Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis

Developing dermatitis therapeutics has been faced with challenges including adverse effects of topical steroid and high cost of new developing drugs. Here, we found the expression levels of dopamine receptor D2 is higher in skin biopsies of dermatitis patients and an oxazolone-induced animal model o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of molecular sciences 2020-05, Vol.21 (9), p.3241, Article 3241
Hauptverfasser: Heo, Min-Jeong, Choi, Soo Young, Lee, Chanmi, Choi, Yeong Min, An, In-sook, Bae, Seunghee, An, Sungkwan, Jung, Jin Hyuk
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 9
container_start_page 3241
container_title International journal of molecular sciences
container_volume 21
creator Heo, Min-Jeong
Choi, Soo Young
Lee, Chanmi
Choi, Yeong Min
An, In-sook
Bae, Seunghee
An, Sungkwan
Jung, Jin Hyuk
description Developing dermatitis therapeutics has been faced with challenges including adverse effects of topical steroid and high cost of new developing drugs. Here, we found the expression levels of dopamine receptor D2 is higher in skin biopsies of dermatitis patients and an oxazolone-induced animal model of dermatitis. We used perphenazine, an FDA-approved dopamine receptor antagonist to determine the therapeutic effect. Two different animal models including 12-o-tetradecanoylphorbol-13-acetate (TPA) and oxazolone (OXA)-induced dermatitis were employed. TPA and OXA-mediated ear swelling was attenuated by perphenazine. Moreover, perphenazine inhibited infiltrated mast cells into lesion area. We found levels of serum IgE, histamine and cytokines are decreased in mice cotreated with perphenazine and OXA compared to OXA-treated mice. Overall, this is a first study showing that the FDA-approved, anti-psychotic drug, perphenazine, alleviates animal models of dermatitis.
doi_str_mv 10.3390/ijms21093241
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_32375285</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_07c5e84370744661b6d1dcd79af9b951</doaj_id><sourcerecordid>2400013895</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-130197a91e191b2f0c07a9d24cbb06678b050946d026776feda549d98de006143</originalsourceid><addsrcrecordid>eNqNkk1vEzEQhlcIREvhxhmtxBEW_LleX5CqUCBSERUKZ8trzyaOdu1ge0Hpr8c0JUpvXGyP55l3PHpdVS8xekepRO_ddkoEI0kJw4-qc8wIaRBqxeOT81n1LKUtQoQSLp9WZ5RQwUnHz6vhBuJuA17fOg_1Zc7gZ50h1XkD9U0MzdIPo54mnUPc198h7YJPJe18_TXMCcpqYUx1GOrVhjSr_a6ojCPEtTP1R4il0GWXnldPBj0meHG_X1Q_Pl2tFl-a62-fl4vL68Yw0eUGU4Sl0BIDlrgnAzKoRJYw0_eobUXXI44kay0irRDtAFZzJq3sLJQxMaMX1fKga4Peql10k457FbRTdxchrpWO2ZkRFBKGQ8eoQIKxtsV9a7E1Vkg9yF5yXLQ-HLR2cz-BNeBz1OMD0YcZ7zZqHX4pQZigdwKv7wVi-DlDymob5ujL_IowhBCmneSFenugTAwpRRiOHTBSfx1Wpw4X_NXpq47wP0sL0B2A39CHIRkH3sARK2055bzDovwGTBYuF4OCX4TZ51L65v9L6R_U0MIw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2400013895</pqid></control><display><type>article</type><title>Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>Web of Science - Science Citation Index Expanded - 2020&lt;img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" /&gt;</source><source>PubMed Central</source><creator>Heo, Min-Jeong ; Choi, Soo Young ; Lee, Chanmi ; Choi, Yeong Min ; An, In-sook ; Bae, Seunghee ; An, Sungkwan ; Jung, Jin Hyuk</creator><creatorcontrib>Heo, Min-Jeong ; Choi, Soo Young ; Lee, Chanmi ; Choi, Yeong Min ; An, In-sook ; Bae, Seunghee ; An, Sungkwan ; Jung, Jin Hyuk</creatorcontrib><description>Developing dermatitis therapeutics has been faced with challenges including adverse effects of topical steroid and high cost of new developing drugs. Here, we found the expression levels of dopamine receptor D2 is higher in skin biopsies of dermatitis patients and an oxazolone-induced animal model of dermatitis. We used perphenazine, an FDA-approved dopamine receptor antagonist to determine the therapeutic effect. Two different animal models including 12-o-tetradecanoylphorbol-13-acetate (TPA) and oxazolone (OXA)-induced dermatitis were employed. TPA and OXA-mediated ear swelling was attenuated by perphenazine. Moreover, perphenazine inhibited infiltrated mast cells into lesion area. We found levels of serum IgE, histamine and cytokines are decreased in mice cotreated with perphenazine and OXA compared to OXA-treated mice. Overall, this is a first study showing that the FDA-approved, anti-psychotic drug, perphenazine, alleviates animal models of dermatitis.