Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters
- Autores
- Hazelhoff, Maria Herminia; Torres, Adriana Monica
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mercury is a widespread pollutant. Mercuric ions uptake into tubular cells is supported by the Organic anion transporter 1 (Oat1) and 3 (Oat3) and its elimination into urine is through the Multidrug resistance-associated protein 2 (Mrp2). We investigated the effect of recombinant human erythropoietin (Epo) on renal function and on renal expression of Oat1, Oat3, and Mrp2 in a model of mercuric chloride (HgCl2)- induced renal damage. Four experimental groups of adult male Wistar rats were used: Control, Epo, HgCl2, and Epo+HgCl2. Epo (3000 IU/kg, b.w., i.p) was administered 24 h before HgCl2 (4 mg/kg, b.w., i.p). Experiments were performed 18 h after the HgCl2 dose. Parameters of renal function and structure were evaluated. The protein expression of Oat1, Oat3 and Mrp2 in renal tissue was assessed by immunoblotting techniques. Mercury levels were determined by cold vapour atomic absorption spectrometry. Pretreatment with Epo ameliorated the HgCl2-induced tubular injury as assessed by histopathology and urinary biomarkers. Immunoblotting showed that pretreatment with Epo regulated the renal expression of mercury transporters in a way to decrease mercury content in the kidney. Epo pretreatment ameliorates HgCl2-induced renal tubular injury by modulation of mercury transporters expression in the kidneys.
Fil: Hazelhoff, Maria Herminia. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina
Fil: Torres, Adriana Monica. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina - Materia
-
ERYTHR0POIETIN
NEPHROTOXICITY
MERCURY
MEMBRANE TRANSPORTERS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/155501
Ver los metadatos del registro completo
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Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transportersHazelhoff, Maria HerminiaTorres, Adriana MonicaERYTHR0POIETINNEPHROTOXICITYMERCURYMEMBRANE TRANSPORTERShttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Mercury is a widespread pollutant. Mercuric ions uptake into tubular cells is supported by the Organic anion transporter 1 (Oat1) and 3 (Oat3) and its elimination into urine is through the Multidrug resistance-associated protein 2 (Mrp2). We investigated the effect of recombinant human erythropoietin (Epo) on renal function and on renal expression of Oat1, Oat3, and Mrp2 in a model of mercuric chloride (HgCl2)- induced renal damage. Four experimental groups of adult male Wistar rats were used: Control, Epo, HgCl2, and Epo+HgCl2. Epo (3000 IU/kg, b.w., i.p) was administered 24 h before HgCl2 (4 mg/kg, b.w., i.p). Experiments were performed 18 h after the HgCl2 dose. Parameters of renal function and structure were evaluated. The protein expression of Oat1, Oat3 and Mrp2 in renal tissue was assessed by immunoblotting techniques. Mercury levels were determined by cold vapour atomic absorption spectrometry. Pretreatment with Epo ameliorated the HgCl2-induced tubular injury as assessed by histopathology and urinary biomarkers. Immunoblotting showed that pretreatment with Epo regulated the renal expression of mercury transporters in a way to decrease mercury content in the kidney. Epo pretreatment ameliorates HgCl2-induced renal tubular injury by modulation of mercury transporters expression in the kidneys.Fil: Hazelhoff, Maria Herminia. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; ArgentinaFil: Torres, Adriana Monica. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; ArgentinaSAGE Publications2021-03-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/155501Hazelhoff, Maria Herminia; Torres, Adriana Monica; Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters; SAGE Publications; Human and Experimental Toxicoloxy; 40; 3; 10-3-2021; 515-5250960-32711477-0903CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://journals.sagepub.com/doi/10.1177/0960327120958109info:eu-repo/semantics/altIdentifier/doi/10.1177%2F0960327120958109info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:09:03Zoai:ri.conicet.gov.ar:11336/155501instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:09:03.914CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
title |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
spellingShingle |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters Hazelhoff, Maria Herminia ERYTHR0POIETIN NEPHROTOXICITY MERCURY MEMBRANE TRANSPORTERS |
title_short |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
title_full |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
