BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis

Abstract Background Patients with interstitial cystitis/bladder pain syndrome (IC/BPS) often grieve over a low quality of life brought about by chronic pain. In our previous studies, we determined that neuroinflammation of the spinal dorsal horn (SDH) was associated with mechanisms of interstitial c...

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Main Authors: Honglu Ding, Jialiang Chen, Minzhi Su, Zhijun Lin, Hailun Zhan, Fei Yang, Wenbiao Li, Juncong Xie, Yong Huang, Xianguo Liu, Bolong Liu, Xiangfu Zhou
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Journal of Neuroinflammation
Subjects:
Online Access:https://doi.org/10.1186/s12974-020-1704-0
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author Honglu Ding
Jialiang Chen
Minzhi Su
Zhijun Lin
Hailun Zhan
Fei Yang
Wenbiao Li
Juncong Xie
Yong Huang
Xianguo Liu
Bolong Liu
Xiangfu Zhou
author_facet Honglu Ding
Jialiang Chen
Minzhi Su
Zhijun Lin
Hailun Zhan
Fei Yang
Wenbiao Li
Juncong Xie
Yong Huang
Xianguo Liu
Bolong Liu
Xiangfu Zhou
author_sort Honglu Ding
collection DOAJ
description Abstract Background Patients with interstitial cystitis/bladder pain syndrome (IC/BPS) often grieve over a low quality of life brought about by chronic pain. In our previous studies, we determined that neuroinflammation of the spinal dorsal horn (SDH) was associated with mechanisms of interstitial cystitis. Moreover, it has been shown that brain-derived neurotrophic factor (BDNF) participates in the regulation of neuroinflammation and pathological pain through BDNF-TrkB signaling; however, whether it plays a role in cyclophosphamide (CYP)-induced cystitis remains unclear. This study aimed to confirm whether BDNF-TrkB signaling modulates neuroinflammation and mechanical allodynia in CYP-induced cystitis and determine how it occurs. Methods Systemic intraperitoneal injection of CYP was performed to establish a rat cystitis model. BDNF-TrkB signaling was modulated by intraperitoneal injection of the TrkB receptor antagonist, ANA-12, or intrathecal injection of exogenous BDNF. Mechanical allodynia in the suprapubic region was assessed using the von Frey filaments test. The expression of BDNF, TrkB, p-TrkB, Iba1, GFAP, p-p38, p-JNK, IL-1β, and TNF-α in the L6-S1 SDH was measured by Western blotting and immunofluorescence analysis. Results BDNF-TrkB signaling was upregulated significantly in the SDH after CYP was injected. Similarly, the expressions of Iba1, GFAP, p-p38, p-JNK, IL-1β, and TNF-α in the SDH were all upregulated. Treatment with ANA-12 could attenuate mechanical allodynia, restrain activation of astrocytes and microglia and alleviate neuroinflammation. Besides, the intrathecal injection of exogenous BDNF further decreased the mechanical withdrawal threshold, promoted activation of astrocytes and microglia, and increased the release of TNF-α and IL-1β in the SDH of our CYP-induced cystitis model. Conclusions In our CYP-induced cystitis model, BDNF promoted the activation of astrocytes and microglia to release TNF-α and IL-1β, aggravating neuroinflammation and leading to mechanical allodynia through BDNF-TrkB-p38/JNK signaling.
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spelling doaj.art-bd02f0850d134321970dbf4d71038b6f2022-12-21T23:15:09ZengBMCJournal of Neuroinflammation1742-20942020-01-0117111310.1186/s12974-020-1704-0BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitisHonglu Ding0Jialiang Chen1Minzhi Su2Zhijun Lin3Hailun Zhan4Fei Yang5Wenbiao Li6Juncong Xie7Yong Huang8Xianguo Liu9Bolong Liu10Xiangfu Zhou11Department of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Rehabilitation, The Third Affiliated Hospital and Lingnan Hospital of the Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityPain Research Center and Department of Physiology, Zhongshan School of Medicine of Sun Yat-sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityDepartment of Urology, the Third Affiliated hospital of Sun Yat-Sen UniversityAbstract Background Patients with interstitial cystitis/bladder pain syndrome (IC/BPS) often grieve over a low quality of life brought about by chronic pain. In our previous studies, we determined that neuroinflammation of the spinal dorsal horn (SDH) was associated with mechanisms of interstitial cystitis. Moreover, it has been shown that brain-derived neurotrophic factor (BDNF) participates in the regulation of neuroinflammation and pathological pain through BDNF-TrkB signaling; however, whether it plays a role in cyclophosphamide (CYP)-induced cystitis remains unclear. This study aimed to confirm whether BDNF-TrkB signaling modulates neuroinflammation and mechanical allodynia in CYP-induced cystitis and determine how it occurs. Methods Systemic intraperitoneal injection of CYP was performed to establish a rat cystitis model. BDNF-TrkB signaling was modulated by intraperitoneal injection of the TrkB receptor antagonist, ANA-12, or intrathecal injection of exogenous BDNF. Mechanical allodynia in the suprapubic region was assessed using the von Frey filaments test. The expression of BDNF, TrkB, p-TrkB, Iba1, GFAP, p-p38, p-JNK, IL-1β, and TNF-α in the L6-S1 SDH was measured by Western blotting and immunofluorescence analysis. Results BDNF-TrkB signaling was upregulated significantly in the SDH after CYP was injected. Similarly, the expressions of Iba1, GFAP, p-p38, p-JNK, IL-1β, and TNF-α in the SDH were all upregulated. Treatment with ANA-12 could attenuate mechanical allodynia, restrain activation of astrocytes and microglia and alleviate neuroinflammation. Besides, the intrathecal injection of exogenous BDNF further decreased the mechanical withdrawal threshold, promoted activation of astrocytes and microglia, and increased the release of TNF-α and IL-1β in the SDH of our CYP-induced cystitis model. Conclusions In our CYP-induced cystitis model, BDNF promoted the activation of astrocytes and microglia to release TNF-α and IL-1β, aggravating neuroinflammation and leading to mechanical allodynia through BDNF-TrkB-p38/JNK signaling.https://doi.org/10.1186/s12974-020-1704-0CystitisBDNFTrkBNeuroinflammationMechanical allodyniaAstrocytes
spellingShingle Honglu Ding
Jialiang Chen
Minzhi Su
Zhijun Lin
Hailun Zhan
Fei Yang
Wenbiao Li
Juncong Xie
Yong Huang
Xianguo Liu
Bolong Liu
Xiangfu Zhou
BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
Journal of Neuroinflammation
Cystitis
BDNF
TrkB
Neuroinflammation
Mechanical allodynia
Astrocytes
title BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
title_full BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
title_fullStr BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
title_full_unstemmed BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
title_short BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis
title_sort bdnf promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide induced cystitis
topic Cystitis
BDNF
TrkB
Neuroinflammation
Mechanical allodynia
Astrocytes
url https://doi.org/10.1186/s12974-020-1704-0
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