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21093241</identifier><identifier>PMID: 32375285</identifier><language>eng</language><publisher>BASEL: Mdpi</publisher><subject>12-O-Tetradecanoylphorbol-13-acetate ; Acetic acid ; Animal models ; Animals ; Biochemistry &amp; Molecular Biology ; Chemistry ; Chemistry, Multidisciplinary ; Cytokines ; Cytokines - metabolism ; Dermatitis ; Dermatitis, Allergic Contact - drug therapy ; Dermatitis, Allergic Contact - etiology ; Dopamine ; Dopamine Antagonists - pharmacology ; Dopamine Antagonists - therapeutic use ; Dopamine D2 receptors ; dopamine receptor D2 ; drug repurposing ; Histamine ; Immunoglobulin E ; Immunoglobulin G - metabolism ; Inflammation ; Laboratory animals ; Life Sciences &amp; Biomedicine ; Lymphocytes ; Lymphocytes T ; Mast cells ; Mast Cells - drug effects ; Mast Cells - immunology ; Metabolism ; Mice ; Mice, Inbred C57BL ; NIH 3T3 Cells ; Oxazolone - toxicity ; Perphenazine ; Perphenazine - pharmacology ; Perphenazine - therapeutic use ; Physical Sciences ; Quarantine ; Science &amp; Technology ; Steroids ; Tetradecanoylphorbol Acetate - toxicity ; Th2 Cells - drug effects ; Th2 Cells - immunology</subject><ispartof>International journal of molecular sciences, 2020-05, Vol.21 (9), p.3241, Article 3241</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>3</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000535581700212</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c478t-130197a91e191b2f0c07a9d24cbb06678b050946d026776feda549d98de006143</citedby><cites>FETCH-LOGICAL-c478t-130197a91e191b2f0c07a9d24cbb06678b050946d026776feda549d98de006143</cites><orcidid>0000-0002-2811-8305</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247351/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247351/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,28253,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32375285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heo, Min-Jeong</creatorcontrib><creatorcontrib>Choi, Soo Young</creatorcontrib><creatorcontrib>Lee, Chanmi</creatorcontrib><creatorcontrib>Choi, Yeong Min</creatorcontrib><creatorcontrib>An, In-sook</creatorcontrib><creatorcontrib>Bae, Seunghee</creatorcontrib><creatorcontrib>An, Sungkwan</creatorcontrib><creatorcontrib>Jung, Jin Hyuk</creatorcontrib><title>Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis</title><title>International journal of molecular sciences</title><addtitle>INT J MOL SCI</addtitle><addtitle>Int J Mol Sci</addtitle><description>Developing dermatitis therapeutics has been faced with challenges including adverse effects of topical steroid and high cost of new developing drugs. Here, we found the expression levels of dopamine receptor D2 is higher in skin biopsies of dermatitis patients and an oxazolone-induced animal model of dermatitis. We used perphenazine, an FDA-approved dopamine receptor antagonist to determine the therapeutic effect. Two different animal models including 12-o-tetradecanoylphorbol-13-acetate (TPA) and oxazolone (OXA)-induced dermatitis were employed. TPA and OXA-mediated ear swelling was attenuated by perphenazine. Moreover, perphenazine inhibited infiltrated mast cells into lesion area. We found levels of serum IgE, histamine and cytokines are decreased in mice cotreated with perphenazine and OXA compared to OXA-treated mice. Overall, this is a first study showing that the FDA-approved, anti-psychotic drug, perphenazine, alleviates animal models of dermatitis.