Lysosomal enzymes are decreased in the kidney of diabetic rats

Detalhes bibliográficos
Autor(a) principal: Peres, Giovani Bravin [UNIFESP]
Data de Publicação: 2013
Outros Autores: Juliano, Maria Aparecida [UNIFESP], Simoes, Manuelde Jesus [UNIFESP], Michelacci, Yara Maria [UNIFESP]
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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spelling 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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