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Are there physiological and pathological convulsive thresholds in brain?

Are there physiological and pathological convulsive thresholds in brain?
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摘要 Objective To investigate changes that occur in the brain when the physiological convulsive threshold becomes pathological,and to determine what differences occur in pathological and physiological convulsive thresholds during the development of epilepsy. Methods In this study,the threshold for convulsions was determined by direct cortical stimulation in rats.The convulsive threshold was measured while recording electroencephalograms and subsequently examining histopathological changes in the hippocampus. Results At the beginning of the experiment,convulsive thresholds were all above 1 100 μA although there were significant individual variations in rats of the same group.But those thresholds quickly declined during the initial 4 weeks of repetitive electrical stimulation.The convulsive thresholds approached a constant level[TLS(430±34)μA,TGS(480±46)μA,TPS(605±70)μA]in the 10th week.There were no significant changes in thresholds when stimulation lasted for longer,the convulsive thresholds and the variations in rats of the same group were significantly lower than that at the beginning of the trial(P<0.01).An interictal discharge was also recorded in the 3rd week in heavy current group and at the 8th week in weak current group respectively which were concomitant with the neuronal da-mage and loss in the hippocampus.There was no abnormality observed in control group. Conclusion These findings indicate that the convulsion threshold in the brain should be divided into two stages:physiological convulsive threshold and pathological convulsive threshold(epileptic threshold).Epileptic threshold is created by pathological acquired factors which give rise to brain damage.The intensity of these pathological acquired factors is correlated with the formation of the pathological convulsive threshold. Objective To investigate changes that occur in the brain when the physiological convulsive threshold becomes pathological, and to determine what differences occur in pathological and physiological convulsive thresholds during the development of epilepsy. Methods In this study,the threshold for convulsions was determined by direct cortical stimulation in rats. The convulsive threshold was measured while recording electroencephalograms and subsequently examining histopathological changes in the hippocampus. Results At the beginning of the experiment, convulsive thresholds were all above 1 100 μA although there were significant individual variations in rats of the same group. But those thresholds quickly declined during the initial 4 weeks of repetitive electrical stimulation. The convulsive thresholds approached a constant level [ TLS (430 ± 34 ) μA, TGS ( 480 ± 46) μA, TPS ( 605 ± 70 ) μA ] in the 10th week. There were no significant changes in thresholds when stimulation lasted for longer, the convulsive thresholds and the variations in rats of the same group were significantly lower than that at the beginning of the trial( P 〈 0.01 ). An interictal discharge was also recorded in the 3rd week in heavy current group and at the 8th week in weak current group respectively which were concomitant with the neuronal damage and loss in the hippocampus. There was no abnormality observed in control group. Conclusion These findings indicate that the convulsion threshold in the brain should be divided into two stages:physiological convulsive threshold and pathological convulsive threshold( epileptic threshold). Epileptic threshold is created by pathological acquired factors which give rise to brain damage. The intensity of these pathological acquired factors is correlated with the formation of the pathological convulsive threshold.
作者 刘玉玺
出处 《山西医科大学学报》 CAS 2009年第9期786-792,共7页 Journal of Shanxi Medical University
关键词 脑部 癫痫 生理学 病理学痉挛 epilepsy physiological convulsive threshold pathological convulsive threshold epileptic threshold cortical stimulation model
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参考文献11

  • 1Goddard GV. The development of epileptic seizures through brain stimulation at low intensity[ J]. Nature, 1967,214 : 1020 - 1021.
  • 2McIntyre DC, Pouher MO, Gilby K. Kinding: some old and some new[ J]. Epilepsy Res ,2002,50:79 - 92.
  • 3Sweet WH. Neurosurgical treatment in psychiatry, pain and epilepsy [ M ]. Baltimore: University Park Press, 1977:651.
  • 4Voskuyl RA, Dingemanse J, Danhof M. Determination of the thrshold for convulsion by direct cortical stimulation [ J ]. Epilepsy Res, 1989,3:120 - 129.
  • 5Voskuyl RA, Hoogerkamp A, Danhof M. Properties of the convulsive threshold determined by direct cortical stimulation in rats [ J ]. Epilepsy Res, 1992,12 : 111 - 120.
  • 6Della Paschoa OE, Kruk MR, Hamstra R, et al. Seizure patterns in kindling and cortical stimulation models of experimental epilepsy [ J ]. Brain Res, 1997,770:221 - 227.
  • 7Voskuyl RA, Beukel IVD. Kinding-like decline of thecortical convulsive threshold with repeated testing [ J ]. Epilepsia, 1996,37 (Suppl 4) :139.
  • 8McNamara JO, Bonhaus DW, Shin C. The kindling model of epilepsy [ M ]//Schwartzkroin PA, editor. Epilepsy: models, mechanisms, and concepts. Cambridge: Cambridge University Press, 1993:27 - 47.
  • 9Walker MC, White HS, Sander JWAS. Disease modification in partial epilepsy[ J]. Brain,2001,125 ( Pt 9 ) : 1937 - 1950.
  • 10Liu Yu Xi, Wang Ming Zheng, Sun Mei Zhen. Rapid arrest of seizures with an inhalation aerosol containing diazepam [ J ]. Epilepsia, 1994,35 ( 2 ) : 357.

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