Stackman Robert W, Cohen Sarah J, Lora Joan C, Rios Lisa M
Department of Psychology, Florida Atlantic University, John D. MacArthur Campus, Jupiter, FL 33458, USA; Center for Complex Systems & Brain Sciences, Florida Atlantic University, Boca Raton, FL 33431, USA.
Center for Complex Systems & Brain Sciences, Florida Atlantic University, Boca Raton, FL 33431, USA.
Neurobiol Learn Mem. 2016 Sep;133:118-128. doi: 10.1016/j.nlm.2016.06.016. Epub 2016 Jun 18.
Recognition of a previously experienced item or object depends upon the successful retrieval of memory for the object. The neural mechanisms that support object recognition memory in the mammalian brain are not well understood. The rodent hippocampus plays a well-established role in spatial memory, and we previously demonstrated that temporary inactivation of the mouse hippocampus impairs object memory, as assessed with a novel object preference (NOP) test. The present studies were designed to test some remaining issues regarding the contribution of the CA1 sub-region of the mouse dorsal hippocampus to long-term object memory. Specifically, we examined whether the retrieval of spatial memory (as assessed by the Morris water maze; MWM) and object recognition memory are differentially sensitive to inactivation of the CA1 region. The current study used pre-test local microinfusion of muscimol directly into the CA1 region of dorsal hippocampus to temporarily interrupt its function during the respective retrieval phases of both behavioral tasks, in order to compare the contribution of the CA1 to object memory and spatial memory. Histological analyses revealed that local intra-CA1 injection of muscimol diffused within, and not beyond, the CA1 region of dorsal hippocampus. The degree of memory retrieval impairment induced by muscimol was comparable in the two tasks, supporting the view that object memory and spatial memory depend similarly on the CA1 region of rodent hippocampus. Further, we confirmed that the muscimol-induced impairment of CA1 function is temporary. First, mice that exhibited impaired object memory retrieval immediately after intra-CA1 muscimol, subsequently exhibited unimpaired retrieval of object memory when tested 24h later. Secondly, a cohort of mice that exhibited impaired object memory retrieval after intra-CA1 muscimol later acquired spatial memory in the MWM comparable to that of control mice. Together, these results offer further support for the involvement of the CA1 region of mouse hippocampus in object recognition memory, and provide evidence to suggest that the NOP task is as much a test of hippocampal function as the classic MWM test.
对先前经历过的物品或物体的识别取决于对该物体记忆的成功提取。哺乳动物大脑中支持物体识别记忆的神经机制尚未得到充分理解。啮齿动物海马体在空间记忆中发挥着既定作用,我们之前证明,小鼠海马体的暂时失活会损害物体记忆,这是通过新颖物体偏好(NOP)测试评估得出的。本研究旨在测试关于小鼠背侧海马体CA1亚区对长期物体记忆贡献的一些遗留问题。具体而言,我们研究了空间记忆的提取(通过莫里斯水迷宫;MWM评估)和物体识别记忆对CA1区失活的敏感性是否存在差异。当前研究在两个行为任务各自的提取阶段,通过将蝇蕈醇预先局部微量注入背侧海马体的CA1区,以暂时中断其功能,从而比较CA1对物体记忆和空间记忆的贡献。组织学分析表明,局部CA1内注射蝇蕈醇在背侧海马体的CA1区内扩散,并未超出该区域。蝇蕈醇诱导的记忆提取损伤程度在两项任务中相当,这支持了物体记忆和空间记忆同样依赖于啮齿动物海马体CA1区的观点。此外,我们证实了蝇蕈醇诱导的CA功能损伤是暂时的。首先,在CA1内注射蝇蕈醇后立即表现出物体记忆提取受损的小鼠,在24小时后测试时,随后表现出物体记忆提取未受损。其次,一组在CA1内注射蝇蕈醇后表现出物体记忆提取受损的小鼠,后来在MWM中获得了与对照小鼠相当的空间记忆。总之,这些结果进一步支持了小鼠海马体CA1区参与物体识别记忆,并提供证据表明NOP任务与经典的MWM测试一样,都是对海马体功能的测试。