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Praziquantel and liposomized glucan-treatment modulated liver fibrogenesis and mastocytosis in mice infected with Mesocestoides vogae (M. corti, Cestoda) tetrathyridia
β–glucans are immunomodulators able to activate innate immunity and to potentiate acquired immune reactions. We investigated the impact of co-administration of liposomized β-glucan on the larvicidal effect of the anthelmintic praziquantel (PZQ) in the livers and peritoneal cavities in mice infected...
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Published in: | Parasitology 2006-04, Vol.132 (4), p.581-594 |
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description | β–glucans are immunomodulators able to activate innate immunity and to potentiate acquired immune reactions. We investigated the impact of co-administration of liposomized β-glucan on the larvicidal effect of the anthelmintic praziquantel (PZQ) in the livers and peritoneal cavities in mice infected with Mesocestoides vogae (M. corti). Also, within 2 weeks following therapy (up to day 29 p.i.) we examined collagen synthesis in the livers of mice by means of biochemical determination of hydroxyprolin concentration, total mast cell counts and cell proliferative capacity using immunohistochemical and radiometrical methods. After co-administration of liposomized glucan (LG) and PZQ efficacy (%) was significantly higher than after treatment with either compond alone, particularly in the peritoneal cavity compared to the liver. In comparison with the control, more intense collagenesis was found in the B-liver parts (high intensity of infection) and lowering of collagen content in the A-parts (very weak infection). This effect was strongest after LG treatment and co-administration of PZQ abolished the pro-fibrotic effect of LG. In all groups, mast cell counts were higher in the B-liver parts than in the A-parts and the dynamics of mastocytosis was profoundly modulated following therapy. Whereas the effect of PZQ was only moderate, early and very strong onset was seen after LG treatment. Administration of PZQ supressed LG induced-elevation of mast cells counts in both liver parts. Using DNA S-phase markers (BrdU and 3H-thymidine) the proliferative capacity was shown to be associated with several kinds of liver cells. Therapy significantly stimulated [3H]-thymidine incorporation (cell proliferation) only in the A-parts over that in control, the most after LG administration. In summary (i) the anthelmintic effect of PZQ could be enhanced after simultaneous administration of the immunomodulator β-glucan entrapped in a liposomal carrier, (ii) intense mastocytosis seen after treatment with LG seems to have a direct role in the glucan′s pro-fibrotic activity and can be abolished after co-administration of PZQ in a time-dependent manner, (iii) the pattern of cell proliferation indicates that in the case of PZQ treatment, the reparative processes of liver parenchyma are enhanced in an inverse correlation with the intensity of infection. |
doi_str_mv | 10.1017/S0031182005009364 |
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We investigated the impact of co-administration of liposomized β-glucan on the larvicidal effect of the anthelmintic praziquantel (PZQ) in the livers and peritoneal cavities in mice infected with Mesocestoides vogae (M. corti). Also, within 2 weeks following therapy (up to day 29 p.i.) we examined collagen synthesis in the livers of mice by means of biochemical determination of hydroxyprolin concentration, total mast cell counts and cell proliferative capacity using immunohistochemical and radiometrical methods. After co-administration of liposomized glucan (LG) and PZQ efficacy (%) was significantly higher than after treatment with either compond alone, particularly in the peritoneal cavity compared to the liver. In comparison with the control, more intense collagenesis was found in the B-liver parts (high intensity of infection) and lowering of collagen content in the A-parts (very weak infection). This effect was strongest after LG treatment and co-administration of PZQ abolished the pro-fibrotic effect of LG. In all groups, mast cell counts were higher