Ferretti Valentina, Florian Cédrick, Costantini Vivian J A, Roullet Pascal, Rinaldi Arianna, De Leonibus Elvira, Oliverio Alberto, Mele Andrea
Dipartimento di Genetica e Biologia Molecolare, Università di Roma La Sapienza, 00185 Rome, Italy.
Psychopharmacology (Berl). 2005 Apr;179(1):108-16. doi: 10.1007/s00213-005-2144-3. Epub 2005 Jan 29.
The nucleus accumbens receives glutamatergic and dopaminergic inputs converging onto common dendrites. Recent behavioral data demonstrated that intra-accumbens administrations of either glutamate or dopamine (DA) antagonist impair spatial memory consolidation. Thus, also based on the biochemical and molecular findings demonstrating interactions among the different receptors subtypes for glutamate and dopamine, it is conceivable that memory consolidation within this structure might be modulated by glutamate-dopamine receptor interactions.
The purpose of this study was to examine the effects of intra-accumbens co-administrations of glutamate and DA antagonists on the consolidation of spatial information.
On day 1, CD1 male mice were placed in an open field containing five different objects and immediately after three sessions of habituation the animals were injected intra-accumbens with either vehicle or low doses of the N-methyl-D: -aspartate (NMDA; AP-5 50 ng/side), the alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA; DNQX 5 ng/side), the D1 (SCH23390 12.5 ng/side) and the D2 (sulpiride 25 ng/side) antagonists that were ineffective alone in disrupting object displacement. Separate groups were then focally injected with a combination of one of the glutamate antagonists with one of the dopamine antagonists. Twenty-four hours later, the ability of mice to discriminate object displacement was assessed.
Controls and mice injected with ineffective doses of the NMDA, the AMPA, the D1 or the D2 antagonists were always able to react to the object displacement. On the contrary, the groups administered with the different combinations (AP-5 and SCH23390, AP-5 and sulpiride, DNQX and SCH23390, DNQX and sulpiride) of glutamate and dopamine antagonists did not discriminate the spatial change.
These results demonstrate that glutamate-dopamine receptor interactions within the accumbens are essential for the consolidation process of spatial information.
伏隔核接收汇聚于共同树突上的谷氨酸能和多巴胺能输入。近期行为学数据表明,向伏隔核内注射谷氨酸或多巴胺(DA)拮抗剂会损害空间记忆巩固。因此,基于证明谷氨酸和多巴胺不同受体亚型之间存在相互作用的生化和分子研究结果,可以推测该结构内的记忆巩固可能受谷氨酸 - 多巴胺受体相互作用的调节。
本研究旨在考察向伏隔核内共同注射谷氨酸和DA拮抗剂对空间信息巩固的影响。
在第1天,将CD1雄性小鼠置于含有五个不同物体的旷场中,在三次适应训练后,立即向小鼠伏隔核内注射溶剂或低剂量的N - 甲基 - D - 天冬氨酸(NMDA;AP - 5 50 ng/侧)、α - 氨基 - 3 - 羟基 - 5 - 甲基 - 4 - 异恶唑丙酸(AMPA;DNQX 5 ng/侧)、D1(SCH23390 12.5 ng/侧)和D2(舒必利25 ng/侧)拮抗剂,这些拮抗剂单独使用时对破坏物体位移无效。然后将单独的组分别局部注射一种谷氨酸拮抗剂与一种多巴胺拮抗剂的组合。24小时后,评估小鼠辨别物体位移的能力。
对照组以及注射无效剂量的NMDA、AMPA、D1或D2拮抗剂的小鼠总能对物体位移做出反应。相反,给予谷氨酸和多巴胺拮抗剂不同组合(AP - 5和SCH23390、AP - 5和舒必利、DNQX和SCH23390、DNQX和舒必利)的组无法辨别空间变化。
这些结果表明,伏隔核内的谷氨酸 - 多巴胺受体相互作用对空间信息的巩固过程至关重要。