배양조건에 의한 일과성 저산소상태 후 신경세포회복의 차이

Difference of Neuronal Recovery by Incubation Condition after Transient Hypoxia

  • 문수현 (건국대학교 의과대학 충주병원 신경외과학교실) ;
  • 오재인 (고려대학교 의과대학 신경외과학교실) ;
  • 박윤관 (고려대학교 의과대학 신경외과학교실) ;
  • 정흥섭 (고려대학교 의과대학 신경외과학교실) ;
  • 이훈갑 (고려대학교 의과대학 신경외과학교실) ;
  • 이기찬 (고려대학교 의과대학 신경외과학교실)
  • Moon, Soo-Hyeon (Department of Neurosurgery, Konkuk University Nedical Center Chungju Hospital) ;
  • Oh, Jae-Inn (Department of Neurosurgery, College of Medicine, Korea University) ;
  • Park, Youn-Kwan (Department of Neurosurgery, College of Medicine, Korea University) ;
  • Chung, Heung-Sub (Department of Neurosurgery, College of Medicine, Korea University) ;
  • Lee, Hoon-Kap (Department of Neurosurgery, College of Medicine, Korea University) ;
  • Lee, Ki-Chan (Department of Neurosurgery, College of Medicine, Korea University)
  • 투고 : 1999.12.22
  • 심사 : 2000.08.03
  • 발행 : 2000.09.28

초록

Objective : The transverse hippocampal slice is one of the most commonly studied in vitro models of mammalian brain physiology. However, despite its broad usage, there has been no standardization of slice preparation techniques or recording condition. It is well known that variations in recording conditions can result in profound different effects to neuronal responses. Evoked field potentials, recorded extracellularly, were used to investigate the effects of variations in hippocampal slice preparation protocol on hypoxia responses of CA1 neurones. Material & Methods : Before hypoxic injury, hippocampal slices were incubated for 4 hours. During incubation period, the slices were placed in a incubation chamber($21^{\circ}C$) for recovery from preparation injury and then transferred to recording chamber($34^{\circ}C$) for more recovery and baseline electric recording with current stimulation(0.1Hz). Various time periods in incubation chamber and recording chamber were applied to each experimental group(group 1=60min : 180min, group 2=90min : 150min, group 3=180min : 60min, time in incubation chamber : time in recording chamber) before 10 min hypoxia produced by replacing 95% $O_2$+5% $CO_2$ mixed gas to 95% $N_2$+5% $CO_2$ gas. Calcium, Magnesium ions and several drugs effecting on glutamate receptor also were studied. Recoveries from hypoxic injury of hippocampal slices were estimated by percent recovery of population spike(PS). Statistic analysis of study were performed using paired t-test. Results : The percent recovery of PS after 10min hypoxia was considerably enhanced by increasing the period of current stimulation during incubation period before hypoxic injury. Temperature effect on the result of this experiment was also studied(group 4) but the result from this showed no statistic significance. Low magnesium ion concentration of artificial CSF(Mg-free aCSF) during incubation period enhanced the recovery of PS but low calcium (calcium-free) and high magnesium ion concentration(2mM) reduced it after hypoxic injury. L-glutamate($100{\mu}M$) and AP-5($50{\mu}M$) had no effect on the recovery of PS but CNQX($10{\mu}M$) in artificial CSF during incubation period markedly enhanced the recovery of PS. Co-treatment of AP-5($50{\mu}M$), CNQX($10{\mu}M$) and high magnesium concentration(2mM) enhanced recovery of PS in immediate following period of hypoxic injury but the effect of cotreatment after then decayed rapidly and lost statistic significance. Conclusions : Judging from above results, the condition of baseline recording is important in observing the recovery of population spike after hypoxia, and the time and the condition should be controled more strictly to obtain reliable results.

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