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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.
Abstract:
Vanadium compounds are known to exert insulin-enhancing activity, normalize elevated blood glucose levels in diabetic subjects, and show significant activity in models of insulin resistance (IR). Faced with insulin resistance, the present work investigates the antidiabetic performance of a known oxidovanadium(IV)-based coordination compound-[VIVO(octd)]-and effects associated with glucocorticoid-induced insulin resistance in mice. The effects of [VIVO(octd)] were evaluated in a female Swiss mice model of insulin resistance induced by seven days of dexamethasone treatment in comparison with groups receiving metformin treatment. Biological assays such as hematological, TyG index, hepatic lipids, glycogen, oxidative stress in the liver, and oral glucose tolerance tests were evaluated. [VIVO(octd)] was characterized with 51V NMR, infrared spectroscopy (FTIR), electron paramagnetic resonance (EPR), electronic absorption spectroscopy, and mass spectrometry (ESI-FT-MS). The [VIVO(octd)] oral treatment (50 mg/kg) had an antioxidant effect, reducing 50% of fast blood glucose (p < 0.05) and 25% of the TyG index, which is used to estimate insulin resistance (p < 0.05), compared with the non-treated group. The oxidovanadium-sulfur compound is a promising antihyperglycemic therapeutic, including in cases aggravated by insulin resistance induced by glucocorticoid treatment.
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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