带有Hv1抑制剂的脑靶向脂质纳米颗粒减轻缺血性卒中后的神经炎症。

IF 10.6 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zeyu Yang, Lei Jin, Longxiang Li, Yu Wu, Wenchao Liu, Xin Feng, Liyan Li, Fa Jin, Yiming Bi, Ran Li, Shenquan Guo, Yanan Wang, Boyang Wei, Yanchao Liu, Xifeng Li, Chuanzhi Duan
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引用次数: 0

摘要

背景:缺血性卒中(IS)是一项重大的全球健康负担。目前的治疗方案面临诸如窗口狭窄和再灌注损伤风险等问题。此外,随着老龄化和危险因素的增加,迫切需要新的治疗策略。NADPH氧化酶(NOX)介导的小胶质细胞氧化应激是驱动神经炎症和细胞死亡的关键机制。Hv1是一种在小胶质细胞中高度表达的电压门控质子通道,它与NOX协同产生活性氧(ROS),加剧脑损伤。YHV984是一种有效的Hv1抑制剂,可缓解is后神经炎症,但由于潜在的毒副作用和溶解度问题,面临临床局限性。为了提高YHV984在脑内特异性抑制Hv1的理化和药代动力学特性,研究人员开发了由t7靶向肽和脂质纳米颗粒(LNP)组成的多功能纳米颗粒来递送YHV984 (T7-LNP@YHV984)。结果:结果表明T7-LNP@YHV984具有良好的稳定性和脑靶向能力,可有效穿过血脑屏障(BBB)并在小胶质细胞内积累。这种靶向递送显著抑制受损大脑中Hv1的表达和NLRP3炎症小体途径的激活。促进小胶质细胞向M2表型极化,增强抗炎因子的释放,减轻神经炎症,改善神经元存活。此外,T7-LNP@YHV984提高了is后小鼠的存活率并促进了神经系统的恢复。结论:T7-LNP@YHV984具有长期稳定性的多功能纳米颗粒是缓解is后再灌注损伤和抑制神经炎症的有效策略。通过精确靶向小胶质细胞中的Hv1,纳米颗粒有效地抑制了小胶质细胞诱导的神经炎症,最大限度地减少了脱靶效应。这项创新为中风治疗和神经保护策略提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain targeted lipid nanoparticles with Hv1 inhibitors alleviate neuroinflammation post-ischemic stroke.

Background: Ischemic stroke (IS) represents a significant global health burden. Current therapeutic options face problems such as window narrowing and reperfusion injury risk. Moreover, with increasing aging and risk factors, novel treatment strategies are urgently needed. NADPH oxidase (NOX)-mediated oxidative stress in microglia is a critical mechanism driving neuroinflammation and cell death. Hv1, a voltage-gated proton channel highly expressed in microglia, synergizes with NOX to generate reactive oxygen species (ROS), exacerbating brain damage. YHV984, a potent Hv1 inhibitor, alleviates post-IS neuroinflammation but faces clinical limitations due to potential toxic side effects and solubility issues. To improve the physicochemical and pharmacokinetic properties of YHV984 for specific Hv1 inhibition in the brain, the multifunctional nanoparticles consisting of a T7-targeting peptide and lipid nanoparticles (LNP) were developed to deliver YHV984 (T7-LNP@YHV984).

Results: The results demonstrated that T7-LNP@YHV984 exhibited good stability and brain targeting capability, effectively crossing the blood-brain barrier (BBB) and accumulating within microglia. This targeted delivery significantly suppressed Hv1 expression and activation of the NLRP3 inflammasome pathway in the damaged brain. Furthermore, it promoted the polarization of microglia towards the M2 phenotype, enhancing the release of anti-inflammatory factors, alleviating neuroinflammation and improved neuronal survival. Additionally, T7-LNP@YHV984 improved survival and facilitated neurological recovery in post-IS mice.

Conclusions: T7-LNP@YHV984 multifunctional nanoparticles with long-term stability emerged as a potent strategy to alleviate reperfusion injury and inhibit neuroinflammation post-IS. By precisely targeting Hv1 in microglia, the nanoparticles effectively suppressed microglia-induced neuroinflammation, minimizing off-target effects. This innovation offers novel insights into stroke treatment and neuroprotective strategies.

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来源期刊
Journal of Nanobiotechnology
Journal of Nanobiotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
13.90
自引率
4.90%
发文量
493
审稿时长
16 weeks
期刊介绍: Journal of Nanobiotechnology is an open access peer-reviewed journal communicating scientific and technological advances in the fields of medicine and biology, with an emphasis in their interface with nanoscale sciences. The journal provides biomedical scientists and the international biotechnology business community with the latest developments in the growing field of Nanobiotechnology.
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