In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum
Adult Toxocara canis and Ascaris suum were incubated in vitro in media containing 0.1, 1, 10 or 100 micro g/ml flubendazole in order to study drug-derived effects. This incubation was done for 8 h and repeated (in some groups) after 24 h for another 8 h. The onset and intensity of flubendazole-deriv...
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description | Adult Toxocara canis and Ascaris suum were incubated in vitro in media containing 0.1, 1, 10 or 100 micro g/ml flubendazole in order to study drug-derived effects. This incubation was done for 8 h and repeated (in some groups) after 24 h for another 8 h. The onset and intensity of flubendazole-derived effects were dosage-dependent and time-dependent, i.e. the same grade of damage was reached when incubating for a longer period at a low dosage or for a shorter period in medium containing a high amount (10 or 100 micro g/ml) of flubendazole. A repeated incubation in drug-containing medium was superior to a single exposure. Flubendazole is apparently able to penetrate into the worm's interior via the cuticle. This became evident in worms with sealed orifices, which showed identical damage to worms which were not sealed. The type of tissue damage due to flubendazole was identical in both worm species when exposed to any of the drug dosages used. The principal mode of action of flubendazole was based on the complete reduction of microtubuli-polymerisation inside the parasite's cells. This apparently led to the complete destruction of the hypodermis, muscle layer and intestine. Flubendazole also stopped the formation of gametes. Summarising, even low concentrations of flubendazole (0.1 micro g/ml) led to significant and irreversible damage in all worms studied. |
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This incubation was done for 8 h and repeated (in some groups) after 24 h for another 8 h. The onset and intensity of flubendazole-derived effects were dosage-dependent and time-dependent, i.e. the same grade of damage was reached when incubating for a longer period at a low dosage or for a shorter period in medium containing a high amount (10 or 100 micro g/ml) of flubendazole. A repeated incubation in drug-containing medium was superior to a single exposure. Flubendazole is apparently able to penetrate into the worm's interior via the cuticle. This became evident in worms with sealed orifices, which showed identical damage to worms which were not sealed. The type of tissue damage due to flubendazole was identical in both worm species when exposed to any of the drug dosages used. The principal mode of action of flubendazole was based on the complete reduction of microtubuli-polymerisation inside the parasite's cells. This apparently led to the complete destruction of the hypodermis, muscle layer and intestine. Flubendazole also stopped the formation of gametes. Summarising, even low concentrations of flubendazole (0.1 micro g/ml) led to significant and irreversible damage in all worms studied.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-002-0668-6</identifier><identifier>PMID: 12474046</identifier><identifier>CODEN: PARREZ</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antinematodal Agents - metabolism ; Antinematodal Agents - pharmacokinetics ; Antinematodal Agents - pharmacology ; Antiparasitic agents ; Ascariasis - drug therapy ; Ascaris suum - cytology ; Ascaris suum - drug effects ; Ascaris suum - ultrastructure ; Biological and medical sciences ; Dogs ; Dose-Response Relationship, Drug ; Female ; Male ; Mebendazole - analogs & derivatives ; Mebendazole - metabolism ; Mebendazole - pharmacokinetics ; Mebendazole - pharmacology ; Medical sciences ; Movement ; Pharmacology. Drug treatments ; Time Factors ; Toxocara canis - cytology ; Toxocara canis - drug effects ; Toxocara canis - ultrastructure ; Toxocariasis - drug therapy</subject><ispartof>Parasitology research (1987), 2003-01, Vol.89 (1), p.63-74</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-a7fb5e9714ecdc834215130da644dd5807e4787e7d56454bf7d5a19a88bb49b83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14643241$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12474046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HANSER, Elena</creatorcontrib><creatorcontrib>MEHLHORN, Heinz</creatorcontrib><creatorcontrib>HOEBEN, Dagmar</creatorcontrib><creatorcontrib>VLAMINCK, Kathleen</creatorcontrib><title>In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><description>Adult Toxocara canis and Ascaris suum were incubated in vitro in media containing 0.1, 1, 10 or 100 micro g/ml flubendazole in order to study drug-derived effects. This incubation was done for 8 h and repeated (in some groups) after 24 h for another 8 h. The onset and intensity of flubendazole-derived effects were dosage-dependent and time-dependent, i.e. the same grade of damage was reached when incubating for a longer period at a low dosage or for a shorter period in medium containing a high amount (10 or 100 micro g/ml) of flubendazole. A repeated incubation in drug-containing medium was superior to a single exposure. Flubendazole is apparently able to penetrate into the worm's interior via the cuticle. This became evident in worms with sealed orifices, which showed identical damage to worms which were not sealed. The type of tissue damage due to flubendazole was identical in both worm species when exposed to any of the drug dosages used. The principal mode of action of flubendazole was based on the complete reduction of microtubuli-polymerisation inside the parasite's cells. This apparently led to the complete destruction of the hypodermis, muscle layer and intestine. Flubendazole also stopped the formation of gametes. Summarising, even low concentrations of flubendazole (0.1 micro g/ml) led to significant and irreversible damage in all worms studied.