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Вопросы реконструктивной и пластической хирургии

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Современные подходы к регенерации периферических нервов и спинного мозга (обзор литературы)

https://doi.org/10.52581/1814-1471/96/09

Аннотация

Цель исследования: обобщить современные подходы к регенерации нервной ткани с акцентом на роль биомиметических и наноструктурированных материалов, определить их потенциал и ограничения для применения в реконструктивной нейрохирургии.

Материал и методы. Проведён нарративный обзор публикаций в базах данных PubMed, Scopus и Web of Science за период 2020–2025 гг. по ключевым словам: «периферические нервы», «спинной мозг», «нейрорегенерация», «биоматериалы», «нервные кондуиты», «наноматериалы». В анализ были включены экспериментальные и клинические исследования, а также обзоры и метаанализы, посвящённые тканевой инженерии и нейрохирургическим методам восстановления. Оценены архитектура материалов, механизмы регенерации и параметры эффективности.

Результаты. Установлено, что наибольший потенциал в направленной регенерации периферических нервов демонстрируют биомиметические материалы, имитирующие внеклеточный матрикс и создающие направляющую структуру для роста аксонов. Наноструктурированные и функционализированные кондуиты, содержащие факторы роста, клеточные элементы и проводящие компоненты, улучшают регенерацию периферических нервов и частично восстанавливают проводимость повреждённого спинного мозга.

Заключение. Биоинженерные подходы на основе наноструктурированных и биомиметических кондуитов расширяют возможности реконструктивной нейрохирургии. Перспективным направлением является определение оптимальных комбинаций материалов и биологически активных факторов, обеспечивающих перенос результатов экспериментальных исследований в клиническую практику.

Об авторах

М. А. Габриянчик
Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)
Россия

Габриянчик Марк Александрович – мл. научн. сотрудник Института кластерной онкологии им. профессора Л.Л. Лёвшина 

119991, г. Москва, ул. Трубецкая, д. 8, стр. 2



О. И. Старцева
Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)
Россия

Старцева Олеся Игоревна – д-р мед. наук, профессор кафедры онкологии, радиотерапии и реконструктивной хирургии Института клинической медицины им. Н.В. Склифосовского; врач-онколог онкологического отделения №1  

119991, г. Москва, ул. Трубецкая, д. 8, стр. 2; 115487, г. Москва, Коломенский проезд, д. 7



М. В. Головань
Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)
Россия

Головань Марина Васильевна – студентка 4-го курса Института клинической медицины им. Н.В. Склифосовского 

119991, г. Москва, ул. Трубецкая, д. 8, стр. 2



В. О. Лысенко
Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)
Россия

Лысенко Владислав Олегович – студент 4-го курса Института клинической медицины им. Н.В. Склифосовского 

119991, г. Москва, ул. Трубецкая, д. 8, стр. 2



К. С. Пирогов
Российский национальный исследовательский медицинский университет им. Н.И. Пирогова
Россия

Пирогов Кирилл Станиславович – студент 4-го курса Института клинической медицины

117513, г. Москва, ул. Островитянова, д. 1



И. В. Решетов
Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)
Россия

Решетов Игорь Владимирович – д-р мед. наук, профессор, академик РАН, директор Института кластерной онкологии им. Л.Л. Левшина, зав. кафедрой онкологии, радиотерапии и реконструктивной хирургии Института клинической медицины им. Н.В. Склифосовского 

119991, г. Москва, ул. Трубецкая, д. 8, стр. 2



Список литературы

1. Li R., Liu Z., Pan Y., Chen L., Zhang Z., Lu L. Peripheral nerve injuries treatment: a systematic review. Cell Biochemistry and Biophysics, 2014;68(3):449-454. https://doi.org/10.1007/s12013-013-9742-1

2. Irisarri C. History of peripheral nerve injuries. The Journal of Hand Surgery, European volume. 2024; 49(6):812-823. https://doi.org/10.1177/17531934231198455

3. Scheib J., Höke A. Advances in peripheral nerve regeneration. Nat Rev Neurol. 2013;9(12):668-676. doi: 10.1038/nrneurol.2013.227

