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关于麻醉和自由活动大鼠海马CA1区长期抑郁的研究。

Studies on long-term depression in area CA1 of the anesthetized and freely moving rat.

作者信息

Staubli U, Scafidi J

机构信息

Center for Neural Science, New York University, New York, New York 10003, USA.

出版信息

J Neurosci. 1997 Jun 15;17(12):4820-8. doi: 10.1523/JNEUROSCI.17-12-04820.1997.

Abstract

Homosynaptic long-term depression (LTD) is reported to occur in field CA1 of hippocampal slices collected from immature brains. Because the effect has been postulated to be a memory storage mechanism, it is of interest to test for its presence in adult, awake animals. Unfortunately, not only has hippocampal LTD proved difficult to obtain reliably in vivo, but the few successful studies vary with respect to protocols and evidence that the depression is input-specific. The present study tested for input-specific (homosynaptic) LTD in field CA1 after application of various stimulation protocols to the Schaffer collateral/commissural projections in freely moving, adult rats. The results indicate that although low-frequency trains do induce decrements in synaptic transmission lasting for hours to several days, the success rate of eliciting input-specific LTD in the awake rat is very modest compared with the ease with which stable potentiation is obtained in the same synapses. Moreover, it is questionable that the effective protocols represent patterns of activity likely to occur during behavior. The stronger the afferent activation during low-frequency stimulation, the greater was the probability of eliciting LTD accompanied by persistent heterosynaptic depression. Clear evidence for the occurrence of LTD, irrespective of stimulation protocol and current intensity, could not be obtained in rats under barbiturate anesthesia. In all, the results do not accord with the suggestion that LTD occurs routinely in the hippocampus in vivo as part of memory encoding.

摘要

据报道,在从未成熟大脑采集的海马切片的CA1区会出现同突触长时程抑制(LTD)。由于这种效应被假定为一种记忆存储机制,因此测试其在成年清醒动物中的存在情况很有意义。不幸的是,不仅海马LTD在体内难以可靠获得,而且少数成功的研究在实验方案以及该抑制是输入特异性的证据方面存在差异。本研究在自由活动的成年大鼠中,对Schaffer侧支/连合投射应用各种刺激方案后,测试了CA1区的输入特异性(同突触)LTD。结果表明,虽然低频串刺激确实会引起持续数小时至数天的突触传递衰减,但与在相同突触中轻松获得稳定增强相比,在清醒大鼠中引发输入特异性LTD的成功率非常低。此外,有效的实验方案是否代表行为过程中可能出现的活动模式也值得怀疑。低频刺激期间传入激活越强,引发LTD并伴有持续性异突触抑制的可能性就越大。在巴比妥类麻醉的大鼠中,无论刺激方案和电流强度如何,都无法获得LTD发生的确切证据。总之,这些结果与LTD作为记忆编码的一部分在体内海马中常规发生的观点不一致。

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