Antiviral Action of Diphenyl Diselenide on Herpes Simplex Virus 2 Infection in Female BALB/c Mice
ABSTRACT Diphenyl diselenide, (PhSe)2, is an organoselenium compound with pharmacological actions mostly related to antioxidant and anti‐inflammatory properties. The study investigated its antiviral and virucidal actions against herpes simplex virus 2 (HSV‐2) infection in vitro and in a vaginal infe...
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Veröffentlicht in: | Journal of cellular biochemistry 2016-07, Vol.117 (7), p.1638-1648 |
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creator | Sartori, Gláubia Jardim, Natália Silva Marcondes Sari, Marcel Henrique Dobrachinski, Fernando Pesarico, Ana Paula Rodrigues Jr, Luiz Carlos Cargnelutti, Juliana Flores, Eduardo F. Prigol, Marina Nogueira, Cristina W. |
description | ABSTRACT
Diphenyl diselenide, (PhSe)2, is an organoselenium compound with pharmacological actions mostly related to antioxidant and anti‐inflammatory properties. The study investigated its antiviral and virucidal actions against herpes simplex virus 2 (HSV‐2) infection in vitro and in a vaginal infection model in mice. The plaque reduction assay indicated that (PhSe)2 showed virucidal and antiviral actions reducing infectivity in 70.8% and 47%, respectively. The antiviral action of (PhSe)2 against HSV‐2 vaginal infection was performed by infecting mice (105 PFU/ml−1) at day 6. The treatment with (PhSe)2 (5 mg/kg/day, intragastric [i.g.]) followed 5 days before and for more 5 days after infection. The extravaginal lesion score was evaluated from days 6 to 10. At day 11, animals were killed, and histological evaluation, determination of viral load, and TNF‐α and IFN‐γ levels were performed in supernatants of homogenized vaginal tissue. The levels of reactive species (RS), protein carbonyl, non‐protein thiols (NPSH), nitrate/nitrite (NOx), and malondialdehyde (MDA), and the activities of myeloperoxidase (MPO), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR) were determined. (PhSe)2 reduced the histological damage, extravaginal lesion scores, the viral load of vaginal tissue, and the activity of MPO, but increased the levels of TNF‐α, IFN‐γ. (PhSe)2 attenuated the increase of RS, MDA, NOx levels and the activity of GR caused by infection. (PhSe)2 also attenuated the reduction of NPSH content and the inhibition of CAT, SOD, and GPx activities. The antiviral action of (PhSe)2 against HSV‐2 infection was related to its immunomodulatory, antioxidant, and anti‐inflammatory properties. J. Cell. Biochem. 117: 1638–1648, 2016. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/jcb.25457 |
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Diphenyl diselenide, (PhSe)2, is an organoselenium compound with pharmacological actions mostly related to antioxidant and anti‐inflammatory properties. The study investigated its antiviral and virucidal actions against herpes simplex virus 2 (HSV‐2) infection in vitro and in a vaginal infection model in mice. The plaque reduction assay indicated that (PhSe)2 showed virucidal and antiviral actions reducing infectivity in 70.8% and 47%, respectively. The antiviral action of (PhSe)2 against HSV‐2 vaginal infection was performed by infecting mice (105 PFU/ml−1) at day 6. The treatment with (PhSe)2 (5 mg/kg/day, intragastric [i.g.]) followed 5 days before and for more 5 days after infection. The extravaginal lesion score was evaluated from days 6 to 10. At day 11, animals were killed, and histological evaluation, determination of viral load, and TNF‐α and IFN‐γ levels were performed in supernatants of homogenized vaginal tissue. The levels of reactive species (RS), protein carbonyl, non‐protein