4. Cristante A.F., Barros Filho T.E., Marcon R.M., Letaif O.B., Rocha I.D. Therapeutic approaches for spinal cord injury. Clinics (Sao Paulo). 2012;67(10):1219-1224. https://doi.org/10.6061/clinics/2012(10)16

5. Yan S., Zhao P., Yu T., Gu N. Current applications and future prospects of nanotechnology in cancer immunotherapy. Cancer Biol Med. 2019;16(3):486-497. https://doi.org/10.20892/j.issn.2095-3941.2018.0493

6. Kang N.U., Lee S.J., Gwak S.J. Fabrication Techniques of Nerve Guidance Conduits for Nerve Regeneration. Yonsei Med J. 2022;63(2):114-123. doi: 10.3349/ymj.2022.63.2.114

7. Büyükuysal O.G., Çağlar Z., Aydın H.M. Biomaterials for Nerve Tissue Engineering. In: Sağlam N., Korkusuz F., Şam M. (eds). Nano-Biomaterials in Tissue Repair and Regeneration. Tissue Repair and Reconstruction. Springer, Singapore, 2024. https://doi.org/10.1007/978-981-97-7600-9_5

8. Gordon T. Electrical Stimulation to Enhance Axon Regeneration After Peripheral Nerve Injuries in Animal Models and Humans. Neurotherapeutics. 2016;13(2):295-310. https://doi.org/10.1007/s13311-015-0415-1

9. Seddon H.J. Surgical Disorders of the Peripheral Nerves. Edinburgh: Churchill Livingstone, 1975.

10. Sunderland S. Nerves and Nerve Injuries. Edinburgh: Churchill Livingstone, 1968.

11. Chen Z.L., Yu W.M., Strickland S. Peripheral regeneration. Annu Rev Neurosci. 2007;30:209-233. doi: 10.1146/annurev.neuro.30.051606.094337

12. Wu D., Murashov A.K. Molecular mechanisms of peripheral nerve regeneration: emerging roles of microRNAs. Front Physiol. 2013;4:55. Published 2013 Apr 1. https://doi.org/10.3389/fphys.2013.00055

13. Zeng C.W., Zhang C.L. Neuronal regeneration after injury: a new perspective on gene therapy. Front Neurosci. 2023;17:1181816. Published 2023 Apr 21. https://doi.org/10.3389/fnins.2023.1181816

14. Jalise S.Z., Habibi S., Fath-Bayati L. et al. Role and Interplay of Different Signaling Pathways Involved in Sciatic Nerve Regeneration. J Mol Neurosci. 2024;74:108. https://doi.org/10.1007/s12031-024-02286-4

15. Si Z.Z., Zou C.J., Mei X., et al. Targeting neuroinflammation in Alzheimer's disease: from mechanisms to clinical applications. Neural Regen Res. 2023;18(4):708-715. https://doi.org/10.4103/1673-5374.353484

16. Gordon T. Physiology of Nerve Regeneration: Key Factors Affecting Clinical Outcomes. Hand Clin. 2024;40(3):337-345. https://doi.org/10.1016/j.hcl.2024.03.001

17. Jahromi M., Razavi S., Bakhtiari A. The advances in nerve tissue engineering: From fabrication of nerve conduit to in vivo nerve regeneration assays. J Tissue Eng Regen Med. 2019;13(11):2077-2100. doi: 10.1002/term.2945

18. Rigby M.J., Gomez T.M., Puglielli L. Glial Cell-Axonal Growth Cone Interactions in Neurodevelopment and Regeneration. Front Neurosci. 2020;14:203. Published 2020 Mar 10. https://doi.org/10.3389/fnins.2020.00203

19. Nocera G., Jacob C. Mechanisms of Schwann cell plasticity involved in peripheral nerve repair after injury. Cell Mol Life Sci. 2020;77(20):3977-3989. https://doi.org/10.1007/s00018-020-03516-9

20. Widodo W., Aprilya D., Satria O. Regenerative Medicine: A New Horizon in Peripheral Nerve Injury and Repair. Orthop Rev (Pavia). 2025;17:133572. Published 2025 Mar 31. https://doi.org/10.52965/001c.133572

