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Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes
The transport of myo-inositol is the main mechanism for the maintenance of its high intracellular levels. We aimed to measure the mRNA and protein levels of myo-inositol cotransporters in the sciatic nerve (SN) and dorsal root ganglia (DRG) during experimental diabetes. Streptozotocin-induced (STZ;...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Associação Brasileira de Divulgação Científica
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556969/ https://www.ncbi.nlm.nih.gov/pubmed/31166385 http://dx.doi.org/10.1590/1414-431X20198589 |
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author | Farias, V.X. Uchoa, P.N. Aquino, C.P. Britto, L.R.G. Fonteles, M.C. Leal-Cardoso, J.H. Silva-Alves, K.S. Havt, A. Prata, M.M.G. Heimark, D.B. Nascimento, N.R.F. Santos, C.F. |
author_facet | Farias, V.X. Uchoa, P.N. Aquino, C.P. Britto, L.R.G. Fonteles, M.C. Leal-Cardoso, J.H. Silva-Alves, K.S. Havt, A. Prata, M.M.G. Heimark, D.B. Nascimento, N.R.F. Santos, C.F. |
author_sort | Farias, V.X. |
collection | PubMed |
description | The transport of myo-inositol is the main mechanism for the maintenance of its high intracellular levels. We aimed to measure the mRNA and protein levels of myo-inositol cotransporters in the sciatic nerve (SN) and dorsal root ganglia (DRG) during experimental diabetes. Streptozotocin-induced (STZ; 4, 8, and 12 weeks; 65 mg/kg; ip) diabetic rats (DB) and age-matched euglycemic (E) rats were used for the analysis of mRNA and protein levels of sodium myo-inositol cotransporters 1, 2 (SMIT1, SMIT2) or H(+)/myo-inositol cotransporter (HMIT). There was a significant reduction in the mRNA levels for SMIT1 in the SN and DRG (by 36.9 and 31.0%) in the 4-week DB (DB4) group compared to the E group. SMIT2 was not expressed in SN. The mRNA level for SMIT2 was up-regulated only in the DRG in the DB4 group. On the other hand, the protein level of SMIT1 decreased by 42.5, 41.3, and 44.8% in the SN after 4, 8, and 12 weeks of diabetes, respectively. In addition, there was a decrease of 64.3 and 58.0% of HMIT in membrane and cytosolic fractions, respectively, in the SN of the DB4 group. In the DRG, there was an increase of 230 and 86.3% for SMIT1 and HMIT, respectively, in the DB12 group. The levels of the main inositol transporters, SMIT1 and HMIT, were greatly reduced in the SN but not in the DRG. SMIT-1 was selectively reduced in the sciatic nerve during experimental STZ-induced diabetes. |
format | Online Article Text |
id | pubmed-6556969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-65569692019-06-21 Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes Farias, V.X. Uchoa, P.N. Aquino, C.P. Britto, L.R.G. Fonteles, M.C. Leal-Cardoso, J.H. Silva-Alves, K.S. Havt, A. Prata, M.M.G. Heimark, D.B. Nascimento, N.R.F. Santos, C.F. Braz J Med Biol Res Research Article The transport of myo-inositol is the main mechanism for the maintenance of its high intracellular levels. We aimed to measure the mRNA and protein levels of myo-inositol cotransporters in the sciatic nerve (SN) and dorsal root ganglia (DRG) during experimental diabetes. Streptozotocin-induced (STZ; 4, 8, and 12 weeks; 65 mg/kg; ip) diabetic rats (DB) and age-matched euglycemic (E) rats were used for the analysis of mRNA and protein levels of sodium myo-inositol cotransporters 1, 2 (SMIT1, SMIT2) or H(+)/myo-inositol cotransporter (HMIT). There was a significant reduction in the mRNA levels for SMIT1 in the SN and DRG (by 36.9 and 31.0%) in the 4-week DB (DB4) group compared to the E group. SMIT2 was not expressed in SN. The mRNA level for SMIT2 was up-regulated only in the DRG in the DB4 group. On the other hand, the protein level of SMIT1 decreased by 42.5, 41.3, and 44.8% in the SN after 4, 8, and 12 weeks of diabetes, respectively. In addition, there was a decrease of 64.3 and 58.0% of HMIT in membrane and cytosolic fractions, respectively, in the SN of the DB4 group. In the DRG, there was an increase of 230 and 86.3% for SMIT1 and HMIT, respectively, in the DB12 group. The levels of the main inositol transporters, SMIT1 and HMIT, were greatly reduced in the SN but not in the DRG. SMIT-1 was selectively reduced in the sciatic nerve during experimental STZ-induced diabetes. Associação Brasileira de Divulgação Científica 2019-06-03 /pmc/articles/PMC6556969/ /pubmed/31166385 http://dx.doi.org/10.1590/1414-431X20198589 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Farias, V.X. Uchoa, P.N. Aquino, C.P. Britto, L.R.G. Fonteles, M.C. Leal-Cardoso, J.H. Silva-Alves, K.S. Havt, A. Prata, M.M.G. Heimark, D.B. Nascimento, N.R.F. Santos, C.F. Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title | Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title_full | Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title_fullStr | Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title_full_unstemmed | Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title_short | Expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
title_sort | expression of myo-inositol cotransporters in the sciatic nerve and dorsal root ganglia in experimental diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556969/ https://www.ncbi.nlm.nih.gov/pubmed/31166385 http://dx.doi.org/10.1590/1414-431X20198589 |
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