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  4. The Effect of Collagen and Fibrin Hydrogels Encapsulated with Adipose Tissue Mesenchymal Stem Cell-Derived Exosomes for Treatment of Spinal Cord Injury in a Rat Model

The Effect of Collagen and Fibrin Hydrogels Encapsulated with Adipose Tissue Mesenchymal Stem Cell-Derived Exosomes for Treatment of Spinal Cord Injury in a Rat Model

Iran. J. Biotechnol., 2023 · DOI: 10.30498/ijb.2023.362229.3505 · Published: July 1, 2023

Regenerative MedicineNeurologyBiomedical

Simple Explanation

This study explores a potential new treatment for spinal cord injuries (SCI) using exosomes derived from mesenchymal stem cells (MSCs). These exosomes, which are tiny vesicles released by cells, are encapsulated within collagen and fibrin hydrogels, which are biocompatible scaffolds. The researchers tested this approach on rats with SCI and compared the results to a control group that did not receive the treatment. They assessed clinical function, histological changes, and molecular markers to evaluate the effectiveness of the hydrogel-encapsulated exosomes. The study found that rats treated with AD-MSC-DE encapsulated into fibrin and collagen groups showed better clinical function than the control group.

Study Duration
4 weeks
Participants
18 adult male Wister rats
Evidence Level
Not specified

Key Findings

  • 1
    AD-MSC-DE encapsulated into fibrin and collagen hydrogels improved clinical function in SCI rats compared to the control group.
  • 2
    The treatment improved SCI-induced polio and leuko-myelomalacia and led to higher expression of NF protein.
  • 3
    AD-MSC-DE in collagen and fibrin hydrogels upregulated the mean levels of NEFL, eNOS, and CK19 mRNAs compared to the control group.

Research Summary

This study investigated the therapeutic potential of AD-MSC-DE encapsulated within collagen and fibrin hydrogels for treating spinal cord injury (SCI) in a rat model. The results demonstrated that AD-MSC-DE, when encapsulated within these hydrogels, promoted nerve regeneration, reduced spinal cord lesion-induced central neuropathic pain, and improved clinical function in SCI rats compared to the control group. The study concludes that AD-MSC-DE combined with hydrogels is a promising method for SCI treatment, with no significant difference between collagen and fibrin hydrogels in terms of therapeutic efficacy.

Practical Implications

Potential SCI Therapy

The use of AD-MSC-DE encapsulated in collagen or fibrin hydrogels presents a potential therapeutic strategy for SCI.

Hydrogel Delivery System

Hydrogels serve as an effective delivery system for exosomes, promoting nerve regeneration and reducing neuropathic pain.

Clinical Translation

Further research is warranted to explore the clinical application of this approach in preclinical or human clinical trials.

Study Limitations

  • 1
    Limited to a rat model; findings may not directly translate to humans.
  • 2
    The exact mechanisms of action of the exosomes and hydrogels need further investigation.
  • 3
    Long-term effects of the treatment were not assessed in this study.

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