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The effect of combined neurolytic blocking agent 5% phenol-glycerol in rat sciatic nerve

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Abstract

Combined 5% phenol-glycerol has been used to treat cancer pain or spasticity and as sympathetic blocks. The major clinical problems have been the unpredictable effects on pain and on the duration of the blocks. Previously we have shown that intraneurally injected phenol induces haemorrhagic necrosis as well as dissolving of the nerve fibres. Glycerol, on the other hand, induces dispersion of nerve fibre debris into the endoneurium. We have now studied the effects of a combination of these two chemically different agents. The endoneurial and epineurial responses of rat peripheral nerve were followed after intraneural and perineural injections. Samples for electron microscopic and immunohistochemical studies were taken at 1–26 weeks after the injection. The intraneural phenol-glycerol injection resulted in gross endoneurial damage with partly or totally dissolved nerve fibres. Totally dissolved nerve fibres showed empty, collapsed basal lamina tubes and partly dissolved nerve fibres showed breaching of remaining degenerative debris into the endoneurial space. Axonal regeneration was delayed and was observed first after 2 weeks and it took 4 months before most of the nerve fibres were myelinated. The perineural injections resulted in partial subperineurial damage of the endoneurium morphologically similar to the results caused by the intraneural injection. An initial high accumulation of epineurial macrophages was noted at 1 and 2 weeks. An invasion of macrophages into the endoneurium occurred within 1 week after the intraneural and perineural injections and the number of endoneurial macrophages remained high for up to 6 months. The present study shows that glycerol added to phenol diminishes the necrotizing effect of phenol after an intraneural injection. Combined phenol-glycerol-induced nerve injury is reversible and the axons regenerate but residual morphological changes can be observed even after 6 months.

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References

  1. Antila H, Kirvelä O (1998) Neurolytic thoracic paravertebral block in cancer pain. Acta Anaesthesiol Scand 42:581–585

    CAS  PubMed  Google Scholar 

  2. Bodine-Fowler SC, Allsing S, Botte MJ (1996) Time course of muscle atrophy and recovery following a phenol-induced nerve block. Muscle Nerve 19:497–504

    CAS  PubMed  Google Scholar 

  3. Bremerich A, Reisert I (1991) Die perineural Leitungsblockade mit Glycerin und Phenol-Glycerin. Dtsch Zahnärtzl Z 46:825–827

    Google Scholar 

  4. Burkel WE, McPhee M (1970) Effect of phenol injections into peripheral nerve of rat: electron microscope studies. Arch Phys Med Rehab 7:391–397

    Google Scholar 

  5. Carroll SL, Frohnert PW (1998) Expression of JE (monocyte chemoattractant protein-1) is induced by sciatic axotomy in wild type rodents but not in C57BL/ Wld(s) mice. J Neuropathol Exp Neurol 57:915–930

    Google Scholar 

  6. Cross FW, Cotton LT (1985) Chemical lumbar sympathectomy for ischemic rest pain. A randomized, prospective controlled trial. Am J Surg 150:341–345

    CAS  PubMed  Google Scholar 

  7. Hansebout RR, Cosgrove JBR (1966) Effects of intrathecal phenol in man—a histological study. Neurology 16:277–282

    CAS  PubMed  Google Scholar 

  8. Kirvelä O, Nieminen S (1990) Treatment of painful neuromas with neurolytic neural blockade. Pain 41:161–165

    Article  PubMed  Google Scholar 

  9. Kirvelä O, Svedström E, Lundbom N (1992) Ultrasonic guidance of lumbar sympathetic and celiac plexus block: a new technique. Pain 17:43–46

    Google Scholar 

  10. Morris JH, Hudson AR, Weddell G (1972) A study of degeneration and regeneration in the rat divided sciatic nerve using electron microscopy. IV. Changes in fascicular microtopography, the perineurium and endoneurial fibroblasts. Z Zellforsch Mikrosk Anat 124:165–203

    CAS  PubMed  Google Scholar 

  11. Ohara S, Takahashi H, Ikuta F (1986) Ultrastructural alteration of perineurial cells in the early stage of Wallerian degeneration. Lab Invest 54:2:213–221

    Google Scholar 

  12. Pal HK, Dinda AK, Roy S, Banerji AK (1989) Acute effects of anhydrous glycerol on peripheral nerve: an experimental study. Br J Neurosurg 3:463–470

