Muller Alexandre Pastoris, Ferreira Gabriela Kozuchovski, da Silva Sabrina, Nesi Renata Tiscoski, de Bem Silveira Gustavo, Mendes Carolini, Pinho Ricardo A, da Silva Paula Marcos Marques, Silveira Paulo Cesar Lock
Laboratório de Fisiologia e Bioquímica do Exercício, Programa de Pós-Graduação em Ciências da Saúde, Universidade do Extremo Sul Catarinense, 88806-00 Criciúma, SC, Brazil.
Laboratório de Farmacologia e Fisiopatologia da Pele, Departamento de Farmacologia, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.
Mater Sci Eng C Mater Biol Appl. 2017 Aug 1;77:1145-1150. doi: 10.1016/j.msec.2017.04.027. Epub 2017 Apr 6.
Gold nanoparticles (GNPs) have antioxidant and anti-inflammatory effects. However, toxicity is still a concern; therefore, it is critical to study both the therapeutic and toxic properties of GNPs. In this study, we evaluated the effects of the intraperitoneal administration of GNPs (20nm, at a concentration of 2.5mg/L for 21days) every 24 or 48h on oxidative stress, antioxidant status, and electron chain transport (ETC) in the brain. Liver histology and blood marker analyses were conducted to establish a time routine of GNP administration. The concentrations of GNP in the brain and liver were similar. Hepatic and serum levels of cholesterol, triglycerides, and transaminases were not altered after the administration of GNP every 24 or 48h. The superoxide and nitric oxide levels were unchanged after administration of GNP. Dichlorodihydrofluorescein (DCFH) levels decreased after the administration of GNP every 48h compared with that in the saline group. Sulfhydryl and carbonyl levels, as well as superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), and glutathione (GSH) activities were not altered in the brain after administration of GNP in the two time periods studied. The GNP 48h group showed increased brain ETC activity. Compared to that in the saline group, the GNP 24h group showed marked parenchyma changes with cell necrosis and leukocyte infiltration. We therefore suggest that a concentration of 2.5mg/L of GNP administered every 48h has potential therapeutic benefits without toxicity.
金纳米颗粒(GNPs)具有抗氧化和抗炎作用。然而,毒性仍是一个令人担忧的问题;因此,研究GNPs的治疗特性和毒性特性至关重要。在本研究中,我们评估了每24小时或48小时腹腔注射GNPs(20纳米,浓度为2.5毫克/升,持续21天)对大脑氧化应激、抗氧化状态和电子链转运(ETC)的影响。进行肝脏组织学和血液标志物分析以确定GNPs给药的时间规律。大脑和肝脏中GNP的浓度相似。每24小时或48小时给予GNP后,肝脏和血清中的胆固醇、甘油三酯和转氨酶水平未发生改变。给予GNP后,超氧化物和一氧化氮水平未发生变化。与生理盐水组相比,每48小时给予GNP后二氯二氢荧光素(DCFH)水平降低。在所研究的两个时间段内,给予GNP后大脑中的巯基和羰基水平以及超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)、过氧化氢酶(CAT)和谷胱甘肽(GSH)活性均未改变。GNP 48小时组的大脑ETC活性增加。与生理盐水组相比,GNP 24小时组出现明显的实质改变,伴有细胞坏死和白细胞浸润。因此,我们认为每48小时给予2.5毫克/升的GNP具有潜在的治疗益处且无毒性。