21. Jeon SM, Pradeep A, Chang D, et al. Skin Reinnervation by Collateral Sprouting Following Spared Nerve Injury in Mice. J Neurosci. 2024;44(15):e1494232024. Published 2024 Apr 10. doi: 10.1523/JNEUROSCI.1494-23.2024

22. Karumbaiah L., Bellamkonda R. Neural Tissue Engineering. In: Neural Engineering. Springer, 2012. P. 765–794. https://doi.org/10.1007/978-1-4614-5227-0_19

23. Duraku L.S., Eberlin K.R., Moore A., et al. Ten Myths in Nerve Surgery. Plast Reconstr Surg Glob Open. 2024;12(8):e6017. Published 2024 Aug 1. https://doi.org/10.1097/GOX.0000000000006017

24. Zhai X., Wang Y. Physical modulation and peripheral nerve regeneration: a literature review. Cell Regen. 2024;13:32. doi: 10.1186/s13619-024-00215-9

25. Mahdian M., Tabatabai T.S., Abpeikar Z., Rezakhani L, Khazaei M. Nerve regeneration using decellularized tissues: challenges and opportunities. Front Neurosci. 2023;17:1295563. Published 2023 Oct 19. https://doi.org/10.3389/fnins.2023.1295563

26. Uyeda A., Muramatsu R. Molecular mechanisms of central nervous system axonal regeneration and remyelination: a review. Int J Mol Sci. 2020;21:8116, https://doi.org/10.3390/ijms21218116

27. Jacobi A., Tran N.M., Yan W., et al. Overlapping transcriptional programs promote survival and axonal regeneration of injured retinal ganglion cells. Neuron. 2022;110(16):2625-2645.e7. https://doi.org/10.1016/j.neuron.2022.06.002

28. Zheng F., Li R., He Q., Koral K., Tao J., Fan L., Xiang R., Ma J., Wang N., Yin Y., Huang Z., Xu P., Xu H. The electrostimulation and scar inhibition effect of chitosan/oxidized hydroxyethyl cellulose/reduced graphene oxide/ asiaticoside liposome based hydrogel on peripheral nerve regeneration in vitro. Materials Science & Engineering. C, Materials for biological applications. 2020;109:110560. https://doi.org/10.1016/j.msec.2019.110560

29. Kaplan B., Levenberg S. The Role of Biomaterials in Peripheral Nerve and Spinal Cord Injury: A Review. International Journal of Molecular Sciences. 2022;23(3):1244. https://doi.org/10.3390/ijms23031244

30. Costăchescu B., Niculescu A.G., Dabija M.G., Teleanu R.I., Grumezescu A.M., Eva L. Novel Strategies for Spinal Cord Regeneration. International Journal of Molecular Sciences. 2022;23(9):4552. doi: 10.3390/ijms23094552

31. Lee J., Nguyen S., Bhattacharya S. Optic nerve regeneration: Potential treatment approaches. Current Opinion in Pharmacology. 2024;74:102428. https://doi.org/10.1016/j.coph.2023.102428

32. Robinson J., Fisher D. Facial Nerve Reconstruction Using Acellular Nerve Allograft. J Craniofac Surg. 2022;33(4):413-414. doi: 10.1097/SCS.0000000000008313

33. Xu T., Liu C., Deng S., Gan L., Zhang Z., Yang G.Y., Tian H., Tang Y. The roles of microglia and astrocytes in myelin phagocytosis in the central nervous system. Journal of Cerebral Blood Flow and Metabolism. 2023;43(3):325-340. https://doi.org/10.1177/0271678X221137762

34. Pettigrew D.B., Singh N., Kirthivasan S., Crutcher K.A. The Role of Tissue Geometry in Spinal Cord Regeneration. Medicina (Kaunas), 2022;58(4):542. https://doi.org/10.3390/medicina58040542

35. Rui J., Zhou Y.J., Zhao X., Li J.F., Gu Y.D., Lao J. Endogenous automatic nerve discharge promotes nerve repair: an optimized animal model. Neural Regeneration Res. 2019;14(2):306-312. https://doi.org/10.4103/1673-5374.244802