thiols (NPSH), nitrate/nitrite (NOx), and malondialdehyde (MDA), and the activities of myeloperoxidase (MPO), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR) were determined. (PhSe)2 reduced the histological damage, extravaginal lesion scores, the viral load of vaginal tissue, and the activity of MPO, but increased the levels of TNF‐α, IFN‐γ. (PhSe)2 attenuated the increase of RS, MDA, NOx levels and the activity of GR caused by infection. (PhSe)2 also attenuated the reduction of NPSH content and the inhibition of CAT, SOD, and GPx activities. The antiviral action of (PhSe)2 against HSV‐2 infection was related to its immunomodulatory, antioxidant, and anti‐inflammatory properties. J. Cell. Biochem. 117: 1638–1648, 2016. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.25457</identifier><identifier>PMID: 26639776</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; Anti-Inflammatory Agents, Non-Steroidal - pharmacology ; Antioxidants - pharmacology ; Antiviral Agents - pharmacology ; Benzene Derivatives - pharmacology ; Dose-Response Relationship, Drug ; Drug Evaluation, Preclinical ; Female ; Herpes Genitalis - blood ; Herpes Genitalis - drug therapy ; Herpes simplex virus 2 ; Herpesvirus 2, Human ; HSV-2 ; IMMUNE SYSTEM ; Immunologic Factors - pharmacology ; INFLAMMATION ; Mice ; Organoselenium Compounds - pharmacology ; OXIDATIVE STRESS ; SELENIUM</subject><ispartof>Journal of cellular biochemistry, 2016-07, Vol.117 (7), p.1638-1648</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5607-bfe9e96473071659cdaa074f1bbb6891b111f2d07965fc18abe7f1014e53fd2a3</citedby><cites>FETCH-LOGICAL-c5607-bfe9e96473071659cdaa074f1bbb6891b111f2d07965fc18abe7f1014e53fd2a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcb.25457$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.25457$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26639776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sartori, Gláubia</creatorcontrib><creatorcontrib>Jardim, Natália Silva</creatorcontrib><creatorcontrib>Marcondes Sari, Marcel Henrique</creatorcontrib><creatorcontrib>Dobrachinski, Fernando</creatorcontrib><creatorcontrib>Pesarico, Ana Paula</creatorcontrib><creatorcontrib>Rodrigues Jr, Luiz Carlos</creatorcontrib><creatorcontrib>Cargnelutti, Juliana</creatorcontrib><creatorcontrib>Flores, Eduardo F.</creatorcontrib><creatorcontrib>Prigol, Marina</creatorcontrib><creatorcontrib>Nogueira, Cristina W.</creatorcontrib><title>Antiviral Action of Diphenyl Diselenide on Herpes Simplex Virus 2 Infection in Female BALB/c Mice</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>ABSTRACT
Diphenyl diselenide, (PhSe)2, is an organoselenium compound with pharmacological actions mostly related to antioxidant and anti‐inflammatory properties. The study investigated its antiviral and virucidal actions against herpes simplex virus 2 (HSV‐2) infection in vitro and in a vaginal infection model in mice. The plaque reduction assay indicated that (PhSe)2 showed virucidal and antiviral actions reducing infectivity in 70.8% and 47%, respectively. The antiviral action of (PhSe)2 against HSV‐2 vaginal infection was performed by infecting mice (105 PFU/ml−1) at day 6. The treatment with (PhSe)2 (5 mg/kg/day, intragastric [i.g.]) followed 5 days before and for more 5 days after infection. The extravaginal lesion score was evaluated from days 6 to 10. At day 11, animals were killed, and histological evaluation, determination of viral load, and TNF‐α and IFN‐γ levels were performed in supernatants of homogenized vaginal tissue. The levels of reactive species (RS), protein carbonyl, non‐protein thiols (NPSH), nitrate/nitrite (NOx), and malondialdehyde (MDA), and