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Anales de Otorrinolaringología Mexicana

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2024, Number 3

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Otorrinolaringología 2024; 69 (3)

Effect of brain derived neurotrophic factor on the regeneration of facial nerve

Cristerna SL, Brulé ACD, Olmos ZJR, Silva MM, Gomes-da Silva RP, Gaxiola GM, Romero RLP
Full text How to cite this article

Language: Spanish
References: 21
Page: 163-174
PDF size: 857.82 Kb.


Key words:

Facial paralysis, Brain derived neurotrophic factor, Myelin basic protein, Glial fibrillary acidic protein.

ABSTRACT

Objective: To evaluate the clinical, macroscopic and histological changes and in the expression of myelin basic protein and glial fibrillary acidic protein postneurorraphy of the facial nerve combined with the application of brain derived neurotrophic factor or placement of a sural nerve graft in guinea pigs.
Materials and Methods: An experimental, prospective, longitudinal and comparative study was done at Unit of Experimental Lung Transplant of National Institute of Respiratory Diseases Ismael Cosio Villegas, Mexico City. In 18 guinea pigs, divided into 3 groups of 6 each one, neurorraphy of the left facial nerve was performed and they were treated as follows: Group I: Facial nerve neurorraphy without treatment. Group II: sural nerve graft placement without treatment. Group III: Facial nerve neurorraphy and brain derived neurotrophic factor. The study lasted 12 weeks and eyelid closure, vibrissa movements, infection, necrosis, adhesions and fibrosis of the anastomosis were evaluated. Study was done from January 1st, 2022 to January 31, 2023.
Results: Group III showed better clinical evolution in a shorter time, less macroscopic and microscopic fibrosis, better axonal regeneration and neovascularization. The 3 groups showed similar expression of myelin basic protein and glial fibrillary acidic protein.
Conclusions: Facial nerve neurorraphy in guinea pigs combined with the application of brain derived neurotrophic factor reduces the degree of facial paralysis in a shorter time and favors the healing of the neurorraphy with less fibrosis and better axonal regeneration than the neurorraphy without treatment and sural graft placement without treatment, but it does not originate changes in the production of basic protein and glial fibrillary acidic protein.


REFERENCES

  1. Ho ML, Juliano A, Eisenberg EL, Moonis G. Anatomy and pathology of the facial nerve. AJR Am J Roentgenol 2015; 204: W612-9. doi: 10.2214/AJR.14.13444

  2. León Rojas DE, León Rodríguez SN, Gutiérrez Ortega FH, Torres Criollo LM. Parálisis facial. En: TorresCriollo LM, Álvarez Ochoa RI, Pérez Ramírez JE. Medicina de Urgencias Tomo 2. 1ª ed. Puerto Madero. LaPlata, Argentina, 2022: 173-183.

  3. Sebben AD, Lichtenfels M, da Silva JL. Peripheral nerve regeneration: cell therapy and neurotrophic factors.Rev Bras Ortop 2015; 46 (6): 643-9. doi: 10.1016/S2255-4971(15)30319-0

  4. Estados Unidos Mexicanos. AFÍA. Especificaciones Técnicas para la Producción, Cuidado y Uso de Animalesde Laboratorio de la Norma Oficial Mexicana NOM-062-ZOO-1999. Diario Oficial de la Federación 6 dic, 1999.

  5. National Institutes of Health USA. Guía para el Cuidado y Uso de los Animales de Laboratorio. Departmentof Health and Human Services, Public Health Service, National Institutes of Health USA. Edición mexicanaauspiciada por la Academia Nacional de Medicina. México, 2002.

  6. Dew LA, Shelton C. Iatrogenic facial nerve injury: prevalence and predisposing factors. Ear Nose Throat J1996; 75 (11): 724-9.

  7. Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG. improving bioscience research reporting: The ARRIVEGuidelines for Reporting Animal Research. PLoSBiol 2010; 8 (6): e1000412. doi:10.1371/journal.pbio.1000412

  8. Veiga A, Rendal M, Matheu G, Andión C, et al. Cambios histopatológicos en arterias humanas sometidas a procesosde isquemia fría y criopreservación. Angiología 2004; 56 (2): 97-105. DOI: 10.1016/S0003-3170(04)74854-3

  9. Zamzam, SM, Hassouna MS, Elsawy MK, Gafaar SH. Correction: Otolaryngologists and iatrogenic facialnerve injury: a meta-analysis. Egypt J Otolaryngol 2023; 39: 85. https://doi.org/10.1186/s43163-023-00450-y

  10. Prats Golczer VE. Efectividad del tratamiento rehabilitador en pacientes con parálisis del nervio facial postparotidectomíay su impacto en la calidad de vida. Tesis Doctoral. Universidad de Sevilla, Sevilla, España, 2015.

  11. Myckatyn TM, Mackinnon SE. The surgical management of facial nerve injury. Clin Plast Surg 2003; 30(2): 307-318. doi: 10.1016/s0094-1298(02)00102-5

  12. Rovak JM, Tung TH, Mackinnon SE. The surgical management of facial nerve injury. Semin Plast Surg.2004; 18(1): 23-30. doi: 10.1055/s-2004-823120

  13. Cui Y, Lu C, Meng D, et al. Collagen scaffolds modified with CNTF and bFGF promote facial nerve regenerationin minipigs. Biomaterials 2014; 35 (27): 7819-27. doi: 10.1016/j.biomaterials.2014.05.065

  14. Shi ZL, Fan ZY, Zhang H, Li ST, et al. Localized delivery of brain derived neurotrophic factor from PLGAmicrospheres promotes peripheral nerve regeneration in rats. J Orthop Surg Res 2022; 17 (1): 172. https://doi.org/10.1186/s13018-022-02985-x

  15. Daradka MH, Bani Ismail ZA, Irsheid MA. Peripheral nerve regeneration: A comparative study of the effectsof autologous bone marrow-derived mesenchymal stem cells, platelet-rich plasma, and lateral saphenousvein graft as a conduit in a dog model. Open Vet J 2021; 11 (4): 686-694. doi: 10.5455/OVJ.2021.v11.i4.20

  16. García Medrano B. Regeneración de las lesiones críticas del nervio periférico con factores de crecimiento.Estudio experimental. Tesis Doctorado. Universidad de Valladolid. Valladolid, España, 2013.

  17. Fletcher JL, Murray SS, Xiao J. Brain-derived neurotrophic factor in central nervous system myelination: A newmechanism to promote myelin plasticity and repair. Int J Mol Sci 2018; 19 (12): 4131. doi: 10.3390/ijms19124131

  18. Moir MS, Wang MZ, To M, Lum J, Terris DJ. Delayed repair of transected nerves: effect of brain-derivedneurotrophic factor. Arch Otolaryngol Head Neck Surg 2000; 126 (4): 501-505. doi: 10.1001/archotol.126.4.501

  19. Yang Z, Wang KK. Glial fibrillary acidic protein: from intermediate filament assembly and gliosis to neurobiomarker.Trends Neurosci 2015; 38 (6): 364-374. doi: 10.1016/j.tins.2015.04.003

  20. Triolo D, Dina G, Lorenzetti I, et al. Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferationand delays nerve regeneration after damage. J Cell Sci 2006; 119 (Pt 19): 3981-3993. doi: 10.1242/jcs.03168

  21. Jessen KR, Mirsky R. The repair Schwann cell and its function in regenerating nerves. J Physiol 2016; 594(13): 3521-3531. doi: 10.1113/JP270874




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Otorrinolaringología. 2024;69