Skip to main content

Advertisement

Log in

The effect of a silicone sheet on sciatic nerve healing in rats

  • Experimental Study
  • Published:
European Journal of Plastic Surgery Aims and scope Submit manuscript

Abstract

Background

Fibrosis occurs during the healing process after nerve injury. Extraneural fibrosis occurs around the epineural sheath. Intraneural fibrosis occurs in the internal structure of the nerve. Prophylactic treatment with silicone gel sheets is effective in preventing severe scarring in the skin. Nerve action potential (NAP) recording is a well established, simple, and useful tool in the surgical treatment of nerve damage. Our aim in this study was to determine the effect of a silicone sheet on biophysical and histopathologic parameters when used in the treatment of peripheral nerve transection (neurotmesis) and crush injuries.

Methods

The study was conducted with 32 Wistar albino male rats. The rats in the neurotmesis and crush injury groups were divided into study and control groups. Before the injury and after 12 weeks, electrophysiological measurements were obtained. The sciatic nerve biopsy specimens were histopathologically evaluated.

Results

After 12 weeks, there was no statistical difference between pre- and post-injury ΔPP values in the PNR+SS group (p = 0.123). There was no statistically significant difference in post-injury ΔPP values between the CI and CI+SS groups (p = 0.201). The mean total histopathological score was significantly higher in the PNR+SS group than in the PNR group (p = 0.023).

Conclusions

In this rat model, a silicone sheet appears to have positive effects on peripheral nerve healing after primer repair and crush injury.

Level of evidence

Not gradable.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Mustoe TA (2008) Evolution of silicone therapy and mechanism of action in scar management. Aesthet Plast Surg 32:82–92

    Article  Google Scholar 

  2. Gold MH, Foster TD, Adair MA, Burlison K (2001) Lewis T Prevention of hypertrophic scars and keloids by the prophylactic use of topical silicone gel sheets following a surgical procedure in an office setting. Dermatol Surg 27:641–644

    CAS  PubMed  Google Scholar 

  3. Quinn KJ, Evans JH, Courtney JM, Gaylor JDS (1985) Nonpressure treatment of hypertrophic scars. Burns 12:102–108

    Article  CAS  Google Scholar 

  4. Wolfram D, Tzankov A, Pülzl P, Piza-Katzer H (2009) Hypertrophic scars and keloids: a review of their pathophysiology, risk factors, and therapeutic management. Dermatol Surg 35:171–181

    Article  CAS  PubMed  Google Scholar 

  5. Zurada JM, Kriegel D, Davis IC (2006) Topical treatments for hypertrophic scars. J Am Acad Dermatol 55:1024–1031

    Article  PubMed  Google Scholar 

  6. Chang CC, Kuo YF, Chiu HC, Lee JL, Wong TW, Jee SH (1995) Hydration, not silicone, modulates the effects of keratinocytes on fibroblasts. J Surg Res 59:705–711

    Article  CAS  PubMed  Google Scholar 

  7. Yagmur C, Akaishi S, Ogawa R, Guneren E (2010) Mechanical receptor–related mechanisms in scar management: a review and hypothesis. Plast Reconstr Surg 126(2):426–434

    Article  CAS  PubMed  Google Scholar 

  8. Akaishi S, Akimoto M, Hyakusoku H, Ogawa R (2010) The tensile reduction effects of silicone gel sheeting. Plast Reconstr Surg 126(2):109e–111e

    Article  PubMed  Google Scholar 

  9. Atkins S, Smith KG, Loescher AR, Boissonade FM, O’Kane S, Ferguson MWJ, Robinson PP (2006) Scarring impedes regeneration at sites of peripheral nerve repair. Neuroreport 17:1245–1249

    Article  CAS  PubMed  Google Scholar 

  10. Wang ML, Rivlin M, Graham JG, Beredjiklian PK (2019) Peripheral nerve injury, scarring, and recovery. Connect Tissue Res 60(1):3–9

