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利用双修饰新型仿生纳米系统通过全身递送白藜芦醇实现阿尔茨海默病的神经元线粒体靶向治疗。

Neuronal mitochondria-targeted therapy for Alzheimer's disease by systemic delivery of resveratrol using dual-modified novel biomimetic nanosystems.

机构信息

School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang, PR China.

Department of stomatology, The Fifth Medical Center of PLA General Hospital, Beijing, PR China.

出版信息

Drug Deliv. 2020 Dec;27(1):502-518. doi: 10.1080/10717544.2020.1745328.

Abstract

Reactive oxygen species (ROS)-induced neuronal mitochondrial dysfunction is a key pathologic factor in sporadic Alzheimer's disease (AD). Neuronal mitochondria have been proposed to be a promising therapeutic target for AD, especially for the failures of phase III clinical trials on conventional amyloid-β (Aβ) targeted therapy. However, the efficient intravenous delivery of therapeutic agents to neuronal mitochondria in the brain remains a major challenge due to the complicated physiological environment. Recently, biomaterials-based nanomedicine has been widely investigated for the treatment of AD. Herein, we devised a strategy for functional antioxidant delivery to neuronal mitochondria by loading antioxidants into red blood cell (RBC) membrane-coated nanostructured lipid carriers (NLC) bearing rabies virus glycoprotein (RVG29) and triphenylphosphine cation (TPP) molecules attached to the RBC membrane surface (RVG/TPP NPs@RBCm). With the advantage of suitable physicochemical properties of NLC and unique biological functions of the RBC membrane, RVG/TPP NPs@RBCm are stabilized and enabled sustained drug release, providing improved biocompatibility and long-term circulation. Under the synergistic effects of RVG29 and TPP, RVG/TPP NPs@RBCm can not only penetrate the blood-brain barrier (BBB) but also target neuron cells and further localize in the mitochondria. After encapsulating Resveratrol (RSV) as the model antioxidant, the data demonstrated that RVG/TPP-RSV NPs@RBCm can relieve AD symptoms by mitigating Aβ-related mitochondrial oxidative stress both and . The memory impairment in APP/PS1 mice is significantly improved following the systemic administration of RVG/TPP-RSV NPs@RBCm. In conclusion, intravenous neuronal mitochondria-targeted dual-modified novel biomimetic nanosystems are a promising therapeutic candidate for ROS-induced mitochondrial dysfunction in AD.

摘要

活性氧(ROS)诱导的神经元线粒体功能障碍是散发性阿尔茨海默病(AD)的关键病理因素。神经元线粒体被认为是 AD 的一个有前途的治疗靶点,特别是对于传统淀粉样蛋白-β(Aβ)靶向治疗的 III 期临床试验失败。然而,由于复杂的生理环境,有效的将治疗剂递送至大脑中的神经元线粒体仍然是一个主要挑战。最近,基于生物材料的纳米医学已被广泛用于 AD 的治疗。在此,我们设计了一种通过将抗氧化剂装载到带有狂犬病病毒糖蛋白(RVG29)和三苯基膦阳离子(TPP)分子的红细胞(RBC)膜包裹的纳米结构脂质载体(NLC)中,从而将功能性抗氧化剂递送至神经元线粒体的策略,这些分子附着在 RBC 膜表面(RVG/TPP NPs@RBCm)。利用 NLC 合适的物理化学性质和 RBC 膜的独特生物学功能,RVG/TPP NPs@RBCm 得到稳定,并能够持续释放药物,提高生物相容性和延长循环时间。在 RVG29 和 TPP 的协同作用下,RVG/TPP NPs@RBCm 不仅可以穿透血脑屏障(BBB),还可以靶向神经元细胞并进一步定位于线粒体。包封白藜芦醇(RSV)作为模型抗氧化剂后,数据表明 RVG/TPP-RSV NPs@RBCm 可以通过减轻 Aβ 相关的线粒体氧化应激来缓解 AD 症状。在 APP/PS1 小鼠中,RVG/TPP-RSV NPs@RBCm 的全身给药显著改善了记忆障碍。综上所述,静脉内神经元线粒体靶向双重修饰新型仿生纳米系统是治疗 AD 中 ROS 诱导的线粒体功能障碍的一种很有前途的治疗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0fa/7170363/ceddc0a5bdc4/IDRD_A_1745328_F0001_C.jpg

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