Microglial and Astrocytic Function in Physiological and Pathological Conditions: Estrogenic Modulation
There are sexual differences in the onset, prevalence, and outcome of numerous neurological diseases. Thus, in Alzheimer's disease, multiple sclerosis, and major depression disorder, the incidence in women is higher than in men. In contrast, men are more likely to present other pathologies, suc...
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description | There are sexual differences in the onset, prevalence, and outcome of numerous neurological diseases. Thus, in Alzheimer's disease, multiple sclerosis, and major depression disorder, the incidence in women is higher than in men. In contrast, men are more likely to present other pathologies, such as amyotrophic lateral sclerosis, Parkinson's disease, and autism spectrum. Although the neurological contribution to these diseases has classically always been studied, the truth is that neurons are not the only cells to be affected, and there are other cells, such as glial cells, that are also involved and could be key to understanding the development of these pathologies. Sexual differences exist not only in pathology but also in physiological processes, which shows how cells are differentially regulated in males and females. One of the reasons these sexual differences may occur could be due to the different action of sex hormones. Many studies have shown an increase in aromatase levels in the brain, which could indicate the main role of estrogens in modulating proinflammatory processes. This review will highlight data about sex differences in glial physiology and how estrogenic compounds, such as estradiol and tibolone, could be used as treatment in neurological diseases due to their anti-inflammatory effects and the ability to modulate glial cell functions. |
doi_str_mv | 10.3390/ijms21093219 |
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Thus, in Alzheimer's disease, multiple sclerosis, and major depression disorder, the incidence in women is higher than in men. In contrast, men are more likely to present other pathologies, such as amyotrophic lateral sclerosis, Parkinson's disease, and autism spectrum. Although the neurological contribution to these diseases has classically always been studied, the truth is that neurons are not the only cells to be affected, and there are other cells, such as glial cells, that are also involved and could be key to understanding the development of these pathologies. Sexual differences exist not only in pathology but also in physiological processes, which shows how cells are differentially regulated in males and females. One of the reasons these sexual differences may occur could be due to the different action of sex hormones. Many studies have shown an increase in aromatase levels in the brain, which could indicate the main role of estrogens in modulating proinflammatory processes. This review will highlight data about sex differences in glial physiology and how estrogenic compounds, such as estradiol and tibolone, could be used as treatment in neurological diseases due to their anti-inflammatory effects and the ability to modulate glial cell functions.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21093219</identifier><identifier>PMID: 32370112</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>17β-Estradiol ; Alzheimer Disease - metabolism ; Alzheimer Disease - pathology ; Alzheimer's disease ; Amyotrophic lateral sclerosis ; Aromatase ; Astrocytes - pathology ; Autism ; Chemokines ; Cytokines ; Depressive Disorder, Major - metabolism ; Depressive Disorder, Major - pathology ; Disease ; Estrogens ; Estrogens - metabolism ; Female ; Gender differences ; Genotype & phenotype ; Glial cells ; Humans ; Immune system ; Inflammation ; Male ; Mental disorders ; Microglia - pathology ; Morphology ; Multiple sclerosis ; Multiple Sclerosis - metabolism ; Multiple Sclerosis - pathology ; Nervous system ; Neurological diseases ; Parkinson's disease ; Physiology ; Review ; Sex differences ; Sex Factors ; Sex hormones ; Sexual behavior ; Testosterone ; Tibolone ; Trauma ; Traumatic brain injury ; Xenoestrogens</subject><ispartof>International journal of molecular sciences, 2020-05, Vol.21 (9), p.3219</ispartof><rights>2020. 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Thus, in Alzheimer's disease, multiple sclerosis, and major depression disorder, the incidence in women is higher than in men. In contrast, men are more likely to present other pathologies, such as amyotrophic lateral sclerosis, Parkinson's disease, and autism spectrum. Although the neurological contribution to these diseases has classically always been studied, the truth is that neurons are not the only cells to be affected, and there are other cells, such as glial cells, that are also involved and could be key to understanding the development of these pathologies. Sexual differences exist not only in pathology but also in physiological processes, which shows how cells are differentially regulated in males and females. One of the reasons these sexual differences may occur could be due to the different action of sex hormones. Many studies have shown an increase in aromatase levels in the brain, which could indicate the main role of estrogens in modulating proinflammatory processes. This review will highlight data about sex differences in glial physiology and how estrogenic compounds, such as estradiol and tibolone, could be used as treatment in neurological diseases due to their anti-inflammatory effects and the ability to modulate glial cell functions.