化学
氧化应激
抗氧化剂
药理学
体内
谷胱甘肽过氧化物酶
超氧化物歧化酶
谷胱甘肽
神经保护
脂质过氧化
小檗碱
细胞毒性
过氧化氢酶
肿瘤坏死因子α
体外
生物化学
酶
免疫学
医学
生物
生物技术
作者
Marjan Heidarzadeh,Mehriar Amininasab,Seyed Mahdi Rezayat,Seyyedeh Elaheh Mousavi
出处
期刊:Current Drug Delivery
[Bentham Science]
日期:2024-11-01
卷期号:21 (9): 1273-1283
被引量:1
标识
DOI:10.2174/0115672018258030230920035222
摘要
Introduction: In the present study, neuroprotective effects of berberine (BBR) and berberine nanomicelle (BBR-NM) against lipopolysaccharides (LPS)-induced stress oxidative were investigated, and compared by evaluating their antioxidant and anti-inflammatory activities in PC12 cells, and rat brains. A fast, green, and simple synthesis method was used to prepare BBR-NMs. Method: The prepared BBR-NMs were then characterized using dynamic light scattering (DLS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). In vitro experiments were carried out on the LPS-treated PC12 cell lines to investigate the anti-cytotoxic and antioxidant properties of BBR-NM and BBR. The results showed that BBR-NMs with a diameter of ~100 nm had higher protective effects against ROS production and cytotoxicity induced by LPS in PC12 cells in comparison with free BBR. Results: Moreover, in vivo experiments indicated that the activity levels of antioxidant enzymes, such as superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), increased in the brain of LPS-treated rats administrated with BBR-NM at the optimum dose of 100 mg.kg-1. BBR-NM administration also resulted in decreased concentration of lipid peroxidation (MDA) and pro-inflammatory cytokines, such as Serum interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α). Conclusion: Overall, BBR-NM demonstrated higher neuroprotective effects than free BBR, making it a promising treatment for improving many diseases caused by oxidative stress and inflammation.
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