Laboratoire d'Imagerie et de Neurosciences Cognitives, FRE 3289, Université de Strasbourg - CNRS, Faculté de Psychologie, 67000 Strasbourg, France.
Hippocampus. 2011 Dec;21(12):1277-89. doi: 10.1002/hipo.20837. Epub 2010 Jul 9.
Studies of the neuropharmacological substrates of spatial memory formation have focused on the contribution of septohippocampal pathways. Although these pathways include, among others, cholinergic and GABAergic fibers innervating the hippocampus, research has essentially been oriented towards the role of their cholinergic component. Recently, a few studies investigated the role of GABAergic septohippocampal projections. These only focused on almost immediate or recent memory and yielded discrepant results. GABAergic lesions impaired learning or had no effects. Given the role of the hippocampus in memory consolidation and the potential modulatory influence of the septum on hippocampal function, it is relevant to study the role of the septohippocampal interface in memory stabilization. We performed investigations with relatively selective lesions of GABAergic (using oxerin-saporin) or/and cholinergic (using 192 IgG-saporin) medial septum/vertical limb of the diagonal band of Broca (MS/vDBB) neurons in rats, and assessed acquisition of a spatial memory and its subsequent recall in the water maze. Following a 6-day training phase during which all groups improved performance to comparable levels, retention was tested 1, 5, or 25 days later. At the 1-day delay, all groups performed above chance and did not differ significantly among each other. At the 5-day delay, only rats with GABAergic or combined lesions exhibited a retention deficit. At the 25-day delay, all three lesion groups performed at chance level; in these groups, performance was significantly lower than that found in sham-operated rats. Immunochemical and histochemical verifications of the lesion extent/selectivity showed extensive GABAergic damage after intraseptal orexin-saporin infusions or cholinergic damage after 192 IgG-saporin infusions, with relatively limited damage to the other neurotransmitter system. Our data show that GABAergic and cholinergic septohippocampal neurons both contribute to memory stabilization, and could do so in a sequential way: GABAergic processes could be engaged at an earlier stage than cholinergic ones during system consolidation of a spatial memory.
研究空间记忆形成的神经药理学基础集中在隔海马通路的贡献上。尽管这些通路包括但不限于支配海马的胆碱能和 GABA 能纤维,但研究基本上是针对其胆碱能成分的作用。最近,一些研究调查了 GABA 能隔海马投射的作用。这些研究只关注几乎是即时或最近的记忆,得出了不一致的结果。GABA 能损伤损害了学习或没有影响。鉴于海马在记忆巩固中的作用以及隔区对海马功能的潜在调节影响,研究隔海马界面在记忆稳定中的作用是相关的。我们在大鼠中进行了相对选择性的 GABA 能(使用 ocrexin-saporin)或/和胆碱能(使用 192 IgG-saporin)内侧隔核/垂直带的 Broca (MS/vDBB)神经元损伤的研究,并评估了空间记忆的获得及其在水迷宫中的随后回忆。在为期 6 天的训练阶段,所有组都将表现提高到可比水平后,在 1、5 或 25 天后进行保留测试。在 1 天的延迟中,所有组的表现都高于机会水平,彼此之间没有显著差异。在 5 天的延迟中,只有 GABA 能或联合损伤的大鼠表现出保留缺陷。在 25 天的延迟中,所有三组损伤组的表现都达到机会水平;在这些组中,表现明显低于假手术组大鼠。损伤程度/选择性的免疫化学和组织化学验证表明,内侧隔核 orexin-saporin 输注后 GABA 能损伤广泛,192 IgG-saporin 输注后胆碱能损伤相对有限,而其他神经递质系统的损伤相对较小。我们的数据表明,GABA 能和胆碱能隔海马神经元都有助于记忆稳定,并且可以以顺序的方式进行:在空间记忆的系统巩固过程中,GABA 能过程可能比胆碱能过程更早参与。