Platelet-rich plasma promotes skeletal muscle regeneration and neuromuscular functional reconstitution in a concentration-dependent manner in a rat laceration model

Biochem Biophys Res Commun. 2023 Sep 10:672:185-192. doi: 10.1016/j.bbrc.2023.05.123. Epub 2023 Jun 10.

Abstract

Abnormal function of injured muscle with innervation loss is a challenge in sports medicine. The difficulty of rehabilitation is regenerating and reconstructing the skeletal muscle tissue and the neuromuscular junction (NMJ). Platelet-rich plasma (PRP) releases various growth factors that may provide an appropriate niche for tissue regeneration. However, the specific mechanism of the PRP's efficacy on muscle healing remains unknown. In this study, we injected PRP with different concentration gradients (800, 1200, 1600 × 109 pl/L) or saline into a rat gastrocnemius laceration model. The results of histopathology and neuromyography show that PRP improved myofibers regeneration, facilitated electrophysiological recovery, and reduced fibrosis in a concentration-dependent manner. Furthermore, we found that PRP promotes the activity of satellite cells by upregulating the expression of the myogenic regulatory factor (MyoD, myogenin). Meanwhile, PRP promotes the regeneration and maturation of acetylcholine receptor (AChR) clusters of the Neuromuscular junction (NMJ) on the regenerative myofibers. Finally, we found that the expression of the Agrin, LRP4, and MuSK was upregulated in the PRP-treated groups, which may contribute to AChR cluster regeneration and functional recovery. The conclusions proposed a hypothesis for PRP treatment's efficacy and mechanism in muscle injuries, indicating promising application prospects.

Keywords: Biomaterial; Platelet-rich plasma; Skeletal muscle injury; Sports medicine.

MeSH terms

  • Animals
  • Lacerations* / metabolism
  • Lacerations* / pathology
  • Muscle, Skeletal / pathology
  • Muscular Diseases* / metabolism
  • Neuromuscular Junction / metabolism
  • Platelet-Rich Plasma* / metabolism
  • Rats
  • Receptors, Cholinergic / metabolism

Substances

  • Receptors, Cholinergic