Early gamma oscillations

Gamma oscillations have long been considered to emerge late in development. However, recent studies have revealed that gamma oscillations are transiently expressed in the rat barrel cortex during the first postnatal week, a "critical" period of sensory-dependent barrel map formation. The mechanisms underlying the generation and physiological roles of early gamma oscillations (EGOs) in the development of thalamocortical circuits will be discussed in this review. In contrast to adult gamma oscillations, synchronized through gamma-rhythmic perisomatic inhibition, EGOs are primarily driven through feedforward gamma-rhythmic excitatory input from the thalamus. The recruitment of cortical interneurons to EGOs and the emergence of feedforward inhibition are observed by the end of the first postnatal week. EGOs facilitate the precise synchronization of topographically aligned thalamic and cortical neurons. The multiple replay of sensory input during EGOs supports long-term potentiation at thalamocortical synapses. We suggest that this early form of gamma oscillations, which is mechanistically different from adult gamma oscillations, guides barrel map formation during the critical developmental period. © 2013 IBRO

Early gamma oscillations

Gamma oscillations have long been considered to emerge late in development. However, recent studies have revealed that gamma oscillations are transiently expressed in the rat barrel cortex during the first postnatal week, a "critical" period of sensory-dependent barrel map formation. The mechanisms underlying the generation and physiological roles of early gamma oscillations (EGOs) in the development of thalamocortical circuits will be discussed in this review. In contrast to adult gamma oscillations, synchronized through gamma-rhythmic perisomatic inhibition, EGOs are primarily driven through feedforward gamma-rhythmic excitatory input from the thalamus. The recruitment of cortical interneurons to EGOs and the emergence of feedforward inhibition are observed by the end of the first postnatal week. EGOs facilitate the precise synchronization of topographically aligned thalamic and cortical neurons. The multiple replay of sensory input during EGOs supports long-term potentiation at thalamocortical synapses. We suggest that this early form of gamma oscillations, which is mechanistically different from adult gamma oscillations, guides barrel map formation during the critical developmental period. © 2013 IBRO

Early gamma oscillations

Gamma oscillations have long been considered to emerge late in development. However, recent studies have revealed that gamma oscillations are transiently expressed in the rat barrel cortex during the first postnatal week, a "critical" period of sensory-dependent barrel map formation. The mechanisms underlying the generation and physiological roles of early gamma oscillations (EGOs) in the development of thalamocortical circuits will be discussed in this review. In contrast to adult gamma oscillations, synchronized through gamma-rhythmic perisomatic inhibition, EGOs are primarily driven through feedforward gamma-rhythmic excitatory input from the thalamus. The recruitment of cortical interneurons to EGOs and the emergence of feedforward inhibition are observed by the end of the first postnatal week. EGOs facilitate the precise synchronization of topographically aligned thalamic and cortical neurons. The multiple replay of sensory input during EGOs supports long-term potentiation at thalamocortical synapses. We suggest that this early form of gamma oscillations, which is mechanistically different from adult gamma oscillations, guides barrel map formation during the critical developmental period. © 2013 IBRO

Early gamma oscillations

Gamma oscillations have long been considered to emerge late in development. However, recent studies have revealed that gamma oscillations are transiently expressed in the rat barrel cortex during the first postnatal week, a "critical" period of sensory-dependent barrel map formation. The mechanisms underlying the generation and physiological roles of early gamma oscillations (EGOs) in the development of thalamocortical circuits will be discussed in this review. In contrast to adult gamma oscillations, synchronized through gamma-rhythmic perisomatic inhibition, EGOs are primarily driven through feedforward gamma-rhythmic excitatory input from the thalamus. The recruitment of cortical interneurons to EGOs and the emergence of feedforward inhibition are observed by the end of the first postnatal week. EGOs facilitate the precise synchronization of topographically aligned thalamic and cortical neurons. The multiple replay of sensory input during EGOs supports long-term potentiation at thalamocortical synapses. We suggest that this early form of gamma oscillations, which is mechanistically different from adult gamma oscillations, guides barrel map formation during the critical developmental period. © 2013 IBRO

Cell-attached recordings of responses evoked by photorelease of GABA in the immature cortical neurons

