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Pyruvate Dehydrogenase Kinase 1 inhibition mediated oxidative phosphorylation enhancement in cartilage promotes osteoarthritis progression. | LitMetric

AI Article Synopsis

  • Osteoarthritis (OA) is characterized by the breakdown of cartilage, with emerging evidence suggesting that glucose metabolism plays a crucial role in maintaining joint health.
  • The study finds that the enzyme Pyruvate Dehydrogenase Kinase 1 (PDK1) is reduced in OA cartilage and its inhibition leads to accelerated cartilage loss and increased inflammation.
  • Overall, PDK1 seems to significantly contribute to OA progression by promoting cartilage degradation and inflammation in the articular cartilage.

Article Abstract

Osteoarthritis (OA) is a common disease characterized by cartilage degradation. Growing evidence showed that glucose metabolism impacts joint homeostasis and an imbalance between glycolysis and oxidative phosphorylation (OXPHOS) may exacerbate OA progression, however, a definitive link is yet to be established. Here, we report that pyruvate metabolism and oxidative phosphorylation pathway is enriched in OA cartilage through gene set enrichment analysis (GSEA) and expression of Pyruvate Dehydrogenase Kinase 1 (PDK1), an enzyme that can phosphorylate Pyruvate Dehydrogenase (PDH), and inhibit pyruvate fluxes into the tricarboxylic acid (TCA) cycle and to OXPHOS, in articular cartilage is notably reduced through destabilization of medial meniscus (DMM). Moreover, by inhibiting PDK1, cartilage loss is markedly accelerated in DMM-induced OA through extracellular matrix (ECM) degradation and apoptosis of chondrocytes. These results indicate that PDK1 is involved in the progression of OA through accelerating cartilage matrix degradation and synovium inflammation to ameliorate cartilage degeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357736PMC
http://dx.doi.org/10.1186/s12891-023-06585-6DOI Listing

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