in the B-liver parts than in the A-parts and the dynamics of mastocytosis was profoundly modulated following therapy. Whereas the effect of PZQ was only moderate, early and very strong onset was seen after LG treatment. Administration of PZQ supressed LG induced-elevation of mast cells counts in both liver parts. Using DNA S-phase markers (BrdU and 3H-thymidine) the proliferative capacity was shown to be associated with several kinds of liver cells. Therapy significantly stimulated [3H]-thymidine incorporation (cell proliferation) only in the A-parts over that in control, the most after LG administration. In summary (i) the anthelmintic effect of PZQ could be enhanced after simultaneous administration of the immunomodulator β-glucan entrapped in a liposomal carrier, (ii) intense mastocytosis seen after treatment with LG seems to have a direct role in the glucan′s pro-fibrotic activity and can be abolished after co-administration of PZQ in a time-dependent manner, (iii) the pattern of cell proliferation indicates that in the case of PZQ treatment, the reparative processes of liver parenchyma are enhanced in an inverse correlation with the intensity of infection.</description><identifier>ISSN: 0031-1820</identifier><identifier>EISSN: 1469-8161</identifier><identifier>DOI: 10.1017/S0031182005009364</identifier><identifier>PMID: 16556345</identifier><identifier>CODEN: PARAAE</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Animals ; Anthelmintics - pharmacology ; Antiparasitic agents ; beta-Glucans - administration & dosage ; beta-Glucans - pharmacology ; Biological and medical sciences ; Bromodeoxyuridine - analysis ; Cell division ; cell proliferation ; Cestode Infections - drug therapy ; Cestode Infections - parasitology ; Cestode Infections - pathology ; Collagen - analysis ; Collagen - metabolism ; Drug Therapy, Combination ; Drugs ; fibrogenesis ; Fundamental and applied biological sciences. Psychology ; General aspects ; General aspects and techniques. Study of several systematic groups. Models ; hydroxyproline ; Hydroxyproline - analysis ; Immunohistochemistry ; Invertebrates ; Liposomes ; Liver ; Liver - chemistry ; Liver - drug effects ; Liver - parasitology ; Liver - pathology ; Liver Cirrhosis - pathology ; Liver Cirrhosis - prevention & control ; Male ; mast cells ; Mast Cells - pathology ; Mastocytosis - pathology ; Mastocytosis - prevention & control ; Mesocestoides - drug effects ; Mesocestoides vogae ; Mice ; Mice, Inbred ICR ; Nemathelminthia. Plathelmintha ; praziquantel ; Praziquantel - administration & dosage ; Praziquantel - pharmacology ; Rodents ; Thymidine - metabolism ; Tissues ; Tolonium Chloride - metabolism ; Tritium ; Wound healing ; β-glucan</subject><ispartof>Parasitology, 2006-04, Vol.132 (4), p.581-594</ispartof><rights>2005 Cambridge University Press</rights><rights>2006 INIST-CNRS</rights><rights>Copyright Cambridge University Press Apr 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-3434aad9ce6258e83005e70eac38929f21dd1a7c8dd0d52850cdcd8bb3b0ea673</citedby><cites>FETCH-LOGICAL-c438t-3434aad9ce6258e83005e70eac38929f21dd1a7c8dd0d52850cdcd8bb3b0ea673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0031182005009364/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,72960</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17642997$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16556345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HRCKOVA, G</creatorcontrib><creatorcontrib>VELEBNY, S</creatorcontrib><creatorcontrib>DAXNEROVA, Z</creatorcontrib><creatorcontrib>SOLAR, P</creatorcontrib><title>Praziquantel and liposomized glucan-treatment modulated liver fibrogenesis and mastocytosis in mice infected with Mesocestoides vogae (M. corti, Cestoda) tetrathyridia</title><title>Parasitology</title><addtitle>Parasitology</addtitle><description>β–glucans are immunomodulators able to activate innate immunity and to potentiate acquired immune reactions. We investigated the impact of co-administration of liposomized β-glucan on the larvicidal effect of the anthelmintic praziquantel (PZQ) in the livers and peritoneal cavities in mice infected with Mesocestoides vogae (M. corti). Also, within 2 weeks following