Reduced amount of olfactory receptor neurons in the rat model of depression

•Atrophic olfactory epithelium presents in the CUMS rat model.•Reduced number of basal cells is shown in the olfactory epithelium of CUMS rat model.•Reduced number of immature olfactory receptor neurons is shown in the olfactory epithelium of CUMS rat model.•Reduced number of mature olfactory recept...

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Veröffentlicht in:Neuroscience letters 2015-08, Vol.603, p.48-54
Hauptverfasser: Li, Qianlu, Yang, Deyu, Wang, Juan, Liu, Li, Feng, Guibo, Li, Juan, Liao, Juan, Wei, Youdong, Li, Zhiwei
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container_title Neuroscience letters
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creator Li, Qianlu
Yang, Deyu
Wang, Juan
Liu, Li
Feng, Guibo
Li, Juan
Liao, Juan
Wei, Youdong
Li, Zhiwei
description •Atrophic olfactory epithelium presents in the CUMS rat model.•Reduced number of basal cells is shown in the olfactory epithelium of CUMS rat model.•Reduced number of immature olfactory receptor neurons is shown in the olfactory epithelium of CUMS rat model.•Reduced number of mature olfactory receptor neurons is shown in the olfactory epithelium of CUMS rat model. Reduced olfactory sensitivity has been reported in depressive disorder. However, the pathological mechanism is still unclear. The reduced olfactory bulb (OB) volume and reduced hippocampal neurogenesis has been unraveled in major depressive disorder (MDD). However, changes in olfactory epithelium (OE) have not been reported, which might contribute to olfactory deficits in MDD. In the context, we investigated the thickness of OE in a chronic unpredictable mild stress (CUMS) rat model of depression using hematoxylin and eosin (HE) staining. Simultaneously, the basal cells (labeled by nerve growth factor receptor (p75NGFR)), immature olfactory receptor neurons (ORNs) (marked by growth-associated protein 43 (GAP43)) and mature ORNs (labeled by olfactory marker protein (OMP)) in OE were detected by immunohistochemistry. The results showed that the thickness of OE, the number of basal cells, immature ORNs as well as mature ORNs decreased dramatically in the OE of CUMS rats. Those findings indicate that the reduced number of ORNs might induce OE atrophy in CUMS rats and the abnormalities of the OE may be partially responsible for the reduced olfactory sensitivity in MDD.
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Reduced olfactory sensitivity has been reported in depressive disorder. However, the pathological mechanism is still unclear. The reduced olfactory bulb (OB) volume and reduced hippocampal neurogenesis has been unraveled in major depressive disorder (MDD). However, changes in olfactory epithelium (OE) have not been reported, which might contribute to olfactory deficits in MDD. In the context, we investigated the thickness of OE in a chronic unpredictable mild stress (CUMS) rat model of depression using hematoxylin and eosin (HE) staining. Simultaneously, the basal cells (labeled by nerve growth factor receptor (p75NGFR)), immature olfactory receptor neurons (ORNs) (marked by growth-associated protein 43 (GAP43)) and mature ORNs (labeled by olfactory marker protein (OMP)) in OE were detected by immunohistochemistry. The results showed that the thickness of OE, the number of basal cells, immature ORNs as well as mature ORNs decreased dramatically in the OE of CUMS rats. Those findings indicate that the reduced number of ORNs might induce OE atrophy in CUMS rats and the abnormalities of the OE may be partially responsible for the reduced olfactory sensitivity in MDD.</description><identifier>ISSN: 0304-3940</identifier><identifier>EISSN: 1872-7972</identifier><identifier>DOI: 10.1016/j.neulet.2015.07.007</identifier><identifier>PMID: 26170245</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Cell Count ; Depressive Disorder, Major - etiology ; Depressive Disorder, Major - metabolism ; Depressive Disorder, Major - pathology ; GAP-43 Protein - metabolism ; Major depressive disorder ; Male ; Olfactory deficits ; Olfactory epithelium ; Olfactory Marker Protein - metabolism ; Olfactory Mucosa - metabolism ; Olfactory Mucosa - pathology ; Olfactory receptor neurons ; Olfactory Receptor Neurons - metabolism ; Olfactory Receptor Neurons - pathology ; Rats, Sprague-Dawley ; Receptors, Nerve Growth Factor - metabolism ; Stress, Psychological - complications</subject><ispartof>Neuroscience letters, 2015-08, Vol.603, p.48-54</ispartof><rights>2015 Elsevier Ireland Ltd</rights><rights>Copyright © 2015 Elsevier Ireland Ltd. 