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藏药硫化汞制剂生物合成纳米颗粒促进内吞作用并实现药物穿越血脑屏障

Biosynthesized nanoparticles of Tibetan medicine mercuric sulfide preparation to promote endocytosis and realize drug crossing through blood brain barrier.

作者信息

Jia Wenjing, Yue Huilan, Liu Liying, Wang Luya, Zhang Lin, Tao Jihong, Zhou Guoying, Wei Lixin, Dong Hongxin, Dhondrup Rinchen, Zhao Xiaohui

机构信息

Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, CAS and Qinghai Provincial Key Laboratory of Tibetan Medicine Research, Qinghai, 810008, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

J Nanobiotechnology. 2025 Jun 16;23(1):445. doi: 10.1186/s12951-025-03525-5.

Abstract

β-HgS as the main component of Tibetan medicine Zuotai (ZT) is widely used in the treatment of central nervous system diseases. Although the synergism of HgS has been clinically verified for more than 2000 years, its synergetic mechanism is still an unsolved mystery and a huge challenge. Notably, we clearly and intuitively demonstrate that Zuotai or β-HgS is auto-synthesized by organisms into spherical HgS nanoparticles with protein corona, with an overall particle size of 30-195 nm and a core of HgS NPs of 5-7 nm. Further research showed that HgS NPs facilitated the transport of Oxiracetam (ORT), Memantine Hydrochloride (MH) and Entinostat (MS-275) across the blood-brain barrier (BBB), especially the brain accumulation of MS-275 increased by more than three times. Meanwhile, HgS NPs enhanced the effect of MS-275 on spatial learning and memory ability of APP/PS1 mice. Further studies confirmed that HgS NPs increased the permeability of the blood-brain barrier (BBB) by regulating endocytosis (Upregulation of caveolin, clathrin, and dynamin, downregulation P-gp) thereby facilitate the transport of drugs across BBB with more than threefold higher brain accumulation and long-lasting efficiency enhancement (4 days). Our findings reveal that these in vivo-generated HgS NPs provide an efficient, convenient, and biocompatible drug delivery platform for crossing the BBB. Importantly, our findings offer new hopes and ideas for in-depth research on highly valuable and mysterious metal preparations in classic Chinese and Tibetan medicine.

摘要

β-硫化汞作为藏药坐台(ZT)的主要成分,被广泛用于治疗中枢神经系统疾病。尽管硫化汞的协同作用已在临床上得到验证达2000多年,但其协同机制仍是一个未解之谜和巨大挑战。值得注意的是,我们清晰直观地证明,坐台或β-硫化汞可被生物体自动合成具有蛋白质冠的球形硫化汞纳米颗粒,其总体粒径为30 - 195纳米,硫化汞纳米颗粒核心粒径为5 - 7纳米。进一步研究表明,硫化汞纳米颗粒促进了奥拉西坦(ORT)、盐酸美金刚(MH)和恩替诺特(MS - 275)跨越血脑屏障(BBB)的运输,尤其是MS - 275的脑内蓄积增加了三倍多。同时,硫化汞纳米颗粒增强了MS - 275对APP/PS1小鼠空间学习和记忆能力的影响。进一步研究证实,硫化汞纳米颗粒通过调节内吞作用(上调小窝蛋白、网格蛋白和发动蛋白,下调P - 糖蛋白)增加血脑屏障(BBB)的通透性,从而促进药物跨越血脑屏障,使脑内蓄积提高三倍以上且长效增强效果(4天)。我们的研究结果表明,这些体内生成的硫化汞纳米颗粒为跨越血脑屏障提供了一个高效、便捷且生物相容的药物递送平台。重要的是,我们的研究结果为深入研究中药和藏药中极具价值且神秘的金属制剂提供了新的希望和思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b846/12168276/645a21f8409b/12951_2025_3525_Fig1_HTML.jpg

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