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中缝核团对从穿通通路经齿状回的神经元传递的影响。

Influence of raphe nuclei on neuronal transmission from perforant pathway through dentate gyrus.

作者信息

Winson J

出版信息

J Neurophysiol. 1980 Nov;44(5):937-50. doi: 10.1152/jn.1980.44.5.937.

DOI:10.1152/jn.1980.44.5.937
PMID:6255111
Abstract
  1. In chronically prepared, freely moving rats, electrical stimulation was applied to the perforant pathway and monosynaptic responses were recorded extracellularly in the ipsilateral dentate gyrus. In some tests a stimulus was also applied to the median raphe nucleus (mr) prior to activating the perforant pathway. Experiments were performed during two behavioral conditions: slow-wave sleep (SWS) and the still, alert state (SAL). Two varieties of evoked responses were recorded: those due to synchronous firing of neuronal action potentials (evoked action potentials or EAPs) and those produced by excitatory synaptic activity (evoked synaptic potentials or ESPs). 2. As reported previously (38), perforant path stimulation elicited EAPs of greater magnitude during SWS than during SAL. The application of a prior stimulus to mr (prestimulation) markedly increased the already elevated EAPs observed during SWS. The EAPs during SAL were unaffected by prestimulation. 3. The minimum delay time (time between mr and perforant path stimuli) at which the augmentation of the EAPs appeared during SWS was approximately 5 ms. The augmentation reached a maximum at delay times of 25-40 ms and was present up to a delay time of 150 ms. 4. As in former experiments (38), ESPs recorded in the molecular layer of the dentate gyrus after perforant path stimulation were found to be greater during SAL than during SWS. Prestimulation of mr had no significant effect on the ESPs at any level of the molecular layer during either SWS or SAL. 5. The perforant path afferent volley was recorded at high gain in the dentate gyrus. Its amplitude was found to be solely dependent on perforant path stimulus intensity and not on behavioral state or the prestimulation of mr. 6. In preparations anesthetized with Chloropent (82% chloral hydrate, 18% pentobarbital; Fort Dodge Laboratories, Fort Dodge, IA), prestimulation was applied at each of a number of loci within the pons and medulla, including mr, As in SWS, prestimulating mr resulted in augmented EAPs with a minimum delay time of 5 ms. Similar augmented responses were observed when stimulation was applied at other raphe nuclei (dorsal raphe, pontis, magnus, and pallidus), but there was no augmentation when stimulation was applied at other brain stem sites. Threshold stimulus intensities for producing augmented EAPs in the raphe nuclei were less than 30 microA. 7. In freely moving animals it was first established that the EAP responses during SWS were markedly greater than during SAL. Midline lesions were then made at the rostrocaudal level of mr. Following the lesions, there was no longer any significant difference in the magnitude of the EAPs recorded during the two behaviors. 8. These findings suggest that tonic influences arising from raphe nuclei during SWS may be involved in the facilitation of neuronal transmission through the dentate gyrus observed during this behavioral state.
摘要
  1. 在长期制备的、自由活动的大鼠中,对穿通通路施加电刺激,并在同侧齿状回细胞外记录单突触反应。在一些试验中,在激活穿通通路之前,也对中缝正中核(mr)施加刺激。实验在两种行为状态下进行:慢波睡眠(SWS)和安静警觉状态(SAL)。记录到两种诱发反应:由神经元动作电位同步发放引起的反应(诱发动作电位或EAPs)和由兴奋性突触活动产生的反应(诱发突触电位或ESPs)。2. 如先前报道(38),穿通通路刺激在慢波睡眠期间比在安静警觉状态下诱发的EAPs幅度更大。对mr施加预先刺激(预刺激)显著增加了在慢波睡眠期间观察到的已经升高的EAPs。安静警觉状态下的EAPs不受预刺激影响。3. 在慢波睡眠期间EAPs增强出现的最小延迟时间(mr和穿通通路刺激之间的时间)约为5毫秒。增强在延迟时间为25 - 40毫秒时达到最大值,并且一直持续到延迟时间为150毫秒。4. 如先前实验(38)一样,在穿通通路刺激后在齿状回分子层记录到的ESPs在安静警觉状态下比在慢波睡眠期间更大。在慢波睡眠或安静警觉状态下,mr的预刺激对分子层任何水平的ESPs均无显著影响。5. 在齿状回以高增益记录穿通通路传入冲动。发现其幅度仅取决于穿通通路刺激强度,而不取决于行为状态或mr的预刺激。6. 在用氯戊巴比妥(82%水合氯醛,18%戊巴比妥;福道奇实验室,爱荷华州福道奇)麻醉的标本中,在脑桥和延髓内的多个位点(包括mr)施加预刺激。与慢波睡眠时一样,预刺激mr导致EAPs增强,最小延迟时间为5毫秒。当在其他中缝核(背侧中缝核、脑桥中缝核、大细胞中缝核和苍白中缝核)施加刺激时观察到类似的增强反应,但在其他脑干位点施加刺激时没有增强。在中缝核产生增强的EAPs的阈刺激强度小于30微安。7. 在自由活动的动物中,首先确定慢波睡眠期间的EAP反应明显大于安静警觉状态下的。然后在mr的前后水平进行中线损伤。损伤后,在两种行为期间记录到的EAPs幅度不再有任何显著差异。8. 这些发现表明,慢波睡眠期间从中缝核产生的紧张性影响可能参与了在这种行为状态下观察到的通过齿状回的神经元传递的促进作用。

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