Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>

<p>Abstract</p> <p>Background</p> <p>There is no published information about the use of different protocols to administer a highly diluted medication.</p> <p>Evaluate the effect of different protocols for treatment with biotherapic <it>T. cruzi</it&...

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Main Authors: Aleixo Denise, Ferraz Fabiana, Ferreira Érika, de Lana Marta, Gomes Mônica, de Abreu Filho Benício, de Araújo Silvana
Format: Article
Language:English
Published: BMC 2012-07-01
Series:BMC Research Notes
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Online Access:http://www.biomedcentral.com/1756-0500/5/352
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spelling doaj-077c6fe82a84436da6f791a5751caff72020-11-25T03:28:30ZengBMCBMC Research Notes1756-05002012-07-015135210.1186/1756-0500-5-352Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>Aleixo DeniseFerraz FabianaFerreira Érikade Lana MartaGomes Mônicade Abreu Filho Beníciode Araújo Silvana<p>Abstract</p> <p>Background</p> <p>There is no published information about the use of different protocols to administer a highly diluted medication.</p> <p>Evaluate the effect of different protocols for treatment with biotherapic <it>T. cruzi</it> 17 dH (BIOT<sub><it>Tc</it>17dH</sub>) on clinical/parasitological evolution of mice infected with <it>T. cruzi-Y</it> strain.</p> <p>Methods</p> <p>A blind, randomized controlled trial was performed twice, using 60 28-day-old male Swiss mice infected with <it>T. cruzi-Y</it> strain, in five treatment groups: CI <it>-</it> treated with a 7% ethanol-water solution, diluted in water (10 μL/mL) <it>ad libitum</it>; <it>BIOT</it><sub><it>PI</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> in water (10 μL/mL) <it>ad libitum</it> during a period that started on the day of infection; <it>BIOT</it><sub><it>4DI</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> in water (10 μL/mL) <it>ad libitum</it> beginning on the 4<sup>th</sup> day of infection; <it>BIOT</it><sub><it>4-5–6</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> by gavage (0.2 mL/ animal/day) on the 4<sup>th</sup>, 5<sup>th</sup> and 6<sup>th</sup> days after infection; <it>BIOT</it><sub><it>7-8–9</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> by gavage (0.2 mL/ animal/day) on the 7<sup>th</sup>, 8<sup>th</sup> and 9<sup>th</sup> days after infection. We evaluated: parasitemia; total parasitemia (P<sub>total</sub>); maximum peak of parasites; prepatent period (PPP) - time from infection to detection of the parasite in blood; patent period (PP) - period when the parasitemia can be detected in blood; clinical aspects; and mortality.</p> <p>Results</p> <p>Parasitological parameters in the BIOT<sub>PI</sub> and mainly in the BIOT<sub>4PI</sub> group showed better evolution of the infection compared to the control group (CI), with lower P<sub>total</sub>, lower maximum peak of parasites, higher PPP, lower PP and longer survival times. These animals showed stable body temperature and higher weight gain and water consumption, with more animals having normal-appearing fur for longer periods. In contrast, groups BIOT<sub>4-5–6</sub> and BIOT<sub>7-8–9</sub> showed worse evolution of the infection compared to the control group, considering both parasitological and clinical parameters. The correlation analysis combined with the other data from this study indicated that the prepatent period is the best parameter to evaluate the effect of a medication in this model.</p> <p>Conclusions</p> <p>The BIOT<sub>4DI</sub> group showed the best clinical and parasitological evolution, with lower parasitemia and a trend toward lower mortality and a longer survival period. The prepatent period was the best parameter to evaluate the effect of a medication in this model.</p> http://www.biomedcentral.com/1756-0500/5/352BiotherapyMice infectionParasitological evaluationClinical evaluationPrepatent period
collection DOAJ
language English
format Article
sources DOAJ
author Aleixo Denise
Ferraz Fabiana
Ferreira Érika
de Lana Marta
Gomes Mônica
de Abreu Filho Benício
de Araújo Silvana
spellingShingle Aleixo Denise
Ferraz Fabiana
Ferreira Érika
de Lana Marta
Gomes Mônica
de Abreu Filho Benício
de Araújo Silvana
Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
BMC Research Notes
Biotherapy
Mice infection
Parasitological evaluation
Clinical evaluation
Prepatent period
author_facet Aleixo Denise
Ferraz Fabiana
Ferreira Érika
de Lana Marta
Gomes Mônica
de Abreu Filho Benício
de Araújo Silvana
author_sort Aleixo Denise
title Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
title_short Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
title_full Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
title_fullStr Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
title_full_unstemmed Highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>Trypanosoma cruzi</it>
title_sort highly diluted medication reduces parasitemia and improves experimental infection evolution by <it>trypanosoma cruzi</it>
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>There is no published information about the use of different protocols to administer a highly diluted medication.</p> <p>Evaluate the effect of different protocols for treatment with biotherapic <it>T. cruzi</it> 17 dH (BIOT<sub><it>Tc</it>17dH</sub>) on clinical/parasitological evolution of mice infected with <it>T. cruzi-Y</it> strain.</p> <p>Methods</p> <p>A blind, randomized controlled trial was performed twice, using 60 28-day-old male Swiss mice infected with <it>T. cruzi-Y</it> strain, in five treatment groups: CI <it>-</it> treated with a 7% ethanol-water solution, diluted in water (10 μL/mL) <it>ad libitum</it>; <it>BIOT</it><sub><it>PI</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> in water (10 μL/mL) <it>ad libitum</it> during a period that started on the day of infection; <it>BIOT</it><sub><it>4DI</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> in water (10 μL/mL) <it>ad libitum</it> beginning on the 4<sup>th</sup> day of infection; <it>BIOT</it><sub><it>4-5–6</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> by gavage (0.2 mL/ animal/day) on the 4<sup>th</sup>, 5<sup>th</sup> and 6<sup>th</sup> days after infection; <it>BIOT</it><sub><it>7-8–9</it></sub> - treated with BIOT<sub><it>Tc</it>17dH</sub> by gavage (0.2 mL/ animal/day) on the 7<sup>th</sup>, 8<sup>th</sup> and 9<sup>th</sup> days after infection. We evaluated: parasitemia; total parasitemia (P<sub>total</sub>); maximum peak of parasites; prepatent period (PPP) - time from infection to detection of the parasite in blood; patent period (PP) - period when the parasitemia can be detected in blood; clinical aspects; and mortality.</p> <p>Results</p> <p>Parasitological parameters in the BIOT<sub>PI</sub> and mainly in the BIOT<sub>4PI</sub> group showed better evolution of the infection compared to the control group (CI), with lower P<sub>total</sub>, lower maximum peak of parasites, higher PPP, lower PP and longer survival times. These animals showed stable body temperature and higher weight gain and water consumption, with more animals having normal-appearing fur for longer periods. In contrast, groups BIOT<sub>4-5–6</sub> and BIOT<sub>7-8–9</sub> showed worse evolution of the infection compared to the control group, considering both parasitological and clinical parameters. The correlation analysis combined with the other data from this study indicated that the prepatent period is the best parameter to evaluate the effect of a medication in this model.</p> <p>Conclusions</p> <p>The BIOT<sub>4DI</sub> group showed the best clinical and parasitological evolution, with lower parasitemia and a trend toward lower mortality and a longer survival period. The prepatent period was the best parameter to evaluate the effect of a medication in this model.</p>
topic Biotherapy
Mice infection
Parasitological evaluation
Clinical evaluation
Prepatent period
url http://www.biomedcentral.com/1756-0500/5/352
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