Cargando…

Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation

BACKGROUND: Brain-derived neurotrophic factor (BDNF) and its receptor, tropomyosin-related kinase B (TrkB), signaling represent potential therapeutic targets for major depressive disorder. The purpose of this study is to examine whether TrkB ligands show antidepressant effects in an inflammation-ind...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Ji-chun, Wu, Jin, Fujita, Yuko, Yao, Wei, Ren, Qian, Yang, Chun, Li, Su-xia, Shirayama, Yukihiko, Hashimoto, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360225/
https://www.ncbi.nlm.nih.gov/pubmed/25628381
http://dx.doi.org/10.1093/ijnp/pyu077
_version_ 1782361517768835072
author Zhang, Ji-chun
Wu, Jin
Fujita, Yuko
Yao, Wei
Ren, Qian
Yang, Chun
Li, Su-xia
Shirayama, Yukihiko
Hashimoto, Kenji
author_facet Zhang, Ji-chun
Wu, Jin
Fujita, Yuko
Yao, Wei
Ren, Qian
Yang, Chun
Li, Su-xia
Shirayama, Yukihiko
Hashimoto, Kenji
author_sort Zhang, Ji-chun
collection PubMed
description BACKGROUND: Brain-derived neurotrophic factor (BDNF) and its receptor, tropomyosin-related kinase B (TrkB), signaling represent potential therapeutic targets for major depressive disorder. The purpose of this study is to examine whether TrkB ligands show antidepressant effects in an inflammation-induced model of depression. METHODS: In this study, we examined the effects of TrkB agonist 7,8-dihydroxyflavone (7,8-DHF) and TrkB antagonist ANA-12 on depression-like behavior and morphological changes in mice previously exposed to lipopolysaccharide (LPS). Protein levels of BDNF, phospho-TrkB (p-TrkB), and TrkB in the brain regions were also examined. RESULTS: LPS caused a reduction of BDNF in the CA3 and dentate gyrus (DG) of the hippocampus and prefrontal cortex (PFC), whereas LPS increased BDNF in the nucleus accumbens (NAc). Dexamethason suppression tests showed hyperactivity of the hypothalamic-pituitary-adrenal axis in LPS-treated mice. Intraperitoneal (i.p.) administration of 7,8-DHF showed antidepressant effects on LPS-induced depression-like behavior, and i.p. pretreatment with ANA-12 blocked its antidepressant effects. Surprisingly, ANA-12 alone showed antidepressant-like effects on LPS-induced depression-like behavior. Furthermore, bilateral infusion of ANA-12 into the NAc showed antidepressant effects. Moreover, LPS caused a reduction of spine density in the CA3, DG, and PFC, whereas LPS increased spine density in the NAc. Interestingly, 7,8-DHF significantly attenuated LPS-induced reduction of p-TrkB and spine densities in the CA3, DG, and PFC, whereas ANA-12 significantly attenuated LPS-induced increases of p-TrkB and spine density in the NAc. CONCLUSIONS: The results suggest that LPS-induced inflammation may cause depression-like behavior by altering BDNF and spine density in the CA3, DG, PFC, and NAc, which may be involved in the antidepressant effects of 7,8-DHF and ANA-12, respectively.
format Online
Article
Text
id pubmed-4360225
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-43602252015-09-01 Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation Zhang, Ji-chun Wu, Jin Fujita, Yuko Yao, Wei Ren, Qian Yang, Chun Li, Su-xia Shirayama, Yukihiko Hashimoto, Kenji Int J Neuropsychopharmacol Research Article BACKGROUND: Brain-derived neurotrophic factor (BDNF) and its receptor, tropomyosin-related kinase B (TrkB), signaling represent potential therapeutic targets for major depressive disorder. The purpose of this study is to examine whether TrkB ligands show antidepressant effects in an inflammation-induced model of depression. METHODS: In this study, we examined the effects of TrkB agonist 7,8-dihydroxyflavone (7,8-DHF) and TrkB antagonist ANA-12 on depression-like behavior and morphological changes in mice previously exposed to lipopolysaccharide (LPS). Protein levels of BDNF, phospho-TrkB (p-TrkB), and TrkB in the brain regions were also examined. RESULTS: LPS caused a reduction of BDNF in the CA3 and dentate gyrus (DG) of the hippocampus and prefrontal cortex (PFC), whereas LPS increased BDNF in the nucleus accumbens (NAc). Dexamethason suppression tests showed hyperactivity of the hypothalamic-pituitary-adrenal axis in LPS-treated mice. Intraperitoneal (i.p.) administration of 7,8-DHF showed antidepressant effects on LPS-induced depression-like behavior, and i.p. pretreatment with ANA-12 blocked its antidepressant effects. Surprisingly, ANA-12 alone showed antidepressant-like effects on LPS-induced depression-like behavior. Furthermore, bilateral infusion of ANA-12 into the NAc showed antidepressant effects. Moreover, LPS caused a reduction of spine density in the CA3, DG, and PFC, whereas LPS increased spine density in the NAc. Interestingly, 7,8-DHF significantly attenuated LPS-induced reduction of p-TrkB and spine densities in the CA3, DG, and PFC, whereas ANA-12 significantly attenuated LPS-induced increases of p-TrkB and spine density in the NAc. CONCLUSIONS: The results suggest that LPS-induced inflammation may cause depression-like behavior by altering BDNF and spine density in the CA3, DG, PFC, and NAc, which may be involved in the antidepressant effects of 7,8-DHF and ANA-12, respectively. Oxford University Press 2015-01-26 /pmc/articles/PMC4360225/ /pubmed/25628381 http://dx.doi.org/10.1093/ijnp/pyu077 Text en © The Author 2015. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Ji-chun
Wu, Jin
Fujita, Yuko
Yao, Wei
Ren, Qian
Yang, Chun
Li, Su-xia
Shirayama, Yukihiko
Hashimoto, Kenji
Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title_full Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title_fullStr Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title_full_unstemmed Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title_short Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation
title_sort antidepressant effects of trkb ligands on depression-like behavior and dendritic changes in mice after inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360225/
https://www.ncbi.nlm.nih.gov/pubmed/25628381
http://dx.doi.org/10.1093/ijnp/pyu077
work_keys_str_mv AT zhangjichun antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT wujin antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT fujitayuko antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT yaowei antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT renqian antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT yangchun antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT lisuxia antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT shirayamayukihiko antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation
AT hashimotokenji antidepressanteffectsoftrkbligandsondepressionlikebehavioranddendriticchangesinmiceafterinflammation