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The mechanical and thermal hypersensitivity were assessed using the von Frey filament, radiant heat and acetone drop tests. Histopathological and apoptotic changes and the level of <jats:styled-content style=\"fixed-case\">FGF<\/jats:styled-content>1, <jats:styled-content style=\"fixed-case\">GFAP<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u03b1 proteins were assessed in the lumbar portion (L4\u2013L6). Moreover, <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> were labelled with <jats:sup>99m<\/jats:sup>Tc \u2010<jats:styled-content style=\"fixed-case\">HMPAO<\/jats:styled-content> and isolated organ counting were performed upon <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> administration.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Administration of <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> attenuated the <jats:styled-content style=\"fixed-case\">CCI<\/jats:styled-content>\u2010induced mechanical and thermal hypersensitivity. Spinal structural alterations and apoptosis were decreased in the <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> group. The injection of either phosphate\u2010buffered saline or normal <jats:styled-content style=\"fixed-case\">NIH<\/jats:styled-content>3T3 fibroblasts could not attenuate the behavioural symptoms of neuropathic pain. Increased genetically engineered cells were counted in the injured sciatic nerve and the elevated levels of <jats:styled-content style=\"fixed-case\">FGF<\/jats:styled-content>1 were detected in the spinal tissue. Stem cell therapy lead to decrement the level of the <jats:styled-content style=\"fixed-case\">CCI<\/jats:styled-content>\u2010induced <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u2010\u03b1 and <jats:styled-content style=\"fixed-case\">GFAP<\/jats:styled-content> expression.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The intravenous administration of <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> could be considered as a potential remedy for the management of neuropathic pain.<\/jats:p><\/jats:sec><jats:sec><jats:title>Significance<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> attenuated the <jats:styled-content style=\"fixed-case\">CCI<\/jats:styled-content>\u2010induced mechanical and thermal hypersensitivity. Spinal structural alterations and apoptosis were significantly decreased in the <jats:styled-content style=\"fixed-case\">AD<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">MSC<\/jats:styled-content>s <jats:styled-content style=\"fixed-case\"><jats:sup>FGF<\/jats:sup><\/jats:styled-content><jats:sup>1<\/jats:sup> group. Elevated levels of <jats:styled-content style=\"fixed-case\">FGF<\/jats:styled-content>1 were detected in the spinal tissue.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ejp.1119","type":"journal-article","created":{"date-parts":[[2017,9,26]],"date-time":"2017-09-26T10:38:47Z","timestamp":1506422327000},"page":"295-310","source":"Crossref","is-referenced-by-count":34,"title":["New approach for the treatment of neuropathic pain: Fibroblast growth factor 1 gene\u2010transfected adipose\u2010derived mesenchymal stem cells"],"prefix":"10.1002","volume":"22","author":[{"given":"F.","family":"Forouzanfar","sequence":"first","affiliation":[{"name":"Department of Pharmacology, Faculty of Medicine Mashhad University of Medical Sciences Mashhad Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B.","family":"Amin","sequence":"additional","affiliation":[{"name":"Cellular and Molecular Research Center, Department of Physiology and Pharmacology, Faculty of Medicine Sabzevar University 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