Skip to main content

Advertisement

Log in

Effects of 660- and 980-nm low-level laser therapy on neuropathic pain relief following chronic constriction injury in rat sciatic nerve

  • Original Article
  • Published:
Lasers in Medical Science Aims and scope Submit manuscript

Abstract

Neuropathic pain (NP) is one of the most suffered conditions in medical disciplines. The role of reactive oxygen species (ROS) and oxidative stress in the induction of NP was studied by many researchers. Neuropathies lead to medical, social, and economic isolation of the patient, so various therapies were used to treat or reduce it. During the recent years, low-level laser therapy (LLLT) has been used in certain areas of medicine and rehabilitation. Chronic constriction injury (CCI) is a well-known model for neuropathic pain studies. In order to find the effects of different wavelengths of LLLT on the injured sciatic nerve, the present research was done. Thirty Wistar adult male rats (230–320 g) were used in this study. The animals were randomly divided into three groups (n = 10). To induce neuropathic pain for the sciatic nerve, the CCI technique was used. Low-level laser of 660 and 980 nm was used for two consecutive weeks. Thermal and mechanical hyperalgesia was done before and after surgery on days 7 and 14, respectively. Paw withdrawal thresholds were also evaluated. CCI decreased the pain threshold, whereas both wavelengths of LLLT for 2 weeks increased mechanical and thermal threshold significantly. A comparison of the mechanical and thermal threshold showed a significant difference between the therapeutic effects of the two groups that received LLLT. Based on our findings, the laser with a 660-nm wavelength had better therapeutic effects than the laser with a 980-nm wavelength, so the former one may be used for clinical application in neuropathic cases; however, it needs more future studies.

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.

Institutional subscriptions

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Merskey H, Bogduk N (1994) Part III: Pain terms, a current list with definitions and notes on usage. In: Merskey H, Bogduk N (eds) Classification of chronic pain: descriptions of chronic pain syndromes and definitions of pain terms. IASP, Seattle, pp 209–214

    Google Scholar 

  2. WangLX WZJ (2003) Animal and cellular models of chronic pain. Adv Drug Deliv Rev 55:949–965

    Article  Google Scholar 

  3. WoolfCJ MRJ (1999) Neuropathic pain: aetiology, symptoms, mechanisms, and management. Lancet 353:1959–1964

    Article  Google Scholar 

  4. Zimmermann M (2001) Pathobiology of neuropathic pain. Eur J Pharmacol 429:23–37

    Article  CAS  PubMed  Google Scholar 

  5. Dubner R (1991) Neuronal plasticity and pain following peripheral tissue inflammation or nerve injury. In: BondMR CJE, Woolf CJ (eds) Proceedings of the VIth World Congress on Pain. Elsevier, Amsterdam, pp 263–276

    Google Scholar 

  6. Woolf CJ (1996) Windup and central sensitization are not equivalent. Pain 66:105–108

    Article  CAS  PubMed  Google Scholar 

  7. Bennett GJ, Xie YK (1988) A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain 33:87–107

    Article  CAS  PubMed  Google Scholar 

  8. Gary J, Bennett G, Chung JM, Honore M, Seltzer Z (2003) Models of neuropathic pain in the rat. Current Protocols in Pharmacology. doi:10.1002/0471141755

    Google Scholar 

  9. Amour FE, Smith D (1941) A method for determining loss of pain sensation. J Pharmacol Exp Ther 72:74–79

    Google Scholar 

  10. Hargreaves K, Dubner R, Brown F, Flores C, Joris J (1988) A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia. Pain 32:77–88

    Article  CAS  PubMed  Google Scholar 

  11. Espejo EF, Mir D (1993) Structure of the rat's behaviour in the hot plate test. Behav Brain Res 56:171–176

    Article  CAS  PubMed  Google Scholar 

  12. Woolfe G, Macdonald AD (1944) The evaluation of the anelgesic action of pethidine hydrochloride (Dermol). J Pharmacol Exp Ther 80:300–307

    CAS  Google Scholar 

  13. Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL (1994) Quantitative assessment of tactile allodynia in the rat paw. J NeurosciMethods 53:55–63

    CAS  Google Scholar 

  14. Dubner R (1989) Methods of assessing pain in animals. In: Textbook of pain Edited by: Wall PD and Melzack R. Edinburgh, Churchville Livingstone: 247-256.

