Two-deoxyglucose-induced long-term potentiation in slices of rat dentrate gyrus.

Jean-Marie Godfraind, Yao-Zhong Xu
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引用次数: 6

Abstract

In keeping with previous observations in the CA1 and the somatosensory neocortex of the brain of rat, 20-min applications of 2-deoxy-D-glucose (2DG; 10 mM, replacing glucose) induced a long-term potentiation (LTP)-like enhancement of field excitatory synaptic potentials (fEPSPs) in the dentate region of hippocampal slices. The effects of 2DG were not identical at synapses of medial and lateral perforant paths (MPP and LPP). At MPP synapses, there was no post-2DG early depression of fEPSPs and the potentiation reached +78.6 +/- 5.7 % (+/- standard error of the mean) 40 min after the return to glucose. In the presence of 50 microM D-amino-phosphono valerate (APV; an N-methyl-D-aspartate [NMDA] receptor antagonist), a marked post-2DG depression appeared and the subsequent LTP was reduced to +34.7 +/- 2.8 % (for both 2DG- and APV-treatment P<0.001 by ANOVA-2W). At LPP synapses, even under control conditions, there was a sharp post-2DG depression followed by LTP (+62.2 +/- 5.7 %) and APV had little effect on either the post-2DG depression or LTP, reducing the latter by only 24 % [the 2DG treatment was very significant (P<0.001) but not the APV treatment]. Thus, 2DG evokes both NMDAR-dependent and -independent components of LTP in the perforant pathways. In view of these findings, the consumption of 2DG could have significant effects on synaptic plasticity and cognitive function.
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二脱氧葡萄糖诱导大鼠齿状回切片的长时程增强。
与之前对大鼠大脑CA1和体感新皮层的观察结果一致,将2-脱氧-d -葡萄糖(2DG;10 mM,替代葡萄糖)诱导海马齿状区场兴奋性突触电位(fEPSPs)的长期增强(LTP)样增强。2DG对内侧和外侧穿通通路(MPP和LPP)突触的作用并不相同。在MPP突触,2dg后fepsp未出现早期抑制,在返回葡萄糖后40分钟增强达到+78.6 +/- 5.7%(平均+/-标准误差)。在50 μ m戊酸d -氨基膦(APV;(n -甲基- d -天冬氨酸[NMDA]受体拮抗剂),2DG后出现明显的抑制,随后LTP降至+34.7 +/- 2.8%(对于2DG-和apv治疗P)
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