We present a novel non-invasive technique to measure the polarity of GABAergic responses based on cell-attached recordings of currents activated by laser-uncaging of GABA. For these recordings, a patch pipette was filled with a solution containing RuBi-GABA, and GABA was released from this complex by a laser beam conducted to the tip of the patch pipette via an optic fiber. In cell-attached recordings from neocortical and hippocampal neurons in postnatal days P2-5 rat brain slices in vitro, we found that laser-uncaging of GABA activates integral cell-attached currents mediated by tens of GABA(A) channels. The initial response was inwardly directed, indicating a depolarizing response to GABA. The direction of the initial response was dependent on the pipette potential and analysis of its slope-voltage relationships revealed a depolarizing driving force of +11 mV for the currents through G. Current-voltage relationships of the currents evoked by Rubi-GABA uncaging using voltage-ramps at the peak of responses not only revealed a bumetanide-sensitive depolarizing reversal potential of the GABA(A) receptor mediated responses, but also showed a strong voltage-dependent hysteresis. Upon desensitization of the uncaged-GABA response, current-voltage relationships of the currents through single GABA(A) channels revealed depolarizing responses with the driving force values similar to those obtained for the initial response. Thus, cell-attached recordings of the responses evoked by local intrapipette GABA uncaging are suitable to assess the polarity of the GABA(A)-Rs mediated signals in small cell compartments. © 2013 Minlebaev, Valeeva, Tcheremiskine, Coustillier and Khazipov

Cell-attached recordings of responses evoked by photorelease of GABA in the immature cortical neurons

We present a novel non-invasive technique to measure the polarity of GABAergic responses based on cell-attached recordings of currents activated by laser-uncaging of GABA. For these recordings, a patch pipette was filled with a solution containing RuBi-GABA, and GABA was released from this complex by a laser beam conducted to the tip of the patch pipette via an optic fiber. In cell-attached recordings from neocortical and hippocampal neurons in postnatal days P2-5 rat brain slices in vitro, we found that laser-uncaging of GABA activates integral cell-attached currents mediated by tens of GABA(A) channels. The initial response was inwardly directed, indicating a depolarizing response to GABA. The direction of the initial response was dependent on the pipette potential and analysis of its slope-voltage relationships revealed a depolarizing driving force of +11 mV for the currents through G. Current-voltage relationships of the currents evoked by Rubi-GABA uncaging using voltage-ramps at the peak of responses not only revealed a bumetanide-sensitive depolarizing reversal potential of the GABA(A) receptor mediated responses, but also showed a strong voltage-dependent hysteresis. Upon desensitization of the uncaged-GABA response, current-voltage relationships of the currents through single GABA(A) channels revealed depolarizing responses with the driving force values similar to those obtained for the initial response. Thus, cell-attached recordings of the responses evoked by local intrapipette GABA uncaging are suitable to assess the polarity of the GABA(A)-Rs mediated signals in small cell compartments. © 2013 Minlebaev, Valeeva, Tcheremiskine, Coustillier and Khazipov

Cell-attached recordings of responses evoked by photorelease of GABA in the immature cortical neurons

We present a novel non-invasive technique to measure the polarity of GABAergic responses based on cell-attached recordings of currents activated by laser-uncaging of GABA. For these recordings, a patch pipette was filled with a solution containing RuBi-GABA, and GABA was released from this complex by a laser beam conducted to the tip of the patch pipette via an optic fiber. In cell-attached recordings from neocortical and hippocampal neurons in postnatal days P2-5 rat brain slices in vitro, we found that laser-uncaging of GABA activates integral cell-attached currents mediated by tens of GABA(A) channels. The initial response was inwardly directed, indicating a depolarizing response to GABA. The direction of the initial response was dependent on the pipette potential and analysis of its slope-voltage relationships revealed a depolarizing driving force of +11 mV for the currents through G. Current-voltage relationships of the currents evoked by Rubi-GABA uncaging using voltage-ramps at the peak of responses not only revealed a bumetanide-sensitive depolarizing reversal potential of the GABA(A) receptor mediated responses, but also showed a strong voltage-dependent hysteresis. Upon desensitization of the uncaged-GABA response, current-voltage relationships of the currents through single GABA(A) channels revealed depolarizing responses with the driving force values similar to those obtained for the initial response. Thus, cell-attached recordings of the responses evoked by local intrapipette GABA uncaging are suitable to assess the polarity of the GABA(A)-Rs mediated signals in small cell compartments. © 2013 Minlebaev, Valeeva, Tcheremiskine, Coustillier and Khazipov