Suppression of knee joint osteoarthritis induced secondary to type 2 diabetes mellitus in rats by resveratrol: role of glycated haemoglobin and hyperlipidaemia and biomarkers of inflammation and oxidative stress.
Hasnaa A EbrahimNorah M AlzamilBahjat Al-AniMohamed A HaidaraAbeer Ibraheem OmarAmal F DawoodPublished in: Archives of physiology and biochemistry (2020)
Background: We investigated whether the anti-inflammatory and antioxidant agent, resveratrol can inhibit type 2 diabetes mellitus (T2DM)-induced osteoarthritis (OA) in rats and whether it is associated with the suppression of glycaemia, dyslipidemia and inflammatory and oxidative stress biomarkers.Materials and methods: T2DM was induced by streptozotocin (50 mg/kg body weight) and high carbohydrate and fat diet (HCFD). The protective group was put on resveratrol (30 mg/kg) 14 days prior to the induction of diabetes and continued on resveratrol and HCFD until being sacrificed at week 12.Results: Diabetic rats showed a substantial damage to the knee joints and loss of proteoglycans from the articular cartilage, which were effectively but not completly protected by resveratrol. Resveratrol also significantly (p ≤ .0029) reduced diabetic up-regulation of HbA1c, hyperlipidaemia, inflammation and oxidative stress.Conclusions: Resveratrol protects against T2DM-induced OA associated with the inhibition of glycated haemoglobin, dyslipidemia, and biomarkers of oxidative stress and inflammation.
Keyphrases
- diabetic rats
- oxidative stress
- ischemia reperfusion injury
- glycemic control
- dna damage
- induced apoptosis
- body weight
- type diabetes
- cardiovascular disease
- total knee arthroplasty
- physical activity
- adipose tissue
- heat shock
- skeletal muscle
- insulin resistance
- high resolution
- atomic force microscopy
- endothelial cells
- heat stress