36. Bellaire C. P., Inglesby D.C., Marayati N.F., Warburton A.J., Melamed E. Trends in Peripheral Nerve Epidemiology and Reconstruction: A State Database Study of Direct Repairs, Grafts, and Conduits. Annals of Plastic Surgery. 2021;87(2):179-186. https://doi.org/10.1097/SAP.0000000000002823

37. Heinzel J.C., Quyen Nguyen M., Kefalianakis L., et al. A systematic review and meta-analysis of studies comparing muscle-in-vein conduits with autologous nerve grafts for nerve reconstruction. Sci Rep.2021;11:11691. https://doi.org/10.1038/s41598-021-90956-3

38. Houschyar K.S., Momeni A., Pyles M.N., Cha J.Y., Maan Z.N., Duscher D., Jew O.S., Siemers F., van Schoonhoven J. The Role of Current Techniques and Concepts in Peripheral Nerve Repair. Plast Surg Int. 2016:4175293. https://doi.org/10.1155/2016/4175293

39. Pan D., Mackinnon S.E., Wood M.D. Advances in the repair of segmental nerve injuries and trends in reconstruction. Muscle Nerve. 2020;61:726-739. https://doi.org/10.1002/mus.26797

40. Heinzel J.C., Oberhauser V., Keibl C., Schädl B., Swiadek N.V., et al. ESWT Diminishes Axonal Regeneration following Repair of the Rat Median Nerve with Muscle-In-Vein Conduits but Not after Autologous Nerve Grafting. Biomedicines. 2022;10:1777. https://doi.org/10.3390/biomedicines10081777

41. Bedar M., Saffari T.M., Mathot F., Shin A.Y. Functional outcomes of nerve allografts augmented with mesenchymal stem cells and surgical angiogenesis in a rat sciatic nerve defect model. J Plast Reconstr Aesthet Surg. 2023;87:329-338. https://doi.org/10.1016/j.bjps.2023.10.054

42. Broeren B.O., Hundepool C.A., Kumas A.H., Duraku L.S., Walbeehm E.T., et al. The effectiveness of acellular nerve allografts compared to autografts in animal models: A systematic review and meta-analysis. PLoS ONE. 2024;19(1):e0279324. https://doi.org/10.1371/journal.pone.0279324

43. Schäfer B., Freund G., Bahm J., Beier J.P. Robotic microsurgery for pediatric peripheral nerve surgery. J Robot Surg. 2024;18(1):388. https://doi.org/10.1007/s11701-024-02140-0

44. Oberlin C., Durand S., Belheyar Z., Shafi M., David E., Asfazadourian H. Nerve transfers in brachial plexus palsies. Chir Main. 2009;28(1):1-9. https://doi.org/10.1016/j.main.2008.11.010

45. Iamaguchi R.B., Arranz M.V., Mattar Junior R. Hand reanimation: functional free gracilis transfer or transfer of the distal tendon of the biceps to the flexor digitorum profundus and flexor pollicis longus as surgical options. Einstein (Sao Paulo). 2024;22:eAO0719. https://doi.org/10.31744/einstein_journal/2024AO0719

46. Koshima I., Narushima M., Mihara M., Uchida G., Nakagawa M. Fascicular turnover flap for nerve gaps. J Plast Reconstr Aesthet Surg. 2010;63(6):1008-14. https://doi.org/10.1016/j.bjps.2009.02.083

47. Ferry A.M., Manfro G., Dias F.L., Teixeira G.V., Cernea C.R., Abu-Ghname A., Maricevich M. Fascicular Turnover Flap: An Approach for Facial Nerve Reconstruction. J Craniofac Surg. 2021;32(6):e560-e562. https://doi.org/10.1097/SCS.0000000000007638

48. Zhang X., Zhang S., Wang T. How the mechanical microenvironment of stem cell growth affects their differentiation: a review. Stem Cell Research & Therapy. 2022;13(1):415. https://doi.org/10.1186/s13287-022-03070-0

49. Maruyama H., Fujiwara K., Kumeta M., Koyama D. Ultrasonic control of neurite outgrowth direction. Scientific Reports. 2021; 11(1):20099. https://doi.org/10.1038/s41598-021-99711-0

