Needle-scalpel therapy inhibits the apoptosis of nucleus pulposus cells via the SDF-1/CXCR4 axis in a rat degenerative cervical intervertebral disc model

Aging (Albany NY). 2024 Jun 20;16(13):10868-10881. doi: 10.18632/aging.205959. Epub 2024 Jun 20.

Abstract

As a common disease, cervical spondylosis (CS) results from the degeneration of the cervical intervertebral disc. However, there are still no effective clinical strategies for the treatment of this disease. Needle-scalpel (Ns), a therapy guided by traditional Chinese medicine theory, alleviates intervertebral disc degradation and is widely used in the clinic to treat CS. Stromal cell-derived factor-1 (SDF-1) and its receptor CXC receptor 4 (CXCR4) in nucleus pulposus cells play an important role in CS onset and development. This study aimed to explore whether Ns can relieve pain and regulate the SDF-1/CXCR4 axis in nucleus pulposus cells to inhibit apoptosis, thereby delaying cervical intervertebral disc degradation in a rat model of CS. It was found that the Ns-treated groups exhibited higher mechanical allodynia scores than the model group, and H&E staining, MRI, and scanning electron microscopy revealed that Ns therapy inhibited intervertebral disc degeneration. Additionally, Ns therapy significantly inhibited increases in the RNA and protein expression levels of SDF-1 and CXCR4. Furthermore, these treatments alleviated the apoptosis of nucleus pulposus cells, which manifested as a decline in the proportion of apoptotic nucleus pulposus cells and inhibition of the decrease in the levels of Bcl-2/Bax. These findings indicated that Ns mitigated CS-induced pain, inhibited the apoptosis of nucleus pulposus cells, and alleviated intervertebral disc degeneration in CS rats. These effects may be mediated by specifically regulating the SDF-1/CXCR4 signaling axis. Based on these findings, we conclude that Ns might serve as a promising therapy for the treatment of CS.

Keywords: Needle-scalpel; SDF-1/CXCR4 axis; apoptosis of nucleus pulposus cells; intervertebral disc degeneration.

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Cervical Vertebrae
  • Chemokine CXCL12* / metabolism
  • Disease Models, Animal*
  • Intervertebral Disc Degeneration* / drug therapy
  • Intervertebral Disc Degeneration* / metabolism
  • Intervertebral Disc Degeneration* / pathology
  • Male
  • Nucleus Pulposus* / drug effects
  • Nucleus Pulposus* / metabolism
  • Nucleus Pulposus* / pathology
  • Rats
  • Rats, Sprague-Dawley*
  • Receptors, CXCR4* / genetics
  • Receptors, CXCR4* / metabolism
  • Signal Transduction / drug effects
  • Spondylosis / metabolism
  • Spondylosis / pathology

Substances

  • Receptors, CXCR4
  • Chemokine CXCL12
  • CXCL12 protein, rat
  • Cxcr4 protein, rat