the activities of myeloperoxidase (MPO), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR) were determined. (PhSe)2 reduced the histological damage, extravaginal lesion scores, the viral load of vaginal tissue, and the activity of MPO, but increased the levels of TNF‐α, IFN‐γ. (PhSe)2 attenuated the increase of RS, MDA, NOx levels and the activity of GR caused by infection. (PhSe)2 also attenuated the reduction of NPSH content and the inhibition of CAT, SOD, and GPx activities. The antiviral action of (PhSe)2 against HSV‐2 infection was related to its immunomodulatory, antioxidant, and anti‐inflammatory properties. J. Cell. Biochem. 117: 1638–1648, 2016. © 2015 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</subject><subject>Antioxidants - pharmacology</subject><subject>Antiviral Agents - pharmacology</subject><subject>Benzene Derivatives - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Evaluation, Preclinical</subject><subject>Female</subject><subject>Herpes Genitalis - blood</subject><subject>Herpes Genitalis - drug therapy</subject><subject>Herpes simplex virus 2</subject><subject>Herpesvirus 2, Human</subject><subject>HSV-2</subject><subject>IMMUNE SYSTEM</subject><subject>Immunologic Factors - pharmacology</subject><subject>INFLAMMATION</subject><subject>Mice</subject><subject>Organoselenium Compounds - pharmacology</subject><subject>OXIDATIVE STRESS</subject><subject>SELENIUM</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtvEzEURi0EoqGw4A8gS2xgMY0fM_Z4mQTSFqWw4NGl5fFcCwfPo3YGmn-PYdoukFjdK93zfbo6CL2k5IwSwpZ725yxqqzkI7SgRMmiFGX5GC2I5KRgnLIT9CylPSFEKc6eohMmBFdSigUyq_7gf_poAl7Zgx96PDj8zo_foT-GvCQI0PsWcL5cQBwh4c--GwPc4m8-TgkzfNk7mKO-x1voTAC8Xu3WS4uvvIXn6IkzIcGLu3mKvm7ff9lcFLtP55eb1a6wlSCyaBwoUKLML0sqKmVbY4gsHW2aRtSKNpRSx1oilaicpbVpQDpKaAkVdy0z_BS9mXvHONxMkA6688lCCKaHYUqaSlVWhKtaZfT1P-h-mGKfv8tULURNiSCZejtTNg4pRXB6jL4z8agp0X-86-xd__We2Vd3jVPTQftA3ovOwHIGfvkAx_836Q-b9X1lMSd8OsDtQ8LEH1pILit9_fFcy2xgu7m61pT_BudHmKw</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Sartori, Gláubia</creator><creator>Jardim, Natália Silva</creator><creator>Marcondes Sari, Marcel Henrique</creator><creator>Dobrachinski, Fernando</creator><creator>Pesarico, Ana Paula</creator><creator>Rodrigues Jr, Luiz Carlos</creator><creator>Cargnelutti, Juliana</creator><creator>Flores, Eduardo F.</creator><creator>Prigol, Marina</creator><creator>Nogueira, Cristina W.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>201607</creationdate><title>Antiviral Action of Diphenyl Diselenide on Herpes Simplex Virus 2 Infection in Female BALB/c Mice</title><author>Sartori, Gláubia ; Jardim, Natália Silva ; Marcondes Sari, Marcel Henrique ; Dobrachinski, Fernando ; Pesarico, Ana Paula ; Rodrigues Jr, Luiz Carlos ; Cargnelutti, Juliana ; Flores, Eduardo F. ; Prigol, Marina ; Nogueira, Cristina W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5607-bfe9e96473071659cdaa074f1bbb6891b111f2d07965fc18abe7f1014e53fd2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</topic><topic>Antioxidants - pharmacology</topic><topic>Antiviral Agents - pharmacology</topic><topic>Benzene Derivatives - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Evaluation, Preclinical</topic><topic>Female</topic><topic>Herpes Genitalis - blood</topic><topic>Herpes Genitalis - drug therapy</topic><topic>Herpes simplex virus 2</topic><topic>Herpesvirus 2, Human</topic><topic>HSV-2</topic><topic>IMMUNE SYSTEM</topic><topic>Immunologic Factors - pharmacology</topic><topic>INFLAMMATION</topic><topic>Mice</topic><topic>Organoselenium Compounds - pharmacology</topic><topic>OXIDATIVE STRESS</topic><topic>SELENIUM</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sartori, Gláubia</creatorcontrib><creatorcontrib>Jardim, Natália Silva</creatorcontrib><creatorcontrib>Marcondes Sari, Marcel Henrique</creatorcontrib><creatorcontrib>Dobrachinski, Fernando</creatorcontrib><creatorcontrib>Pesarico, Ana Paula</creatorcontrib><creatorcontrib>Rodrigues Jr, Luiz Carlos</creatorcontrib><creatorcontrib>Cargnelutti, Juliana</creatorcontrib><creatorcontrib>Flores, Eduardo F.