Cargando…
Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight
Neurons are well suited for computations on millisecond timescales, but some neuronal circuits set behavioral states over long time periods, such as those involved in energy homeostasis. We found that multiple types of hypothalamic neurons, including those that oppositely regulate body weight, are s...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912688/ https://www.ncbi.nlm.nih.gov/pubmed/27315482 http://dx.doi.org/10.1016/j.cell.2016.05.019 |
_version_ | 1782438303517114368 |
---|---|
author | Branco, Tiago Tozer, Adam Magnus, Christopher J. Sugino, Ken Tanaka, Shinsuke Lee, Albert K. Wood, John N. Sternson, Scott M. |
author_facet | Branco, Tiago Tozer, Adam Magnus, Christopher J. Sugino, Ken Tanaka, Shinsuke Lee, Albert K. Wood, John N. Sternson, Scott M. |
author_sort | Branco, Tiago |
collection | PubMed |
description | Neurons are well suited for computations on millisecond timescales, but some neuronal circuits set behavioral states over long time periods, such as those involved in energy homeostasis. We found that multiple types of hypothalamic neurons, including those that oppositely regulate body weight, are specialized as near-perfect synaptic integrators that summate inputs over extended timescales. Excitatory postsynaptic potentials (EPSPs) are greatly prolonged, outlasting the neuronal membrane time-constant up to 10-fold. This is due to the voltage-gated sodium channel Na(v)1.7 (Scn9a), previously associated with pain-sensation but not synaptic integration. Scn9a deletion in AGRP, POMC, or paraventricular hypothalamic neurons reduced EPSP duration, synaptic integration, and altered body weight in mice. In vivo whole-cell recordings in the hypothalamus confirmed near-perfect synaptic integration. These experiments show that integration of synaptic inputs over time by Na(v)1.7 is critical for body weight regulation and reveal a mechanism for synaptic control of circuits regulating long term homeostatic functions. |
format | Online Article Text |
id | pubmed-4912688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49126882016-06-28 Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight Branco, Tiago Tozer, Adam Magnus, Christopher J. Sugino, Ken Tanaka, Shinsuke Lee, Albert K. Wood, John N. Sternson, Scott M. Cell Article Neurons are well suited for computations on millisecond timescales, but some neuronal circuits set behavioral states over long time periods, such as those involved in energy homeostasis. We found that multiple types of hypothalamic neurons, including those that oppositely regulate body weight, are specialized as near-perfect synaptic integrators that summate inputs over extended timescales. Excitatory postsynaptic potentials (EPSPs) are greatly prolonged, outlasting the neuronal membrane time-constant up to 10-fold. This is due to the voltage-gated sodium channel Na(v)1.7 (Scn9a), previously associated with pain-sensation but not synaptic integration. Scn9a deletion in AGRP, POMC, or paraventricular hypothalamic neurons reduced EPSP duration, synaptic integration, and altered body weight in mice. In vivo whole-cell recordings in the hypothalamus confirmed near-perfect synaptic integration. These experiments show that integration of synaptic inputs over time by Na(v)1.7 is critical for body weight regulation and reveal a mechanism for synaptic control of circuits regulating long term homeostatic functions. Cell Press 2016-06-16 /pmc/articles/PMC4912688/ /pubmed/27315482 http://dx.doi.org/10.1016/j.cell.2016.05.019 Text en © 2016 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Branco, Tiago Tozer, Adam Magnus, Christopher J. Sugino, Ken Tanaka, Shinsuke Lee, Albert K. Wood, John N. Sternson, Scott M. Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title | Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title_full | Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title_fullStr | Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title_full_unstemmed | Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title_short | Near-Perfect Synaptic Integration by Na(v)1.7 in Hypothalamic Neurons Regulates Body Weight |
title_sort | near-perfect synaptic integration by na(v)1.7 in hypothalamic neurons regulates body weight |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912688/ https://www.ncbi.nlm.nih.gov/pubmed/27315482 http://dx.doi.org/10.1016/j.cell.2016.05.019 |
work_keys_str_mv | AT brancotiago nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT tozeradam nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT magnuschristopherj nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT suginoken nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT tanakashinsuke nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT leealbertk nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT woodjohnn nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight AT sternsonscottm nearperfectsynapticintegrationbynav17inhypothalamicneuronsregulatesbodyweight |