Effects of Electrical Stimulation of Brainstem Nuclei on Dorsal Horn Neuron Responses to Mechanical Stimuli in a Rat Model of Neuropathic Pain

신경병증성 통증 모델 쥐에서 뇌간 핵의 전기자극이 후각세포의 기계자극에 대한 반응도에 미치는 영향

  • Leem Joong-Woo (Department of Physiology, Yonsei University College of Medicine) ;
  • Choi Yoon (Department of Anesthesiology, Ulsan University College of Medicine) ;
  • Gwak Young-Seob (Department of Physiology, Yonsei University College of Medicine) ;
  • Nam Taik-Sang (Department of Physiology, Yonsei University College of Medicine) ;
  • Paik Kwang-Se (Department of Physiology, Yonsei University College of Medicine)
  • 임중우 (연세대학교 의과대학 생리학교실) ;
  • 최윤 (울산대학교 의과대학 마취과학교실) ;
  • 곽영섭 (연세대학교 의과대학 생리학교실) ;
  • 남택상 (연세대학교 의과대학 생리학교실) ;
  • 백광세 (연세대학교 의과대학 생리학교실)
  • Published : 1997.06.01

Abstract

The aim of the present study is to examine the brainstem sites where the electrical stimulation produces a suppression of dorsal horn neuron responses of neuropathic rats. An experimental neuropathy was induced by a unilateral ligation of L5-L6 spinal nerves of rats. Ten to 15 days after surgery, the spinal cord was exposed and single-unit recording was made on wide dynamic range (WDR) neurons in the dorsal horn. Neuronal responses to mechanical stimuli applied to somatic receptive fields were examined to see if they were modulated by electrical stimulation of various brainstem sites. Electrical stimulation of periaqueductal gray (PAG), n. raphe magnus (RMg) or n. reticularis gigantocellularis (Gi) significantly suppressed responses of WDR neurons -to both noxious and non-noxious stimuli. Electrical stimulation of other brainstem areas, such as locus coeruleus. (LC) and n. reticularis paragigantocellularis lateralis (LPGi), produced little or no suppression. Microinjection of morphine into PAG, RMg, or Gi also produced a suppression as similar pattern to the case of electrical stimulation, whereas morphine injection into LC or LPGi exerted no effects. The results suggest that PAG, NRM and Gi are the principle brainstem nuclei involved in the descending inhibitory systems responsible for the control of neuropathic pain. These systems are likely activated by endogenous opioids and exert their inhibitory effect by acting on WDR neurons in the spinal cord.

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