therapy (up to day 29 p.i.) we examined collagen synthesis in the livers of mice by means of biochemical determination of hydroxyprolin concentration, total mast cell counts and cell proliferative capacity using immunohistochemical and radiometrical methods. After co-administration of liposomized glucan (LG) and PZQ efficacy (%) was significantly higher than after treatment with either compond alone, particularly in the peritoneal cavity compared to the liver. In comparison with the control, more intense collagenesis was found in the B-liver parts (high intensity of infection) and lowering of collagen content in the A-parts (very weak infection). This effect was strongest after LG treatment and co-administration of PZQ abolished the pro-fibrotic effect of LG. In all groups, mast cell counts were higher in the B-liver parts than in the A-parts and the dynamics of mastocytosis was profoundly modulated following therapy. Whereas the effect of PZQ was only moderate, early and very strong onset was seen after LG treatment. Administration of PZQ supressed LG induced-elevation of mast cells counts in both liver parts. Using DNA S-phase markers (BrdU and 3H-thymidine) the proliferative capacity was shown to be associated with several kinds of liver cells. Therapy significantly stimulated [3H]-thymidine incorporation (cell proliferation) only in the A-parts over that in control, the most after LG administration. In summary (i) the anthelmintic effect of PZQ could be enhanced after simultaneous administration of the immunomodulator β-glucan entrapped in a liposomal carrier, (ii) intense mastocytosis seen after treatment with LG seems to have a direct role in the glucan′s pro-fibrotic activity and can be abolished after co-administration of PZQ in a time-dependent manner, (iii) the pattern of cell proliferation indicates that in the case of PZQ treatment, the reparative processes of liver parenchyma are enhanced in an inverse correlation with the intensity of infection.</description><subject>Animals</subject><subject>Anthelmintics - pharmacology</subject><subject>Antiparasitic agents</subject><subject>beta-Glucans - administration & dosage</subject><subject>beta-Glucans - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Bromodeoxyuridine - analysis</subject><subject>Cell division</subject><subject>cell proliferation</subject><subject>Cestode Infections - drug therapy</subject><subject>Cestode Infections - parasitology</subject><subject>Cestode Infections - pathology</subject><subject>Collagen - analysis</subject><subject>Collagen - metabolism</subject><subject>Drug Therapy, Combination</subject><subject>Drugs</subject><subject>fibrogenesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>General aspects and techniques. Study of several systematic groups. Models</subject><subject>hydroxyproline</subject><subject>Hydroxyproline - analysis</subject><subject>Immunohistochemistry</subject><subject>Invertebrates</subject><subject>Liposomes</subject><subject>Liver</subject><subject>Liver - chemistry</subject><subject>Liver - drug effects</subject><subject>Liver - parasitology</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver Cirrhosis - prevention & control</subject><subject>Male</subject><subject>mast cells</subject><subject>Mast Cells - pathology</subject><subject>Mastocytosis - pathology</subject><subject>Mastocytosis - prevention & control</subject><subject>Mesocestoides - drug effects</subject><subject>Mesocestoides vogae</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Nemathelminthia. Plathelmintha</subject><subject>praziquantel</subject><subject>Praziquantel - administration & dosage</subject><subject>Praziquantel - pharmacology</subject><subject>Rodents</subject><subject>Thymidine - metabolism</subject><subject>Tissues</subject><subject>Tolonium Chloride - metabolism</subject><subject>Tritium</subject><subject>Wound