Response sensitivity of barrel neuron subpopulations to simulated thalamic input.
نویسندگان
چکیده
Our goal is to examine the relationship between neuron- and network-level processing in the context of a well-studied cortical function, the processing of thalamic input by whisker-barrel circuits in rodent neocortex. Here we focus on neuron-level processing and investigate the responses of excitatory and inhibitory barrel neurons to simulated thalamic inputs applied using the dynamic clamp method in brain slices. Simulated inputs are modeled after real thalamic inputs recorded in vivo in response to brief whisker deflections. Our results suggest that inhibitory neurons require more input to reach firing threshold, but then fire earlier, with less variability, and respond to a broader range of inputs than do excitatory neurons. Differences in the responses of barrel neuron subtypes depend on their intrinsic membrane properties. Neurons with a low input resistance require more input to reach threshold but then fire earlier than neurons with a higher input resistance, regardless of the neuron's classification. Our results also suggest that the response properties of excitatory versus inhibitory barrel neurons are consistent with the response sensitivities of the ensemble barrel network. The short response latency of inhibitory neurons may serve to suppress ensemble barrel responses to asynchronous thalamic input. Correspondingly, whereas neurons acting as part of the barrel circuit in vivo are highly selective for temporally correlated thalamic input, excitatory barrel neurons acting alone in vitro are less so. These data suggest that network-level processing of thalamic input in barrel cortex depends on neuron-level processing of the same input by excitatory and inhibitory barrel neurons.
منابع مشابه
Response sensitivity of barrel neuron sub - populations 6 to simulated thalamic input 7 8 9 10
1 2 3 4 5 Response sensitivity of barrel neuron sub-populations 6 to simulated thalamic input 7 8 9 10 Michael J. Pesavento Cynthia D. Rittenhouse, David J Pinto 11 12 13 14 Department of Neurobiology and Anatomy, 15 Department of Biomedical Engineering, 16 Department of Neurology 17 University of Rochester School of Medicine 18 Rochester, NY, 15642 19 20 21 22 23 Running Title: Barrel neuron r...
متن کامل1 Network and neuronal membrane properties in hybrid networks reciprocally 2 regulate selectivity to rapid thalamocortical inputs
33 Rapidly changing environments require rapid processing from sensory inputs. Varying deflection 34 velocities of a rodent’s primary facial vibrissa cause varying temporal neuronal activity profiles within the 35 ventral posteromedial thalamic nucleus. Local neuron populations in a single somatosensory layer 4 barrel 36 transform sparsely coded input into a spike count based on the input’s tem...
متن کاملNetwork and neuronal membrane properties in hybrid networks reciprocally regulate selectivity to rapid thalamocortical inputs.
Rapidly changing environments require rapid processing from sensory inputs. Varying deflection velocities of a rodent's primary facial vibrissa cause varying temporal neuronal activity profiles within the ventral posteromedial thalamic nucleus. Local neuron populations in a single somatosensory layer 4 barrel transform sparsely coded input into a spike count based on the input's temporal profil...
متن کاملCortical damping: analysis of thalamocortical response transformations in rodent barrel cortex.
In the whisker-barrel system, layer IV excitatory neurons respond preferentially to high-velocity deflections of their principal whisker, and these responses are inhibited by deflections of adjacent whiskers. Thalamic input neurons are amplitude and velocity sensitive and have larger excitatory and weaker inhibitory receptive fields than cortical neurons. Computational models based on known fea...
متن کاملWeaker feedforward inhibition accounts for less pronounced thalamocortical response transformation in mouse vs. rat barrels.
Feedforward inhibition is a common motif of thalamocortical circuits. Strong engagement of inhibitory neurons by thalamic inputs enhances response differentials between preferred and nonpreferred stimuli. In rat whisker-barrel cortex, robustly driven inhibitory barrel neurons establish a brief epoch during which synchronous or near-synchronous thalamic firing produces larger responses to prefer...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of neurophysiology
دوره 103 6 شماره
صفحات -
تاریخ انتشار 2010