Lysosomal enzymes are decreased in the kidney of diabetic rats
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.bbadis.2012.09.011 http://repositorio.unifesp.br/handle/11600/35643 |
Resumo: | The objective of the present study was to investigate the expression and activities of lysosomal enzymes that act upon proteins and sulfated polysaccharides in diabetic rat kidney. Cathepsins, glycosidases and sulfatases were studied on the 10th (DM-10) and on the 30th (DM-30) day of streptozotocin-induced diabetes mellitus (DM). the activity of cathepsin B, the main kidney cysteine protease, was decreased both in DM-10 and DM-30. Gel filtration chromatography of urinary proteins has shown the prevalence of low molecular weight peptides in normal and DM-10 urine, in contrast to the prevalence of high molecular weight peptides and intact proteins in DM-30. These results show that the decrease in lysosomal proteases could explain, at least in part, the increased albuminuria detected by radial immunodiffusion (RID), due to the excretion of less degraded or intact albumin. Concerning sulfated polysaccharides, the activities of beta-glucuronidase, N-acetyl-beta-D-glucosaminidase, and N-acetyl-beta-D-galactosaminidase were also decreased in DM-30, while aryl sulfatases did not vary. Increased toluidine blue metachromatic staining of the tissue suggests that the lower activities of glycosidases could lead to intracellular deposition of partially digested molecules, and this could explain the decreased urinary excretion and increased tissue buildup of these molecules. the main morphological changes observed in kidney were proximal convoluted tubules with thinner walls and thinner brush border. Immunohistochemistry revealed that most of cathepsin B was located in the brush border of proximal tubular cells, highlighting the involvement of proximal convoluted tubules in diabetic nephropathy. (C) 2012 Elsevier B.V. All rights reserved. |
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Lysosomal enzymes are decreased in the kidney of diabetic ratsDiabetes mellitusLysosomeCathepsinGlycosidaseKidneyTubular cellsThe objective of the present study was to investigate the expression and activities of lysosomal enzymes that act upon proteins and sulfated polysaccharides in diabetic rat kidney. Cathepsins, glycosidases and sulfatases were studied on the 10th (DM-10) and on the 30th (DM-30) day of streptozotocin-induced diabetes mellitus (DM). the activity of cathepsin B, the main kidney cysteine protease, was decreased both in DM-10 and DM-30. Gel filtration chromatography of urinary proteins has shown the prevalence of low molecular weight peptides in normal and DM-10 urine, in contrast to the prevalence of high molecular weight peptides and intact proteins in DM-30. These results show that the decrease in lysosomal proteases could explain, at least in part, the increased albuminuria detected by radial immunodiffusion (RID), due to the excretion of less degraded or intact albumin. Concerning sulfated polysaccharides, the activities of beta-glucuronidase, N-acetyl-beta-D-glucosaminidase, and N-acetyl-beta-D-galactosaminidase were also decreased in DM-30, while aryl sulfatases did not vary. Increased toluidine blue metachromatic staining of the tissue suggests that the lower activities of glycosidases could lead to intracellular deposition of partially digested molecules, and this could explain the decreased urinary excretion and increased tissue buildup of these molecules. the main morphological changes observed in kidney were proximal convoluted tubules with thinner walls and thinner brush border. Immunohistochemistry revealed that most of cathepsin B was located in the brush border of proximal tubular cells, highlighting the involvement of proximal convoluted tubules in diabetic nephropathy. (C) 2012 Elsevier B.V. All rights reserved.Universidade Federal de São Paulo, Disciplina Biol Mol, Dept Bioquim, Escola Paulista Med, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, Escola Paulista Med, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morfol, Escola Paulista Med, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Disciplina Biol Mol, Dept Bioquim, Escola Paulista Med, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, Escola Paulista Med, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Morfol, Escola Paulista Med, BR-04044020 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)FAPESP: 2010/16022-5FAPESP: 2009/11817-2CNPq: 308642/2010-4Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Peres, Giovani Bravin [UNIFESP]Juliano, Maria Aparecida [UNIFESP]Simoes, Manuelde Jesus [UNIFESP]Michelacci, Yara Maria [UNIFESP]2016-01-24T14:28:11Z2016-01-24T14:28:11Z2013-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion85-95application/pdfhttp://dx.doi.org/10.1016/j.bbadis.2012.09.011Biochimica Et Biophysica Acta-molecular Basis of Disease. Amsterdam: Elsevier B.V., v. 1832, n. 1, p. 85-95, 2013.10.1016/j.bbadis.2012.09.011WOS000313932000010.pdf0925-4439http://repositorio.unifesp.br/handle/11600/35643WOS:000313932000010engBiochimica Et Biophysica Acta-molecular Basis of Diseaseinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T04:13:46Zoai:repositorio.unifesp.br/:11600/35643Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-01T04:13:46Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