healing</subject><subject>β-glucan</subject><issn>0031-1820</issn><issn>1469-8161</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kV9v0zAUxSMEYmXwAXhBFtIQk8iw48RxHlHFOlArGH-eoxv7pvNI4s52Bt0X4mvi0IpKIJ6u5PM71rn3JMlTRs8YZeXrz5RyxmRGaUFpxUV-L5mxXFSpZILdT2aTnE76UfLI-2tKqeAie5gcMVEUgufFLPn50cGduRlhCNgRGDTpzMZ625s71GTdjQqGNDiE0OMQSG_12EHACbtFR1rTOLvGAb3xv909-GDVNtjpwQykNwrjbFFNpu8mXJEVeqswYkajJ7d2DUhers6Isi6YV2Q-SRpOScDgIFxtndEGHicPWug8PtnP4-Tr-dsv84t0-WHxbv5mmaqcy5DynOcAulIoskKi5PE0WFIExWWVVW3GtGZQKqk11UUmC6q00rJpeBMhUfLj5MXu342zN2OMUvfGK-w6GNCOvhZlKamkWQSf_wVe29ENMVudxQ5YJaWIENtBylnvHbb1xpke3LZmtJ4qrP-pMHqe7T8emx71wbHvLAInewC8gq51MCjjD1wp8qyqplXSHWd8wB9_dHDf4ha8LGqxuKwXy_fzy098VZ9Hnu_DQt_Eo6_xsNL_4_4CimPFgw</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>HRCKOVA, G</creator><creator>VELEBNY, S</creator><creator>DAXNEROVA, Z</creator><creator>SOLAR, P</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>IQODW</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>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20060401</creationdate><title>Praziquantel and liposomized glucan-treatment modulated liver fibrogenesis and mastocytosis in mice infected with Mesocestoides vogae (M. corti, Cestoda) tetrathyridia</title><author>HRCKOVA, G ; VELEBNY, S ; DAXNEROVA, Z ; SOLAR, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-3434aad9ce6258e83005e70eac38929f21dd1a7c8dd0d52850cdcd8bb3b0ea673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Anthelmintics - pharmacology</topic><topic>Antiparasitic agents</topic><topic>beta-Glucans - administration & dosage</topic><topic>beta-Glucans - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Bromodeoxyuridine - analysis</topic><topic>Cell division</topic><topic>cell proliferation</topic><topic>Cestode Infections - drug therapy</topic><topic>Cestode Infections - parasitology</topic><topic>Cestode Infections - pathology</topic><topic>Collagen - analysis</topic><topic>Collagen - metabolism</topic><topic>Drug Therapy, Combination</topic><topic>Drugs</topic><topic>fibrogenesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>General aspects and techniques. Study of several systematic groups. Models</topic><topic>hydroxyproline</topic><topic>Hydroxyproline - analysis</topic><topic>Immunohistochemistry</topic><topic>Invertebrates</topic><topic>Liposomes</topic><topic>Liver</topic><topic>Liver - chemistry</topic><topic>Liver - drug effects</topic><topic>Liver - parasitology</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver Cirrhosis - prevention & control</topic><topic>Male</topic><topic>mast cells</topic><topic>Mast Cells - pathology</topic><topic>Mastocytosis - pathology</topic><topic>Mastocytosis - prevention & control</topic><topic>Mesocestoides - drug effects</topic><topic>Mesocestoides vogae</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Nemathelminthia. Plathelmintha</topic><topic>praziquantel</topic><topic>Praziquantel - administration & dosage</topic><topic>Praziquantel - pharmacology</topic><topic>Rodents</topic><topic>Thymidine - metabolism</topic><topic>Tissues</topic><topic>Tolonium Chloride - metabolism</topic><topic>Tritium</topic><topic>Wound healing</topic><topic>β-glucan</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HRCKOVA, G</creatorcontrib><creatorcontrib>VELEBNY, S</creatorcontrib><creatorcontrib>DAXNEROVA, Z</creatorcontrib><creatorcontrib>SOLAR, P</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HRCKOVA, G</au><au>VELEBNY, S</au><au>DAXNEROVA, Z</au><au>SOLAR, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Praziquantel and liposomized glucan-treatment modulated liver fibrogenesis and mastocytosis in mice infected with Mesocestoides vogae (M. corti, Cestoda) tetrathyridia</atitle><jtitle>Parasitology</jtitle><addtitle>Parasitology</addtitle><date>2006-04-01</date><risdate>2006</risdate><volume>132</volume><issue>4</issue><spage>581</spage><epage>594</epage><pages>581-594</pages><issn>0031-1820</issn><eissn>1469-8161</eissn><coden>PARAAE</coden><abstract>β–glucans are immunomodulators able to activate innate immunity and to potentiate acquired immune reactions. We investigated the impact of co-administration of liposomized β-glucan on the larvicidal effect of the anthelmintic praziquantel (PZQ) in the livers and peritoneal cavities in mice infected with Mesocestoides vogae (M. corti). Also, within 2 weeks following therapy (up to day 29 p.i.) we examined collagen synthesis in the livers of mice by means of biochemical determination of hydroxyprolin concentration, total mast cell counts and