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Anti-inflammatory effects of C-peptide on kidney of type 1 diabetes mellitus animal model

  • Michelle T. Alves
  • Amanda C. S. Chaves
  • Ana Paula M. Almeida
  • Ana Cristina Simões e Silva
  • Stanley de A. Araújo
  • Ana Paula L. Mota
  • Thiago R. dos Mares-Guia
  • Ana Paula Fernandes
  • Karina B. GomesEmail author
Short Communication
  • 41 Downloads

Abstract

Type 1 diabetes mellitus (T1DM) is characterized by C-peptide deficiency and elevated levels of pro-inflammatory cytokines. The aim of this study was to investigate the role of C-peptide in renal and inflammatory complications in streptozotocin (STZ)-diabetic mice model of T1DM with kidney disease. The study was performed in 8-week old male C57BL/6 mice. Two streptozotocin-diabetic groups (a T1DM animal model), after 4 weeks of diabetes, were treated with subcutaneous infusion of either vehicle (n = 12) or C-peptide (n = 11). Two non-diabetic groups (vehicle, n = 10; C-peptide, n = 9) were treated using the same protocol as described for the diabetic mice. The treatment with C-peptide in the diabetic group reduced the urinary levels of IL17 and TNFα, as well as IL4 and IL10 (p < 0.05). Contrary, the diabetic + C-peptide group presented higher IL10 gene expression in kidney. Besides, it displayed a reduction of TNFα gene expression. The data suggest that C-peptide may modulate pro- and anti-inflammatory signalling pathways, resulting in attenuation of kidney inflammation in T1DM animal model.

Keywords

C-peptide Type 1 diabetes mellitus Inflammation Kidney disease 

Notes

Acknowledgements

ACSS, APF and KBG are grateful to CNPq Research Fellowship (PQ). This work was supported by FAPEMIG, CNPq/Brazil and CAPES.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer Nature B.V. 2019

Authors and Affiliations

  • Michelle T. Alves
    • 1
  • Amanda C. S. Chaves
    • 1
  • Ana Paula M. Almeida
    • 1
  • Ana Cristina Simões e Silva
    • 2
  • Stanley de A. Araújo
    • 3
  • Ana Paula L. Mota
    • 1
  • Thiago R. dos Mares-Guia
    • 4
  • Ana Paula Fernandes
    • 1
  • Karina B. Gomes
    • 1
    Email author
  1. 1.Departamento de Análises Clínicas e Toxicológicas, Faculdade de FarmáciaUniversidade Federal de Minas GeraisBelo HorizonteBrazil
  2. 2.Departamento de Pediatria, Faculdade de MedicinaUniversidade Federal de Minas GeraisBelo HorizonteBrazil
  3. 3.Hospital das Clínicas, Universidade Federal de Minas GeraisBelo HorizonteBrazil
  4. 4.Núcleo de Terapia Celular e Molecular (NUCEL/NETCEM)Universidade de São PauloSão PauloBrazil

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