4.7 Article

Agathisflavone as a Single Therapy or in Association With Mesenchymal Stem Cells Improves Tissue Repair in a Spinal Cord Injury Model in Rats

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FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.858190

关键词

MSCs; mesenchymal stem cells; agathisflavone; acute spinal cord injury; neurotrophins; regeneration

资金

  1. Foundation for Research Support of the State of Bahia (FAPESB) [RED0016/2013, INT 0016/2016]
  2. Coordination of Personnel Improvement of Higher Level (CAPES) [88881.117666/2016-01]
  3. National Council for Scientific and Technological Development (CNPq, EU Edital MCTI/CNPq/Universal Process EU) [443723/2014-1]
  4. Post-Graduation Program in Biotechnology-State University of Feira de Santana
  5. CAPES [0001]
  6. CNPq [205792/2017-0, 307539/2018-0]
  7. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-Brazil (CAPES) [001]
  8. National Council for Scientific and Technological Development (CNPq, INCT for Excitotoxicity and Neuroprotection)
  9. National Council for Scientific and Technological Development (CNPq, INCT-Translational Neuroscience)

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The study found that Agathisflavone can protect injured spinal cord tissue and exhibit therapeutic effects in a rat model of acute spinal cord injury. It also promotes neurogenesis and increases the expression of neurotrophins while reducing inflammation.
Agathisflavone is a flavonoid with anti-neuroinflammatory and myelinogenic properties, being also capable to induce neurogenesis. This study evaluated the therapeutic effects of agathisflavone-both as a pharmacological therapy administered in vivo and as an in vitro pre-treatment aiming to enhance rat mesenchymal stem cells (r)MSCs properties-in a rat model of acute spinal cord injury (SCI). Adult male Wistar rats (n = 6/group) underwent acute SCI with an F-2 Fogarty catheter and after 4 h were treated daily with agathisflavone (10 mg/kg ip, for 7 days), or administered with a single i.v. dose of 1 x 10(6) rMSCs either unstimulated cells (control) or pretreated with agathisflavone (1 mu M, every 2 days, for 21 days in vitro). Control rats (n = 6/group) were treated with a single dose methylprednisolone (MP, 60 mg/kg ip). BBB scale was used to evaluate the motor functions of the animals; after 7 days of treatment, the SCI area was analyzed after H&E staining, and RT-qPCR was performed to analyze the expression of neurotrophins and arginase. Treatment with agathisflavone alone or with of 21-day agathisflavone-treated rMSCs was able to protect the injured spinal cord tissue, being associated with increased expression of NGF, GDNF and arginase, and reduced macrophage infiltrate. In addition, treatment of animals with agathisflavone alone was able to protect injured spinal cord tissue and to increase expression of neurotrophins, modulating the inflammatory response. These results support a pro-regenerative effect of agathisflavone that holds developmental potential for clinical applications in the future.

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