    CAS  PubMed  Google Scholar 

  13. Patt RB, Cousins MJ (1998) Techniques for neurolytic neural blockade. In: Cousins MJ, Bridenbaugh PO (eds) Neural blockade in clinical anaesthesia and management of pain, 3rd edn. Lippincott-Raven, Philadelphia, pp 1007–1061

  14. Rengachary SS, Watanabe IS, Singer P, Bopp WJ (1983) Effect of glycerol on peripheral nerve: an experimental study. Neurosurgery 13:681–688

    CAS  PubMed  Google Scholar 

  15. Reynolds JEF (1989) Glycerol, glygols and macrogols. In: Reynolds JEF (ed) Martindale. The extra pharmacopoeai, 29th edn. London Pharmaceutical press, London, p 1128

  16. Röyttä M, Horwitz SB, Raine CS (1984) Taxol-induced neuropathy: short-term effects of local injection. J Neurocytol 13:685–701

    PubMed  Google Scholar 

  17. Röyttä M, Salonen V, Peltonen J (1987) Reversible endoneurial changes after nerve transection. Acta Neuropathol (Berl) 73:323–329

    Google Scholar 

  18. Siironen J, Collan Y, Röyttä M (1994) Axonal reinnervation does not influence Schwann cell proliferation after rat sciatic nerve transection. Brain Res 654:303–311

    CAS  PubMed  Google Scholar 

  19. Smith MC (1964) Histological findings following intrathecal injections of phenol solutions for relief of pain. Br J Anaesth 36:387–405

    CAS  Google Scholar 

  20. Stajčić Z (1990) Effects of glycerol on the rat infraorbital nerve. An experimental study. Br J Max Fac Surg 29:90–93

    Google Scholar 

  21. Swerdlow M (1979) Subarachnoid and extradural neurolytic blocks. Adv Pain Res Ther 2:325–337

    Google Scholar 

  22. Taskinen HS, Röyttä M (1997) The dynamics of macrophage recruitment after nerve transection. Acta Neuropathol 93:252–259

    Article  CAS  PubMed  Google Scholar 

  23. Taskinen HS, Röyttä M (2000) Cyclosporin A retards macrophages and axonal degeneration. Neurotrauma 17:431–440

    CAS  Google Scholar 

  24. Vallat JM, Leboutet MJ, Loubet A, Hugon J, Moreau JJ (1988) Effects of glycerol injection into rat sciatic nerve. Muscle Nerve 11:540–545

    CAS  PubMed  Google Scholar 

  25. Vuorinen V, Röyttä M, Raine CS (1989) The long-term effects of a single injection of taxol upon peripheral nerve axons. J Neurocytol 18:775–783

    CAS  PubMed  Google Scholar 

  26. Westerlund T, Vuorinen V, Kirvelä O, Röyttä M (1999) The endoneurial response to neurolytic agents is highly dependent on the mode of application. Reg Anesth Pain Med 24:294–302

    CAS  PubMed  Google Scholar 

  27. Westerlund T, Vuorinen V, Röyttä M (2001) Same axonal regeneration rate after different endoneurial response to intraneural glycerol and phenol injection. Acta Neuropathol 102:41–54

    CAS  PubMed  Google Scholar 

  28. Wilkinson HA (1999) Trigeminal nerve peripheral branch phenol/glycerol injections for tic douloureux. J Neurosurg 90:828–832

    CAS  PubMed  Google Scholar 

  29. Wood KM (1978) The use of phenol as a neurolytic agent:a review. Pain 5:205–229

    CAS  PubMed  Google Scholar 

  30. Woolsey RM, Taylor JJ, Nagel JH (1974) Acute effects of topical ethyl alcohol on the sciatic nerve of the mouse. Arch Phys Med Rehabil 53:410–414

    Google Scholar 

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Acknowledgements

We are deeply grateful to the Institute of Neurosciences, Southern General Hospital in Glasgow for letting us use their electron microscope facilities. We would also like to thank Mr. Jaakko Liippo for skilled photography as well as Ms. Paula Lehtinen and Pirkko Huuskonen, M.A., for correcting the language. This work was supported by an EVO Grant to Turku University Hospital and Turku University Foundation.

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Correspondence to Matias Röyttä.

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Westerlund, T., Vuorinen, V. & Röyttä, M. The effect of combined neurolytic blocking agent 5% phenol-glycerol in rat sciatic nerve. Acta Neuropathol 106, 261–270 (2003). https://doi.org/10.1007/s00401-003-0730-1

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  • DOI: https://doi.org/10.1007/s00401-003-0730-1

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