</description><subject>17β-Estradiol</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer's disease</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Aromatase</subject><subject>Astrocytes - pathology</subject><subject>Autism</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Depressive Disorder, Major - metabolism</subject><subject>Depressive Disorder, Major - pathology</subject><subject>Disease</subject><subject>Estrogens</subject><subject>Estrogens - metabolism</subject><subject>Female</subject><subject>Gender differences</subject><subject>Genotype & phenotype</subject><subject>Glial cells</subject><subject>Humans</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>Male</subject><subject>Mental disorders</subject><subject>Microglia - pathology</subject><subject>Morphology</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - metabolism</subject><subject>Multiple Sclerosis - pathology</subject><subject>Nervous system</subject><subject>Neurological diseases</subject><subject>Parkinson's disease</subject><subject>Physiology</subject><subject>Review</subject><subject>Sex differences</subject><subject>Sex Factors</subject><subject>Sex hormones</subject><subject>Sexual behavior</subject><subject>Testosterone</subject><subject>Tibolone</subject><subject>Trauma</subject><subject>Traumatic brain injury</subject><subject>Xenoestrogens</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkT1PwzAQhi0EgvKxMaNILAwUzmenThiQqqp8SFR0gNlyHKd1ldolTpD670mgVIXJ1vnRc3d-CTmncMNYCrd2sQxIIWVI0z3SoxyxDzAQ-zv3I3IcwgIAGcbpITliyARQij1STKyu_Ky0qoyUy6NhqCuv17XV0UPjdG29i6yLpvN1sL70M6s34FTV821h5F1uOzbcRePOMDOuNUx83pSqq5-Sg0KVwZxtzhPy_jB-Gz31X14fn0fDl77mcVz3U-CGQUq5yZkGLRLBYh4bwwqFSQ6ZQM4h08poLjTSAjMqNGRJBlwMEhDshNz_eFdNtjS5Nq6uVClXlV2qai29svLvi7NzOfOfsjW3vZJWcLURVP6jMaGWSxu0KUvljG-CRJamGHOBXa_Lf-jCN5Vr1_um4sEgQWyp6x-q_eYQKlNsh6EguwDlboAtfrG7wBb-TYx9AVhnmD8</recordid><startdate>20200502</startdate><enddate>20200502</enddate><creator>Crespo-Castrillo, Andrea</creator><creator>Arevalo, Maria-Angeles</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4303-9576</orcidid></search><sort><creationdate>20200502</creationdate><title>Microglial and Astrocytic Function in Physiological and Pathological Conditions: Estrogenic Modulation</title><author>Crespo-Castrillo, Andrea ; Arevalo, Maria-Angeles</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-904e30914ed3c0c7873545ee3fa28d0b72440bcaec47c21f2b17c0b8b04768073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>17β-Estradiol</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer's disease</topic><topic>Amyotrophic lateral sclerosis</topic><topic>Aromatase</topic><topic>Astrocytes - pathology</topic><topic>Autism</topic><topic>Chemokines</topic><topic>Cytokines</topic><topic>Depressive Disorder, Major - metabolism</topic><topic>Depressive Disorder, Major - pathology</topic><topic>Disease</topic><topic>Estrogens</topic><topic>Estrogens - metabolism</topic><topic>Female</topic><topic>Gender differences</topic><topic>Genotype & phenotype</topic><topic>Glial cells</topic><topic>Humans</topic><topic>Immune system</topic><topic>Inflammation</topic><topic>Male</topic><topic>Mental disorders</topic><topic>Microglia - pathology</topic><topic>Morphology</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - metabolism</topic><topic>Multiple Sclerosis - pathology</topic><topic>Nervous system</topic><topic>Neurological diseases</topic><topic>Parkinson's disease</topic><topic>Physiology</topic><topic>Review</topic><topic>Sex differences</topic><topic>Sex Factors</topic><topic>Sex hormones</topic><topic>Sexual behavior</topic><topic>Testosterone</topic><topic>Tibolone</topic><topic>Trauma</topic><topic>Traumatic brain injury</topic><topic>Xenoestrogens</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Crespo-Castrillo, Andrea</creatorcontrib><creatorcontrib>Arevalo, Maria-Angeles</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Crespo-Castrillo, Andrea</au><au>Arevalo, Maria-Angeles</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microglial and Astrocytic Function in Physiological and Pathological Conditions: Estrogenic Modulation</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-05-02</date><risdate>2020</risdate><volume>21</volume><issue>9</issue><spage>3219</spage><pages>3219-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>There are sexual differences in the onset, prevalence, and outcome of numerous neurological diseases. Thus, in Alzheimer's disease, multiple sclerosis, and major depression disorder, the incidence in women is higher than in men. In contrast, men are more likely to present other pathologies, such as amyotrophic lateral sclerosis, Parkinson's disease, and autism spectrum. Although the neurological contribution to these diseases has classically always been studied, the truth is that neurons are not the only cells to be affected, and there are other cells, such as glial cells, that are also involved and could be key to understanding the development of these pathologies. Sexual differences exist not only in pathology but also in physiological processes, which shows how cells are differentially regulated in males and females. One of the reasons these sexual differences may occur could be due to the different action of sex hormones. Many studies have shown an increase in aromatase levels in the brain, which could indicate the main role of estrogens in modulating proinflammatory processes. 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subjects | 17β-Estradiol Alzheimer Disease - metabolism Alzheimer Disease - pathology Alzheimer's disease Amyotrophic lateral sclerosis Aromatase Astrocytes - pathology Autism Chemokines Cytokines Depressive Disorder, Major - metabolism Depressive Disorder, Major - pathology Disease Estrogens Estrogens - metabolism Female Gender differences Genotype & phenotype Glial cells Humans Immune system Inflammation Male Mental disorders Microglia - pathology Morphology Multiple sclerosis Multiple Sclerosis - metabolism Multiple Sclerosis - pathology Nervous system Neurological diseases Parkinson's disease Physiology Review Sex differences Sex Factors Sex hormones Sexual behavior Testosterone Tibolone Trauma Traumatic brain injury Xenoestrogens |
title | Microglial and Astrocytic Function in Physiological and Pathological Conditions: Estrogenic Modulation |
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