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Experimental model of nephropathy associated with diabetes mellitus in mice

PURPOSE: Nontransmissible chronic diseases, such as diabetes mellitus (DM) and nephropathy, affect a significant portion of the population, often treated due to injuries that require healing and regeneration. To create an experimental model of associated comorbidities, for healing and regeneration s...

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Autores principales: Silva, Pâmela Henrique, Silva, Patrícia Henrique, Corazza, Adalberto Vieira, da Silva, Josivaldo Godoy, Silva, Iandara Schettert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158849/
https://www.ncbi.nlm.nih.gov/pubmed/37132755
http://dx.doi.org/10.1590/acb381123
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author Silva, Pâmela Henrique
Silva, Patrícia Henrique
Corazza, Adalberto Vieira
da Silva, Josivaldo Godoy
Silva, Iandara Schettert
author_facet Silva, Pâmela Henrique
Silva, Patrícia Henrique
Corazza, Adalberto Vieira
da Silva, Josivaldo Godoy
Silva, Iandara Schettert
author_sort Silva, Pâmela Henrique
collection PubMed
description PURPOSE: Nontransmissible chronic diseases, such as diabetes mellitus (DM) and nephropathy, affect a significant portion of the population, often treated due to injuries that require healing and regeneration. To create an experimental model of associated comorbidities, for healing and regeneration studies, protocols for induction of nephropathy by ischemia and reperfusion (I/R) and induction of DM by injection of streptozotocin (STZ) were associated. METHODS: Sixty-four mice (Mus musculus), female, adult, Swiss strain, weighing approximately 20 g, were divided into four groups: G1: control (n = 24), G2: nephropathy group (N) (n = 7), G3, DM (n = 9), and G4: N+DM (n = 24). Arteriovenous stenosis (I/R) of the left kidney was performed as the first protocol. The animals received a hyperlipidemic diet for 7 days after the injection of STZ (150 mg/kg, via i.p.) and an aqueous glucose solution (10%) for 24 h. The animals in the G3 and G4 groups were observed for 14 days before receiving the diet and STZ. The evolution of nephropathy was observed using a urine test strip and the DM, through the analysis of blood glucose with a reagent strip on a digital monitor. RESULTS: The ischemic induction protocols of nephropathy and DM with STZ, associated, were sustainable, low-cost, and without deaths. There were alterations compatible with initial renal alterations, in the first 14 days, such as increased urinary density, pH alteration, presence of glucose, proteins and leukocytes, when compared to the control group. DM was confirmed by the presence of hyperglycemia 7 days after induction and its evolution after 14 days. The animals in the G4 group showed constant weight loss when compared to the other groups. It was possible to observe morphological alterations in the kidneys submitted to I/R, regarding coloration, during surgery and after the end of the observation period, in the volume and size of the left kidney, when compared to the contralateral kidney. CONCLUSIONS: It was possible to induce nephropathy and DM associated in the same animal, in a simple way, confirmed with rapid tests, without losses, providing a basis for future studies.
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spelling pubmed-101588492023-05-05 Experimental model of nephropathy associated with diabetes mellitus in mice Silva, Pâmela Henrique Silva, Patrícia Henrique Corazza, Adalberto Vieira da Silva, Josivaldo Godoy Silva, Iandara Schettert Acta Cir Bras Original Article PURPOSE: Nontransmissible chronic diseases, such as diabetes mellitus (DM) and nephropathy, affect a significant portion of the population, often treated due to injuries that require healing and regeneration. To create an experimental model of associated comorbidities, for healing and regeneration studies, protocols for induction of nephropathy by ischemia and reperfusion (I/R) and induction of DM by injection of streptozotocin (STZ) were associated. METHODS: Sixty-four mice (Mus musculus), female, adult, Swiss strain, weighing approximately 20 g, were divided into four groups: G1: control (n = 24), G2: nephropathy group (N) (n = 7), G3, DM (n = 9), and G4: N+DM (n = 24). Arteriovenous stenosis (I/R) of the left kidney was performed as the first protocol. The animals received a hyperlipidemic diet for 7 days after the injection of STZ (150 mg/kg, via i.p.) and an aqueous glucose solution (10%) for 24 h. The animals in the G3 and G4 groups were observed for 14 days before receiving the diet and STZ. The evolution of nephropathy was observed using a urine test strip and the DM, through the analysis of blood glucose with a reagent strip on a digital monitor. RESULTS: The ischemic induction protocols of nephropathy and DM with STZ, associated, were sustainable, low-cost, and without deaths. There were alterations compatible with initial renal alterations, in the first 14 days, such as increased urinary density, pH alteration, presence of glucose, proteins and leukocytes, when compared to the control group. DM was confirmed by the presence of hyperglycemia 7 days after induction and its evolution after 14 days. The animals in the G4 group showed constant weight loss when compared to the other groups. It was possible to observe morphological alterations in the kidneys submitted to I/R, regarding coloration, during surgery and after the end of the observation period, in the volume and size of the left kidney, when compared to the contralateral kidney. CONCLUSIONS: It was possible to induce nephropathy and DM associated in the same animal, in a simple way, confirmed with rapid tests, without losses, providing a basis for future studies. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2023-05-01 /pmc/articles/PMC10158849/ /pubmed/37132755 http://dx.doi.org/10.1590/acb381123 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 Original Article
Silva, Pâmela Henrique
Silva, Patrícia Henrique
Corazza, Adalberto Vieira
da Silva, Josivaldo Godoy
Silva, Iandara Schettert
Experimental model of nephropathy associated with diabetes mellitus in mice
title Experimental model of nephropathy associated with diabetes mellitus in mice
title_full Experimental model of nephropathy associated with diabetes mellitus in mice
title_fullStr Experimental model of nephropathy associated with diabetes mellitus in mice
title_full_unstemmed Experimental model of nephropathy associated with diabetes mellitus in mice
title_short Experimental model of nephropathy associated with diabetes mellitus in mice
title_sort experimental model of nephropathy associated with diabetes mellitus in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158849/
https://www.ncbi.nlm.nih.gov/pubmed/37132755
http://dx.doi.org/10.1590/acb381123
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