cell proliferative capacity using immunohistochemical and radiometrical methods. After co-administration of liposomized glucan (LG) and PZQ efficacy (%) was significantly higher than after treatment with either compond alone, particularly in the peritoneal cavity compared to the liver. In comparison with the control, more intense collagenesis was found in the B-liver parts (high intensity of infection) and lowering of collagen content in the A-parts (very weak infection). This effect was strongest after LG treatment and co-administration of PZQ abolished the pro-fibrotic effect of LG. In all groups, mast cell counts were higher in the B-liver parts than in the A-parts and the dynamics of mastocytosis was profoundly modulated following therapy. Whereas the effect of PZQ was only moderate, early and very strong onset was seen after LG treatment. Administration of PZQ supressed LG induced-elevation of mast cells counts in both liver parts. Using DNA S-phase markers (BrdU and 3H-thymidine) the proliferative capacity was shown to be associated with several kinds of liver cells. Therapy significantly stimulated [3H]-thymidine incorporation (cell proliferation) only in the A-parts over that in control, the most after LG administration. In summary (i) the anthelmintic effect of PZQ could be enhanced after simultaneous administration of the immunomodulator β-glucan entrapped in a liposomal carrier, (ii) intense mastocytosis seen after treatment with LG seems to have a direct role in the glucan′s pro-fibrotic activity and can be abolished after co-administration of PZQ in a time-dependent manner, (iii) the pattern of cell proliferation indicates that in the case of PZQ treatment, the reparative processes of liver parenchyma are enhanced in an inverse correlation with the intensity of infection.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>16556345</pmid><doi>10.1017/S0031182005009364</doi><tpages>14</tpages></addata></record> |
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subjects | Animals Anthelmintics - pharmacology Antiparasitic agents beta-Glucans - administration & dosage beta-Glucans - pharmacology Biological and medical sciences Bromodeoxyuridine - analysis Cell division cell proliferation Cestode Infections - drug therapy Cestode Infections - parasitology Cestode Infections - pathology Collagen - analysis Collagen - metabolism Drug Therapy, Combination Drugs fibrogenesis Fundamental and applied biological sciences. Psychology General aspects General aspects and techniques. Study of several systematic groups. Models hydroxyproline Hydroxyproline - analysis Immunohistochemistry Invertebrates Liposomes Liver Liver - chemistry Liver - drug effects Liver - parasitology Liver - pathology Liver Cirrhosis - pathology Liver Cirrhosis - prevention & control Male mast cells Mast Cells - pathology Mastocytosis - pathology Mastocytosis - prevention & control Mesocestoides - drug effects Mesocestoides vogae Mice Mice, Inbred ICR Nemathelminthia. Plathelmintha praziquantel Praziquantel - administration & dosage Praziquantel - pharmacology Rodents Thymidine - metabolism Tissues Tolonium Chloride - metabolism Tritium Wound healing β-glucan |
title | Praziquantel and liposomized glucan-treatment modulated liver fibrogenesis and mastocytosis in mice infected with Mesocestoides vogae (M. corti, Cestoda) tetrathyridia |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T13%3A43%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Praziquantel%20and%20liposomized%20glucan-treatment%20modulated%20liver%20fibrogenesis%20and%20mastocytosis%20in%20mice%20infected%20with%20Mesocestoides%20vogae%20(M.%20corti,%20Cestoda)%20tetrathyridia&rft.jtitle=Parasitology&rft.au=HRCKOVA,%20G&rft.date=2006-04-01&rft.volume=132&rft.issue=4&rft.spage=581&rft.epage=594&rft.pages=581-594&rft.issn=0031-1820&rft.eissn=1469-8161&rft.coden=PARAAE&rft_id=info:doi/10.1017/S0031182005009364&rft_dat=%3Cproquest_cross%3E1456790011%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c438t-3434aad9ce6258e83005e70eac38929f21dd1a7c8dd0d52850cdcd8bb3b0ea673%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=214619886&rft_id=info:pmid/16556345&rft_cupid=10_1017_S0031182005009364&rfr_iscdi=true |