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新生大鼠齿状回长时程增强和长时程抑制的体内记录。

In vivo recordings of long-term potentiation and long-term depression in the dentate gyrus of the neonatal rat.

作者信息

O'Boyle Michael P, Do Viet, Derrick Brian E, Claiborne Brenda J

机构信息

Department of Biology, The University of Texas at San Antonio, San Antonio, Texas 78249, USA.

出版信息

J Neurophysiol. 2004 Feb;91(2):613-22. doi: 10.1152/jn.00307.2003. Epub 2003 Nov 26.

Abstract

Previous in vitro studies demonstrated that long-term potentiation (LTP) could be elicited at medial perforant path (MPP) synapses onto hippocampal granule cells in slices from 7-day-old rats. In contrast, in vivo studies suggested that LTP at perforant path synapses could not be induced until at least days 9 or 10 and then in only a small percentage of animals. Because several characteristics of the oldest granule cells are adult-like on day 7, we re-examined the possibility of eliciting LTP in 7-day-old rats in vivo. We also recorded from 8- and 9-day-old rats to further elucidate the occurrence and magnitude of LTP in neonates. With halothane anesthesia, all animals in each age group exhibited synaptic plasticity of the excitatory postsynaptic potential following high-frequency stimulation of the MPP. In 7-day-old rats, LTP was elicited in 40% of the animals and had an average magnitude of 143%. Long-term depression (LTD) alone (magnitude of 84%) was induced in 40% of the animals, while short-term potentiation (STP) alone (magnitude of 123%) was induced in 10%. STP followed by LTD was elicited in the remaining 10%. Data were similar for all ages combined. In addition, the N-methyl-d-aspartate (NMDA) antagonist (R,S)-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) blocked the occurrence of LTP at each age and doubled the percentage of animals expressing LTD alone for all ages combined. These results demonstrate that tetanic stimulation can elicit LTP or LTD at MPP synapses in 7-day-old rats, supporting our premise that at least a portion of the dentate gyrus is functional at this early age.

摘要

以往的体外研究表明,在7日龄大鼠脑片上,内侧穿通通路(MPP)与海马颗粒细胞之间的突触可引发长时程增强(LTP)。相比之下,体内研究表明,穿通通路突触处的LTP至少要到第9天或第10天才能够诱导产生,而且只有一小部分动物能诱导产生。由于最老的颗粒细胞的几个特征在第7天时就类似成年细胞,我们重新研究了在7日龄大鼠体内诱发LTP的可能性。我们还记录了8日龄和9日龄大鼠的情况,以进一步阐明新生大鼠LTP的发生情况及幅度。使用氟烷麻醉后,每个年龄组的所有动物在高频刺激MPP后均表现出兴奋性突触后电位的突触可塑性。在7日龄大鼠中,40%的动物诱发了LTP,平均幅度为143%。40%的动物单独诱发了长时程抑制(LTD)(幅度为84%),而10%的动物单独诱发了短时程增强(STP)(幅度为123%)。其余10%的动物诱发了先STP后LTD。所有年龄组的数据相似。此外,N-甲基-D-天冬氨酸(NMDA)拮抗剂(R,S)-3-(2-羧基哌嗪-4-基)丙基-1-膦酸(CPP)在各个年龄组均阻断了LTP的发生,并使所有年龄组合中单独表达LTD的动物百分比增加了一倍。这些结果表明,强直刺激可在7日龄大鼠的MPP突触处诱发LTP或LTD,支持了我们的假设,即齿状回的至少一部分在这个早期阶段就具有功能。

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