Early Experimental Results of Nerve Gap Bridging with Silicon Microwires

Authors

DOI:

https://doi.org/10.20535/ibb.2019.3.3.176925

Keywords:

Peripheral nerve injury, Nerve tissue, Peripheral nerve grafting

Abstract

Background. The incidence of severe peripheral nerves and plexus injuries tends to grow. Autoneurografting is considered as a golden standard method of nerve gap bridging, but existing shortcomings such as additional surgery measures, denervation of other segments of the body, discordance of the neurovascular structure of the damaged nerve and autograft stipulate the development of new material and treatment methods.

Objective. The current study is aimed at estimation of the impact of silicon wires on early morphological changes of the parts of the damaged peripheral nerve after nerve injury and grafting with the use of silicon wires.

Methods. Study was performed on Wistar rats that were divided into groups: I (n = 10) was sham-operated, II (n = 10) with 10 mm sciatic nerve gap bridged with autoneurograft, III (n = 10) with nerve gap bridged with freeze-thaw decellularized allogenic aorta filled with 4% carboxymethylcellulose hydrogel, IV (n = 10) with nerve gap bridged with same conduit as III along with longitudinal oriented silicon wires (p-type, Boron-ligated). Parts of the sciatic nerve were harvested for histologic study: 1 week postoperatively the proximal nerve stump, proximal stump-to-graft site and graft site itself were analyzed. 3 weeks after surgery the proximal nerve-to-graft junction and graft site were analyzed. Longitudinal frozen sections were stained with nitric silver via modified Bielschowsky method. The number of nerve fibers was statistically measured and compared.

Results. It is stated that 1 week after surgery rats from groups II, III, and IV demonstrated signs of nerve fibers irritation in proximal nerve stump. Proximal nerve-to-graft junction contained thin nerve fibers and moderate amount of cells in group II, but a substantial amount of cells, blood vessels and newly-formed nerve fibers in groups III and IV. Graft site contained degenerated nerve fibers in group II, homogeneous semi-transparent masses in group III and same masses with silicon wires in group IV. 3 weeks after surgery rats from group II demonstrated heterogeneous chaotic distribution of nerve fibers at the proximal nerve-to-junction site and heterogeneous distribution of nerve fibers at the graft site. Group III had proximal neuroma site that was composed of substantial amount of chaotically oriented nerve fibers. Graft site contained thin heterogeneously distributed nerve fibers inside the conduit, which were situated alongside the conduit wall or close to vessels. Group IV had proximal neuroma site that was composed of newly-formed nerve fibers that were situated in certain order and mixed with cells and vessels. At the conduit site, thin nerve fibers grow inside conduit lumen, mixed with vessels, and shift towards the silicon wires.

Conclusions. It can be concluded about the possible tendency of the pro-regenerative effect of silicon wires, used as a component of the nerve graft, as evidenced by more homogeneous and complete graft site neurotization along with the possible appearance of the nerve interface "nerve fiber–silicone microwire".

References

Patroclo C, Ramalho B, Maia J, Rangel M, Torres F, Souza L, et al. A public database on traumatic brachial plexus injury. 2018. DOI: 10.1101/399824

Castillo-Galvan ML, Martinez-Ruiz FM, de la Garza-Castro. Estudio de la lesion nerviosa periferica en pacientes atendidos por traumatismos. Gaceta Medica de Mexico. 2014;150:527-32.

Missios S, Bekelis K, Spinner R. Traumatic peripheral nerve injuries in children: epidemiology and socioeconomics. J Neurosurg Pediatrics. 2014;14(6):688-94. DOI: 10.3171/2014.8.PEDS14112

Rivera J, Glebus G, Cho M. Disability following combat-sustained nerve injury of the upper limb. The Bone Joint J. 2014;96-B(2):254-58. DOI: 10.1302/0301-620X.96B2.31798

Strafun S, Borzykh N, Haiko O, Borzykh O, Gayovich V, Tsymbaliuk Y. Priority directions of surgical treatment of patients with damage to the peripheral nerves of the upper limb in polystructural injuries. Trauma. 2018;19(3):75-80. DOI: 10.22141/1608-1706.3.19.2018.136410

Bahm J, Esser T, Sellhaus B, El-kazzi W, Schuind F. Tension in peripheral nerve suture. In: Vanaclocha V, Sáiz-Sapena N, editors. Treatment of Brachial Plexus Injuries. IntechOpen; 2019. p. 2-9. DOI: 10.5772/intechopen.78722

Hunt T, Wiesel S. Operative techniques in hand, wrist, and forearm surgery. Philadelphia: Lippincott Williams & Wilkins; 2011.

