» Articles » PMID: 37810956

Rapamycin Responds to Alzheimer's Disease: A Potential Translational Therapy

Overview
Publisher Dove Medical Press
Specialty Geriatrics
Date 2023 Oct 9
PMID 37810956
Authors
Affiliations
Soon will be listed here.
Abstract

Alzheimer's disease (AD) is a sporadic or familial neurodegenerative disease of insidious onset with progressive cognitive decline. Although numerous studies have been conducted or are underway on AD, there are still no effective drugs to reverse the pathological features and clinical manifestations of AD. Rapamycin is a macrolide antibiotic produced by . As a classical mechanistic target of rapamycin (mTOR) inhibitor, rapamycin has been shown to be beneficial in a variety of AD mouse and cells models, both before the onset of disease symptoms and the early stage of disease. Although many basic studies have demonstrated the therapeutic effects of rapamycin in AD, many questions and controversies remain. This may be due to the variability of experimental models, different modes of administration, dose, timing, frequency, and the availability of drug-targeting vehicles. Rapamycin may delay the development of AD by reducing β-amyloid (Aβ) deposition, inhibiting tau protein hyperphosphorylation, maintaining brain function in gene carriers, clearing chronic inflammation, and improving cognitive dysfunction. It is thus expected to be one of the candidates for the treatment of Alzheimer's disease.

Citing Articles

Mikhail 'Misha' Blagosklonny's enduring legacy in geroscience: the hyperfunction theory and the therapeutic potential of rapamycin.

Barzilai D Aging (Albany NY). 2025; 17(1):1-15.

PMID: 39808121 PMC: 11810056. DOI: 10.18632/aging.206189.


Hearing modulation affects Alzheimer's disease progression linked to brain inflammation: a study in mouse models.

Ko Y, Ryu Y, Han S, Park H, Choi M, Kim B Mol Med. 2024; 30(1):276.

PMID: 39725872 PMC: 11670416. DOI: 10.1186/s10020-024-01040-1.


Cellular senescence in Alzheimer's disease: from physiology to pathology.

Zhu J, Wu C, Yang L Transl Neurodegener. 2024; 13(1):55.

PMID: 39568081 PMC: 11577763. DOI: 10.1186/s40035-024-00447-4.


FBXO22 inhibits colitis and colorectal carcinogenesis by regulating the degradation of the S2448-phosphorylated form of mTOR.

Li M, Chen X, Qu P, Shao Z, Shi L, Quan H Proc Natl Acad Sci U S A. 2024; 121(45):e2402035121.

PMID: 39485803 PMC: 11551398. DOI: 10.1073/pnas.2402035121.


Microglial AKAP8L: a key mediator in diabetes-associated cognitive impairment via autophagy inhibition and neuroinflammation triggering.

Zhang W, Wei Q, Zhang T, Wang C, Chen J, Wang J J Neuroinflammation. 2024; 21(1):177.

PMID: 39033121 PMC: 11264944. DOI: 10.1186/s12974-024-03170-z.


References
1.
Kam T, Gwon Y, Jung Y . Amyloid beta receptors responsible for neurotoxicity and cellular defects in Alzheimer's disease. Cell Mol Life Sci. 2014; 71(24):4803-13. PMC: 11113744. DOI: 10.1007/s00018-014-1706-0. View

2.
Mandrioli J, DAmico R, Zucchi E, Gessani A, Fini N, Fasano A . Rapamycin treatment for amyotrophic lateral sclerosis: Protocol for a phase II randomized, double-blind, placebo-controlled, multicenter, clinical trial (RAP-ALS trial). Medicine (Baltimore). 2018; 97(24):e11119. PMC: 6024184. DOI: 10.1097/MD.0000000000011119. View

3.
Li X, An W, Alafuzoff I, Soininen H, Winblad B, Pei J . Phosphorylated eukaryotic translation factor 4E is elevated in Alzheimer brain. Neuroreport. 2004; 15(14):2237-40. DOI: 10.1097/00001756-200410050-00019. View

4.
Shen W, Lu K, Wang J, Wu A, Yue Y . Activation of mTOR signaling leads to orthopedic surgery-induced cognitive decline in mice through β-amyloid accumulation and tau phosphorylation. Mol Med Rep. 2016; 14(4):3925-34. DOI: 10.3892/mmr.2016.5700. View

5.
Spilman P, Podlutskaya N, Hart M, Debnath J, Gorostiza O, Bredesen D . Inhibition of mTOR by rapamycin abolishes cognitive deficits and reduces amyloid-beta levels in a mouse model of Alzheimer's disease. PLoS One. 2010; 5(4):e9979. PMC: 2848616. DOI: 10.1371/journal.pone.0009979. View