Weak before strong: dissociating synaptic tagging and plasticity-factor accounts of late-LTP

被引:175
作者
Frey, U
Morris, RGM
机构
[1] Leibniz Inst Neurobiol, D-39008 Magdeburg, Germany
[2] Univ Edinburgh, Sch Med, Dept Pharmacol, Edinburgh EH8 9LE, Midlothian, Scotland
[3] Univ Edinburgh, Sch Med, Ctr Neurosci, Edinburgh EH8 9LE, Midlothian, Scotland
关键词
synaptic tagging; plasticity; long-term potentiation (LTP); late-LTP; protein synthesis; variable persistence of LTP;
D O I
10.1016/S0028-3908(98)00040-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Experiments were conducted using hippocampal slices in vitro to compare two accounts of the mechanisms by which input-specific protein synthesis-dependent long-term potentiation (late-LTP) may be realised. The synaptic tag hypothesis (Frey and Morris, 1997) predicts that the expression of early-LTP following a weak tetanus can be stabilised into late-LTP by subsequent strong tetanisation of a separate pathway, provided the interval between the two tetanisation episodes is within the decay time-course of a putative synaptic tag. An alternative plasticity-factors hypothesis requires that strong tetanisation should always precede weak tetanisation for stabilisation of early-LTP to occur. Our results indicate that weak tetanisation of pathway S2 at intervals of 5 min or 1 h prior to strong tetanisation on pathway S1 does result in late-LTP on pathway S2. Stabilisation was weaker or did not occur at intervals of 2 and 4 h. This stabilisation effect was shown to depend on protein synthesis during the strong tetanisation of S1. These findings uphold a key prediction of the synaptic tag hypothesis and have implications for the functional role of synaptic tagging for cortical plasticity. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:545 / 552
页数:8
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