    Article  PubMed  Google Scholar 

  11. Tiel RL, Happel LT Jr, Kline DG (1996) Nerve action potential recording method and equipment. Neurosurgery 39(1):103–108

    Article  CAS  PubMed  Google Scholar 

  12. Alvites R, Caseiro AR, Pedrosa SS, Branquinho MV, Ronchi G, Geuna S, Varejão ASP, Maurício AC (2018) Peripheral nerve injury and axonotmesis: state of the art and recent advances. Cogent Medicine 5(1):1466404

    Article  Google Scholar 

  13. Pan HC, Yang DY, Chiu YT, Lai SZ, Wang YC, Chang MH, Cheng FC (2006) Enhanced regeneration in injured sciatic nerve by human amniotic mesenchymal stem cell. J Clin Neurosci 13(5):570–575

    Article  PubMed  Google Scholar 

  14. Frostick SP (1995) The physiology and metabolic consequence of muscle denervation. Int Angiol 14:278–287

    CAS  PubMed  Google Scholar 

  15. Ma HE, Omura T, Cobos EJ, Latrémolière A, Ghasemlou N, Brenner GJ, van Veen BL, Sawada T, Gao F, Coppola G, Gertler F, Costigan M, Geschwind D, Woolf CJ (2011) Accelerating axonal growth promotes motor recovery after peripheral nerve injury in mice. J Clin Invest 121:4332–4347

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Mathieu L, Adam C, Legagneux J, Bruneval P, Masmejean E (2012) Reduction of neural scarring after peripheral nerve suture: an experimental study about collagen membrane and autologous vein wrapping. Chir Main 31:311–317

    Article  CAS  PubMed  Google Scholar 

  17. Ngeow WC (2010) Scar less: a review of methods of scar reduction at sites of peripheral nerve repair, Oral Surg. Oral Med Oral Pathol Oral Radiol Endod 109:357–366

    Article  Google Scholar 

  18. Kaplan T, Kafa IM, Cansev M, Bekar A, Karli N, Taskapilioglu MO, Kanar F (2014) Investigation of the dose-dependency of citicoline effects on nerve regeneration and functional recovery in a rat model of sciatic nerve injury. Turk Neurosurg 24:54–62

    PubMed  Google Scholar 

  19. Ozay R, Bekar A, Kocaeli H, Karli N, Filiz G, Ulus IH (2007) Citicoline improves functional recovery, promotes nerve regeneration, and reduces postoperative scarring after peripheral nerve surgery in rats. Surg Neurol 68:615–622

    Article  PubMed  Google Scholar 

  20. Sarhane KA, Ibrahim Z, Martin R, Krick K, Cashman CR, Tuffaha SH, Broyles JM, Prasad N, Yao ZC, Cooney DS, Mi R, Lee WA, Hoke A, Mao HQ (2019) Brandacher GMacroporous nanofiber wraps promote axonal regeneration and functional recovery in nerve repair by limiting fibrosis. Acta Biomater 88:332–345

    Article  CAS  PubMed  Google Scholar 

  21. Pleasure D, Bora FW, Lane J (1974) Prockop D Regeneration after nerve transection: effect of inhibition of collagen synthesis. Exp Neurol 45:72–78

    Article  CAS  PubMed  Google Scholar 

  22. Soller EC, Tzeranis DS, Miu K, So PT, Yannas IV (2012) Common features of optimal collagen scaffolds that disrupt wound contraction and enhance regeneration both in peripheral nerves and in skin. Biomaterials 33:4783–4791

    Article  CAS  PubMed  Google Scholar 

  23. Schaefer C, Sadosky A, Mann R, Daniel S, Parsons B, Tuchman M, Anschel A, Stacey BR, Nalamachu S (2014) Nieshoff EPain severity and the economic burden of neuropathic pain in the United States: BEAT Neuropathic Pain Observational Study. Clin Outcomes Res 6:483–496

    Google Scholar 

  24. Sauer SK, Bove GM, Averbeck B, Reeh PW (1999) Rat peripheral nerve components release calcitonin gene-related peptide and prostaglandin E2 in response to noxious stimuli: evidence that nervi nervorum are nociceptors. Neuroscience 92(1):319–325

    Article  CAS  PubMed  Google Scholar 

  25. Bove GM (2008) Epi-perineurial anatomy, innervation, and axonal nociceptive mechanisms. J Bodyw Mov Ther 12(3):185–190

    Article  PubMed  PubMed Central  Google Scholar 

  26. Teixeira MJ, Almeida DB, Yeng LT (2016) Concept of acute neuropathic pain. The role of nervi nervorum in the distinction between acute nociceptive and neuropathic pain. Rev Dor São Paulo 17(1):5–10

    Google Scholar 

  27. Bove GM, Light AR (1995) Calcitonin gene-related peptide and peripherin immunoreactivity in nerve sheaths. Somatosens Mot Res 12:49–57

    Article  CAS  PubMed  Google Scholar 

  28. Schoonhoven R, Stegeman DF (1991) Models and analysis of compound nerve action potentials. Crit Rev Biomed Eng 19(1):47–111

    CAS  PubMed  Google Scholar 

  29. Lee HJ (2001) Compound nerve action potential of common peroneal nerve recorded at fibular neck ıts clinical usefulness am. J Phys Med Rehabil Am J Phys Med Rehabil 80(2):108–112

    Article  CAS  Google Scholar 

  30. Lim TK, Shi XQ, Johnson JM, Rone MB, Antel JP, David S, Zhang J (2015) Peripheral nerve injury induces persistent vascular dysfunction and endoneurial hypoxia, contributing to the genesis of neuropathic pain. J Neurosci 35(8):3346–33459

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Gao Y, Weng C (2013) Changes in nerve microcirculation following peripheral nerve compression. Neural Regen Res 8(11):1041–1047

    PubMed  PubMed Central  Google Scholar 

  32. Saika T, Senba E, Noguchi K, Sato M, Yoshida S, Kubo T, Matsunaga T, Tohyama M (1991) Effects of nerve crush and transection on mRNA levels for nerve growth factor receptor in the rat facial motoneurons. Res Mol Brain Res 9(1-2):157–160

    Article  CAS  PubMed  Google Scholar 

  33. Yetiser S, Kahraman E (2008) An analysis of time-dependent changes of neurotrophic factors (BDNF, CNTF) in traumatic facial nerve ınjury of a nerve-cut and nerve-crush model in rats. Otol Neurotol 29(3):392–396

    Article  PubMed  Google Scholar 

  34. Gutmann E, Guteman L, Medawar PB, Young JZ (1942) The rate of regeneration of nerve. J Exp Biol 19:14–44

    Article  Google Scholar 

  35. Haftek J, Thomas PK (1968) Electron-microscope observations on the effects of localized crush injuries on the connective tissues of peripheral nerve. J Anat 103(Pt 2):233–243

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Niemi JP, DeFrancesco-Lisowitz A, Roldán-Hernández L, Lindborg JA, Mandell D, Zigmond RE (2013) A critical role for macrophages near axotomized neuronal cell bodies in stimulating nerve regeneration. J Neurosci 33(41):16236–16248

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Shashkin P, Dragulev B, Ley K (2005) Macrophage differentiation to foam cells. Curr Pharm Des 11:3061–3072

    Article  CAS  PubMed  Google Scholar 

Download references

Funding

Financial assistance was received from Sivas Cumhuriyet University Scientific Research Project.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Handan Derebaşınlıoğlu.

Ethics declarations

Ethical approval

All procedures performed in studies involving animal subjects were in accordance with the ethical standards of the institutional and/or national research committee. This study was also performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals. The Cumhuriyet University Ethical Comittee approved this study (decision No: 65202830-050 04 04-243).

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Derebaşınlıoğlu, H., Demirkazık, A., Çiçek Doğan, İ. et al. The effect of a silicone sheet on sciatic nerve healing in rats. Eur J Plast Surg 46, 453–463 (2023). https://doi.org/10.1007/s00238-023-02071-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00238-023-02071-3

Keywords

Navigation