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发育中大鼠新皮层的自发性癫痫样放电和持续电位变化。

Spontaneous ictal-like discharges and sustained potential shifts in the developing rat neocortex.

作者信息

Hablitz J J

机构信息

Department of Neurology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Neurophysiol. 1987 Nov;58(5):1052-65. doi: 10.1152/jn.1987.58.5.1052.

DOI:10.1152/jn.1987.58.5.1052
PMID:3694244
Abstract
  1. Intra- and extracellular recording techniques were used to study epileptogenesis in in vitro slices of immature rat neocortex. Slices of sensorimotor cortex were prepared from animals 5-60 days old. Epileptiform activity was induced by bath application of 50 microM picrotoxin. 2. Convulsant-induced paroxysmal activity was observed only rarely in the youngest age group (5-7 days) and consisted of orthodromically evoked bursts of low-amplitude isolated discharges. This activity was labile and could be evoked only at long interstimulus intervals (greater than 10 s). 3. Extracellular recordings in slices from 8- to 15-day-old rats showed spontaneous epileptiform activity consisting of 10- to 30-s paroxysms of repetitive spike discharges superimposed on a 3- to 5-mV negative steady potential. This steady potential declined slightly during the course of the prolonged discharge and returned quickly to base line following the last spike discharge. 4. Laminar analysis of epileptiform activity in 8- to 15-day-old rats showed that the spike discharges were negative and superimposed on a positive slow wave in superficial cortical layers. At 100 micron below the pial surface, the slow potential reversed polarity and remained negative throughout the remainder of the cortex. Spike discharges reversed polarity 800 micron below the pial surface. 5. In intracellular recordings from slices obtained from 9- to 14-day-old animals, each paroxysm began with a sharply rising membrane depolarization (paroxysmal depolarizing shift, or PDS). A second PDS occurred before the cells repolarized to their resting potential. A series of PDSs then followed, superimposed on a sustained membrane depolarization. This was associated with a 33% decrease in input resistance. Afterhyperpolarizations (AHPs) following termination of the depolarization were low in amplitude or absent. 6. In the 16- to 30-day-old age group, extracellular recordings showed paroxysmal activity consisting of 3-10 initial spikes followed by a sustained, slow, negative-potential shift. This slow potential could be as great as 30 mV in amplitude and could last as long as 180 s. Paroxysmal events recurred spontaneously at intervals of 4-11 min. Spontaneous PDSs and slow, negative-potential shifts were not observed after 30 days of age, although PDSs could still be evoked by orthodromic stimulation. 7. Intracellular recordings in the 16- to 30-day-old group revealed that each paroxysmal event consisted of an initial period of increased synaptic activity and cellular firing, followed by a marked, long-lasting depolarization (LLD), culminating in an AHP.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用细胞内和细胞外记录技术研究未成熟大鼠新皮质体外脑片的癫痫发生机制。从5至60日龄的动物制备感觉运动皮质脑片。通过浴加50微摩尔苦味毒诱导癫痫样活动。

  2. 在最年幼的年龄组(5至7日龄)中仅很少观察到惊厥诱导的阵发活动,其由正向诱发的低幅孤立放电爆发组成。这种活动不稳定,仅在长的刺激间隔(大于10秒)时才能诱发。

  3. 对8至15日龄大鼠脑片的细胞外记录显示,自发癫痫样活动由10至30秒的重复棘波放电阵发组成,叠加在3至5毫伏的负向稳定电位上。在长时间放电过程中,该稳定电位略有下降,并在最后一次棘波放电后迅速恢复至基线。

  4. 对8至15日龄大鼠癫痫样活动的层分析表明,棘波放电为负向,叠加在皮质浅层的正向慢波上。在软脑膜表面以下100微米处,慢电位极性反转,并在皮质其余部分始终保持负向。棘波放电在软脑膜表面以下800微米处极性反转。

  5. 在从9至14日龄动物获取的脑片的细胞内记录中,每次阵发开始时伴有膜去极化急剧上升(阵发去极化偏移,或PDS)。在细胞复极化至静息电位之前出现第二个PDS。随后是一系列PDS,叠加在持续的膜去极化上。这与输入电阻降低33%相关。去极化终止后的超极化后电位(AHP)幅度低或不存在。

  6. 在16至30日龄组中,细胞外记录显示阵发活动由3至10个初始棘波组成,随后是持续的、缓慢的负向电位偏移。该慢电位幅度可达30毫伏,可持续长达180秒。阵发事件以4至11分钟的间隔自发复发。30日龄后未观察到自发PDS和缓慢的负向电位偏移,尽管仍可通过正向刺激诱发PDS。

  7. 16至30日龄组的细胞内记录显示,每次阵发事件包括突触活动和细胞放电增加的初始阶段,随后是明显的、持久的去极化(LLD),最终导致AHP。(摘要截断于400字)

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