scholarly journals Anticipatory Changes in Regional Cerebral Hemodynamics: A New Role for Dopamine?

2009 ◽  
Vol 101 (6) ◽  
pp. 2738-2740 ◽  
Author(s):  
Can Ozan Tan

Recently, adaptively timed, anticipatory changes in hemodynamic responses, independent of neural activity, were described in primate primary visual cortex. Task-related properties of these responses point to a possible link between regional cerebral microcirculation and dopaminergic signaling. In this report, this link is elaborated on the basis of known physiological data and further experiments are proposed to test the possible role of dopamine in task-dependent, “on-demand” allocation of metabolic resources.

2008 ◽  
Vol 20 (7) ◽  
pp. 1847-1872 ◽  
Author(s):  
Mark C. W. van Rossum ◽  
Matthijs A. A. van der Meer ◽  
Dengke Xiao ◽  
Mike W. Oram

Neurons in the visual cortex receive a large amount of input from recurrent connections, yet the functional role of these connections remains unclear. Here we explore networks with strong recurrence in a computational model and show that short-term depression of the synapses in the recurrent loops implements an adaptive filter. This allows the visual system to respond reliably to deteriorated stimuli yet quickly to high-quality stimuli. For low-contrast stimuli, the model predicts long response latencies, whereas latencies are short for high-contrast stimuli. This is consistent with physiological data showing that in higher visual areas, latencies can increase more than 100 ms at low contrast compared to high contrast. Moreover, when presented with briefly flashed stimuli, the model predicts stereotypical responses that outlast the stimulus, again consistent with physiological findings. The adaptive properties of the model suggest that the abundant recurrent connections found in visual cortex serve to adapt the network's time constant in accordance with the stimulus and normalizes neuronal signals such that processing is as fast as possible while maintaining reliability.


1994 ◽  
Vol 34 (6) ◽  
pp. 709-720 ◽  
Author(s):  
Michela Fagiolini ◽  
Tommaso Pizzorusso ◽  
Nicoletta Berardi ◽  
Luciano Domenici ◽  
Lamberto Maffei

2016 ◽  
Vol 23 (5) ◽  
pp. 529-541 ◽  
Author(s):  
Sara Ajina ◽  
Holly Bridge

Damage to the primary visual cortex removes the major input from the eyes to the brain, causing significant visual loss as patients are unable to perceive the side of the world contralateral to the damage. Some patients, however, retain the ability to detect visual information within this blind region; this is known as blindsight. By studying the visual pathways that underlie this residual vision in patients, we can uncover additional aspects of the human visual system that likely contribute to normal visual function but cannot be revealed under physiological conditions. In this review, we discuss the residual abilities and neural activity that have been described in blindsight and the implications of these findings for understanding the intact system.


1998 ◽  
Vol 10 (2) ◽  
pp. 353-371 ◽  
Author(s):  
Paul Mineiro ◽  
David Zipser

The relative contributions of feedforward and recurrent connectivity to the direction-selective responses of cells in layer IVB of primary visual cortex are currently the subject of debate in the neuroscience community. Recently, biophysically detailed simulations have shown that realistic direction-selective responses can be achieved via recurrent cortical interactions between cells with nondirection-selective feedforward input (Suarez et al., 1995; Maex & Orban, 1996). Unfortunately these models, while desirable for detailed comparison with biology, are complex and thus difficult to analyze mathematically. In this article, a relatively simple cortical dynamical model is used to analyze the emergence of direction-selective responses via recurrent interactions. A comparison between a model based on our analysis and physiological data is presented. The approach also allows analysis of the recurrently propagated signal, revealing the predictive nature of the implementation.


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