Study on the nNOS Expression in the Rat Spinal Cord of the Spinal Nerve Ligation Model with Neuropathic Pain and the Dorsal Rhizotomy

척수신경 결찰 만성통증모델 및 후신경근 절단 백서의 척수에서 Neuronal Nitric Oxide Synthase(nNOS) 발현에 관한 연구

  • Youm, Jin Young (Department of Neurosurgery, College of Medicine, Chungnam National University) ;
  • Kim, Youn (Department of Neurosurgery, College of Medicine, Chungnam National University)
  • 염진영 (충남대학교 의과대학 신경외과학교실) ;
  • 김윤 (충남대학교 의과대학 신경외과학교실)
  • Received : 2000.01.11
  • Accepted : 2000.03.27
  • Published : 2000.07.28

Abstract

Objective : The NOS inhibitors exhibit antinociceptive activity in rat model of neuropathic pain. NOS activity increases in the dorsal root ganglia(DRG) in neurop-athic pain. However, NOS activity decreases in the dorsal horn of spinal cord in the nerve injury models of neuropathic pain. To investigate whether the mechanism of decrease of NOS expression in the dorsal horn is related to a secondary effect resulting from increased NO production and likewise in the spinal DRG in the spinal nerve ligation model of neuropathic pain. Methods : We conducted behavioral tests for neuropathic pain, and nNOS immunohistochemistry and NADPH-diaphorase histochemistry after tight ligation of the 5th lumbar(L5) and 6th lumbar(L6) spinal nerves and L5 dorsal rhizotomy. Results : Typical neuropathic pain behaviors occurred 7 days after post-ligation in the neuropathic surgery group, but neuropathic pain behaviors in the dorsal rhizotomy group were absent or weak 7 days after post-operation. There was a decrease in the number of nNOS immunoreactive dorsal horn neurons on the both side(especially ipsilateral side) 7 days after post-ligation. The number of nNOS immunoreactive neurons in both side of the dorsal horn was not decreased 7 days after L5 dorsal rhizotomy. Conclusion : These data indicate that the changes in the injured DRG is essential for development and maintenance of neuropathic pain, and mechanism of decrease of nNOS expression in the dorsal horn is a secondary effect against the changes in the DRG including increased NO production in the spinal nerve ligation model of neuropathic pain.

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