Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism

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Standard

Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism. / Perrier, Jean-François; Rasmussen, Hanne B; Jørgensen, Lone K; Berg, Rune W.

I: Frontiers in Neural Circuits, Bind 11, 111, 2018.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Perrier, J-F, Rasmussen, HB, Jørgensen, LK & Berg, RW 2018, 'Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism' Frontiers in Neural Circuits, bind 11, 111. https://doi.org/10.3389/fncir.2017.00111

APA

Perrier, J-F., Rasmussen, H. B., Jørgensen, L. K., & Berg, R. W. (2018). Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism. Frontiers in Neural Circuits, 11, [111]. https://doi.org/10.3389/fncir.2017.00111

Vancouver

Perrier J-F, Rasmussen HB, Jørgensen LK, Berg RW. Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism. Frontiers in Neural Circuits. 2018;11. 111. https://doi.org/10.3389/fncir.2017.00111

Author

Perrier, Jean-François ; Rasmussen, Hanne B ; Jørgensen, Lone K ; Berg, Rune W. / Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism. I: Frontiers in Neural Circuits. 2018 ; Bind 11.

Bibtex

@article{896808b8a0b04b89b94addb0a439d001,
title = "Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism",
abstract = "Motor fatigue occurring during prolonged physical activity has both peripheral and central origins. It was previously demonstrated that the excitability of motoneurons was decreased when a spillover of serotonin could activate extrasynaptic 5-HT1A receptors at the axon initial segment (AIS) of motoneurons. Here we investigated the impact of massive synaptic release of serotonin on motor behavior in an integrated preparation of the adult turtle performing fictive scratching behaviors. We found that a prolonged electrical stimulation of the raphe spinal pathway induced a reversible inhibition of the motor behavior that lasted several tens of seconds. The effect disappeared when the spinal cord was perfused with an antagonist for 5-HT1A receptors. By demonstrating a direct impact of serotonin on motor behavior, we suggest a central role of this monoamine behind central fatigue.",
author = "Jean-Fran{\cc}ois Perrier and Rasmussen, {Hanne B} and J{\o}rgensen, {Lone K} and Berg, {Rune W}",
year = "2018",
doi = "10.3389/fncir.2017.00111",
language = "English",
volume = "11",
journal = "Frontiers in Neural Circuits",
issn = "1662-5110",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism

AU - Perrier, Jean-François

AU - Rasmussen, Hanne B

AU - Jørgensen, Lone K

AU - Berg, Rune W

PY - 2018

Y1 - 2018

N2 - Motor fatigue occurring during prolonged physical activity has both peripheral and central origins. It was previously demonstrated that the excitability of motoneurons was decreased when a spillover of serotonin could activate extrasynaptic 5-HT1A receptors at the axon initial segment (AIS) of motoneurons. Here we investigated the impact of massive synaptic release of serotonin on motor behavior in an integrated preparation of the adult turtle performing fictive scratching behaviors. We found that a prolonged electrical stimulation of the raphe spinal pathway induced a reversible inhibition of the motor behavior that lasted several tens of seconds. The effect disappeared when the spinal cord was perfused with an antagonist for 5-HT1A receptors. By demonstrating a direct impact of serotonin on motor behavior, we suggest a central role of this monoamine behind central fatigue.

AB - Motor fatigue occurring during prolonged physical activity has both peripheral and central origins. It was previously demonstrated that the excitability of motoneurons was decreased when a spillover of serotonin could activate extrasynaptic 5-HT1A receptors at the axon initial segment (AIS) of motoneurons. Here we investigated the impact of massive synaptic release of serotonin on motor behavior in an integrated preparation of the adult turtle performing fictive scratching behaviors. We found that a prolonged electrical stimulation of the raphe spinal pathway induced a reversible inhibition of the motor behavior that lasted several tens of seconds. The effect disappeared when the spinal cord was perfused with an antagonist for 5-HT1A receptors. By demonstrating a direct impact of serotonin on motor behavior, we suggest a central role of this monoamine behind central fatigue.

U2 - 10.3389/fncir.2017.00111

DO - 10.3389/fncir.2017.00111

M3 - Journal article

VL - 11

JO - Frontiers in Neural Circuits

JF - Frontiers in Neural Circuits

SN - 1662-5110

M1 - 111

ER -

ID: 189622240