Long-term treatment with senolytic drugs Dasatinib and Quercetin ameliorates age-dependent intervertebral disc degeneration in mice

Nat Commun. 2021 Sep 3;12(1):5213. doi: 10.1038/s41467-021-25453-2.

Abstract

Intervertebral disc degeneration is highly prevalent within the elderly population and is a leading cause of chronic back pain and disability. Due to the link between disc degeneration and senescence, we explored the ability of the Dasatinib and Quercetin drug combination (D + Q) to prevent an age-dependent progression of disc degeneration in mice. We treated C57BL/6 mice beginning at 6, 14, and 18 months of age, and analyzed them at 23 months of age. Interestingly, 6- and 14-month D + Q cohorts show lower incidences of degeneration, and the treatment results in a significant decrease in senescence markers p16INK4a, p19ARF, and SASP molecules IL-6 and MMP13. Treatment also preserves cell viability, phenotype, and matrix content. Although transcriptomic analysis shows disc compartment-specific effects of the treatment, cell death and cytokine response pathways are commonly modulated across tissue types. Results suggest that senolytics may provide an attractive strategy to mitigating age-dependent disc degeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggrecans / metabolism
  • Aging / drug effects*
  • Aging / metabolism
  • Animals
  • Annulus Fibrosus / drug effects
  • Annulus Fibrosus / metabolism
  • Annulus Fibrosus / pathology
  • Cell Survival / drug effects
  • Cellular Senescence / drug effects
  • Dasatinib / therapeutic use*
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Fibrosis
  • Inflammation
  • Intervertebral Disc Degeneration / drug therapy*
  • Intervertebral Disc Degeneration / metabolism
  • Intervertebral Disc Degeneration / pathology
  • Mice
  • Mice, Inbred C57BL
  • Nucleus Pulposus / drug effects
  • Nucleus Pulposus / metabolism
  • Nucleus Pulposus / pathology
  • Phenotype
  • Quercetin / therapeutic use*
  • Transcriptome / drug effects

Substances

  • Aggrecans
  • Quercetin
  • Dasatinib