  15. Mendonça AC, Barbieri CH, Mazzer N (2003) Directly applied low intensity direct electric current enhances peripheral nerve regeneration in rats. J Neurosci Methods 129:183–190. doi:10.1016/S0165-0270(03)00207-3

    Article  PubMed  Google Scholar 

  16. Gigo-Benato D, Geuna S, Rochkind S (2005) Phototherapy for enhancing peripheral nerve repair: a review of the literature. Muscle Nerve 31:694–701. doi:10.1002/mus.20305

    Article  PubMed  Google Scholar 

  17. Raso VVM, Barbieri CH, Mazzer N, Fasan VS (2005) Can therapeutic ultrasound influence the regeneration of the peripheral nerves. J Neurosci Methods 142:185–192

    Article  PubMed  Google Scholar 

  18. Ohshiro T, Calderhead RG (1988) Low-level laser therapy: a practical introduction. Wiley, New York, pp 17, 28–30, 33, 34.

  19. Huang Y, Chen ACH, Carroll JD, Hamblin MR (2009) Biphasic dose response in low-level light therapy. Dose Response 7:358–383

    Article  PubMed Central  PubMed  Google Scholar 

  20. Kitchen SS, Partridge CJ (1991) A review of low level laser therapy, part I: background, physiological effects and hazards. Physiotherapy 77:161–163

    Article  Google Scholar 

  21. Karu TI, Pyatibrat L, Kalendo G (1995) Irradiation with He-Ne laser increases ATP level in cells cultivated in vitro. J Photochem Photobiol B 27:219–233

    Article  CAS  PubMed  Google Scholar 

  22. Khullar SM, Brodin P, Fristad I, Kvinnsland IH (1999) Enhanced sensory reinnervation of dental target tissues in rats following low level laser (LLL) irradiation. Lasers Med Sci 14:177–184

    Article  Google Scholar 

  23. Schindl A, Schindl M, Schindl L, Jurecka W, Hönigsmann H, Breier F (1999) Increased dermal angiogenesis after low-intensity laser therapy for a chronic radiation ulcer determined by a video measuring system. J Am AcadDermatol 40:481–484

    Article  CAS  Google Scholar 

  24. Manteifel V, Bakeeva L, Karu T (1997) Ultrastructural changes in chondriome of human lymphocytes after irradiation with He-Ne laser: appearance of giant mitochondria. J Photochem Photobiol B 38:25–30

    Article  CAS  PubMed  Google Scholar 

  25. Reis FA, Belchior ACG, Carvalho PTC, Silva BAK, Pereira DM, Silva IS, Nicolau RA (2009) Effects of laser therapy (660 nm) on recovery of the sciatic nerve in rats after injury through neurotmesis followed by epineural anastomosis. Lasers Med Sci 24:741–747

    Article  PubMed  Google Scholar 

  26. Belchior ACG, Reis FA, Nicolau RA, Silva IS, Pereira DM, Carvalho PTC (2009) Influence of laser (660 nm) on functional recovery of the sciatic nerve in rats following crushing lesion. Lasers Med Sci 24:893–899

    Article  PubMed  Google Scholar 

  27. Barbosa RI, MarcolinoAM GRRJ, MazzerN BCH, Fonseca MCR (2010) Comparative effects of wavelengths of low-power laser in regeneration of sciatic nerve in rats following crushing lesion. Lasers Med Sci 25:423–430

    Article  PubMed  Google Scholar 

  28. HsiehYL CLW, ChangPL YCC, KaoMJ HCZ (2012) Low-level laser therapy alleviates neuropathic pain and promotes function recovery in rats with chronic constriction injury: possible involvements in hypoxia-inducible factor 1a (HIF-1a). The Journal of Comparative Neurology Research in Systems Neuroscience 520:2903–2916

