Dexamethasone-Induced Insulin Resistance Attenuation by Oral Sulfur-Oxidovanadium(IV) Complex Treatment in Mice

Eucilene K Batista1, Lidiane M A de Lima2, Dayane A Gomes1

  • 1Departamento de Fisiologia e Farmacologia, Centro de Biociências, Universidade Federal de Pernambuco, Recife 50670-901, PE, Brazil.

Insights

This study shows that the oxidovanadium(IV) compound [VIVO(octd)] effectively lowers blood glucose and insulin resistance in mice. It offers a promising therapeutic for diabetes, even when complicated by glucocorticoid-induced insulin resistance.

Area of Science:

  • Inorganic Chemistry
  • Biochemistry
  • Pharmacology

Background:

  • Vanadium compounds exhibit insulin-enhancing and anti-diabetic properties.
  • Insulin resistance (IR) is a key factor in diabetes development and progression.
  • Glucocorticoids can induce or exacerbate insulin resistance.

Purpose of the Study:

  • To investigate the anti-diabetic effects of the oxidovanadium(IV) compound [VIVO(octd)] in a mouse model of glucocorticoid-induced insulin resistance.
  • To evaluate the compound's impact on key metabolic and oxidative stress markers.
  • To compare its efficacy against metformin.

Main Methods:

  • Characterization of [VIVO(octd)] using spectroscopic techniques (51V NMR, FTIR, EPR, UV-Vis, ESI-FT-MS).
  • Induction of insulin resistance in female Swiss mice using dexamethasone.
  • Oral administration of [VIVO(octd)] and metformin.
  • Assessment of hematological parameters, TyG index, hepatic lipids, glycogen, oxidative stress, and oral glucose tolerance tests.

Main Results:

  • [VIVO(octd)] demonstrated significant antioxidant effects.
  • Oral treatment (50 mg/kg) reduced fasting blood glucose by 50% (p < 0.05) and the TyG index by 25% (p < 0.05) compared to controls.
  • The compound showed comparable or beneficial effects to metformin in certain assays.

Conclusions:

  • The oxidovanadium-sulfur compound [VIVO(octd)] is a potent antihyperglycemic agent.
  • It is effective in managing diabetes, particularly in cases of glucocorticoid-induced insulin resistance.
  • This compound represents a promising therapeutic candidate for type 2 diabetes treatment.

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