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

Author:

He Xiaofei1,Peng Yuan2,Huang Sicong3,Xiao Zecong4,Li Ge5,Zuo Zejie1,Zhang Liying1,Shuai Xintao4ORCID,Zheng Haiqing1,Hu Xiquan1

Affiliation:

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

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

3. School of Materials Science and Engineering Sun Yat‐sen University Guangzhou 510275 China

4. Nanomedicine Research Center The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou 510630 China

5. Guangdong Provincial Key Laboratory of Laboratory Animals Guangdong Laboratory Animals Monitoring Institute 11 Fengxin Road Guangzhou Guangdong 510663 China

Abstract

AbstractAlzheimer's disease (AD) is the most common age‐related neurodegenerative disorder leading to cognitive decline. Excessive cytosolic calcium (Ca2+) 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.

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

Wiley

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