    Article  Google Scholar 

  29. Bertolini GR, Artifon EL, Silva TS, Cunha DM, Vigo PR (2011) Low-level laser therapy, at 830 nm, for pain reduction in experimental model of rats with sciatica. Arq Neuro Psiquiatr 69:356–359

    Article  Google Scholar 

  30. RandallLO SJJ (1957) A method for measurement of analgesic activity on inflamed tissue. Arch Int Pharmacodyn Ther 111:409–419

    Google Scholar 

  31. Cui JG, holmin S, mathiesen T (2000) Possible role of inflammatory mediators in tactile hypersensitivity in rat models of mononeuropathy. Pain 88(3):239–248

    Article  CAS  PubMed  Google Scholar 

  32. Martucci C, Trovato AE, Costa B, Borsani E, Franchi S, Magnaghi V, Panerai AE, Rodella LF, Valsecchi AE, Sacerdote P, Colleoni M (2008) The purinergic antagonist PPADS reduces pain related behaviours and interleukin-1 beta, interleukin-6, iNOS and nNOS overproduction in central and peripheral nervous system after peripheral neuropathy in mice. Pain 137:81–95

    Article  CAS  PubMed  Google Scholar 

  33. Sommer C, Kress M (2004) Recent findings on how proinflammatory cytokines cause pain: peripheral mechanisms in inflammatory and neuropathic hyperalgesia. Neurosci Lett 361:184–187

    Article  CAS  PubMed  Google Scholar 

  34. leung l, Cahill CM (2010) TNF-alpha and neuropathic pain--a review. J Neuroinflammation 7:27

    Article  PubMed Central  PubMed  Google Scholar 

  35. Ferreira SH, Nakamura M, Abreu Castro MS (1978) The hyperalgesic effects of prostacyclin and prostaglandin E2. Prostaglandins 16(1):31–37

    Article  CAS  PubMed  Google Scholar 

  36. Higgs EA, Moncada S, Vane JR (1978) Inflammatory effects of prostacyclin (PGI2) and 6-oxo-PGF1[alpha] in the rat paw. Prostaglandins 16(2):153–162

    Article  CAS  PubMed  Google Scholar 

  37. Schepelmann K, Linger K, Schaibleh G (1992) Inflammatory mediators and nociception in the joint: excitation and sensitization of slowly conducting afferent fibers of cat's knee by prostaglandin I2. Neuroscience 50(1):237–247

    Article  CAS  PubMed  Google Scholar 

  38. DevorM WDM, Goetzl EJ (1992) Eicosanoids, but not tachykinins, excite C-fiber endings in rat sciatic nerve-end neuromas. Neuroreport 3(1):21–24

    Article  Google Scholar 

  39. Cuzzocrea S, Thiemermann C, Salvemini D (2004) Potential therapeutic effect of antioxidant therapy in shock and inflammation. Curr Med Chem 11:1147–1162

    Article  CAS  PubMed  Google Scholar 

  40. Torres SH, De Sanctis JB, Briceño ML, Hernandez N, Finol H (2004) Inflammation and nitric oxide production in skeletal muscle of type 2 diabetic patients. J Endocrinol 181:419–427

    Article  CAS  PubMed  Google Scholar 

  41. Adams V, Nehrhoff B, Spate U, Linke A, Schulze PC, Baur A, Gielen S, Hambrecht R, Schuler G (2002) Induction of iNOS expression in skeletal muscle by IL-1b and NF-kB activation: An in vitro and in vivo study. Cardiovasc Res 54:95–104

    Article  CAS  PubMed  Google Scholar 

  42. Gomez-Cabrera MC, Borras C, Pallardo FV, Sastre J, Ji LL, Vina J (2005) Decreasing xanthine oxidase-mediated oxidative stress prevents useful cellular adaptations to exercise in rats. J Physiol 15:113–120

