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Surgical Bone Implantation Technique for Rat Tibia Models of Diabetes and Osteoporosis
Published on: July 5, 2024
Insulin and vanadium protect against osteoarthritis development secondary to diabetes mellitus in rats
Abbas O El Karib1, Bahjat Al-Ani1, Fahaid Al-Hashem1
1a Department of Physiology .
Objective:
Diabetic complications such as cardiovascular disease and osteoarthritis (OA) are among the common public health problems. The effect of insulin on OA secondary to diabetes has not been investigated before in animal models. Therefore, we sought to determine whether insulin and the insulin-mimicking agent, vanadium can protect from developing OA in diabetic rats.
Methods:
Type 1 diabetes mellitus (T1DM) was induced in Sprague-Dawley rats and treated with insulin and/or vanadium. Tissues harvested from the articular cartilage of the knee joint were examined by scanning electron microscopy, and blood samples were assayed for oxidative stress and inflammatory biomarkers.
Results:
Eight weeks following the induction of diabetes, a profound damage to the knee joint compared to the control non-diabetic group was observed. Treatment of diabetic rats with insulin and/or vanadium differentially protected from diabetes-induced cartilage damage and deteriorated fibrils of collagen fibers. The relative biological potencies were insulin + vanadium >> insulin > vanadium. Furthermore, there was about 2- to 5-fold increase in TNF-α (from 31.02 ± 1.92 to 60.5 ± 1.18 pg/ml, p < 0.0001) and IL-6 (from 64.67 ± 8.16 to 338.0 ± 38.9 pg/ml, p < 0.0001) cytokines and free radicals measured as TBARS (from 3.21 ± 0.37 to 11.48 ± 1.5 µM, p < 0.0001) in the diabetic group, which was significantly reduced with insulin and or vanadium. Meanwhile, SOD decreased (from 17.79 ± 8.9 to 8.250.29, p < 0.0001) and was increased with insulin and vanadium. The relative potencies of the treating agents on inflammatory and oxidative stress biomarkers were insulin + vanadium >> insulin > vanadium.
Conclusion:
The present study demonstrates that co-administration of insulin and vanadium to T1DM rats protect against diabetes-induced OA possibly by lowering biomarkers of inflammation and oxidative stress.
Insights
Insulin and vanadium protect diabetic rats from osteoarthritis by reducing inflammation and oxidative stress. Combined treatment showed the greatest protective effect on cartilage and collagen fibers.
Area of Science:
- Biomedical Science
- Endocrinology
- Orthopedics
Background:
- Diabetic complications, including osteoarthritis (OA), pose significant public health challenges.
- The impact of insulin on diabetes-related OA has not been previously studied in animal models.
Purpose of the Study:
- To investigate the protective effects of insulin and vanadium, an insulin-mimicking agent, against osteoarthritis in diabetic rats.
Main Methods:
- Type 1 diabetes mellitus (T1DM) was induced in Sprague-Dawley rats.
- Rats were treated with insulin and/or vanadium.
- Articular cartilage tissues were analyzed using scanning electron microscopy.
- Blood samples were assessed for oxidative stress and inflammatory biomarkers.
Main Results:
- Diabetic rats exhibited significant knee joint damage compared to controls.
- Insulin and/or vanadium treatment protected against cartilage damage and collagen fiber deterioration.
- The combination of insulin and vanadium demonstrated the highest potency, followed by insulin, then vanadium.
- Treatment significantly reduced elevated levels of TNF-α, IL-6, and TBARS, while increasing SOD levels.
Conclusions:
- Co-administration of insulin and vanadium protects against diabetes-induced osteoarthritis in T1DM rats.
- This protection is likely mediated by the reduction of inflammation and oxidative stress biomarkers.
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