乳铁蛋白修饰的纳米乳增强了弓形虫诱导的神经损伤的脑靶向性和治疗效果。

Jing-Mei Lu, Guang-Nan Jin, Yan Xin, Jing-Wen Ma, Xin-Yu Shen, Yan-Zhu Quan, Yi-Ming Liu, Jin-Yi Zhou, Bing-Zhe Wang, Ying-Biao Li, Xiang Xu, Lian-Xun Piao
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引用次数: 0

摘要

刚地弓形虫是一种嗜神经原生动物寄生虫,影响中枢神经系统并引起各种神经系统疾病。以往的研究表明,Arctigenin (AG)具有抗t。并减少弓形虫感染引起的抑郁样行为。本研究旨在通过制备含AG的乳铁蛋白修饰纳米乳(Lf-AG-NEs)来提高AG的脑靶向性和治疗效果。利用弓形虫RH菌株体内和体外感染模型,以及BV2小胶质细胞和原代神经元细胞共培养系统,制备了lf修饰的纳米乳剂,并对其进行了评估。通过实时定量PCR、western blotting、免疫荧光、流式细胞术、免疫组织化学、尼氏染色等方法,探讨Lf-AG-NEs对刚地弓形虫诱导的神经损伤的影响,并阐明其可能的分子机制。体外评估显示,Lf-AG-NEs显著增加细胞摄取和血脑屏障穿透。这些纳米乳明显抑制了弓形虫在脑组织和BV2细胞中的增殖,超过了游离AG或AG- nes的作用。此外,Lf-AG-NEs通过下调TLR4/NF-κB和TNFR1/NF-κB信号通路,显著缓解神经病理改变,减少小胶质细胞活化和神经炎症。BV2细胞与原代皮质神经元共培养表明,与CLI-095和R7050类似,Lf-AG-NEs可以减弱弓形虫诱导的小胶质细胞激活和随后的神经元损伤。综上所述,成功制备的Lf-AG-NEs不仅增强了抗t。同时还通过调节小胶质信号通路,增强了对弓形虫诱导的神经元损伤的保护作用。
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Lactoferrin-modified nanoemulsions enhance brain-targeting and therapeutic efficacy of arctigenin against Toxoplasma gondii-induced neuronal injury.

Toxoplasma gondii, a neurotropic protozoan parasite, affects the central nervous system and causes various neurological disorders. Previous studies have demonstrated that Arctigenin (AG) exhibits anti-T. gondii activity and reduces depression-like behaviors induced by T. gondii infection. This study aimed to enhance AG's brain-targeting and therapeutic efficacy by developing lactoferrin-modified nanoemulsions loaded with AG (Lf-AG-NEs). Lf-modified nanoemulsions were prepared and assessed using in vivo and in vitro infection models with the T. gondii RH strain, and a co-culture system of BV2 microglia and primary neuron cells. The effects of Lf-AG-NEs on T. gondii-induced neuronal injury were examined, and potential molecular mechanisms were elucidated through real-time quantitative PCR, western blotting, immunofluorescence, flow cytometry, immunohistochemistry, and Nissl staining. In vitro assessments showed significant increases in cellular uptake and blood-brain barrier penetration by Lf-AG-NEs. These nanoemulsions notably inhibited T. gondii proliferation in brain tissue and BV2 cells, surpassing the effects of free AG or AG-NEs alone. Additionally, Lf-AG-NEs substantially alleviated neuropathological changes and reduced microglial activation and neuroinflammation by downregulating the TLR4/NF-κB and TNFR1/NF-κB signaling pathways. Co-culturing BV2 cells with primary cortical neurons indicated that Lf-AG-NEs, similarly to CLI-095 and R7050, attenuated T. gondii-induced microglial activation and subsequent neuronal injury. In conclusion, the successfully prepared Lf-AG-NEs not only enhanced the anti-T. gondii effect but also strengthened the protective impact against neuronal injury induced by T. gondii, through the modulation of microglial signaling pathways.

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来源期刊
CiteScore
7.90
自引率
7.50%
发文量
31
审稿时长
48 days
期刊介绍: The International Journal for Parasitology – Drugs and Drug Resistance is one of a series of specialist, open access journals launched by the International Journal for Parasitology. It publishes the results of original research in the area of anti-parasite drug identification, development and evaluation, and parasite drug resistance. The journal also covers research into natural products as anti-parasitic agents, and bioactive parasite products. Studies can be aimed at unicellular or multicellular parasites of human or veterinary importance.
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