Literature DB >> 9522378

Somatotopic redistribution of c-fos expressing neurons in the superficial dorsal horn after peripheral nerve injury.

C Molander1, J Hongpaisan, P Shortland.   

Abstract

The functional somatotopic reorganization of the lumbar spinal cord dorsal horn after nerve injury was studied in the rat by mapping the stimulus-evoked distribution of neurons expressing proto-oncogene c-fos. In three different nerve injury paradigms, the saphenous nerve was electrically stimulated at C-fibre strength at survival times ranging from 40 h to more than six months: 1) Saphenous nerve stimulation from three weeks onwards after ipsilateral sciatic nerve transection resulted in an increase in the number of Fos-immunoreactive neurons within the dorsal horn saphenous territory in laminae I-II, and an expansion of the saphenous territory into the denervated sciatic territory until 14 weeks postinjury. 2) Saphenous nerve stimulation from five days onwards after ipsilateral sciatic nerve section combined with saphenous nerve crush resulted in an increase in the number of Fos-immunoreactive neurons within the dorsal horn saphenous nerve territory, and an expansion of the saphenous nerve territory into the denervated sciatic nerve territory. 3) Stimulation of the crushed nerve (without previous adjacent nerve section) at five days, but not at eight months resulted in a temporary increase in the number of Fos-immunoreactive neurons within the territory of the injured nerve, and no change in area at either survival time. The results indicate that nerve injury results in an increased capacity of afferents in an adjacent uninjured, or regenerating nerve, to excite neurons both in its own and in the territory of the permanently injured nerve in the dorsal horn. The onset and duration of the increased postsynaptic excitability and expansion depends on the types of nerve injuries involved. These findings indicate the complexity of the central changes that follows in nerve injuries that contain a mixture of uninjured, regenerating and permanently destroyed afferents.

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Year:  1998        PMID: 9522378     DOI: 10.1016/s0306-4522(97)00375-8

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  3 in total

1.  Fos protein-like immunoreactive neurons induced by electrical stimulation in the trigeminal sensory nuclear complex of rats with chronically injured peripheral nerve.

Authors:  Naoko Fujisawa; Ryuji Terayama; Daisuke Yamaguchi; Shinji Omura; Takashi Yamashiro; Tomosada Sugimoto
Journal:  Exp Brain Res       Date:  2012-03-29       Impact factor: 1.972

2.  Nerve injury-induced tactile allodynia is present in the absence of FOS labeling in retrogradely labeled post-synaptic dorsal column neurons.

Authors:  En-Tan Zhang; Michael H Ossipov; Dong-Qin Zhang; Josephine Lai; Frank Porreca
Journal:  Pain       Date:  2006-12-06       Impact factor: 6.961

3.  Neuritis and vinblastine-induced axonal transport disruption lead to signs of altered dorsal horn excitability.

Authors:  Ieva Satkeviciute; Andrew Dilley
Journal:  Mol Pain       Date:  2018-08-21       Impact factor: 3.395

  3 in total

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