Pentavalent antimonial nephrotoxicity in the rat

Detalhes bibliográficos
Autor(a) principal: Veiga, Joel Paulo R.
Data de Publicação: 1990
Outros Autores: Khanam, Rashida, Rosa, Tânia T., Junqueira Jr., Luiz F., Brant, Plínio C., Raick, Alberto N., Friedman, Horacio, Marsden, Phillip D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista do Instituto de Medicina Tropical de São Paulo
Texto Completo: https://www.revistas.usp.br/rimtsp/article/view/28750
Resumo: Aspects of the renal function were assessed in rats treated with the pentavalent antimonials Glucantime (Meglumine Antimoniate, Rhodia) or Pentostam (Sodium Stibogluconate, Wellcome). In dose of 30 mg of Sb v (Glucantime or Pentostam) by 100 mg of weight by day for 30 days, renal functional changes were observed consisting of disturbances in urine concentrating capacity. Such disturbances were expressed by significantly low values of urine osmolality as compared to the basal values previous to the drugs. The decrease in urine osmolality was associated to a significant increase in urinary flow and in negative free-water clearance. There was no alteration in osmolar clearance and in fractional excretion of sodium. These observations suggest an interference of the drugs in the action of the antidiuretic hormone. The disturbance in urine concentration was reversible after a seven days period without the drugs administration. No significant histopathological alterations were observed in the kidneys of the rats treated with the drugs. On the other hand, the rats treated with a high dose of Pentostam (200 mg/100 grams of weight/day) showed the functional and the histopathological alterations of the acute tubular necrosis.
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spelling Pentavalent antimonial nephrotoxicity in the rat Disfunção tubular renal em ratos tratados com antimoniais pentavalentes Pentavalent antimonialRenal functionUrinary concentrating capacityAcute tubular necrosisRat Aspects of the renal function were assessed in rats treated with the pentavalent antimonials Glucantime (Meglumine Antimoniate, Rhodia) or Pentostam (Sodium Stibogluconate, Wellcome). In dose of 30 mg of Sb v (Glucantime or Pentostam) by 100 mg of weight by day for 30 days, renal functional changes were observed consisting of disturbances in urine concentrating capacity. Such disturbances were expressed by significantly low values of urine osmolality as compared to the basal values previous to the drugs. The decrease in urine osmolality was associated to a significant increase in urinary flow and in negative free-water clearance. There was no alteration in osmolar clearance and in fractional excretion of sodium. These observations suggest an interference of the drugs in the action of the antidiuretic hormone. The disturbance in urine concentration was reversible after a seven days period without the drugs administration. No significant histopathological alterations were observed in the kidneys of the rats treated with the drugs. On the other hand, the rats treated with a high dose of Pentostam (200 mg/100 grams of weight/day) showed the functional and the histopathological alterations of the acute tubular necrosis. Estudou-se a função renal de ratos tratados com Glucantime (Antimoniato de Meglumine, Rhodia) e Pentostam (Estibogluconato de Sódio, Wellcome) na dose de 30 mg de Sb v por 100 g de peso por dia, durante 30 dias. Observou-se um distúrio na concentração urinária, que foi reversível 7 dias após cessada a administração das drogas. O estudo histopatológico do rim, por meio da microscopia óptica, não evidenciou alterações significativas. Por outro lado, ratos tratados com altas doses dos antimoniais (200 mg de Sb v por 100 g de peso por dia) mostraram alterações funcionais e histopatológicas renais compatíveis com necrose tubular aguda. Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo1990-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/rimtsp/article/view/28750Revista do Instituto de Medicina Tropical de São Paulo; Vol. 32 No. 4 (1990); 304-309 Revista do Instituto de Medicina Tropical de São Paulo; Vol. 32 Núm. 4 (1990); 304-309 Revista do Instituto de Medicina Tropical de São Paulo; v. 32 n. 4 (1990); 304-309 1678-99460036-4665reponame:Revista do Instituto de Medicina Tropical de São Pauloinstname:Instituto de Medicina Tropical (IMT)instacron:IMTenghttps://www.revistas.usp.br/rimtsp/article/view/28750/30603Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Pauloinfo:eu-repo/semantics/openAccessVeiga, Joel Paulo R.Khanam, RashidaRosa, Tânia T.Junqueira Jr., Luiz F.Brant, Plínio C.Raick, Alberto N.Friedman, HoracioMarsden, Phillip D.2012-07-02T01:28:24Zoai:revistas.usp.br:article/28750Revistahttp://www.revistas.usp.br/rimtsp/indexPUBhttps://www.revistas.usp.br/rimtsp/oai||revimtsp@usp.br1678-99460036-4665opendoar:2022-12-13T16:50:30.298183Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)true
dc.title.none.fl_str_mv Pentavalent antimonial nephrotoxicity in the rat
Disfunção tubular renal em ratos tratados com antimoniais pentavalentes
title Pentavalent antimonial nephrotoxicity in the rat
spellingShingle Pentavalent antimonial nephrotoxicity in the rat
Veiga, Joel Paulo R.
