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在顶叶后皮质受损后,头部方向细胞在很大程度上仍能维持地标控制和自我运动线索的更新。

Landmark control and updating of self-movement cues are largely maintained in head direction cells after lesions of the posterior parietal cortex.

作者信息

Calton Jeffrey L, Turner Carol S, Cyrenne De-Laine M, Lee Brian R, Taube Jeffrey S

机构信息

Department of Psychology, California State University-Sacramento, CA, USA.

出版信息

Behav Neurosci. 2008 Aug;122(4):827-40. doi: 10.1037/0735-7044.122.4.827.

DOI:10.1037/0735-7044.122.4.827
PMID:18729636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2771080/
Abstract

Head direction (HD) cells discharge as a function of the rat's directional orientation with respect to its environment. Because animals with posterior parietal cortex (PPC) lesions exhibit spatial and navigational deficits, and the PPC is indirectly connected to areas containing HD cells, we determined the effects of bilateral PPC lesions on HD cells recorded in the anterodorsal thalamus. HD cells from lesioned animals had similar firing properties compared to controls and their preferred firing directions shifted a corresponding amount following rotation of the major visual landmark. Because animals were not exposed to the visual landmark until after surgical recovery, these results provide evidence that the PPC is not necessary for visual landmark control or the establishment of landmark stability. Further, cells from lesioned animals maintained a stable preferred firing direction when they foraged in the dark and were only slightly less stable than controls when they self-locomoted into a novel enclosure. These findings suggest that PPC does not play a major role in the use of landmark and self-movement cues in updating the HD cell signal, or in its generation.

摘要

头部方向(HD)细胞的放电是大鼠相对于其环境的定向取向的函数。由于患有顶叶后皮质(PPC)损伤的动物表现出空间和导航缺陷,并且PPC与包含HD细胞的区域间接相连,因此我们确定了双侧PPC损伤对在前背侧丘脑记录的HD细胞的影响。与对照组相比,来自损伤动物的HD细胞具有相似的放电特性,并且在主要视觉地标旋转后,它们的首选放电方向相应地发生了偏移。由于动物直到手术恢复后才接触视觉地标,这些结果提供了证据,表明PPC对于视觉地标控制或地标稳定性的建立不是必需的。此外,来自损伤动物的细胞在黑暗中觅食时保持稳定的首选放电方向,并且当它们自行进入新的围栏时,其稳定性仅略低于对照组。这些发现表明,PPC在利用地标和自我运动线索更新HD细胞信号或其产生过程中不发挥主要作用。

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