50. Tominami K., Kudo T.A., Noguchi T., Hayashi Y., Luo Y.R., Tanaka T., Matsushita A., Izumi S., Sato H., Gengyo-Ando K., Matsuzawa A., Hong G., Nakai J. Physical Stimulation Methods Developed for In Vitro Neuronal Differentiation Studies of PC12 Cells: A Comprehensive Review. International Journal of Molecular Sciences. 2024;25(2):772. https://doi.org/10.3390/ijms25020772

51. Zuo K.J., Gordon T., Chan K.M., Borschel G.H. Electrical stimulation to enhance peripheral nerve regeneration: Update in molecular investigations and clinical translation. Experimental Neurology. 2020;332:113397. https://doi.org/10.1016/j.expneurol.2020.113397

52. Uz M., Hondred J., Donta M., Jung J., Kozik E., Green J., Sandquist E., Sakaguchi D., Claussen J., Mallapragada S. Determination of Electrical Stimuli Parameters To Transdifferentiate Genetically Engineered Mesenchymal Stem Cells into Neuronal or Glial Lineages. Regenerative Engineering and Translational Medicine. 2019;6. https://doi.org/10.1007/s40883-019-00126-1

53. King E.S., Tang A.D. Intrinsic Plasticity Mechanisms of Repetitive Transcranial Magnetic Stimulation. The Neuroscientist: a review journal bringing neurobiology, neurology and psychiatry. 2024;30(2):260-274. https://doi.org/10.1177/10738584221118262

54. Fu Y., Wang X., Chen X., Wu S. Transcranial iTBS Combined With Trans-Spinal iTBS Targeting PDE1A/cAMP/PKA Axis Regulates Neural Regeneration After Spinal Cord Injury. CNS Neuroscience & Therapeutics. 2025;31(7):e70525. https://doi.org/10.1111/cns.70525

55. Yoo M.C., Chon J., Jung J., Kim S.S., Bae S., Kim S. H., Yeo S.G. Potential Therapeutic Strategies and Substances for Facial Nerve Regeneration Based on Preclinical Studies. International journal of molecular sciences. 2021;22(9):4926. https://doi.org/10.3390/ijms22094926

56. Sharifi M., Kamalabadi-Farahani M., Salehi M., Ebrahimi-Brough S., Alizadeh M. Recent perspectives on the synergy of mesenchymal stem cells with micro/nano strategies in peripheral nerve regeneration-a review. Frontiers in Bioengineering and Biotechnology. 2024;12: 1401512. https://doi.org/10.3389/fbioe.2024.1401512

57. Wan T., Li Q.C., Zhang F.S., Zhang X.M., Han N., Zhang P.X. Biomimetic ECM nerve guidance conduit with dynamic 3D interconnected porous network and sustained IGF-1 delivery for enhanced peripheral nerve regeneration and immune modulation. Materials Today. Bio. 2024;30:101403. https://doi.org/10.1016/j.mtbio.2024.101403

58. Daeschler S.C., So K.J.W., Feinberg K., Manoraj M., Cheung J., Zhang J., Mirmoeini K., Santerre J.P., Gordon T., Borschel G.H. A functional tacrolimus-releasing nerve wrap for enhancing nerve regeneration following surgical nerve repair. Neural Regeneration Research. 2025;20(1):291-304. https://doi.org/10.4103/NRR.NRRD-22-01198

59. Al-Saedi H.F., Panahi Y., Ghanimi H.A., Abdolmaleki A., Asadi A. Enhancement of nerve regeneration with nimodipine treatment after sciatic nerve injury. Fundamental & Clinical Pharmacology. 2023;37(1):107-115. https://doi.org/10.1111/fcp.12827

60. Evaniew N., Noonan V.K., Fallah N., Kwon B.K., Rivers C.S., Ahn H., Bailey C.S., Christie S.D., Fourney D.R., Hurlbert R.J., Linassi A.G., Fehlings M.G., Dvorak M.F., & RHSCIR Network. Methylprednisolone for the Treatment of Patients with Acute Spinal Cord Injuries: A Propensity Score-Matched Cohort Study from a Canadian Multi-Center Spinal Cord Injury Registry. Journal of Neurotrauma. 2015;32(21):1674-1683. https://doi.org/10.1089/neu.2015.3963

