Correlation Engine 2.0
Clear Search sequence regions


  • cases (1)
  • cellular (1)
  • help (1)
  • necrosis (1)
  • rats (3)
  • rats wistar (1)
  • streptozocin (2)
  • streptozocin (3)
  • therapies (1)
  • Sizes of these terms reflect their relevance to your search.

    Diabetes mellitus (DM) is a worldwide health concern, and projections state that cases will reach 578 million by 2030. Adjuvant therapies that can help the standard treatment and mitigate DM effects are necessary, especially those using nutritional supplements to improve glycemic control. Previous studies suggest creatine supplementation as a possible adjuvant therapy for DM, but they lack the evaluation of potential morphological parameters alterations and tissue injury caused by this compound. The present study aimed to elucidate clinical, histomorphometric, and histopathological consequences and the cellular oxidative alterations of creatine supplementation in streptozotocin (STZ)-induced type 1 DM rats. We could estimate whether the findings are due to DM or the supplementation from a factorial experimental design. Although creatine supplementation attenuated some biochemical parameters, the morphological analyses of pancreatic and renal tissues made clear that the supplementation did not improve the STZ-induced DM1 injuries. Moreover, creatine-supplemented non-diabetic animals were diagnosed with pancreatitis and showed renal tubular necrosis. Therefore, even in the absence of clinical symptoms and unaltered biochemical parameters, creatine supplementation as adjuvant therapy for DM should be carefully evaluated.

    Citation

    Meline Gomes Gonçalves, Matheus Anselmo Medeiros, Licyanne Ingrid Carvalho de Lemos, Lucia de Fátima Campos Pedrosa, Pedro Paulo de Andrade Santos, Bento João Abreu, João Paulo Matos Santos Lima. Effects of Creatine Supplementation on Histopathological and Biochemical Parameters in the Kidney and Pancreas of Streptozotocin-Induced Diabetic Rats. Nutrients. 2022 Jan 19;14(3)

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35276790

    View Full Text