Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark

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Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark. / Rotem, Naama; Sestieri, Emanuel; Hounsgaard, Jørn Dybkjær; Yarom, Yosef.

In: Frontiers in Cellular Neuroscience, Vol. 8, 72, 2014, p. 1-12.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rotem, N, Sestieri, E, Hounsgaard, JD & Yarom, Y 2014, 'Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark', Frontiers in Cellular Neuroscience, vol. 8, 72, pp. 1-12. https://doi.org/10.3389/fncel.2014.00072

APA

Rotem, N., Sestieri, E., Hounsgaard, J. D., & Yarom, Y. (2014). Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark. Frontiers in Cellular Neuroscience, 8, 1-12. [72]. https://doi.org/10.3389/fncel.2014.00072

Vancouver

Rotem N, Sestieri E, Hounsgaard JD, Yarom Y. Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark. Frontiers in Cellular Neuroscience. 2014;8:1-12. 72. https://doi.org/10.3389/fncel.2014.00072

Author

Rotem, Naama ; Sestieri, Emanuel ; Hounsgaard, Jørn Dybkjær ; Yarom, Yosef. / Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark. In: Frontiers in Cellular Neuroscience. 2014 ; Vol. 8. pp. 1-12.

Bibtex

@article{a07d03b5d59f4c2b9f9b3bb15ce9fba4,
title = "Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark",
abstract = "High impulse rate in afferent nerves is a common feature in many sensory systems that serve to accommodate a wide dynamic range. However, the first stage of integration should be endowed with specific properties that enable efficient handling of the incoming information. In elasmobranches, the afferent nerve originating from the ampullae of Lorenzini targets specific neurons located at the Dorsal Octavolateral Nucleus (DON), the first stage of integration in the electroreception system. Using intracellular recordings in an isolated brainstem preparation from the shark we analyze the properties of this afferent pathway. We found that stimulating the afferent nerve activates a mixture of excitatory and inhibitory synapses mediated by AMPA-like and GABAA receptors, respectively. The excitatory synapses that are extremely efficient in activating the postsynaptic neurons display unusual voltage dependence, enabling them to operate as a current source. The inhibitory input is powerful enough to completely eliminate the excitatory action of the afferent nerve but is ineffective regarding other excitatory inputs. These observations can be explained by the location and efficiency of the synapses. We conclude that the afferent nerve provides powerful and reliable excitatory input as well as a feed-forward inhibitory input, which is partially presynaptic in origin. These results question the cellular location within the DON where cancelation of expected incoming signals occurs.",
author = "Naama Rotem and Emanuel Sestieri and Hounsgaard, {J{\o}rn Dybkj{\ae}r} and Yosef Yarom",
year = "2014",
doi = "10.3389/fncel.2014.00072",
language = "English",
volume = "8",
pages = "1--12",
journal = "Frontiers in Cellular Neuroscience",
issn = "1662-5102",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Excitatory and inhibitory synaptic mechanisms at the first stage of integration in the electroreception system of the shark

AU - Rotem, Naama

AU - Sestieri, Emanuel

AU - Hounsgaard, Jørn Dybkjær

AU - Yarom, Yosef

PY - 2014

Y1 - 2014

N2 - High impulse rate in afferent nerves is a common feature in many sensory systems that serve to accommodate a wide dynamic range. However, the first stage of integration should be endowed with specific properties that enable efficient handling of the incoming information. In elasmobranches, the afferent nerve originating from the ampullae of Lorenzini targets specific neurons located at the Dorsal Octavolateral Nucleus (DON), the first stage of integration in the electroreception system. Using intracellular recordings in an isolated brainstem preparation from the shark we analyze the properties of this afferent pathway. We found that stimulating the afferent nerve activates a mixture of excitatory and inhibitory synapses mediated by AMPA-like and GABAA receptors, respectively. The excitatory synapses that are extremely efficient in activating the postsynaptic neurons display unusual voltage dependence, enabling them to operate as a current source. The inhibitory input is powerful enough to completely eliminate the excitatory action of the afferent nerve but is ineffective regarding other excitatory inputs. These observations can be explained by the location and efficiency of the synapses. We conclude that the afferent nerve provides powerful and reliable excitatory input as well as a feed-forward inhibitory input, which is partially presynaptic in origin. These results question the cellular location within the DON where cancelation of expected incoming signals occurs.

AB - High impulse rate in afferent nerves is a common feature in many sensory systems that serve to accommodate a wide dynamic range. However, the first stage of integration should be endowed with specific properties that enable efficient handling of the incoming information. In elasmobranches, the afferent nerve originating from the ampullae of Lorenzini targets specific neurons located at the Dorsal Octavolateral Nucleus (DON), the first stage of integration in the electroreception system. Using intracellular recordings in an isolated brainstem preparation from the shark we analyze the properties of this afferent pathway. We found that stimulating the afferent nerve activates a mixture of excitatory and inhibitory synapses mediated by AMPA-like and GABAA receptors, respectively. The excitatory synapses that are extremely efficient in activating the postsynaptic neurons display unusual voltage dependence, enabling them to operate as a current source. The inhibitory input is powerful enough to completely eliminate the excitatory action of the afferent nerve but is ineffective regarding other excitatory inputs. These observations can be explained by the location and efficiency of the synapses. We conclude that the afferent nerve provides powerful and reliable excitatory input as well as a feed-forward inhibitory input, which is partially presynaptic in origin. These results question the cellular location within the DON where cancelation of expected incoming signals occurs.

U2 - 10.3389/fncel.2014.00072

DO - 10.3389/fncel.2014.00072

M3 - Journal article

C2 - 24639631

VL - 8

SP - 1

EP - 12

JO - Frontiers in Cellular Neuroscience

JF - Frontiers in Cellular Neuroscience

SN - 1662-5102

M1 - 72

ER -

ID: 138803945