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Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi

Bibliographic Details
Main Author: Oliveira C.B.
Publication Date: 2014
Other Authors: Rigo L.A., Franca R.T., Gressler L.T., Dalla Rosa L., Ourique A.F., Oliveira D.T., Doyle R.L., Moreira K.L.D.S., Veiga M.L., Lopes S.T.A., Beck R.C.R., Da Silva A.S.*, Monteiro S.G.
Format: Article
Language: eng
Source: Repositório Institucional da Udesc
dARK ID: ark:/33523/001300000psbp
Download full: https://repositorio.udesc.br/handle/UDESC/8320
Summary: © 2014 Elsevier GmbH.The aim of this study was to evaluate the effect of treatment with liposomal (L-DMZ) and conventional (C-DMZ) diminazene aceturate formulations on hepatic and renal functions of rats, experimentally infected with Trypanosoma evansi. For this purpose, 72 Wistar rats (Rattus norvegicus) were divided into six groups (A, B, C, D, E, and F). Each group was subdivided into two other subgroups in order to assess the biochemical and histological results on days 7 and 40 post-treatment (PT). Treatments were carried out based on two different therapeutic protocols: L-DMZ and C-DMZ at 3.5mg/kg-1, single dose (groups C and D), and five successive doses within intervals of 24h (groups E and F). Groups A and B corresponded to uninfected and infected (without treatment) animals, respectively. Sample collections were held on days 7 and 40 PT for the assessment of hepatic [alkaline phosphatase (AP), alanine transferase (ALT), albumin, gamma glutamil transferase (GGT) and renal functions (creatinine and urea). Additionally, the histology of fragments of liver, kidney, and spleen was performed. Animals in group B showed a significant increase in AP, GGT, ALT, and urea when compared with group A. On day 7 post-inoculation (PI), the biochemical analysis showed a reduction (P<0.05) of AP and GGT, while the levels of urea were increased in groups C, D, E, F. On day 40 PT, ALT was increased in these same groups when compared with group A. In histopathology, changes in liver samples were observed on day 7 PT in groups D and F, especially regarding the area and density of the hepatocytes. Renal analysis exhibited changes in glomerular space, glomerular, and corpuscular areas in group E. Therefore, these results allowed us to conclude that the treatment with L-DMZ and C-DMZ led to variable biochemical changes, which defined the functions of the liver and kidneys of treated animals, since the main histopathology alterations were observed in animals treated with liposomes, at their higher dosages. Thus, treatments with L-DMZ and C-DMZ in five consecutive doses were effective although being followed by liver toxicity.
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spelling Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi© 2014 Elsevier GmbH.The aim of this study was to evaluate the effect of treatment with liposomal (L-DMZ) and conventional (C-DMZ) diminazene aceturate formulations on hepatic and renal functions of rats, experimentally infected with Trypanosoma evansi. For this purpose, 72 Wistar rats (Rattus norvegicus) were divided into six groups (A, B, C, D, E, and F). Each group was subdivided into two other subgroups in order to assess the biochemical and histological results on days 7 and 40 post-treatment (PT). Treatments were carried out based on two different therapeutic protocols: L-DMZ and C-DMZ at 3.5mg/kg-1, single dose (groups C and D), and five successive doses within intervals of 24h (groups E and F). Groups A and B corresponded to uninfected and infected (without treatment) animals, respectively. Sample collections were held on days 7 and 40 PT for the assessment of hepatic [alkaline phosphatase (AP), alanine transferase (ALT), albumin, gamma glutamil transferase (GGT) and renal functions (creatinine and urea). Additionally, the histology of fragments of liver, kidney, and spleen was performed. Animals in group B showed a significant increase in AP, GGT, ALT, and urea when compared with group A. On day 7 post-inoculation (PI), the biochemical analysis showed a reduction (P<0.05) of AP and GGT, while the levels of urea were increased in groups C, D, E, F. On day 40 PT, ALT was increased in these same groups when compared with group A. In histopathology, changes in liver samples were observed on day 7 PT in groups D and F, especially regarding the area and density of the hepatocytes. Renal analysis exhibited changes in glomerular space, glomerular, and corpuscular areas in group E. Therefore, these results allowed us to conclude that the treatment with L-DMZ and C-DMZ led to variable biochemical changes, which defined the functions of the liver and kidneys of treated animals, since the main histopathology alterations were observed in animals treated with liposomes, at their higher dosages. Thus, treatments with L-DMZ and C-DMZ in five consecutive doses were effective although being followed by liver toxicity.2024-12-06T14:03:54Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlep. 840 - 8461618-063110.1016/j.prp.2014.08.010https://repositorio.udesc.br/handle/UDESC/8320ark:/33523/001300000psbpPathology Research and Practice21012Oliveira C.B.Rigo L.A.Franca R.T.Gressler L.T.Dalla Rosa L.Ourique A.F.Oliveira D.T.Doyle R.L.Moreira K.L.D.S.Veiga M.L.Lopes S.T.A.Beck R.C.R.Da Silva A.S.*Monteiro S.G.engreponame:Repositório Institucional da Udescinstname:Universidade do Estado de Santa Catarina (UDESC)instacron:UDESCinfo:eu-repo/semantics/openAccess2024-12-07T20:57:06Zoai:repositorio.udesc.br:UDESC/8320Biblioteca Digital de Teses e Dissertaçõeshttps://pergamumweb.udesc.br/biblioteca/index.phpPRIhttps://repositorio-api.udesc.br/server/oai/requestri@udesc.bropendoar:63912024-12-07T20:57:06Repositório Institucional da Udesc - Universidade do Estado de Santa Catarina (UDESC)false
dc.title.none.fl_str_mv Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
title Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
spellingShingle Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
Oliveira C.B.
