School of Clinical Medicine, Hebei University, Baoding, 071000, China.
Key Laboratory of Precise Diagnosis and Treatment of Glioma in Hebei Province, Baoding, 071000, China.
Sci Rep. 2024 Oct 5;14(1):23229. doi: 10.1038/s41598-024-74546-7.
Glioma is the most prevalent malignant brain tumor in adults. The development of engineered nanomaterials (ENMs) has led to the emergence of innovative therapeutic strategies for gliomas. Therefore, our aim is to investigate the therapeutic effect of CuO nanoparticles (NPs) on glioma and provide data support for future research. The therapeutic effect of CuO NPs on glioma rats was explored through the detection of inflammatory factors, oxidase, pathological sections, immunofluorescence, neurotransmitter, glioma biomarker proteins and genes, and rat behavioral tests. Additionally, the application prospect of CuO NPs was evaluated by treating U87MG human glioma cell line. In this study, it was found that CuO NPs can alleviate the inflammatory reaction in the hippocampus tissue of glioma rats, promote the production of ·OH and lead to the up-regulation of catalase (CAT) and superoxide dismutase (SOD) enzyme activities. Treatment with CuO NPs also inhibited the expression of matrix metalloproteinase-9 (MMP-9) biomarkers in model rats and glioma cells. Moreover, it enhanced the release of neurotransmitters, which subsequently improved spatial recognition and memory ability of glioma rats. In conclusion, CuO NPs is a potential glioma treatment for ENMs, but still needs modification and modification strategies to improve its biocompatibility and targeted delivery.
脑胶质瘤是成年人中最常见的恶性脑肿瘤。工程纳米材料(ENMs)的发展为脑胶质瘤的治疗带来了创新的治疗策略。因此,我们旨在研究氧化铜纳米颗粒(CuO NPs)对脑胶质瘤的治疗效果,为未来的研究提供数据支持。通过检测炎症因子、氧化酶、病理切片、免疫荧光、神经递质、脑胶质瘤生物标志物蛋白和基因以及大鼠行为测试,探讨了 CuO NPs 对脑胶质瘤大鼠的治疗效果。此外,通过治疗 U87MG 人胶质瘤细胞系评估了 CuO NPs 的应用前景。在这项研究中,发现 CuO NPs 可以减轻脑胶质瘤大鼠海马组织中的炎症反应,促进·OH 的产生,并导致过氧化氢酶(CAT)和超氧化物歧化酶(SOD)酶活性上调。CuO NPs 处理还抑制了模型大鼠和胶质瘤细胞中基质金属蛋白酶-9(MMP-9)生物标志物的表达。此外,它增强了神经递质的释放,随后改善了脑胶质瘤大鼠的空间识别和记忆能力。总之,CuO NPs 是一种有潜力的脑胶质瘤治疗用 ENMs,但仍需要修饰和修饰策略来提高其生物相容性和靶向递送。