In vitro models for neuropathic pain phenotypic screening in brain therapeutics

被引:1
作者
Martinez, A. L. [1 ,2 ,3 ]
Brea, J. [1 ,2 ,3 ]
Lopez, D. [1 ,2 ]
Cosme, N. [1 ,2 ]
Barro, M. [1 ,2 ]
Monroy, X. [4 ]
Burgueno, J. [4 ]
Merlos, M. [4 ]
Loza, M. I. [1 ,2 ,3 ]
机构
[1] Univ Santiago de Compostela, Ctr Singular Invest Med Mol & Enfermidades Cron CI, BioFarma Res Grp, Santiago De Compostela, Spain
[2] Inst Invest Sanitarias Santiago de Compostela IDIS, Santiago De Compostela, Spain
[3] Univ Santiago de Compostela, Dept Farmacol Farm & Tecnol Farmaceut, Fac Farm, Santiago De Compostela, Spain
[4] WeLab Barcelona, Parc Cient Barcelona, Barcelona, Spain
关键词
Phenotypic screening; Immortalized cell lines; In vitro models; Neuropathic pain; In vitro pharmacology; Early drug discovery; INDUCED PERIPHERAL NEUROPATHY; PLURIPOTENT STEM-CELLS; SODIUM-CHANNELS; DRUG DISCOVERY; NEURONAL CELL; MICROFLUIDICS; CURRENTS; THERAPY; DIFFERENTIATION; IDENTIFICATION;
D O I
10.1016/j.phrs.2024.107111
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The discovery of brain therapeutics faces a significant challenge due to the low translatability of preclinical results into clinical success. To address this gap, several efforts have been made to obtain more translatable neuronal models for phenotypic screening. These models allow the selection of active compounds without predetermined knowledge of drug targets. In this review, we present an overview of various existing models within the field, examining their strengths and limitations, particularly in the context of neuropathic pain research. We illustrate the usefulness of these models through a comparative review in three crucial areas: i) the development of novel phenotypic screening strategies specifically for neuropathic pain, ii) the validation of the models for both primary and secondary screening assays, and iii) the use of the models in target deconvolution processes.
引用
收藏
页数:11
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