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Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi

The aim of this study was to investigate the effects of Trypanosoma evansi infections on arterial blood gases of experimentally infected rats. Two groups with eight animals each were used; group A (uninfected) and group B (infected). Infected animals were daily monitored through blood smears that sh...

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Autores principales: Baldissera, Matheus D., Vaucher, Rodrigo A., Oliveira, Camila B., Rech, Virginia C., Sagrillo, Michele R., Stainki, Daniel R., França, Raqueli T., Machado, Gustavo, Lopes, Sonia T.A., Monteiro, Silvia G., Stefani, Lenita M., Da Silva, Aleksandro S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642149/
https://www.ncbi.nlm.nih.gov/pubmed/26644945
http://dx.doi.org/10.1016/j.jare.2014.12.001
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author Baldissera, Matheus D.
Vaucher, Rodrigo A.
Oliveira, Camila B.
Rech, Virginia C.
Sagrillo, Michele R.
Stainki, Daniel R.
França, Raqueli T.
Machado, Gustavo
Lopes, Sonia T.A.
Monteiro, Silvia G.
Stefani, Lenita M.
Da Silva, Aleksandro S.
author_facet Baldissera, Matheus D.
Vaucher, Rodrigo A.
Oliveira, Camila B.
Rech, Virginia C.
Sagrillo, Michele R.
Stainki, Daniel R.
França, Raqueli T.
Machado, Gustavo
Lopes, Sonia T.A.
Monteiro, Silvia G.
Stefani, Lenita M.
Da Silva, Aleksandro S.
author_sort Baldissera, Matheus D.
collection PubMed
description The aim of this study was to investigate the effects of Trypanosoma evansi infections on arterial blood gases of experimentally infected rats. Two groups with eight animals each were used; group A (uninfected) and group B (infected). Infected animals were daily monitored through blood smears that showed high parasitemia with 30 trypanosomes per field (1000×) on average, 5 days post-infection (PI). Arterial blood was collected at 5 days PI for blood gas analysis using an automated method based on dry-chemistry. Hydrogen potential (pH), partial oxygen pressure (pO(2)), oxygen saturation (sO(2)), sodium (Na), ionic calcium (Ca ionic), chlorides (Cl), partial dioxide carbon pressure (pCO(2)), base excess (BE), base excess in the extracellular fluid (BEecf), bicarbonate (cHCO(3)), potassium (K), lactate, and blood total dioxide the carbon (tCO(2)) were evaluated. The levels of pH, pCO(2), BE, BEecf, cHCO(3), and tCO(2) were significantly decreased (P < 0.05) in group B compared to group A. Additionally, the same group showed increases in Cl and lactate levels when compared to uninfected group. Therefore, it is possible to state that the infection caused by T. evansi led to alterations in the acid–base status, findings that are correlated to metabolic acidosis.
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spelling pubmed-46421492015-12-07 Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi Baldissera, Matheus D. Vaucher, Rodrigo A. Oliveira, Camila B. Rech, Virginia C. Sagrillo, Michele R. Stainki, Daniel R. França, Raqueli T. Machado, Gustavo Lopes, Sonia T.A. Monteiro, Silvia G. Stefani, Lenita M. Da Silva, Aleksandro S. J Adv Res Short Communication The aim of this study was to investigate the effects of Trypanosoma evansi infections on arterial blood gases of experimentally infected rats. Two groups with eight animals each were used; group A (uninfected) and group B (infected). Infected animals were daily monitored through blood smears that showed high parasitemia with 30 trypanosomes per field (1000×) on average, 5 days post-infection (PI). Arterial blood was collected at 5 days PI for blood gas analysis using an automated method based on dry-chemistry. Hydrogen potential (pH), partial oxygen pressure (pO(2)), oxygen saturation (sO(2)), sodium (Na), ionic calcium (Ca ionic), chlorides (Cl), partial dioxide carbon pressure (pCO(2)), base excess (BE), base excess in the extracellular fluid (BEecf), bicarbonate (cHCO(3)), potassium (K), lactate, and blood total dioxide the carbon (tCO(2)) were evaluated. The levels of pH, pCO(2), BE, BEecf, cHCO(3), and tCO(2) were significantly decreased (P < 0.05) in group B compared to group A. Additionally, the same group showed increases in Cl and lactate levels when compared to uninfected group. Therefore, it is possible to state that the infection caused by T. evansi led to alterations in the acid–base status, findings that are correlated to metabolic acidosis. Elsevier 2015-11 2014-12-09 /pmc/articles/PMC4642149/ /pubmed/26644945 http://dx.doi.org/10.1016/j.jare.2014.12.001 Text en © 2014 Production and hosting by Elsevier B.V. on behalf of Cairo University. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Short Communication
Baldissera, Matheus D.
Vaucher, Rodrigo A.
Oliveira, Camila B.
Rech, Virginia C.
Sagrillo, Michele R.
Stainki, Daniel R.
França, Raqueli T.
Machado, Gustavo
Lopes, Sonia T.A.
Monteiro, Silvia G.
Stefani, Lenita M.
Da Silva, Aleksandro S.
Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title_full Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title_fullStr Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title_full_unstemmed Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title_short Blood gas analyses and other components involved in the acid–base metabolism of rats infected by Trypanosoma evansi
title_sort blood gas analyses and other components involved in the acid–base metabolism of rats infected by trypanosoma evansi
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642149/
https://www.ncbi.nlm.nih.gov/pubmed/26644945
http://dx.doi.org/10.1016/j.jare.2014.12.001
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