Slovin Hamutal, Arieli Amos, Hildesheim Rina, Grinvald Amiram
Department of Neurobiology and Grodetsky Center for Studies of Higher Brain Function, The Weizmann Institute of Science, 76100 Rehovot, Israel.
J Neurophysiol. 2002 Dec;88(6):3421-38. doi: 10.1152/jn.00194.2002.
A novel method of chronic optical imaging based on new voltage-sensitive dyes (VSDs) was developed to facilitate the explorations of the spatial and temporal patterns underlying higher cognitive functions in the neocortex of behaving monkeys. Using this system, we were able to explore cortical dynamics, with high spatial and temporal resolution, over period of <or=1 yr from the same patch of cortex. The visual cortices of trained macaques were stained one to three times a week, and immediately after each staining session, the monkey started to perform the behavioral task, while the primary and secondary visual areas (V1 and V2) were imaged with a fast optical imaging system. Long-term repeated VSD imaging (VSDI) from the same cortical area did not disrupt the normal cortical architecture as confirmed repeatedly by optical imaging based on intrinsic signals. The spatial patterns of functional maps obtained by VSDI were essentially identical to those obtained from the same patch of cortex by imaging based on intrinsic signals. On comparing the relative amplitudes of the evoked signals and differential map obtained using these two different imaging methodologies, we found that VSDI emphasizes subthreshold activity more than imaging based on intrinsic signals, that emphasized more spiking activity. The latency of the VSD-evoked response in V1 ranged from 46 to 68 ms in the different monkeys. The amplitude of the V2 response was only 20-60% of that in V1. As expected from the anatomy, the retinotopic responses to local visual stimuli spread laterally across the cortical surface at a spreading velocity of 0.15-0.19 m/s over a larger area than that expected by the classical magnification factor, reaching its maximal anisotropic spatial extent within approximately 40 ms. We correlated the observed dynamics of cortical activation patterns with the monkey's saccadic eye movements and found that due to the slow offset of the cortical response relative to its onset, there was a short period of simultaneous activation of two distinct patches of cortex following a saccade to the visual stimulus. We also found that a saccade to a small stimulus was followed by direct transient activation of a cortical region in areas of V1 and V2, located retinotopically within the saccadic trajectory.
基于新型电压敏感染料(VSDs)开发了一种新型慢性光学成像方法,以促进对行为猴子新皮层中更高认知功能潜在的空间和时间模式的探索。使用该系统,我们能够在长达1年的时间里,以高空间和时间分辨率从同一皮层区域探索皮层动力学。对训练有素的猕猴的视觉皮层每周进行1至3次染色,每次染色后立即让猴子开始执行行为任务,同时用快速光学成像系统对初级和次级视觉区域(V1和V2)进行成像。基于内在信号的光学成像反复证实,从同一皮层区域进行长期重复的VSD成像(VSDI)不会破坏正常的皮层结构。通过VSDI获得的功能图谱的空间模式与通过基于内在信号的成像从同一皮层区域获得的空间模式基本相同。在比较使用这两种不同成像方法获得的诱发信号的相对幅度和差异图谱时,我们发现VSDI比基于内在信号的成像更强调阈下活动,后者更强调尖峰活动。在不同猴子中,V1中VSD诱发反应的潜伏期为46至68毫秒。V2反应的幅度仅为V1中的20%-60%。正如从解剖学上预期的那样,对局部视觉刺激的视网膜拓扑反应以0.15-0.19米/秒的传播速度在皮层表面横向传播,传播面积比经典放大因子预期的更大,在大约40毫秒内达到其最大各向异性空间范围。我们将观察到的皮层激活模式的动力学与猴子的扫视眼动相关联,发现由于皮层反应相对于其起始的缓慢偏移,在向视觉刺激进行扫视后,有一小段时间两个不同的皮层区域会同时激活。我们还发现,向小刺激进行扫视后,V1和V2区域中位于扫视轨迹视网膜拓扑位置的皮层区域会直接短暂激活。