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  4. Modified black phosphorus quantum dots promotes spinal cord injury repair by targeting the AKT signaling pathway

Modified black phosphorus quantum dots promotes spinal cord injury repair by targeting the AKT signaling pathway

Journal of Tissue Engineering, 2023 · DOI: 10.1177/20417314231180033 · Published: June 1, 2023

Spinal Cord InjuryBiomedical

Simple Explanation

Spinal cord injury (SCI) is a serious condition affecting the central nervous system, often caused by trauma. Current treatments have limitations due to inflammation and nerve cell dysfunction. This study explores a new approach using hydrogels containing black phosphorus quantum dots (BPQDs) and Epigallocatechin-3-gallate (EGCG) (E@BP) to reduce inflammation and promote nerve regeneration after SCI. The research demonstrates that E@BP can improve motor function recovery in rats with SCI by reducing inflammation, promoting nerve regeneration, and activating the AKT signaling pathway.

Study Duration
8 weeks
Participants
Male Sprague–Dawley rats (12 weeks old, 320–350 g)
Evidence Level
Not specified

Key Findings

  • 1
    E@BP treatment enhances the structural and functional integrity of spinal cord tracts, leading to improved motor neuron function in SCI rats.
  • 2
    E@BP reduces inflammation in SCI tissues by decreasing the accumulation of astrocytes, microglia, macrophages, and oligodendrocytes.
  • 3
    The mechanism behind E@BP's regenerative and anti-inflammatory effects involves promoting the phosphorylation of key proteins in the AKT signaling pathway.

Research Summary

This study introduces a novel therapeutic approach for spinal cord injury (SCI) using black phosphorus quantum dots (BPQDs) encapsulated within Epigallocatechin-3-gallate (EGCG) hydrogels (E@BP). E@BP demonstrates significant potential in reducing inflammation and promoting neuronal regeneration in SCI rats, leading to improved motor function recovery. The therapeutic effects of E@BP are attributed to the modulation of the AKT signaling pathway, highlighting its potential as a promising treatment option for SCI.

Practical Implications

Potential Therapeutic Agent

E@BP could be further developed as a therapeutic agent for SCI, offering a new approach to reduce inflammation and promote neural regeneration.

AKT Signaling Pathway Target

The study highlights the AKT signaling pathway as a key target for SCI treatment, providing insights for future drug development and therapeutic strategies.

Hydrogel Delivery System

The use of hydrogels as a delivery system for nanomaterials demonstrates a promising approach for targeted drug delivery and tissue engineering applications in SCI.

Study Limitations

  • 1
    The retention time of E@BP in the injury site was limited to less than a week after transplantation.
  • 2
    Sensory function was not assessed.
  • 3
    Potential off-target effects of E@BP were not investigated.

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