61. Kato K., Liu H., Kikuchi S., Myers R.R., Shubayev V.I. Immediate anti-tumor necrosis factor-alpha (etanercept) therapy enhances axonal regeneration after sciatic nerve crush. Journal of Neuroscience Research. 2010;88(2):360-368. https://doi.org/10.1002/jnr.22202

62. Leonardi R., Villari L., Bernasconi G., Piacentini C., Baciliero U., Travali S. Cellular S-100 protein immunostaining in human dysfunctional temporomandibular joint discs. Archives of Oral Biology, 2000;45(5):411-418. https://doi.org/10.1016/s0003-9969(99)00144-2

63. Sanchez Rezza A., Kulahci Y., Gorantla V.S., Zor F., Drzeniek N.M. Implantable Biomaterials for Peripheral Nerve Regeneration-Technology Trends and Translational Tribulations. Frontiers in Bioengineering and Biotechnology. 2022;10:863969. https://doi.org/10.3389/fbioe.2022.863969

64. Mendibil U., Ruiz-Hernandez R., Retegi-Carrion S., Garcia-Urquia N., Olalde-Graells B., Abarrategi A. Tissue-Specific Decellularization Methods: Rationale and Strategies to Achieve Regenerative Compounds. International Journal of Molecular Sciences. 2020;21(15):5447. https://doi.org/10.3390/ijms21155447

65. Khazaei F., Rezakhani L., Alizadeh M., Mahdavian E., Khazaei M. Exosomes and exosome-loaded scaffolds: Characterization and application in modern regenerative medicine. Tissue & Cell. 2023;80:102007. https://doi.org/10.1016/j.tice.2022.102007

66. Gareev K.G., Grouzdev D.S., Koziaeva V.V., Sitkov N.O., Gao H., Zimina T.M., Shevtsov M. Biomimetic Nanomaterials: Diversity, Technology, and Biomedical Applications. Nanomaterials (Basel, Switzerland). 2022;12(14):2485. https://doi.org/10.3390/nano12142485

67. Perrelle J.M., Boreland A.J., Gamboa J.M., Gowda P., Murthy N.S. Biomimetic Strategies for Peripheral Nerve Injury Repair: An Exploration of Microarchitecture and Cellularization. Biomedical Materials & Devices (New York.). 2023;1(1):21-37. https://doi.org/10.1007/s44174-022-00039-8

68. Stocco E., Barbon S., Zamuner A., Confalonieri M., Tiengo C., De Caro R., Macchi V., Dettin M., Porzionato A. Self-assembling peptides for sciatic nerve regeneration: a review of conduit microenvironment modeling strategies in preclinical studies. Front. Cell Dev. Biol. 2025;3:1637189. https://doi.org/10.3389/fcell.2025.1637189

69. Sandoval-Castellanos A.M., Claeyssens F., Haycock J.W. Biomimetic surface delivery of NGF and BDNF to enhance neurite outgrowth. Biotechnology and Bioengineering, 2020;117(10):3124-3135. https://doi.org/10.1002/bit.27466

70. Tauser R.G., Lupascu F.G., Profire B.S., Iacob A.T., Vasincu I.M., Apotrosoaei M., Chirliu O.M., Lupascu D., Profire L. Aptamer-Nanoconjugates as Potential Theranostics in Major Neuro-Oncological and Neurodegenerative Disorders. Pharmaceutics. 2025;17(9):1106. https://doi.org/10.3390/pharmaceutics17091106

71. Ahmed Z., Morgan-Warren P.J., Berry M., Scott R. A.H., Logan A. Effects of siRNA-Mediated Knockdown of GSK3β on Retinal Ganglion Cell Survival and Neurite/Axon Growth. Cells. 2019;8(9):956. https://doi.org/10.3390/cells8090956

72. Ahmed Z., Suggate E.L., Logan A., Berry M. Retinal Ganglion Cell Survival and Axon Regeneration after Optic Nerve Transection is Driven by Cellular Intravitreal Sciatic Nerve Grafts. Cells. 2020:9(6),1335. https://doi.org/10.3390/cells9061335