title_short Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
title_full Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
title_fullStr Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
title_full_unstemmed Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
title_sort Diminazene Aceturate Liposomes: Morphometric and Biochemical Liver, Kidney, and Spleen of Rats Infected with Trypanosoma evansi
author Oliveira C.B.
author_facet Oliveira C.B.
Rigo L.A.
Franca R.T.
Gressler L.T.
Dalla Rosa L.
Ourique A.F.
Oliveira D.T.
Doyle R.L.
Moreira K.L.D.S.
Veiga M.L.
Lopes S.T.A.
Beck R.C.R.
Da Silva A.S.*
Monteiro S.G.
author_role author
author2 Rigo L.A.
Franca R.T.
Gressler L.T.
Dalla Rosa L.
Ourique A.F.
Oliveira D.T.
Doyle R.L.
Moreira K.L.D.S.
Veiga M.L.
Lopes S.T.A.
Beck R.C.R.
Da Silva A.S.*
Monteiro S.G.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira C.B.
Rigo L.A.
Franca R.T.
Gressler L.T.
Dalla Rosa L.
Ourique A.F.
Oliveira D.T.
Doyle R.L.
Moreira K.L.D.S.
Veiga M.L.
Lopes S.T.A.
Beck R.C.R.
Da Silva A.S.*
Monteiro S.G.
description © 2014 Elsevier GmbH.The aim of this study was to evaluate the effect of treatment with liposomal (L-DMZ) and conventional (C-DMZ) diminazene aceturate formulations on hepatic and renal functions of rats, experimentally infected with Trypanosoma evansi. For this purpose, 72 Wistar rats (Rattus norvegicus) were divided into six groups (A, B, C, D, E, and F). Each group was subdivided into two other subgroups in order to assess the biochemical and histological results on days 7 and 40 post-treatment (PT). Treatments were carried out based on two different therapeutic protocols: L-DMZ and C-DMZ at 3.5mg/kg-1, single dose (groups C and D), and five successive doses within intervals of 24h (groups E and F). Groups A and B corresponded to uninfected and infected (without treatment) animals, respectively. Sample collections were held on days 7 and 40 PT for the assessment of hepatic [alkaline phosphatase (AP), alanine transferase (ALT), albumin, gamma glutamil transferase (GGT) and renal functions (creatinine and urea). Additionally, the histology of fragments of liver, kidney, and spleen was performed. Animals in group B showed a significant increase in AP, GGT, ALT, and urea when compared with group A. On day 7 post-inoculation (PI), the biochemical analysis showed a reduction (P<0.05) of AP and GGT, while the levels of urea were increased in groups C, D, E, F. On day 40 PT, ALT was increased in these same groups when compared with group A. In histopathology, changes in liver samples were observed on day 7 PT in groups D and F, especially regarding the area and density of the hepatocytes. Renal analysis exhibited changes in glomerular space, glomerular, and corpuscular areas in group E. Therefore, these results allowed us to conclude that the treatment with L-DMZ and C-DMZ led to variable biochemical changes, which defined the functions of the liver and kidneys of treated animals, since the main histopathology alterations were observed in animals treated with liposomes, at their higher dosages. Thus, treatments with L-DMZ and C-DMZ in five consecutive doses were effective although being followed by liver toxicity.
publishDate 2014
dc.date.none.fl_str_mv 2014
2024-12-06T14:03:54Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv 1618-0631
10.1016/j.prp.2014.08.010
https://repositorio.udesc.br/handle/UDESC/8320
dc.identifier.dark.fl_str_mv ark:/33523/001300000psbp
identifier_str_mv 1618-0631
10.1016/j.prp.2014.08.010
ark:/33523/001300000psbp
url https://repositorio.udesc.br/handle/UDESC/8320
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pathology Research and Practice
210
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv p. 840 - 846
dc.source.none.fl_str_mv reponame:Repositório Institucional da Udesc
instname:Universidade do Estado de Santa Catarina (UDESC)
instacron:UDESC
instname_str Universidade do Estado de Santa Catarina (UDESC)
instacron_str UDESC
institution UDESC
reponame_str Repositório Institucional da Udesc
collection Repositório Institucional da Udesc
repository.name.fl_str_mv Repositório Institucional da Udesc - Universidade do Estado de Santa Catarina (UDESC)
repository.mail.fl_str_mv ri@udesc.br
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