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Reduced olfactory sensitivity has been reported in depressive disorder. However, the pathological mechanism is still unclear. The reduced olfactory bulb (OB) volume and reduced hippocampal neurogenesis has been unraveled in major depressive disorder (MDD). However, changes in olfactory epithelium (OE) have not been reported, which might contribute to olfactory deficits in MDD. In the context, we investigated the thickness of OE in a chronic unpredictable mild stress (CUMS) rat model of depression using hematoxylin and eosin (HE) staining. Simultaneously, the basal cells (labeled by nerve growth factor receptor (p75NGFR)), immature olfactory receptor neurons (ORNs) (marked by growth-associated protein 43 (GAP43)) and mature ORNs (labeled by olfactory marker protein (OMP)) in OE were detected by immunohistochemistry. The results showed that the thickness of OE, the number of basal cells, immature ORNs as well as mature ORNs decreased dramatically in the OE of CUMS rats. Those findings indicate that the reduced number of ORNs might induce OE atrophy in CUMS rats and the abnormalities of the OE may be partially responsible for the reduced olfactory sensitivity in MDD.</description><subject>Animals</subject><subject>Cell Count</subject><subject>Depressive Disorder, Major - etiology</subject><subject>Depressive Disorder, Major - metabolism</subject><subject>Depressive Disorder, Major - pathology</subject><subject>GAP-43 Protein - metabolism</subject><subject>Major depressive disorder</subject><subject>Male</subject><subject>Olfactory deficits</subject><subject>Olfactory epithelium</subject><subject>Olfactory Marker Protein - metabolism</subject><subject>Olfactory Mucosa - metabolism</subject><subject>Olfactory Mucosa - pathology</subject><subject>Olfactory receptor neurons</subject><subject>Olfactory Receptor Neurons - metabolism</subject><subject>Olfactory Receptor Neurons - pathology</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Nerve Growth Factor - metabolism</subject><subject>Stress, Psychological - complications</subject><issn>0304-3940</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVJqF2n_yAEHXPZ7ejL0l4CwSRpqaEQ2rOQpVm6ZnflSLuB_PvIOMkxp5nD887LPIRcMqgZsPWPfT3i3ONUc2CqBl0D6C9kyYzmlW40PyNLECAr0UhYkG857wFAMSW_kgVfMw1cqiX5_Yhh9hioG-I8TjS2NPat81NMLzShx0PZaGlKccy0G-n0H2lyEx1iwP6IBzwkzLmL4wU5b12f8fvbXJF_93d_Nz-r7Z-HX5vbbeUlN1NltHANrs2uAYVeoGoYaGaYUV744D2YoJxvhS6Dt1ILFoxxslWeCc5bJ1bk-nT3kOLTjHmyQ5c99r0bMc7Zlt-0UlquVUHlCfUp5pywtYfUDS69WAb2qNHu7UmjPWq0oG3RWGJXbw3zbsDwEXr3VoCbE4Dlz-cOk82-w7GI7Iq0yYbYfd7wCnPJhao</recordid><startdate>20150831</startdate><enddate>20150831</enddate><creator>Li, Qianlu</creator><creator>Yang, Deyu</creator><creator>Wang, Juan</creator><creator>Liu, Li</creator><creator>Feng, Guibo</creator><creator>Li, Juan</creator><creator>Liao, Juan</creator><creator>Wei, Youdong</creator><creator>Li, Zhiwei</creator><general>Elsevier Ireland Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150831</creationdate><title>Reduced amount of olfactory receptor neurons in the rat model of depression</title><author>Li, Qianlu ; 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Reduced olfactory sensitivity has been reported in depressive disorder. However, the pathological mechanism is still unclear. The reduced olfactory bulb (OB) volume and reduced hippocampal neurogenesis has been unraveled in major depressive disorder (MDD). However, changes in olfactory epithelium (OE) have not been reported, which might contribute to olfactory deficits in MDD. In the context, we investigated the thickness of OE in a chronic unpredictable mild stress (CUMS) rat model of depression using hematoxylin and eosin (HE) staining. Simultaneously, the basal cells (labeled by nerve growth factor receptor (p75NGFR)), immature olfactory receptor neurons (ORNs) (marked by growth-associated protein 43 (GAP43)) and mature ORNs (labeled by olfactory marker protein (OMP)) in OE were detected by immunohistochemistry. The results showed that the thickness of OE, the number of basal cells, immature ORNs as well as mature ORNs decreased dramatically in the OE of CUMS rats. 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subjects Animals
Cell Count
Depressive Disorder, Major - etiology
Depressive Disorder, Major - metabolism
Depressive Disorder, Major - pathology
GAP-43 Protein - metabolism
Major depressive disorder
Male
Olfactory deficits
Olfactory epithelium
Olfactory Marker Protein - metabolism
Olfactory Mucosa - metabolism
Olfactory Mucosa - pathology
Olfactory receptor neurons
Olfactory Receptor Neurons - metabolism
Olfactory Receptor Neurons - pathology
Rats, Sprague-Dawley
Receptors, Nerve Growth Factor - metabolism
Stress, Psychological - complications
title Reduced amount of olfactory receptor neurons in the rat model of depression
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