Pentavalent antimonial nephrotoxicity in the rat
Autor(a) principal: | |
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Data de Publicação: | 1990 |
Outros Autores: | , , , , , , |
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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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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1798951638371663872 |