The protein kinase A signaling pathway mediates the effect of electroacupuncture on excessive contraction of the bladder detrusor in a rat model of neurogenic bladder

Acupunct Med. 2024 Feb;42(1):32-38. doi: 10.1177/09645284231206154. Epub 2023 Oct 29.

Abstract

Background: Neurogenic bladder (NB) is a form of neurological bladder dysfunction characterized by excessive contraction of the bladder detrusor. Protein kinase A (PKA) signaling is involved in the contraction of the detrusor muscle.

Aims: To investigate whether PKA signaling mediates the effect of electroacupuncture (EA) on the excessive contraction of the bladder detrusor in NB.

Methods: Sixty rats were randomly divided into control, sham, NB, NB + EA, and NB + EA + H89 (a PKA receptor antagonist) groups. The modified Hassan Shaker spinal cord transection method was used to generate a NB model. After EA intervention for one week, urodynamic tests were used to evaluate bladder function, hematoxylin and eosin staining was conducted to assess morphological changes, enzyme-linked immunosorbent assay (ELISA) was performed to measure the concentration of PKA, and Western blotting was conducted to measure the protein levels of phosphorylated myosin light chain kinase (p-MLCK)/p-MLC.

Results: The results showed that NB resulted in morphological disruption, impairment of urodynamics, and decreases in the concentration of PKA and the protein levels of p-MLCK/p-MLC. EA reversed the changes induced by NB dysfunction. However, the improvement in urodynamics and the increases in the concentration of PKA and the protein levels of p-MLCK/p-MLC were inhibited by H89.

Conclusion: Our findings indicate that the PKA signaling pathway mediates the beneficial effect of EA on excessive contraction of the bladder detrusor in a rat model of NB.

Keywords: PKA signaling; electroacupuncture; neurogenic bladder; p-MLC; p-MLCK; spinal cord injury.

MeSH terms

  • Animals
  • Cyclic AMP-Dependent Protein Kinases
  • Electroacupuncture*
  • Rats
  • Signal Transduction
  • Spinal Cord Injuries*
  • Urinary Bladder
  • Urinary Bladder, Neurogenic* / etiology
  • Urinary Bladder, Neurogenic* / therapy

Substances

  • N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide
  • Cyclic AMP-Dependent Protein Kinases