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Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain

Although activation of microglial cells is critical in developing brain disorders, their role in anxiety-like behaviors in pain is still vague. This study indicates that alteration of microglia’s neuronal spine engulfment capacity in ventral zona incerta (ZI(V)) leads to significant pain and anxiety...

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Autores principales: Farzinpour, Zahra, Liu, An, Cao, Peng, Mao, Yu, Zhang, Zhi, Jin, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337222/
https://www.ncbi.nlm.nih.gov/pubmed/35910255
http://dx.doi.org/10.3389/fncel.2022.898346
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author Farzinpour, Zahra
Liu, An
Cao, Peng
Mao, Yu
Zhang, Zhi
Jin, Yan
author_facet Farzinpour, Zahra
Liu, An
Cao, Peng
Mao, Yu
Zhang, Zhi
Jin, Yan
author_sort Farzinpour, Zahra
collection PubMed
description Although activation of microglial cells is critical in developing brain disorders, their role in anxiety-like behaviors in pain is still vague. This study indicates that alteration of microglia’s neuronal spine engulfment capacity in ventral zona incerta (ZI(V)) leads to significant pain and anxiety-like behaviors in mice 1-day post-injection of Complete Freud’s Adjuvant (CFA1D). Performing whole-cell patch-clamp recordings in GABAergic neurons in the ZI(V) (ZI(V)(GABA)) in brain slices, we observed decreased activity in ZIv(GABA) and reduced frequency of the miniature excitatory postsynaptic currents (mEPSCs) in ZI(V)(GABA) of CFA1D mice compared with the saline1D mice. Besides, chemogenetic activation of ZI(V)(GABA) significantly relieved pain and anxiety-like behaviors in CFA1D mice. Conversely, in naïve mice, chemogenetic inhibition of ZI(V)(GABA) induced pain and anxiety-like behaviors. Interestingly, we found changes in the density and morphology of ZI(V)(Microglia) and increased microglial engulfment of spines in ZI(V) of CFA1D mice. Furthermore, pain sensitization and anxiety-like behaviors were reversed when the ZI(V)(Microglia) of CFA1D-treated mice were chemically inhibited by intra-ZI(V) minocycline injection, accompanied by the recovery of decreased ZI(V)(GABA) excitability. Conclusively, our results provide novel insights that dysregulation of microglial engulfment capacity encodes maladaptation of ZI(V)(GABA), thus promoting the development of anxiety-like behaviors in acute pain.
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spelling pubmed-93372222022-07-30 Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain Farzinpour, Zahra Liu, An Cao, Peng Mao, Yu Zhang, Zhi Jin, Yan Front Cell Neurosci Neuroscience Although activation of microglial cells is critical in developing brain disorders, their role in anxiety-like behaviors in pain is still vague. This study indicates that alteration of microglia’s neuronal spine engulfment capacity in ventral zona incerta (ZI(V)) leads to significant pain and anxiety-like behaviors in mice 1-day post-injection of Complete Freud’s Adjuvant (CFA1D). Performing whole-cell patch-clamp recordings in GABAergic neurons in the ZI(V) (ZI(V)(GABA)) in brain slices, we observed decreased activity in ZIv(GABA) and reduced frequency of the miniature excitatory postsynaptic currents (mEPSCs) in ZI(V)(GABA) of CFA1D mice compared with the saline1D mice. Besides, chemogenetic activation of ZI(V)(GABA) significantly relieved pain and anxiety-like behaviors in CFA1D mice. Conversely, in naïve mice, chemogenetic inhibition of ZI(V)(GABA) induced pain and anxiety-like behaviors. Interestingly, we found changes in the density and morphology of ZI(V)(Microglia) and increased microglial engulfment of spines in ZI(V) of CFA1D mice. Furthermore, pain sensitization and anxiety-like behaviors were reversed when the ZI(V)(Microglia) of CFA1D-treated mice were chemically inhibited by intra-ZI(V) minocycline injection, accompanied by the recovery of decreased ZI(V)(GABA) excitability. Conclusively, our results provide novel insights that dysregulation of microglial engulfment capacity encodes maladaptation of ZI(V)(GABA), thus promoting the development of anxiety-like behaviors in acute pain. Frontiers Media S.A. 2022-07-14 /pmc/articles/PMC9337222/ /pubmed/35910255 http://dx.doi.org/10.3389/fncel.2022.898346 Text en Copyright © 2022 Farzinpour, Liu, Cao, Mao, Zhang and Jin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Farzinpour, Zahra
Liu, An
Cao, Peng
Mao, Yu
Zhang, Zhi
Jin, Yan
Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title_full Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title_fullStr Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title_full_unstemmed Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title_short Microglial Engulfment of Spines in the Ventral Zona Incerta Regulates Anxiety-Like Behaviors in a Mouse Model of Acute Pain
title_sort microglial engulfment of spines in the ventral zona incerta regulates anxiety-like behaviors in a mouse model of acute pain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9337222/
https://www.ncbi.nlm.nih.gov/pubmed/35910255
http://dx.doi.org/10.3389/fncel.2022.898346
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