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用于阿尔茨海默病治疗的脂质体多奈哌齐、美金刚和 BACE-1siRNA 经鼻脑递释的体内评价。

In Vivo Evaluation of Nose-to-Brain Delivery of Liposomal Donepezil, Memantine, and BACE-1 siRNA for Alzheimer's Disease Therapy.

机构信息

Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.

Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, USA.

出版信息

Int J Mol Sci. 2024 Sep 26;25(19):10357. doi: 10.3390/ijms251910357.

Abstract

Our study took an innovative approach by evaluating, in vivo, the efficacy of intranasal (IN) administration of liposomal formulations of donepezil, memantine, and beta-site amyloid precursor protein-cleaving enzyme (BACE-1) siRNA, and their combination as a "triple-drug therapy" in treating Alzheimer's disease (AD). Female APP/PS1 homozygous, transgenic mice were used as an AD model. The spatial short-term memory of the APP/PS1 mice was evaluated by a Y-maze behavioral test. IN-administered formulations demonstrated better short-term memory recovery than oral administration. Triple-drug therapy induced short-term memory recovery and lowered beta-amyloid (Aβ) 40 and 42 peptide levels and BACE-1 mRNA expression. Additionally, inflammatory cytokine mRNA expression was downregulated. This innovative approach opens new possibilities for Alzheimer's disease treatment and nose-to-brain delivery.

摘要

我们的研究采用了一种创新的方法,通过体内评估鼻腔内给予多奈哌齐、美金刚和β-淀粉样前体蛋白裂解酶(BACE-1)siRNA 的脂质体制剂及其组合作为“三联药物治疗”在治疗阿尔茨海默病(AD)中的功效。雌性 APP/PS1 纯合子转基因小鼠被用作 AD 模型。通过 Y 迷宫行为测试评估 APP/PS1 小鼠的空间短期记忆。鼻腔给药制剂显示出比口服给药更好的短期记忆恢复。三联药物治疗诱导短期记忆恢复,并降低β-淀粉样蛋白(Aβ)40 和 42 肽水平和 BACE-1 mRNA 表达。此外,下调了炎症细胞因子 mRNA 表达。这种创新方法为阿尔茨海默病治疗和鼻内递药开辟了新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ad/11476875/b1ac10481c1a/ijms-25-10357-g001.jpg

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