Farhadieh R, Bulstrode N, Cugno S. Plastic and reconstructive surgery. Wiley-Blackwell; 2015.

Pi H, Gao Y, Wang Y, Kong D, Qu B, Su X, et al. Nerve autografts and tissue-engineered materials for the repair of peri­pheral nerve injuries: a 5-year bibliometric analysis. Neural Regen Res. 2015;10(6):1003. DOI: 10.4103/1673-5374.158369

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. J R Soc Interf. 2011;9(67):202-221. DOI: 10.1098/rsif.2011.0438

Huang J, Patel N, Lyon K. An update-tissue engineered nerve grafts for the repair of peripheral nerve injuries. Neural Regen Res. 2018;13(5):764. DOI: 10.4103/1673-5374.232458

Schoenfeld A, Dunn J, Belmont P. Pelvic, spinal and extremity wounds among combat-specific personnel serving in Iraq and Afghanistan (2003–2011): A new paradigm in military musculoskeletal medicine. Injury. 2013;44(12):1866-70. DOI: 10.1016/j.injury.2013.08.001

Tsema E, Khomenko І, Bespalenko А, Buryanov О, Міshalov V, Kіkh А. Clinico-statistical investigation of the extremity amputation level in wounded persons. Klinicheskaia Khirurgiia. 2017;10:51. DOI: 10.26779/2522-1396.2017.10.51

Varma P, Stineman M, Dillingham T. Epidemiology of limb loss. Phys Med Rehabil Clin N Am. 2014;25(1):1-8. DOI: 10.1016/j.pmr.2013.09.001

Seo M, Kim H, Choi Y. Human mimetic forearm mechanism towards bionic arm. In: Proceedings of International Confe­rence on Rehabilitation Robotics; 2017; London. p. 1171-76. DOI: 10.1109/icorr.2017.8009408

Dhillon G, Lawrence S, Hutchinson D, Horch K. Residual function in peripheral nerve stumps of amputees: implications for neural control of artificial limbs. J Hand Surg. 2004;29(4):605-15. DOI: 10.1016/j.jhsa.2004.02.006

Ghafoor U, Kim S, Hong K. Selectivity and longevity of peripheral-nerve and machine interfaces: a review. Front Neurorobot. 2017;11:59. DOI: 10.3389/fnbot.2017.00059

Merrill D, Bikson M, Jefferys J. Electrical stimulation of excitable tissue: design of efficacious and safe protocols. J Neurosci Methods. 2005;141(2):171-98. DOI: 10.1016/j.jneumeth.2004.10.020

Du J, Chen H, Qing L, Yang X, Jia X. Biomimetic neural scaffolds: a crucial step towards optimal peripheral nerve regeneration. Biomater Sci. 2018;6(6):1299-311. DOI: 10.1039/c8bm00260f

Siemionow M. Plastic and reconstructive surgery. London: Springer; 2015.

Chaikovsky YB. Regenerative neuroma. Morphologia. 1999;1(15):55-67.

Flecknell P. Laboratory animal anaesthesia. 4th ed. Academic Press; 2015.

Angius D, Wang H, Spinner R, Gutierrez-Cotto Y, Yaszemski M, Windebank A. A systematic review of animal models used to study nerve regeneration in tissue-engineered scaffolds. Biomaterials. 2012;33(32):8034-9. DOI: 10.1016/j.biomaterials.2012.07.056

Tos P, Ronchi G, Papalia I, Sallen V, Legagneux J, Geuna S, et al. Chapter 4: methods and protocols in peripheral nerve regeneration experimental research: part I—experimental models. Int Rev Neurobiol. 2009;87:47-79. DOI: 10.1016/S0074-7742(09)87004-9

Rodriguez M, Juran C, McClendon M, Eyadiel C, McFetridge P. Development of a mechanically tuneable 3D scaffold for vascular reconstruction. J Biomed Mater Resh Part A. 2012;100A(12):3480-9. DOI: 10.1002/jbm.a.34267

