Chinese Journal of Tissue Engineering Research ›› 2023, Vol. 27 ›› Issue (16): 2518-2524.doi: 10.12307/2023.168

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Repair effect of poly(lactic-co-glycolic acid) nanospheres with sustained-release of neurotrophin-3 and ganglioside GD1a on spinal cord injury in rats

Xia Yu1, 2, Sun Jia2, Qi Zhengyan1, 2, Ma Lin1, 2, Ma Wenqian2, Niu Jianguo1, 2, Wen Yujun1, 2   

  1. 1Department of Human Anatomy and Histology Embryology, School of Basic Medicine, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China; 2Ningxia Key Laboratory of Craniocerebral Diseases, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China
  • Received:2022-04-09 Accepted:2022-06-08 Online:2023-06-08 Published:2022-11-10
  • Contact: Wen Yujun, Professor, Master’s supervisor, Department of Human Anatomy and Histology Embryology, School of Basic Medicine, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China; Ningxia Key Laboratory of Craniocerebral Diseases, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China
  • About author:Xia Yu, Master candidate, Department of Human Anatomy and Histology Embryology, School of Basic Medicine, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China; Ningxia Key Laboratory of Craniocerebral Diseases, Ningxia Medical University, Yinchuan 750004, Ningxia Hui Autonomous Region, China
  • Supported by:
    Ningxia Natural Science Foundation Project, No. 2020AAC03182 (to WYJ); National Natural Science Foundation of China, No. 81660216 (to WYJ); Ningxia Key Research & Development Program, No. 2021BEG03096 (to WYJ)

Abstract: BACKGROUND: Non-invasive treatment of spinal cord injury needs to be developed urgently. Nanomaterials have obvious advantages, which can deliver drugs and improve the therapeutic effect.
OBJECTIVE: To fabricate sustained-release nanospheres containing neurotrophin-3 and ganglioside GD1a by poly(lactic-co-glycolic acid) and investigate their effects on the repair of spinal cord injury in rats.
METHODS: Poly(lactic-co-glycolic acid) nanospheres encapsulated with neurotrophin-3 and ganglioside GD1a were prepared using oil-water emulsion volatile organic solvent method. The sustained release properties of microspheres were tested. Sixty female adult SD rats were randomly divided into five groups with 12 rats in each group. In the sham operation group, the lamina was opened and sutured directly. In the spinal cord injury group, a spinal cord T9 impingement injury model was established. In the neurotrophin group, the nanosphere suspension of slow-release neurotrophin-3 was injected into the injured area of spinal cord T9. In the ganglioside GD1a group, the sustained-release ganglioside GD1a nanosphere suspension was injected into the spinal cord T9 injury area. The experimental group was injected with nanosphere suspension of sustained-release neurotrophin-3 and ganglioside GD1a in the injured area of spinal cord T9. Open field test and BBB scoring were conducted weekly after operation. The sections were taken 4 and 8 weeks after surgery for morphological observation.
RESULTS AND CONCLUSION: (1) After soaking in PBS for 14 days in vitro, the sustained-release nanospheres could continuously release neurotrophin-3 and ganglioside GD1a. (2) At 7 and 8 weeks after surgery, compared with the spinal cord injury group, the BBB score and the total open field distance of the rats increased in the neurotrophin group and the experimental group (P < 0.05). The results of Nissl staining showed that at 4 and 8 weeks after surgery, the number of motor neurons increased in the anterior horn of caudal gray matter in the experimental group compared with the spinal cord injury group (P < 0.05). At 8 weeks after surgery, the number of motor neurons increased in the anterior horn of caudal gray matter in the neurotrophin group compared with the spinal cord injury group (P < 0.05). The results of immunofluorescence staining showed that compared with the spinal cord injury group, the neurotrophin group at 8 weeks and the experimental group at 4 and 8 weeks had increased spinal white matter ventral nerve fibers (P < 0.05); the expression of myelin basic protein on the ventral side of the spinal cord white matter increased at 4 and 8 weeks in the ganglioside GD1a and experimental groups (P < 0.05); the expression of myelin basic protein in the neurotrophin group increased at 8 weeks after operation (P < 0.05); the descending propriospinal tract increased in the neurotrophin group and the experimental group at 8 weeks (P < 0.05). (3) The results showed that neurotrophin-3 microspheres alone or in combination with ganglioside GD1a microspheres could promote the survival of motor neurons and nerve fibers around the spinal cord injury site and improve the motor function of the hind limbs of rats.

Key words: spinal cord injury, neurotrophin-3, gangliosides, poly(lactic-co-glycolic acid), tissue engineering, nerve regeneration

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