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Neuroprotective Effects of Celastrol in Neurodegenerative Diseases-Unscramble Its Major Mechanisms of Action and Targets

Overview
Journal Aging Dis
Specialty Geriatrics
Date 2022 Jun 3
PMID 35656110
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Abstract

There are rarely new therapeutic breakthroughs present for neurodegenerative diseases in the last decades. Thus, new effective drugs are urgently needed for millions of patients with neurodegenerative diseases. Celastrol, a pentacyclic triterpenoid compound, is one of the main active ingredients isolated from Hook. f. that has multiple biological activities. Recently, amount evidence indicates that celastrol exerts neuroprotective effects and holds therapeutic potential to serve as a novel agent for neurodegenerative diseases. This review focuses on the therapeutic efficacy and major regulatory mechanisms of celastrol to rescue damaged neurons, restore normal cognitive and sensory motor functions in neurodegenerative diseases. Importantly, we highlight recent progress regarding identification of the drug targets of celastrol by using advanced quantitative chemical proteomics technology. Overall, this review provides novel insights into the pharmacological activities and therapeutic potential of celastrol for incurable neurodegenerative diseases.

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References
1.
Nakamichi K, Kitani H, Takayama-Ito M, Morimoto K, Kurane I, Saijo M . Celastrol suppresses morphological and transcriptional responses in microglial cells upon stimulation with double-stranded RNA. Int J Neurosci. 2010; 120(4):252-7. DOI: 10.3109/00207451003615763. View

2.
Lu C, Zhang X, Zhang D, Pei E, Xu J, Tang T . Short time tripterine treatment enhances endothelial progenitor cell function via heat shock protein 32. J Cell Physiol. 2014; 230(5):1139-47. DOI: 10.1002/jcp.24849. View

3.
Nakazono A, Adachi N, Takahashi H, Seki T, Hamada D, Ueyama T . Pharmacological induction of heat shock proteins ameliorates toxicity of mutant PKCγ in spinocerebellar ataxia type 14. J Biol Chem. 2018; 293(38):14758-14774. PMC: 6153279. DOI: 10.1074/jbc.RA118.002913. View

4.
Zhang X, Zhao W, Liu X, Huang Z, Shan R, Huang C . Celastrol ameliorates inflammatory pain and modulates HMGB1/NF-κB signaling pathway in dorsal root ganglion. Neurosci Lett. 2018; 692:83-89. DOI: 10.1016/j.neulet.2018.11.002. View

5.
Yang H, Wang H, Andersson U . Targeting Inflammation Driven by HMGB1. Front Immunol. 2020; 11:484. PMC: 7099994. DOI: 10.3389/fimmu.2020.00484. View