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In a case report study, light\u2010emitting diode therapy (\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      ) has shown analgesic activity as well as reduced the expression of pro\u2010inflammatory cytokines in a rabbit osteoarthritis model and in calcaneal tendinitis in rats. Although\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      stimulated morphofunctional recovery after nerve injury in rats, its effect against neuropathic pain has not been tested.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      To that purpose, mice under anaesthesia were subjected to the sciatic nerve crush (\n                      <jats:styled-content style=\"fixed-case\">SNC<\/jats:styled-content>\n                      ) model. On the seventh post\u2010operative day, after determining analgesic dose (energy density in joules),\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      (950\u2009nm, 80\u2009m\n                      <jats:styled-content style=\"fixed-case\">W<\/jats:styled-content>\n                      \/cm\n                      <jats:sup>2<\/jats:sup>\n                      , 2.5\u2009\n                      <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>\n                      \/cm\n                      <jats:sup>2<\/jats:sup>\n                      ) was irradiated, daily for a period of 15 days, on the skin over the crush site.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Compared with the\n                      <jats:styled-content style=\"fixed-case\">SNC<\/jats:styled-content>\n                      group,\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      reduced mechanical hypersensitivity but not cold hypersensitivity which is induced by\n                      <jats:styled-content style=\"fixed-case\">SNC<\/jats:styled-content>\n                      , decreased spinal cord and sciatic nerve levels of tumour necrosis factor alpha (\n                      <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\n                      \u2010\u03b1) but did not alter interleukin (\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      )\u20101\u03b2 and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u201010 levels, and finally, failed to accelerate motor functional recovery and morphological nerve regeneration.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Taken together, these data provide first\u2010hand evidence of\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      effectiveness against neuropathic pain induced by\n                      <jats:styled-content style=\"fixed-case\">SNC<\/jats:styled-content>\n                      , with corresponding decrease of pro\u2010inflammatory cytokine levels, both in the sciatic nerve and in the spinal cord, although at a small analgesic dose,\n                      <jats:styled-content style=\"fixed-case\">LEDT<\/jats:styled-content>\n                      failed to accelerate nerve regeneration.\n                    <\/jats:p>\n                  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