    Article  Google Scholar 

  43. Gilad E, Wong HR, Zingarelli B, Virag L, O'Connor M, Salzman AL, Szabo C (1998) Melatonin inhibits expression of the inducible isoform of nitric oxide synthase in murine macrophages: Role of inhibition of NFkappaB activation. FASEB J 12:685–693

    CAS  PubMed  Google Scholar 

  44. RabeloSB VAB, NicolauR SMC, MeloMdaS PMT (2006) Comparison between wound healing in induced diabetic and nondiabetic rats after low-level laser therapy. Photomed Laser Surg 24(4):474–479

    Article  Google Scholar 

  45. AlbertiniR AFS, CorreaFI RW, CogoJC AE, TeixeiraSA DNGHC, NetoCF ZRA, Lopes-Martins RA (2004) Effects of different protocol doses of low power gallium–aluminum–arsenate (Ga–Al–As) laser radiation (650 nm) on carrageenan induced rat paw oedema. J Photochem Photobiol B 74(2–3):101–107

    Article  Google Scholar 

  46. FerreiraDM ZRA, VillaverdeAB CY, FrigoL PG, LongoI BDG (2005) Analgesic effect of He–Ne (632.8 nm) low-level laser therapy on acute inflammatory pain. Photomed Laser Surg 23(2):177–181

    Article  Google Scholar 

  47. AlbertiniR VAB, AimbireF SMAC, BjordalJM ALP, MuninE CMS (2007) Anti-inflammatory effects of low-level laser therapy (LLLT) with two different red wavelengths (660 nm and 684 nm) in carrageenan-induced rat paw edema. J Photochem Photobiol B Biol 89:50–55

    Article  Google Scholar 

  48. RizziCF, MaurizJL, Freitas CorreaDS, MoreiraAJ, ZettlerCG, FilippinLI, MarroniNP, Gonzalez-GallegoJ (2006) Effects of low-level laser therapy (LLLT) on the nuclear factor (NF)-kappaB signaling pathway in traumatized muscle, Lasers Surg. Med.

  49. Moriyama Y, Moriyama EH, Blackmore K, Akens MK, Lilge L (2005) In vivo study of the inflammatory modulating effects of low level laser therapy on iNOS expression using bioluminescence imaging. Photochem Photobiol 81(6):1351–1355

    Article  CAS  PubMed  Google Scholar 

  50. Gavish L, Asher Y, Becker Y, Kleinman Y (2004) Low level laser irradiation stimulates mitochondrial membrane potential and disperses subnuclear promyelocytic leukemia protein. Lasers Surg Med 35(5):369–376

    Article  PubMed  Google Scholar 

  51. Gavish L, Perez L, Gertz SD (2006) Low-level laser irradiation modulates matrix metalloproteinase activity and gene expression in porcine aortic smooth muscle cells. Lasers Surg Med 38:779–786

    Article  PubMed  Google Scholar 

  52. Aimbire F, Albertini R, Pacheco MT, Castro-Faria-Neto HC, Leonardo PS, Iversen VV, Lopes-Martins RA, Bjordal JM (2006) Low-level laser therapy induces dose-dependent reduction of TNF alpha levels in acute inflammation. Photomed Laser Surg 24(1):33–37

    Article  CAS  PubMed  Google Scholar 

  53. Sakurai Y, Yamaguchi M, Abiko Y (2000) Inhibitory effect of low-level laser irradiation on LPS-stimulated prostaglandin E2 production and cyclooxygenase-2 in human gingival fibroblasts. Eur J Oral Sci 108(1):29–34

    Article  CAS  PubMed  Google Scholar 

  54. Storz P (2007) Mitochondrial ROS—radical detoxification, mediated by protein kinase D. Trends Cell Biol 17:13–18

    Article  CAS  PubMed  Google Scholar 

  55. Brondon P, Stadler I, Lanzafame RJ (2005) A study of the effects of phototherapy dose interval on photobiomodulation of cell cultures. Lasers Surg Med 36:409–413

    Article  PubMed  Google Scholar 

  56. Karu T (1999) Primary and secondary mechanisms of action of visible to near-IR radiation on cells. J Photochem Photobiol B 49:1–17