title_fullStr |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
title_full_unstemmed |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
title_sort |
Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters |
dc.creator.none.fl_str_mv |
Hazelhoff, Maria Herminia Torres, Adriana Monica |
author |
Hazelhoff, Maria Herminia |
author_facet |
Hazelhoff, Maria Herminia Torres, Adriana Monica |
author_role |
author |
author2 |
Torres, Adriana Monica |
author2_role |
author |
dc.subject.none.fl_str_mv |
ERYTHR0POIETIN NEPHROTOXICITY MERCURY MEMBRANE TRANSPORTERS |
topic |
ERYTHR0POIETIN NEPHROTOXICITY MERCURY MEMBRANE TRANSPORTERS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.3 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Mercury is a widespread pollutant. Mercuric ions uptake into tubular cells is supported by the Organic anion transporter 1 (Oat1) and 3 (Oat3) and its elimination into urine is through the Multidrug resistance-associated protein 2 (Mrp2). We investigated the effect of recombinant human erythropoietin (Epo) on renal function and on renal expression of Oat1, Oat3, and Mrp2 in a model of mercuric chloride (HgCl2)- induced renal damage. Four experimental groups of adult male Wistar rats were used: Control, Epo, HgCl2, and Epo+HgCl2. Epo (3000 IU/kg, b.w., i.p) was administered 24 h before HgCl2 (4 mg/kg, b.w., i.p). Experiments were performed 18 h after the HgCl2 dose. Parameters of renal function and structure were evaluated. The protein expression of Oat1, Oat3 and Mrp2 in renal tissue was assessed by immunoblotting techniques. Mercury levels were determined by cold vapour atomic absorption spectrometry. Pretreatment with Epo ameliorated the HgCl2-induced tubular injury as assessed by histopathology and urinary biomarkers. Immunoblotting showed that pretreatment with Epo regulated the renal expression of mercury transporters in a way to decrease mercury content in the kidney. Epo pretreatment ameliorates HgCl2-induced renal tubular injury by modulation of mercury transporters expression in the kidneys. Fil: Hazelhoff, Maria Herminia. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina Fil: Torres, Adriana Monica. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Ciencias Fisiológicas. Área Farmacología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina |
description |
Mercury is a widespread pollutant. Mercuric ions uptake into tubular cells is supported by the Organic anion transporter 1 (Oat1) and 3 (Oat3) and its elimination into urine is through the Multidrug resistance-associated protein 2 (Mrp2). We investigated the effect of recombinant human erythropoietin (Epo) on renal function and on renal expression of Oat1, Oat3, and Mrp2 in a model of mercuric chloride (HgCl2)- induced renal damage. Four experimental groups of adult male Wistar rats were used: Control, Epo, HgCl2, and Epo+HgCl2. Epo (3000 IU/kg, b.w., i.p) was administered 24 h before HgCl2 (4 mg/kg, b.w., i.p). Experiments were performed 18 h after the HgCl2 dose. Parameters of renal function and structure were evaluated. The protein expression of Oat1, Oat3 and Mrp2 in renal tissue was assessed by immunoblotting techniques. Mercury levels were determined by cold vapour atomic absorption spectrometry. Pretreatment with Epo ameliorated the HgCl2-induced tubular injury as assessed by histopathology and urinary biomarkers. Immunoblotting showed that pretreatment with Epo regulated the renal expression of mercury transporters in a way to decrease mercury content in the kidney. Epo pretreatment ameliorates HgCl2-induced renal tubular injury by modulation of mercury transporters expression in the kidneys. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-03-10 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/155501 Hazelhoff, Maria Herminia; Torres, Adriana Monica; Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters; SAGE Publications; Human and Experimental Toxicoloxy; 40; 3; 10-3-2021; 515-525 0960-3271 1477-0903 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/155501 |
identifier_str_mv |
Hazelhoff, Maria Herminia; Torres, Adriana Monica; Effect of erythropoietin on mercury-induced nephrotoxicity: Role of membrane transporters; SAGE Publications; Human and Experimental Toxicoloxy; 40; 3; 10-3-2021; 515-525 0960-3271 1477-0903 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://journals.sagepub.com/doi/10.1177/0960327120958109 info:eu-repo/semantics/altIdentifier/doi/10.1177%2F0960327120958109 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
SAGE Publications |
publisher.none.fl_str_mv |
SAGE Publications |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |