Atorvastatin: In-Vivo Synergy with Metronidazole as Anti-Blastocystis Therapy

is an enteric Straminopile in tropical, subtropical and developing countries. Metronidazole has been a chemotheraputic for blastocystosis. Failures in its regimens were reported and necessitate new studies searching for alternative therapeutic agents. Aim of current study is to investigate potential...

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Published inKorean journal of parasitology Vol. 56; no. 2; pp. 105 - 112
Main Authors Basyoni, Maha M A, Fouad, Shawky A, Amer, Marwa F, Amer, Ahmed Fathy, Ismail, Dalia Ibrahim
Format Journal Article
LanguageEnglish
Published Korea (South) 대한기생충학열대의학회 01.04.2018
The Korean Society for Parasitology and Tropical Medicine
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Summary:is an enteric Straminopile in tropical, subtropical and developing countries. Metronidazole has been a chemotheraputic for blastocystosis. Failures in its regimens were reported and necessitate new studies searching for alternative therapeutic agents. Aim of current study is to investigate potential effects of Atorvastatin (AVA) compared to the conventional chemotherapeutic MTZ in experimentally -infected mice. Anti- efficacy of AVA was evaluated parasitologically, histopathologically and by transmission electron microscopy using MTZ (10 mg/kg) as a control. Therapeutic efficacy of AVA was apparently dose-dependent. Regimens of AVA (20 and 40 mg/kg) proved effective against infections with high reduction in shedding (93.4-97.9%) compared to MTZ (79.3%). The highest reductions (98.1% and 99.4%) were recorded in groups of combination treatments AVA 20-40 mg/kg and MTZ 10 mg/kg. was nearly eradicated by the 20th day post infection. Genotype analysis revealed that genotype I was most susceptible, genotype III was less. Histopathologic and ultrastructural studies revealed apoptotic changes in and significant improvement of intestinal histopathological changes more remarkable in combinational therapy groups. Thus, the present study offers AVA as a potential candidate for therapy combined with MTZ.
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ISSN:0023-4001
1738-0006
DOI:10.3347/kjp.2018.56.2.105