    Article  CAS  PubMed  Google Scholar 

  57. Alexandratou E, Yova D, Handris P, Kletsas D, Loukas S (2002) Human fibroblast alterations induced by low power laser irradiation at the single cell level using confocal microscopy. PhotochemPhotobiolSci 1:547–552

    CAS  Google Scholar 

  58. Chen AC-H, Arany PR, Huang YY, Tomkinson EM, Saleem T, Yull FE, Blackwell TS, and Hamblin MR (2009) Low level laser therapy activates NF-κB via generation of reactive oxygen species in mouse embryonic fibroblasts. Proc SPIE in press.

  59. Lavi R, Shainberg A, Friedmann H, Shneyvays V, Rickover O, Eichler M, Kaplan D, Lubart R (2003) Low energy visible light induces reactive oxygen species generation and stimulates anincrease of intracellular calcium concentration in cardiac cells. J Biol Chem 278:40917–40922

    Article  CAS  PubMed  Google Scholar 

  60. Lubart R, Eichler M, Lavi R, Friedman H, Shainberg A (2005) Low-energy laser irradiation promotes cellular redox activity. Photomed Laser Surg 23:3–9

    Article  CAS  PubMed  Google Scholar 

  61. Pal G, Dutta A, Mitra K, Grace MS, Romanczyk TB, Wu X, Chakrabarti K, Anders J, Gorman E, Waynant RW, Tata DB (2007) Effect of low intensity laser interaction with human skin fibroblast cells using fiber-optic nano-probes. J Photochem Photobiol B 86:252–261

    Article  CAS  PubMed  Google Scholar 

  62. Zhang J, Xing D, Gao X (2008) Low-power laser irradiation activates Src tyrosine kinase through reactive oxygen species-mediated signaling pathway. J Cell Physiol 217:518–528

    Article  CAS  PubMed  Google Scholar 

  63. Wu Q, Huang YY, Dhital S, Hamblin MR, Anders JJ, Waynant RW (2010) Low level laser therapy for traumatic brain injury. Mechanisms for Low-Light Therapy V. Proc SPIE. 7552 Article No. 755206.

  64. Amat A, Rigau J, Waynant RW, Ilev IK, Anders JJ (2006) The electric field induced by light can explain cellular responses to electromagnetic energy: a hypothesis of mechanism. J Photochem Photobiol B 82:152–160

    Article  CAS  PubMed  Google Scholar 

  65. Vladimirov Yu A In: Chikin S (1994) Efferent medicine. Institute of Biomedical Chemistry, Russian Academy of Medical Sciences, Moscow,pp.51–66.

  66. Manteifel VM, Karu TI (2005) Structure of mitochondria and activity of their respiratory chain in successive generations of yeast cells exposed to He-Ne laser light. Izv Akad Nauk Ser Bioll 32:556–566

    CAS  Google Scholar 

  67. Hrnjak M, Kuljic-Kapulica N, Budisin A, Giser A (1995) Stimulatory effect of low-power density He-Ne laser radiation on human fibroblasts in vitro. Vojnosanit Pregl 52:539–546

    CAS  PubMed  Google Scholar 

  68. Romm AR, Sherstnev MP, Volkov VV, Vladimirov Yu A (1986) The action of laser irradiation of peroxide chemiluminescence of wound exudation. Byul EkspBiol Med 102:426–428

    CAS  Google Scholar 

Download references

Acknowledgements

The authors would like to thank the Medical Basic Sciences Laboratory (Faculty of Allied Medicine, TUMS) and Pain Laboratory (Faculty of Medicine, TUMS).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. B. Jameie.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Masoumipoor, M., Jameie, S.B., Janzadeh, A. et al. Effects of 660- and 980-nm low-level laser therapy on neuropathic pain relief following chronic constriction injury in rat sciatic nerve. Lasers Med Sci 29, 1593–1598 (2014). https://doi.org/10.1007/s10103-014-1552-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10103-014-1552-1

Keywords

Navigation