Pentavalent antimonial
Renal function
Urinary concentrating capacity
Acute tubular necrosis
Rat
title_short Pentavalent antimonial nephrotoxicity in the rat
title_full Pentavalent antimonial nephrotoxicity in the rat
title_fullStr Pentavalent antimonial nephrotoxicity in the rat
title_full_unstemmed Pentavalent antimonial nephrotoxicity in the rat
title_sort Pentavalent antimonial nephrotoxicity in the rat
author Veiga, Joel Paulo R.
author_facet Veiga, Joel Paulo R.
Khanam, Rashida
Rosa, Tânia T.
Junqueira Jr., Luiz F.
Brant, Plínio C.
Raick, Alberto N.
Friedman, Horacio
Marsden, Phillip D.
author_role author
author2 Khanam, Rashida
Rosa, Tânia T.
Junqueira Jr., Luiz F.
Brant, Plínio C.
Raick, Alberto N.
Friedman, Horacio
Marsden, Phillip D.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Veiga, Joel Paulo R.
Khanam, Rashida
Rosa, Tânia T.
Junqueira Jr., Luiz F.
Brant, Plínio C.
Raick, Alberto N.
Friedman, Horacio
Marsden, Phillip D.
dc.subject.por.fl_str_mv Pentavalent antimonial
Renal function
Urinary concentrating capacity
Acute tubular necrosis
Rat
topic Pentavalent antimonial
Renal function
Urinary concentrating capacity
Acute tubular necrosis
Rat
description Aspects of the renal function were assessed in rats treated with the pentavalent antimonials Glucantime (Meglumine Antimoniate, Rhodia) or Pentostam (Sodium Stibogluconate, Wellcome). In dose of 30 mg of Sb v (Glucantime or Pentostam) by 100 mg of weight by day for 30 days, renal functional changes were observed consisting of disturbances in urine concentrating capacity. Such disturbances were expressed by significantly low values of urine osmolality as compared to the basal values previous to the drugs. The decrease in urine osmolality was associated to a significant increase in urinary flow and in negative free-water clearance. There was no alteration in osmolar clearance and in fractional excretion of sodium. These observations suggest an interference of the drugs in the action of the antidiuretic hormone. The disturbance in urine concentration was reversible after a seven days period without the drugs administration. No significant histopathological alterations were observed in the kidneys of the rats treated with the drugs. On the other hand, the rats treated with a high dose of Pentostam (200 mg/100 grams of weight/day) showed the functional and the histopathological alterations of the acute tubular necrosis.
publishDate 1990
dc.date.none.fl_str_mv 1990-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/28750
url https://www.revistas.usp.br/rimtsp/article/view/28750
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/28750/30603
dc.rights.driver.fl_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
dc.source.none.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo; Vol. 32 No. 4 (1990); 304-309
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 32 Núm. 4 (1990); 304-309
Revista do Instituto de Medicina Tropical de São Paulo; v. 32 n. 4 (1990); 304-309
1678-9946
0036-4665
reponame:Revista do Instituto de Medicina Tropical de São Paulo
instname:Instituto de Medicina Tropical (IMT)
instacron:IMT
instname_str Instituto de Medicina Tropical (IMT)
instacron_str IMT
institution IMT
reponame_str Revista do Instituto de Medicina Tropical de São Paulo
collection Revista do Instituto de Medicina Tropical de São Paulo
repository.name.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)
repository.mail.fl_str_mv ||revimtsp@usp.br
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