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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
Main Authors: HRCKOVA, G, VELEBNY, S, DAXNEROVA, Z, SOLAR, P
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DAXNEROVA, Z
SOLAR, P
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.
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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 &amp; 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 &amp; control ; Male ; mast cells ; Mast Cells - pathology ; Mastocytosis - pathology ; Mastocytosis - prevention &amp; control ; Mesocestoides - drug effects ; Mesocestoides vogae ; Mice ; Mice, Inbred ICR ; Nemathelminthia. Plathelmintha ; praziquantel ; Praziquantel - administration &amp; 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17642997$$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). 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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.</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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1469-8161
language eng
recordid cdi_proquest_miscellaneous_67780802
source Cambridge University Press
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
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