Dang Y, Waxman S, Wang C, Jensen A, Loewen R, Bilonick R, et al. Freeze-thaw decellularization of the trabecular meshwork in an ex vivo eye perfusion model. PeerJ. 2017;5:1-5. DOI: 10.7717/peerj.3629

Klimovskaya A, Kalashnyk Y, Voroshchenko A, Oberemok O, Pedchenko Y, Lytvyn P. Growth of silicon self-assembled nanowires by using gold-enhanced CVD technology. Semiconductor Physics, Quantum Electronics and Optoelectronics. 2018;21(3):282-7. DOI: 10.15407/spqeo21.03.282

Reinhardt K, Kern W. Handbook of silicon wafer cleaning technology. Norwich, NY: William Andrew; 2008.

Belkas J, Shoichet M, Midha R. Peripheral nerve regeneration through guidance tubes. Neurolog Res. 2004;26(2):151-60. DOI: 10.1179/016164104225013798

Kolomiitsev AK, Chaikovsky YB, Tereschenko TL. Fast method of peripheral nervous system nitric silver impregnation suitable for celloidine and parafine slices. Archives of Anatomy, Histology and Embryology. 1981;8:93-6.

Uchihara T. Silver diagnosis in neuropathology: principles, practice and revised interpretation. Acta Neuropathol. 2007;113(5):483-99. DOI: 10.1007/s00401-007-0200-2

Raimondo S, Fornaro M, Di Scipio F, Ronchi G, Giacobini-Robecchi M, Geuna S. Chapter 5: methods and protocols in peripheral nerve regeneration experimental research. Int Rev Neurobiol. 2009;87:81-103. doi: 10.1016/S0074-7742(09)87005-0

Petrie A, Sabin C. Medical statistics at a glance. Wiley; 2008.

Cajal RS. Degeneration and regeneration of the nervous system. London: Oxford University Press; 1928. DOI: 10.1093/acprof:oso/9780195065169.001.0001

Geuna S, Raimondo S, Ronchi G, Di Scipio F, Tos P, Czaja K, et al. Chapter 3: histology of the peripheral nerve and changes occurring during nerve regeneration. Int Rev Neurobiol. 2009;87:27-46. DOI: 10.1016/S0074-7742(09)87003-7

Aebischer P, Valentini R, Dario P, Domenici C, Galletti P. Piezoelectric guidance channels enhance regeneration in the mouse sciatic nerve after axotomy. Brain Res. 1987;436(1):165-8. DOI: 10.1016/0006-8993(87)91570-8

Fine E, Valentini R, Bellamkonda R, Aebischer P. Improved nerve regeneration through piezoelectric vinylidenefluoride-trifluoroethylene copolymer guidance channels. Biomaterials. 1991;12(8):775-80. DOI: 10.1016/0142-9612(91)90029-a

Valentini R, Vargo T, Gardellajr J, Aebischer P. Electrically charged polymeric substrates enhance nerve fibre outgrowth in vitro. Biomaterials. 1992;13(3):183-90. DOI: 10.1016/0142-9612(92)90069-z

Jaffe L, Poo M. Neurites grow faster towards the cathode than the anode in a steady field. J Exp Zool. 1979;209(1):115-27. DOI: 10.1002/jez.1402090114

McCaig C. Nerve growth in a small applied electric field and the effects of pharmacological agents on rate and orientation. J Cell Sci. 1990;95:617-22.

Patel N, Poo M. Orientation of neurite growth by extracellular electric fields. J Neurosci. 1982;2(4):483-96. DOI: 10.1523/jneurosci.02-04-00483.1982

Dahlin L, Johansson F, Lindwall C, Kanje M. Chapter 28: future perspective in peripheral nerve reconstruction. Int Rev Neurobiol. 2009;87:507-30. DOI: 10.1016/S0074-7742(09)87028-1

Downloads

Published

2019-09-27

How to Cite

1.
Likhodiievskyi V. Early Experimental Results of Nerve Gap Bridging with Silicon Microwires. Innov Biosyst Bioeng [Internet]. 2019Sep.27 [cited 2024Apr.24];3(3):168-75. Available from: http://ibb.kpi.ua/article/view/176925

Issue

Section

Articles