AI Article Synopsis

  • Type 2 diabetes and osteoarthritis (OA) commonly occur together, leading researchers to study plasma IL-6, chondrocyte MMP-13, and col10a expression in obese diabetic mice to better understand OA development.
  • Genistein was tested as a dietary supplement along with an exercise training regimen to see if they could reduce OA symptoms; 100 mice were divided into groups for control and treatment.
  • The study found that while genistein improved key biomarkers related to OA, exercise training had no significant impact on these outcomes in diabetic mice.

Article Abstract

Type 2 diabetes mellitus and osteoarthritis (OA) often present as comorbidities. We examined the role of plasma IL-6, chondrocyte MMP-13, and col10a expression in the development of OA in obese diabetic mice. We further investigated dietary genistein and exercise training as potential mitigators of OA. One hundred adult mice (50 females, 50 males) aged 6 weeks were randomized into 5 groups, including lean controls, obese diabetic controls, and obese diabetic mice treated with genistein, exercise training, and genistein plus exercise training. The obese diabetic state was induced by feeding the mice a high-fat, high-sugar diet. Genistein was incorporated into the diet at a concentration of 600 mg genistein/kg. Exercise training was performed on a treadmill and consisted of daily 30 min sessions at 12 m/min, 5 days/week for a 12-week period. After treatment, plasma was collected, and proximal tibias were removed for analysis. Plasma IL-6 and MMP-13 were elevated while col10a was reduced in obese diabetic mice in comparison to lean controls. Dietary genistein treatment reduced IL-6 and MMP-13 expression and increased col10a expression. Histological examination of articular cartilage showed reduced thickness of the uncalcified zones and proteoglycan content in the cartilage of diabetic mice in comparison to mice fed genistein. Exercise training had no significant effect. In conclusion, genistein (and not exercise training) attenuates OA by reducing IL-6 and MMP-13 expression in diabetic mice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10534591PMC
http://dx.doi.org/10.3390/metabo13091014DOI Listing

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