</description><subject>12-O-Tetradecanoylphorbol-13-acetate</subject><subject>Acetic acid</subject><subject>Animal models</subject><subject>Animals</subject><subject>Biochemistry &amp; Molecular Biology</subject><subject>Chemistry</subject><subject>Chemistry, Multidisciplinary</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Dermatitis</subject><subject>Dermatitis, Allergic Contact - drug therapy</subject><subject>Dermatitis, Allergic Contact - etiology</subject><subject>Dopamine</subject><subject>Dopamine Antagonists - pharmacology</subject><subject>Dopamine Antagonists - therapeutic use</subject><subject>Dopamine D2 receptors</subject><subject>dopamine receptor D2</subject><subject>drug repurposing</subject><subject>Histamine</subject><subject>Immunoglobulin E</subject><subject>Immunoglobulin G - metabolism</subject><subject>Inflammation</subject><subject>Laboratory animals</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Mast cells</subject><subject>Mast Cells - drug effects</subject><subject>Mast Cells - immunology</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>NIH 3T3 Cells</subject><subject>Oxazolone - toxicity</subject><subject>Perphenazine</subject><subject>Perphenazine - pharmacology</subject><subject>Perphenazine - therapeutic use</subject><subject>Physical Sciences</subject><subject>Quarantine</subject><subject>Science &amp; Technology</subject><subject>Steroids</subject><subject>Tetradecanoylphorbol Acetate - toxicity</subject><subject>Th2 Cells - drug effects</subject><subject>Th2 Cells - immunology</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>AOWDO</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1vEzEQhlcIREvhxhmtxBEW_LleX5CqUCBSERUKZ8trzyaOdu1ge0Hpr8c0JUpvXGyP55l3PHpdVS8xekepRO_ddkoEI0kJw4-qc8wIaRBqxeOT81n1LKUtQoQSLp9WZ5RQwUnHz6vhBuJuA17fOg_1Zc7gZ50h1XkD9U0MzdIPo54mnUPc198h7YJPJe18_TXMCcpqYUx1GOrVhjSr_a6ojCPEtTP1R4il0GWXnldPBj0meHG_X1Q_Pl2tFl-a62-fl4vL68Yw0eUGU4Sl0BIDlrgnAzKoRJYw0_eobUXXI44kay0irRDtAFZzJq3sLJQxMaMX1fKga4Peql10k457FbRTdxchrpWO2ZkRFBKGQ8eoQIKxtsV9a7E1Vkg9yF5yXLQ-HLR2cz-BNeBz1OMD0YcZ7zZqHX4pQZigdwKv7wVi-DlDymob5ujL_IowhBCmneSFenugTAwpRRiOHTBSfx1Wpw4X_NXpq47wP0sL0B2A39CHIRkH3sARK2055bzDovwGTBYuF4OCX4TZ51L65v9L6R_U0MIw</recordid><startdate>20200503</startdate><enddate>20200503</enddate><creator>Heo, Min-Jeong</creator><creator>Choi, Soo Young</creator><creator>Lee, Chanmi</creator><creator>Choi, Yeong Min</creator><creator>An, In-sook</creator><creator>Bae, Seunghee</creator><creator>An, Sungkwan</creator><creator>Jung, Jin Hyuk</creator><general>Mdpi</general><general>MDPI AG</general><general>MDPI</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><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>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2811-8305</orcidid></search><sort><creationdate>20200503</creationdate><title>Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis</title><author>Heo, Min-Jeong ; Choi, Soo Young ; Lee, Chanmi ; Choi, Yeong Min ; An, In-sook ; Bae, Seunghee ; An, Sungkwan ; Jung, Jin Hyuk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-130197a91e191b2f0c07a9d24cbb06678b050946d026776feda549d98de006143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>12-O-Tetradecanoylphorbol-13-acetate</topic><topic>Acetic acid</topic><topic>Animal models</topic><topic>Animals</topic><topic>Biochemistry &amp; Molecular Biology</topic><topic>Chemistry</topic><topic>Chemistry, Multidisciplinary</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>Dermatitis</topic><topic>Dermatitis, Allergic Contact - drug therapy</topic><topic>Dermatitis, Allergic Contact - etiology</topic><topic>Dopamine</topic><topic>Dopamine Antagonists - pharmacology</topic><topic>Dopamine Antagonists - therapeutic use</topic><topic>Dopamine D2 receptors</topic><topic>dopamine receptor D2</topic><topic>drug repurposing</topic><topic>Histamine</topic><topic>Immunoglobulin E</topic><topic>Immunoglobulin G - metabolism</topic><topic>Inflammation</topic><topic>Laboratory animals</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Mast cells</topic><topic>Mast Cells - drug effects</topic><topic>Mast Cells - immunology</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>NIH 3T3 Cells</topic><topic>Oxazolone - toxicity</topic><topic>Perphenazine</topic><topic>Perphenazine - pharmacology</topic><topic>Perphenazine - therapeutic use</topic><topic>Physical Sciences</topic><topic>Quarantine</topic><topic>Science &amp; Technology</topic><topic>Steroids</topic><topic>Tetradecanoylphorbol Acetate - toxicity</topic><topic>Th2 Cells - drug effects</topic><topic>Th2 Cells - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heo, Min-Jeong</creatorcontrib><creatorcontrib>Choi, Soo