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  4. Systemic Administration of Fibroblast Growth Factor 21 Improves the Recovery of Spinal Cord Injury (SCI) in Rats and Attenuates SCI-Induced Autophagy

Systemic Administration of Fibroblast Growth Factor 21 Improves the Recovery of Spinal Cord Injury (SCI) in Rats and Attenuates SCI-Induced Autophagy

Frontiers in Pharmacology, 2021 · DOI: 10.3389/fphar.2020.628369 · Published: January 27, 2021

Spinal Cord InjuryPharmacologyRegenerative Medicine

Simple Explanation

Spinal cord injury (SCI) leads to nerve cell death, hindering recovery. Nerve growth factors can help reduce this death and improve healing. This study explores the potential of fibroblast growth factor 21 (FGF21) in promoting SCI repair in rats. The study found that FGF21, when administered systemically, significantly improved the functional recovery of SCI in rats. This improvement was observed through various assessments, including the BBB scale and inclined plane test. The mechanism behind this improvement involves FGF21's ability to restrain injury-induced cell autophagy. This suggests that systemic administration of FGF21 holds therapeutic potential for SCI repair.

Study Duration
60 days
Participants
40 adult female SD rats
Evidence Level
Not specified

Key Findings

  • 1
    Systemic administration of FGF21 significantly promoted the functional recovery of SCI in rats, as assessed by BBB scale and inclined plane test.
  • 2
    FGF21 attenuated cell death in the injured area, accompanied by increased expression of NeuN, GAP43 and NF200, and decreased expression of GFAP.
  • 3
    FGF21 was found to attenuate the elevated expression level of the autophagy marker LC3-II induced by SCI in a dose-dependent manner.

Research Summary

This study investigates the therapeutic effect of systemic administration of FGF21 on spinal cord injury (SCI) in rats. The results demonstrate that FGF21 promotes functional recovery from SCI, protects neurons and axons, and inhibits SCI-induced autophagy. The study found that FGF21 treatment improves the recovery of spinal cord appearance and hindlimb function. FGF21 treated groups exhibited improved locomotor function, when compared with SCI group. FGF21 administration attenuates autophagy induced by SCI. The expression level LC3-II protein was decreased in FGF21 treated groups in a dose dependent manner, when compared with SCI group.

Practical Implications

Therapeutic Potential for SCI Repair

Systemic administration of FGF21 could serve as a promising therapeutic strategy for spinal cord injury repair.

Targeting Autophagy

FGF21's ability to inhibit SCI-induced autophagy suggests a novel mechanism for neuroprotection in SCI.

Clinical Translation

Further research is warranted to explore the safety and efficacy of FGF21 in human SCI patients.

Study Limitations

  • 1
    The study was conducted on rats, and the results may not be directly applicable to humans.
  • 2
    Further studies are needed to fully elucidate the mechanisms underlying FGF21's therapeutic effects.
  • 3
    The long-term effects of FGF21 administration on SCI recovery were not investigated.

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