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阿兹海默病中,非洛地平纳米药物经血脑屏障递呈改善焦虑样行为和认知障碍。

Blood Brain Barrier-Crossing Delivery of Felodipine Nanodrug Ameliorates Anxiety-Like Behavior and Cognitive Impairment in Alzheimer's Disease.

机构信息

Department of Rehabilitation Medicine, The Third Affiliated Hospital, Sun Yat-sen University, 600 Tianhe Road, Guangzhou, Guangdong, 510630, China.

Department of Rehabilitation Medicine, Guangzhou First People's Hospital, Guangzhou, 510180, China.

出版信息

Adv Sci (Weinh). 2024 Sep;11(34):e2401731. doi: 10.1002/advs.202401731. Epub 2024 Jul 9.

Abstract

Alzheimer's disease (AD) is the most common age-related neurodegenerative disorder leading to cognitive decline. Excessive cytosolic calcium (Ca) accumulation plays a critical role in the pathogenesis of AD since it activates the NOD-like receptor family, pyrin domain containing 3 (NLRP3), switches the endoplasmic reticulum (ER) unfolded protein response (UPR) toward proapoptotic signaling and promotes Aβ seeding. Herein, a liposomal nanodrug (felodipine@LND) is developed incorporating a calcium channel antagonist felodipine for Alzheimer's disease treatment through a low-intensity pulse ultrasound (LIPUS) irradiation-assisted blood brain barrier (BBB)-crossing drug delivery. The multifunctional felodipine@LND is effectively delivered to diseased brain through applying a LIPUS irradiation to the skull, which resulted in a series of positive effects against AD. Markedly, the nanodrug treatment switched the ER UPR toward antioxidant signaling, prevented the surface translocation of ER calreticulin (CALR) in microglia, and inhibited the NLRP3 activation and Aβ seeding. In addition, it promoted the degradation of damaged mitochondria via mitophagy, thereby inhibiting the neuronal apoptosis. Therefore, the anxiety-like behavior and cognitive impairment of 5xFAD mice with AD is significantly ameliorated, which manifested the potential of LIPUS - assisted BBB-crossing delivery of felodipine@LND to serve as a paradigm for AD therapy based on the well-recognized clinically available felodipine.

摘要

阿尔茨海默病(AD)是最常见的与年龄相关的神经退行性疾病,导致认知能力下降。细胞溶质钙(Ca)的过度积累在 AD 的发病机制中起着关键作用,因为它激活了 NOD 样受体家族、富含吡喃结构域的 3(NLRP3),将内质网(ER)未折叠蛋白反应(UPR)转向促凋亡信号,并促进 Aβ 播种。在此,开发了一种包含钙通道拮抗剂非洛地平的脂质体纳米药物(felodipine@LND),通过低强度脉冲超声(LIPUS)辐照辅助血脑屏障(BBB)穿透药物递送系统治疗阿尔茨海默病。多功能 felodipine@LND 通过对颅骨施加 LIPUS 辐射,有效地递送到患病大脑,从而对 AD 产生了一系列积极影响。值得注意的是,纳米药物治疗将 ER UPR 转向抗氧化信号,防止微胶质细胞中 ER 钙网蛋白(CALR)的表面易位,并抑制 NLRP3 的激活和 Aβ 的播种。此外,它通过线粒体自噬促进受损线粒体的降解,从而抑制神经元凋亡。因此,5xFAD 型 AD 小鼠的焦虑样行为和认知障碍得到了显著改善,这表明 LIPUS 辅助 BBB 穿透 felodipine@LND 的递送具有作为 AD 治疗范例的潜力,基于已被广泛认可的临床可用的非洛地平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d536/11425895/4ae80687f8f3/ADVS-11-2401731-g004.jpg

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