Mitochondria targeting fluorescent probe for MAO-A and the application in the development of drug candidate for neuroinflammation.


Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
22 Mar 2022
Historique:
received: 23 11 2021
revised: 13 01 2022
accepted: 02 02 2022
entrez: 1 3 2022
pubmed: 2 3 2022
medline: 3 3 2022
Statut: ppublish

Résumé

Monoamine oxidase A (MAO-A), as a vital drug target for various central nervous system diseases, locates in mitochondria and is mainly responsible for the oxidative inactivation of neurotransmitter amines. In the present work, a Mito-targeting fluorescent probe (HCCP) was developed to selectively and sensitively detect MAO-A activity, and successfully applied for the real-time monitoring endogenous MAO-A in living cells and tissues. Additionally, a high-throughput screening platform was established using HCCP and the inhibitory effects of 210 kinds of Herbal medicines toward MAO-A were evaluated. Evocarpine as a novel inhibitor for MAO-A was discovered from Evodia rutaecarpa, which possessed the preferred anti-neuroinflammation activity by suppressing the iNOS expression and NO production in LPS-induced BV2 cells bioactivation. In summary, HCCP was a novel Mito-targeting tool for the real-time imaging of MAO-A, provided an efficient method for real-time exploring of physiological functions of MAO-A and developing potential inhibitors of MAO-A.

Identifiants

pubmed: 35227389
pii: S0003-2670(22)00144-1
doi: 10.1016/j.aca.2022.339573
pii:
doi:

Substances chimiques

Fluorescent Dyes 0
Monoamine Oxidase Inhibitors 0
Pharmaceutical Preparations 0
Monoamine Oxidase EC 1.4.3.4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

339573

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Jiarong Wu (J)

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221004, China.

Chaoyan Han (C)

College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China.

Xudong Cao (X)

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221004, China.

Zhuang Lv (Z)

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221004, China.

Chao Wang (C)

College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China.

Xiaokui Huo (X)

College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China.

Lei Feng (L)

College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China; School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, China. Electronic address: leifeng@dmu.edu.cn.

Baojing Zhang (B)

College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China.

Xiangge Tian (X)

Department of Pharmacy, Peking University Shenzhen Hospital, Shenzhen, 518036, China. Electronic address: tianxiangge1990@163.com.

Xiaochi Ma (X)

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221004, China; College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian, China. Electronic address: maxc1978@163.com.

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Classifications MeSH