Young</creatorcontrib><creatorcontrib>Lee, Chanmi</creatorcontrib><creatorcontrib>Choi, Yeong Min</creatorcontrib><creatorcontrib>An, In-sook</creatorcontrib><creatorcontrib>Bae, Seunghee</creatorcontrib><creatorcontrib>An, Sungkwan</creatorcontrib><creatorcontrib>Jung, Jin Hyuk</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</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>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heo, Min-Jeong</au><au>Choi, Soo Young</au><au>Lee, Chanmi</au><au>Choi, Yeong Min</au><au>An, In-sook</au><au>Bae, Seunghee</au><au>An, Sungkwan</au><au>Jung, Jin Hyuk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis</atitle><jtitle>International journal of molecular sciences</jtitle><stitle>INT J MOL SCI</stitle><addtitle>Int J Mol Sci</addtitle><date>2020-05-03</date><risdate>2020</risdate><volume>21</volume><issue>9</issue><spage>3241</spage><pages>3241-</pages><artnum>3241</artnum><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Developing dermatitis therapeutics has been faced with challenges including adverse effects of topical steroid and high cost of new developing drugs. Here, we found the expression levels of dopamine receptor D2 is higher in skin biopsies of dermatitis patients and an oxazolone-induced animal model of dermatitis. We used perphenazine, an FDA-approved dopamine receptor antagonist to determine the therapeutic effect. Two different animal models including 12-o-tetradecanoylphorbol-13-acetate (TPA) and oxazolone (OXA)-induced dermatitis were employed. TPA and OXA-mediated ear swelling was attenuated by perphenazine. Moreover, perphenazine inhibited infiltrated mast cells into lesion area. We found levels of serum IgE, histamine and cytokines are decreased in mice cotreated with perphenazine and OXA compared to OXA-treated mice. Overall, this is a first study showing that the FDA-approved, anti-psychotic drug, perphenazine, alleviates animal models of dermatitis.</abstract><cop>BASEL</cop><pub>Mdpi</pub><pmid>32375285</pmid><doi>10.3390/ijms21093241</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2811-8305</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1422-0067
ispartof International journal of molecular sciences, 2020-05, Vol.21 (9), p.3241, Article 3241
issn 1422-0067
1661-6596
1422-0067
language eng
recordid cdi_pubmed_primary_32375285
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; MDPI - Multidisciplinary Digital Publishing Institute; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; PubMed Central
subjects 12-O-Tetradecanoylphorbol-13-acetate
Acetic acid
Animal models
Animals
Biochemistry & Molecular Biology
Chemistry
Chemistry, Multidisciplinary
Cytokines
Cytokines - metabolism
Dermatitis
Dermatitis, Allergic Contact - drug therapy
Dermatitis, Allergic Contact - etiology
Dopamine
Dopamine Antagonists - pharmacology
Dopamine Antagonists - therapeutic use
Dopamine D2 receptors
dopamine receptor D2
drug repurposing
Histamine
Immunoglobulin E
Immunoglobulin G - metabolism
Inflammation
Laboratory animals
Life Sciences & Biomedicine
Lymphocytes
Lymphocytes T
Mast cells
Mast Cells - drug effects
Mast Cells - immunology
Metabolism
Mice
Mice, Inbred C57BL
NIH 3T3 Cells
Oxazolone - toxicity
Perphenazine
Perphenazine - pharmacology
Perphenazine - therapeutic use
Physical Sciences
Quarantine
Science & Technology
Steroids
Tetradecanoylphorbol Acetate - toxicity
Th2 Cells - drug effects
Th2 Cells - immunology
title Perphenazine Attenuates the Pro-Inflammatory Responses in Mouse Models of Th2-Type Allergic Dermatitis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T15%3A57%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Perphenazine%20Attenuates%20the%20Pro-Inflammatory%20Responses%20in%20Mouse%20Models%20of%20Th2-Type%20Allergic%20Dermatitis&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Heo,%20Min-Jeong&rft.date=2020-05-03&rft.volume=21&rft.issue=9&rft.spage=3241&rft.pages=3241-&rft.artnum=3241&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms21093241&rft_dat=%3Cproquest_pubme%3E2400013895%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2400013895&rft_id=info:pmid/32375285&rft_doaj_id=oai_doaj_org_article_07c5e84370744661b6d1dcd79af9b951&rfr_iscdi=true