</description><subject>Animals</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antinematodal Agents - metabolism</subject><subject>Antinematodal Agents - pharmacokinetics</subject><subject>Antinematodal Agents - pharmacology</subject><subject>Antiparasitic agents</subject><subject>Ascariasis - drug therapy</subject><subject>Ascaris suum - cytology</subject><subject>Ascaris suum - drug effects</subject><subject>Ascaris suum - ultrastructure</subject><subject>Biological and medical sciences</subject><subject>Dogs</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Male</subject><subject>Mebendazole - analogs & derivatives</subject><subject>Mebendazole - metabolism</subject><subject>Mebendazole - pharmacokinetics</subject><subject>Mebendazole - pharmacology</subject><subject>Medical sciences</subject><subject>Movement</subject><subject>Pharmacology. Drug treatments</subject><subject>Time Factors</subject><subject>Toxocara canis - cytology</subject><subject>Toxocara canis - drug effects</subject><subject>Toxocara canis - ultrastructure</subject><subject>Toxocariasis - drug therapy</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkV1LwzAUhoMobk5_gDeSG72rnjRpkl4O8WMw8GbiZUjzoZU2nU0r6q83Y4VBIG_Ccw4nTxC6JHBLAMRdBGCUZwB5BpzLjB-hOWE0z0hZFMdoDmXKQAidobMYPwGI4IydohnJmWDA-By9rQL-roe-w3EYbe0i7gIePhx23jszpKPHvhkrF6z-6xqH9buuQxzwpvvpjO41NjrUEetg8TKmi5TjOLbn6MTrJrqLaV-g18eHzf1ztn55Wt0v15mhuRgyLXxVuFIQ5ow1krKcFISC1WlOawsJwjEhhRO24KxglU9Bk1JLWVWsrCRdoJt9323ffY0uDqqto3FNo4PrxqhELtMCkkCyB03fxdg7r7Z93er-VxFQO5tqb1Mlm2pnU_FUczU1H6vW2UPFpC8B1xOg09sb3-tg6njgGE-_wQj9Bw7pfKQ</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>HANSER, Elena</creator><creator>MEHLHORN, Heinz</creator><creator>HOEBEN, Dagmar</creator><creator>VLAMINCK, Kathleen</creator><general>Springer</general><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>7X8</scope></search><sort><creationdate>20030101</creationdate><title>In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum</title><author>HANSER, Elena ; MEHLHORN, Heinz ; HOEBEN, Dagmar ; VLAMINCK, Kathleen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-a7fb5e9714ecdc834215130da644dd5807e4787e7d56454bf7d5a19a88bb49b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antinematodal Agents - metabolism</topic><topic>Antinematodal Agents - pharmacokinetics</topic><topic>Antinematodal Agents - pharmacology</topic><topic>Antiparasitic agents</topic><topic>Ascariasis - drug therapy</topic><topic>Ascaris suum - cytology</topic><topic>Ascaris suum - drug effects</topic><topic>Ascaris suum - ultrastructure</topic><topic>Biological and medical sciences</topic><topic>Dogs</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Male</topic><topic>Mebendazole - analogs & derivatives</topic><topic>Mebendazole - metabolism</topic><topic>Mebendazole - pharmacokinetics</topic><topic>Mebendazole - pharmacology</topic><topic>Medical sciences</topic><topic>Movement</topic><topic>Pharmacology. Drug treatments</topic><topic>Time Factors</topic><topic>Toxocara canis - cytology</topic><topic>Toxocara canis - drug effects</topic><topic>Toxocara canis - ultrastructure</topic><topic>Toxocariasis - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HANSER, Elena</creatorcontrib><creatorcontrib>MEHLHORN, Heinz</creatorcontrib><creatorcontrib>HOEBEN, Dagmar</creatorcontrib><creatorcontrib>VLAMINCK, Kathleen</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HANSER, Elena</au><au>MEHLHORN, Heinz</au><au>HOEBEN, Dagmar</au><au>VLAMINCK, Kathleen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum</atitle><jtitle>Parasitology research (1987)</jtitle><addtitle>Parasitol Res</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>89</volume><issue>1</issue><spage>63</spage><epage>74</epage><pages>63-74</pages><issn>0932-0113</issn><eissn>1432-1955</eissn><coden>PARREZ</coden><abstract>Adult Toxocara canis and Ascaris suum were incubated in vitro in media containing 0.1, 1, 10 or 100 micro g/ml flubendazole in order to study drug-derived effects. This incubation was done for 8 h and repeated (in some groups) after 24 h for another 8 h. The onset and intensity of flubendazole-derived effects were dosage-dependent and time-dependent, i.e. the same grade of damage was reached when incubating for a longer period at a low dosage or for a shorter period in medium containing a high amount (10 or 100 micro g/ml) of flubendazole. A repeated incubation in drug-containing medium was superior to a single exposure. Flubendazole is apparently able to penetrate into the worm's interior via the cuticle. This became evident in worms with sealed orifices, which showed identical damage to worms which were not sealed. The type of tissue damage due to flubendazole was identical in both worm species when exposed to any of the drug dosages used. The principal mode of action of flubendazole was based on the complete reduction of microtubuli-polymerisation inside the parasite's cells. This apparently led to the complete destruction of the hypodermis, muscle layer and intestine. Flubendazole also stopped the formation of gametes. Summarising, even low concentrations of flubendazole (0.1 micro g/ml) led to significant and irreversible damage in all worms studied.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>12474046</pmid><doi>10.1007/s00436-002-0668-6</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Antibiotics. Antiinfectious agents. Antiparasitic agents Antinematodal Agents - metabolism Antinematodal Agents - pharmacokinetics Antinematodal Agents - pharmacology Antiparasitic agents Ascariasis - drug therapy Ascaris suum - cytology Ascaris suum - drug effects Ascaris suum - ultrastructure Biological and medical sciences Dogs Dose-Response Relationship, Drug Female Male Mebendazole - analogs & derivatives Mebendazole - metabolism Mebendazole - pharmacokinetics Mebendazole - pharmacology Medical sciences Movement Pharmacology. Drug treatments Time Factors Toxocara canis - cytology Toxocara canis - drug effects Toxocara canis - ultrastructure Toxocariasis - drug therapy |
title | In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum |
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