</creatorcontrib><creatorcontrib>Prigol, Marina</creatorcontrib><creatorcontrib>Nogueira, Cristina W.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sartori, Gláubia</au><au>Jardim, Natália Silva</au><au>Marcondes Sari, Marcel Henrique</au><au>Dobrachinski, Fernando</au><au>Pesarico, Ana Paula</au><au>Rodrigues Jr, Luiz Carlos</au><au>Cargnelutti, Juliana</au><au>Flores, Eduardo F.</au><au>Prigol, Marina</au><au>Nogueira, Cristina W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antiviral Action of Diphenyl Diselenide on Herpes Simplex Virus 2 Infection in Female BALB/c Mice</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>2016-07</date><risdate>2016</risdate><volume>117</volume><issue>7</issue><spage>1638</spage><epage>1648</epage><pages>1638-1648</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>ABSTRACT
Diphenyl diselenide, (PhSe)2, is an organoselenium compound with pharmacological actions mostly related to antioxidant and anti‐inflammatory properties. The study investigated its antiviral and virucidal actions against herpes simplex virus 2 (HSV‐2) infection in vitro and in a vaginal infection model in mice. The plaque reduction assay indicated that (PhSe)2 showed virucidal and antiviral actions reducing infectivity in 70.8% and 47%, respectively. The antiviral action of (PhSe)2 against HSV‐2 vaginal infection was performed by infecting mice (105 PFU/ml−1) at day 6. The treatment with (PhSe)2 (5 mg/kg/day, intragastric [i.g.]) followed 5 days before and for more 5 days after infection. The extravaginal lesion score was evaluated from days 6 to 10. At day 11, animals were killed, and histological evaluation, determination of viral load, and TNF‐α and IFN‐γ levels were performed in supernatants of homogenized vaginal tissue. The levels of reactive species (RS), protein carbonyl, non‐protein thiols (NPSH), nitrate/nitrite (NOx), and malondialdehyde (MDA), and the activities of myeloperoxidase (MPO), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR) were determined. (PhSe)2 reduced the histological damage, extravaginal lesion scores, the viral load of vaginal tissue, and the activity of MPO, but increased the levels of TNF‐α, IFN‐γ. (PhSe)2 attenuated the increase of RS, MDA, NOx levels and the activity of GR caused by infection. (PhSe)2 also attenuated the reduction of NPSH content and the inhibition of CAT, SOD, and GPx activities. The antiviral action of (PhSe)2 against HSV‐2 infection was related to its immunomodulatory, antioxidant, and anti‐inflammatory properties. J. Cell. Biochem. 117: 1638–1648, 2016. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26639776</pmid><doi>10.1002/jcb.25457</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents, Non-Steroidal - pharmacology Antioxidants - pharmacology Antiviral Agents - pharmacology Benzene Derivatives - pharmacology Dose-Response Relationship, Drug Drug Evaluation, Preclinical Female Herpes Genitalis - blood Herpes Genitalis - drug therapy Herpes simplex virus 2 Herpesvirus 2, Human HSV-2 IMMUNE SYSTEM Immunologic Factors - pharmacology INFLAMMATION Mice Organoselenium Compounds - pharmacology OXIDATIVE STRESS SELENIUM |
title | Antiviral Action of Diphenyl Diselenide on Herpes Simplex Virus 2 Infection in Female BALB/c Mice |
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