Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway

Abstract Background Peripheral nerve injury (PNI) causes motor and sensory defects, has strong impact on life quality and still has no effective therapy. Miconazole is one of the most widely used antifungal drugs; the aims of the study were to investigate the effects of miconazole during sciatic ner...

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Main Authors: Liangliang Zhang, Xiuju Chen, Zengyun Liu, Qingluan Han, Liguo Tang, Zhen Tian, Zhiyong Ren, Cunmin Rong, Hui Xu
Format: Article
Language:English
Published: Wiley 2019-10-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.1400
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spelling doaj-f9646131aa9d4778ac09c5ff4c1ba7012020-11-25T03:35:34ZengWileyBrain and Behavior2162-32792019-10-01910n/an/a10.1002/brb3.1400Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathwayLiangliang Zhang0Xiuju Chen1Zengyun Liu2Qingluan Han3Liguo Tang4Zhen Tian5Zhiyong Ren6Cunmin Rong7Hui Xu8Department of Hand Surgery Affiliated Hospital of Jining Medical University Jining Shandong ChinaDepartment of Neurology Tianjin Nankai Hospital Tianjin ChinaDepartment of Orthopaedic Sunshine Union Hospital Weifang Shandong ChinaDepartment of Hand Surgery Affiliated Hospital of Jining Medical University Jining Shandong ChinaDepartment of Orthopaedic Sunshine Union Hospital Weifang Shandong ChinaDepartment of Orthopaedic Sunshine Union Hospital Weifang Shandong ChinaDepartment of Orthopaedic Sunshine Union Hospital Weifang Shandong ChinaDepartment of Hand Surgery Affiliated Hospital of Jining Medical University Jining Shandong ChinaDepartment of Hand Surgery Affiliated Hospital of Jining Medical University Jining Shandong ChinaAbstract Background Peripheral nerve injury (PNI) causes motor and sensory defects, has strong impact on life quality and still has no effective therapy. Miconazole is one of the most widely used antifungal drugs; the aims of the study were to investigate the effects of miconazole during sciatic nerve regeneration in a mouse model of sciatic nerve crush injury. Methods We established peripheral nerve crush model and investigated the effects of miconazole by multiple aspects. We further studied the potential mechanism of action of miconazole by Western blotting, fluorescence immunohistochemistry, and PCR analysis. Results Miconazole improves the symptoms of crushed nerve by improving inflammatory cell infiltration and demyelinating myelin of sciatic nerve. Affected by miconazole, the proportion of inflammatory M1 macrophages in the distal part of the sciatic nerve was reduced, and the proportion of anti‐inflammatory M2 macrophages was increased. Finally, the neuroprotective properties of miconazole may be regulated by the nuclear factor (NF)‐κB pathway. Conclusions Our data suggest that miconazole can effectively alleviate PNI, and the mechanism involves mediating a phenotype change of M1/ M2 macrophages. Thus, miconazole may represent a potential therapeutic intervention for nerve crush injury.https://doi.org/10.1002/brb3.1400macrophagemiconazoleNF‐κBperipheral nerve injurypolarization
collection DOAJ
language English
format Article
sources DOAJ
author Liangliang Zhang
Xiuju Chen
Zengyun Liu
Qingluan Han
Liguo Tang
Zhen Tian
Zhiyong Ren
Cunmin Rong
Hui Xu
spellingShingle Liangliang Zhang
Xiuju Chen
Zengyun Liu
Qingluan Han
Liguo Tang
Zhen Tian
Zhiyong Ren
Cunmin Rong
Hui Xu
Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
Brain and Behavior
macrophage
miconazole
NF‐κB
peripheral nerve injury
polarization
author_facet Liangliang Zhang
Xiuju Chen
Zengyun Liu
Qingluan Han
Liguo Tang
Zhen Tian
Zhiyong Ren
Cunmin Rong
Hui Xu
author_sort Liangliang Zhang
title Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
title_short Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
title_full Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
title_fullStr Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
title_full_unstemmed Miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the NF‐κB pathway
title_sort miconazole alleviates peripheral nerve crush injury by mediating a macrophage phenotype change through the nf‐κb pathway
publisher Wiley
series Brain and Behavior
issn 2162-3279
publishDate 2019-10-01
description Abstract Background Peripheral nerve injury (PNI) causes motor and sensory defects, has strong impact on life quality and still has no effective therapy. Miconazole is one of the most widely used antifungal drugs; the aims of the study were to investigate the effects of miconazole during sciatic nerve regeneration in a mouse model of sciatic nerve crush injury. Methods We established peripheral nerve crush model and investigated the effects of miconazole by multiple aspects. We further studied the potential mechanism of action of miconazole by Western blotting, fluorescence immunohistochemistry, and PCR analysis. Results Miconazole improves the symptoms of crushed nerve by improving inflammatory cell infiltration and demyelinating myelin of sciatic nerve. Affected by miconazole, the proportion of inflammatory M1 macrophages in the distal part of the sciatic nerve was reduced, and the proportion of anti‐inflammatory M2 macrophages was increased. Finally, the neuroprotective properties of miconazole may be regulated by the nuclear factor (NF)‐κB pathway. Conclusions Our data suggest that miconazole can effectively alleviate PNI, and the mechanism involves mediating a phenotype change of M1/ M2 macrophages. Thus, miconazole may represent a potential therapeutic intervention for nerve crush injury.
topic macrophage
miconazole
NF‐κB
peripheral nerve injury
polarization
url https://doi.org/10.1002/brb3.1400
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