroinflammation and sertraline toxicity.
本研究旨在评估舍曲林与金纳米粒子(AuNPs)联合应用对体外细胞活力和焦虑症小鼠模型体内行为和炎症生物标志物的影响。合成并对舍曲林与 AuNPs 进行了表征。在体外研究中,用不同剂量的舍曲林、AuNPs 和舍曲林+AuNPs 处理 NIH3T3 和 HT-22 细胞,并通过 MTT 法评估其活力。在体内研究中,妊娠瑞士小鼠在妊娠第 9 天给予单次脂多糖(LPS)处理。在 PND60 将雌性和雄性仔鼠分为 5 个治疗组,并进行 28 天的慢性治疗。对动物进行行为测试,然后处死。收集其大脑并分析炎症生物标志物。与 AuNPs 结合的舍曲林表现出显著的表面特征变化和直径增加。与单独的舍曲林相比,不同剂量的舍曲林+AuNPs 在 NIH3T3 和 HT-22 细胞中显示出更高的细胞活力。LPS 处理的母鼠的仔鼠在成年期表现出焦虑样行为和神经炎症生物标志物变化,这些变化通过舍曲林+AuNPs 治疗得到改善。治疗反应具有性别依赖性和脑区特异性。这些结果表明,AuNPs 具有与其他分子结合的潜力、低毒性和减轻炎症的作用,与舍曲林联合使用可以通过减少神经炎症和舍曲林毒性来提高药物疗效和安全性。