73. Jongkees B.J., Hommel B., Kühn S., Colzato L.S. Effect of tyrosine supplementation on clinical and healthy populations under stress or cognitive demands – A review. Journal of Psychiatric Research. 2015;70:50-57. doi: 10.1016/j.jpsychires.2015.08.014

74. Wang J., Fang J., Weng Z., Nan L., Chen Y., Shan J., Chen F., Liu J. Advanced development of conductive biomaterials for enhanced peripheral nerve regeneration: a review. RSC advances. 2025;15(17):12997-13009. https://doi.org/10.1039/d5ra01107h

75. Daly W., Yao L., Zeugolis D., Windebank A., Pandit A. A biomaterials approach to peripheral nerve regeneration: bridging the peripheral nerve gap and enhancing functional recovery. Journal of the Royal Society. Interface. 2012;9(67):202-221. https://doi.org/10.1098/rsif.2011.0438

76. Fornasari B.E., Carta G., Gambarotta G., Raimondo S. Natural-Based Biomaterials for Peripheral Nerve Injury Repair. Frontiers in bioengineering and biotechnology. 2020;8: 554257. https://doi.org/10.3389/fbioe.2020.554257

77. Zhang M., Li C., Zhou L.P., Pi W., Zhang P.X. Polymer Scaffolds for Biomedical Applications in Peripheral Nerve Reconstruction. Molecules (Basel, Switzerland). 2021;26(9): 2712. https://doi.org/10.3390/molecules26092712

78. Puranik N., Tiwari S., Kumari M., Yadav S.K., Dhakal T., Song M. Advanced Bioactive Polymers and Materials for Nerve Repair: Strategies and Mechanistic Insights. Journal of Functional Biomaterials. 2025;16(7):255. https://doi.org/10.3390/jfb16070255

79. Zhang S., Sun X., Yang X., Fan Y., Liang Y., Li J., Ling J. Research progress on composite nerve guidance conduits with immune-regulatory functions. Frontiers in immunology. 2025;16:1622508. doi: 10.3389/fimmu.2025.1622508

80. Jiang Z., Zhang Y., Wang Y., Wang S., Chang J., Liu W., Han B. Multichannel nerve conduit based on chitosan derivates for peripheral nerve regeneration and Schwann cell survival. Carbohydrate Polymers. 2023;301 (Pt B):120327. https://doi.org/10.1016/j.carbpol.2022.120327

81. Wan T., Wang Y.L., Zhang F.S., Zhang X.M., Zhang Y.C., Jiang H.R., Zhang M., Zhang P.X. The Porous Structure of Peripheral Nerve Guidance Conduits: Features, Fabrication, and Implications for Peripheral Nerve Regeneration. International Journal of Molecular Sciences. 2023;24(18):14132. doi: 10.3390/ijms241814132

82. Park D., Kim D., Park S.J., Choi J.H., Seo Y., Kim D.H., Lee S.H., Hyun J.K., Yoo J., Jung Y., Kim S.H. Micropattern-based nerve guidance conduit with hundreds of microchannels and stem cell recruitment for nerve regeneration. NPJ Regenerative medicine. 2022;7(1):62. https://doi.org/10.1038/s41536-022-00257-0


Рецензия

Для цитирования:


Габриянчик М.А., Старцева О.И., Головань М.В., Лысенко В.О., Пирогов К.С., Решетов И.В. Современные подходы к регенерации периферических нервов и спинного мозга (обзор литературы). Вопросы реконструктивной и пластической хирургии. 2026;29(1):80-97. https://doi.org/10.52581/1814-1471/96/09

For citation:


Gabriyanchik M.A., Startseva O.I., Golovan M.V., Lysenko V.O., Pirogov K.S., Reshetov I.V. Current approaches to peripheral nerve and spinal cord regeneration (literature review). Issues of Reconstructive and Plastic Surgery. 2026;29(1):80-97. (In Russ.) https://doi.org/10.52581/1814-1471/96/09

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ISSN 1814-1471 (Print)