title |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
spellingShingle |
Lysosomal enzymes are decreased in the kidney of diabetic rats Peres, Giovani Bravin [UNIFESP] Diabetes mellitus Lysosome Cathepsin Glycosidase Kidney Tubular cells |
title_short |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
title_full |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
title_fullStr |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
title_full_unstemmed |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
title_sort |
Lysosomal enzymes are decreased in the kidney of diabetic rats |
author |
Peres, Giovani Bravin [UNIFESP] |
author_facet |
Peres, Giovani Bravin [UNIFESP] Juliano, Maria Aparecida [UNIFESP] Simoes, Manuelde Jesus [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
author_role |
author |
author2 |
Juliano, Maria Aparecida [UNIFESP] Simoes, Manuelde Jesus [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Peres, Giovani Bravin [UNIFESP] Juliano, Maria Aparecida [UNIFESP] Simoes, Manuelde Jesus [UNIFESP] Michelacci, Yara Maria [UNIFESP] |
dc.subject.por.fl_str_mv |
Diabetes mellitus Lysosome Cathepsin Glycosidase Kidney Tubular cells |
topic |
Diabetes mellitus Lysosome Cathepsin Glycosidase Kidney Tubular cells |
description |
The objective of the present study was to investigate the expression and activities of lysosomal enzymes that act upon proteins and sulfated polysaccharides in diabetic rat kidney. Cathepsins, glycosidases and sulfatases were studied on the 10th (DM-10) and on the 30th (DM-30) day of streptozotocin-induced diabetes mellitus (DM). the activity of cathepsin B, the main kidney cysteine protease, was decreased both in DM-10 and DM-30. Gel filtration chromatography of urinary proteins has shown the prevalence of low molecular weight peptides in normal and DM-10 urine, in contrast to the prevalence of high molecular weight peptides and intact proteins in DM-30. These results show that the decrease in lysosomal proteases could explain, at least in part, the increased albuminuria detected by radial immunodiffusion (RID), due to the excretion of less degraded or intact albumin. Concerning sulfated polysaccharides, the activities of beta-glucuronidase, N-acetyl-beta-D-glucosaminidase, and N-acetyl-beta-D-galactosaminidase were also decreased in DM-30, while aryl sulfatases did not vary. Increased toluidine blue metachromatic staining of the tissue suggests that the lower activities of glycosidases could lead to intracellular deposition of partially digested molecules, and this could explain the decreased urinary excretion and increased tissue buildup of these molecules. the main morphological changes observed in kidney were proximal convoluted tubules with thinner walls and thinner brush border. Immunohistochemistry revealed that most of cathepsin B was located in the brush border of proximal tubular cells, highlighting the involvement of proximal convoluted tubules in diabetic nephropathy. (C) 2012 Elsevier B.V. All rights reserved. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01-01 2016-01-24T14:28:11Z 2016-01-24T14:28:11Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.bbadis.2012.09.011 Biochimica Et Biophysica Acta-molecular Basis of Disease. Amsterdam: Elsevier B.V., v. 1832, n. 1, p. 85-95, 2013. 10.1016/j.bbadis.2012.09.011 WOS000313932000010.pdf 0925-4439 http://repositorio.unifesp.br/handle/11600/35643 WOS:000313932000010 |
url |
http://dx.doi.org/10.1016/j.bbadis.2012.09.011 http://repositorio.unifesp.br/handle/11600/35643 |
identifier_str_mv |
Biochimica Et Biophysica Acta-molecular Basis of Disease. Amsterdam: Elsevier B.V., v. 1832, n. 1, p. 85-95, 2013. 10.1016/j.bbadis.2012.09.011 WOS000313932000010.pdf 0925-4439 WOS:000313932000010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Biochimica Et Biophysica Acta-molecular Basis of Disease |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
85-95 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268392791605248 |