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Updated: Jan 15, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
Short-Term: Cellular Metabolism and Gene Expression During the Onset of Diabetic Kidney Disease: A Diabetes Mellitus
Jéssica Encinas1, Glaucia Veiga1, Joyce Raimundo1
1Laboratório de Análises Clínicas, Centro Universitário FMABC, Santo André 09060-870, Brazil.
Abstract:
Diabetes is a chronic disease with a rising global prevalence. Research focuses on understanding its metabolic implications and early signaling of disease onset and complications, particularly the interconnected effects on the kidneys and brain. The objective of this study was to evaluate the expression profile in the genes Mct1, Mct4, Cd147, Hif-1α and Vegf for different biological matrices in rats induced to diabetes in the determined periods of 7, 21, 30 and 40 days. Methods: Wistar rats (160-180g, n = 68), divided into sham and diabetic groups, were evaluated according to tissue samples from the brain and kidney, using classical biochemical analyses and assessing temporal intergroup differential gene expression by qPCR. Additionally, immunohistochemical analysis was performed on kidney samples to evaluate collagen deposition. In the renal tissues, we observed a decrease in the expression of Hif-1α (21 vs. 30 days) and Vegf (21 vs. 40 days), accompanied by an increase in collagen deposition. In the brain, alterations were observed in all evaluated genes when comparing the early group (7 days) to the later groups (30 and 40 days). We observed that the evaluated genes, as well as the collagen deposition analyzed by immunohistochemistry, are related to metabolic changes that, over time, contribute to the worsening of diabetes and the progression of secondary diseases directly and/or indirectly involving the studied tissues.
Insights
This study investigated diabetes-related gene expression in rat kidneys and brains. Findings show altered gene profiles and collagen deposition, indicating progressive metabolic changes contributing to diabetes complications.
Area of Science:
- Metabolic research
- Nephrology
- Neuroscience
Background:
- Diabetes mellitus is a chronic disease with increasing global incidence.
- Understanding its metabolic effects, especially on kidneys and brain, is crucial for early detection and management.
- Interconnected pathophysiology between diabetes, kidney, and brain requires further investigation.
Purpose of the Study:
- To evaluate the gene expression profiles of Mct1, Mct4, Cd147, Hif-1α, and Vegf in rat brain and kidney tissues.
- To assess temporal changes in gene expression and collagen deposition in diabetic rat models over 40 days.
- To correlate observed molecular changes with the progression of diabetes and secondary complications.
Main Methods:
- Wistar rats were induced with diabetes and divided into sham and diabetic groups (n=68).
- Gene expression was analyzed using quantitative polymerase chain reaction (qPCR) in brain and kidney tissues at 7, 21, 30, and 40 days post-induction.
- Immunohistochemistry was used to evaluate collagen deposition in renal tissues.
Main Results:
- In renal tissues, a decrease in Hif-1α (21 vs. 30 days) and Vegf (21 vs. 40 days) expression was observed, alongside increased collagen deposition.
- In brain tissues, significant alterations in the expression of all evaluated genes were noted when comparing early (7 days) to later time points (30 and 40 days).
- A correlation was found between altered gene expression, increased collagen deposition, and progressive metabolic changes.
Conclusions:
- The evaluated genes and collagen deposition are linked to metabolic alterations in diabetes.
- These molecular changes contribute to the worsening of diabetes and the progression of secondary diseases affecting the kidneys and brain over time.
- The study highlights the complex interplay between metabolic dysregulation and tissue-specific molecular responses in diabetic complications.
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