Cargando…

Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla

The rostral ventrolateral medulla (RVLM) is an important brain region involved in both resting and reflex regulation of the sympathetic nervous system. Anatomical evidence suggests that as a bilateral structure, each RVLM innervates sympathetic preganglionic neurons on both sides of the spinal cord....

Descripción completa

Detalles Bibliográficos
Autores principales: Kulkarni, Soumya S., Mischel, Nicholas A., Mueller, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887112/
https://www.ncbi.nlm.nih.gov/pubmed/36733693
http://dx.doi.org/10.3389/fphys.2022.1099513
_version_ 1784880266371661824
author Kulkarni, Soumya S.
Mischel, Nicholas A.
Mueller, Patrick J.
author_facet Kulkarni, Soumya S.
Mischel, Nicholas A.
Mueller, Patrick J.
author_sort Kulkarni, Soumya S.
collection PubMed
description The rostral ventrolateral medulla (RVLM) is an important brain region involved in both resting and reflex regulation of the sympathetic nervous system. Anatomical evidence suggests that as a bilateral structure, each RVLM innervates sympathetic preganglionic neurons on both sides of the spinal cord. However, the functional importance of ipsilateral versus contralateral projections from the RVLM is lacking. Similarly, during hypotension, the RVLM is believed to rely primarily on withdrawal of tonic gamma aminobutyric acid (GABA) inhibition to increase sympathetic outflow but whether GABA withdrawal mediates increased activity of functionally different sympathetic nerves is unknown. We sought to test the hypothesis that activation of the ipsilateral versus contralateral RVLM produces differential increases in splanchnic versus adrenal sympathetic nerve activities, as representative examples of functionally different sympathetic nerves. We also tested whether GABA withdrawal is responsible for hypotension-induced increases in splanchnic and adrenal sympathetic nerve activity. To test our hypothesis, we measured splanchnic and adrenal sympathetic nerve activity simultaneously in Inactin-anesthetized, male Sprague-Dawley rats during ipsilateral or contralateral glutamatergic activation of the RVLM. We also produced hypotension (sodium nitroprusside, i.v.) before and after bilateral blockade of GABA(A) receptors in the RVLM (bicuculline, 5 mM 90 nL). Glutamate (100 mM, 30 nL) injected into the ipsilateral or contralateral RVLM produced equivalent increases in splanchnic sympathetic nerve activity, but increased adrenal sympathetic nerve activity by more than double with ipsilateral injections versus contralateral injections (p < 0.05; n = 6). In response to hypotension, increases in adrenal sympathetic nerve activity were similar after bicuculline (p > 0.05), but splanchnic sympathetic nerve activity responses were eliminated (p < 0.05; n = 5). These results provide the first functional evidence that the RVLM has predominantly ipsilateral innervation of adrenal nerves. In addition, baroreflex-mediated increases in splanchnic but not adrenal sympathetic nerve activity are mediated by GABA(A) receptors in the RVLM. Our studies provide a deeper understanding of neural control of sympathetic regulation and insight towards novel treatments for cardiovascular disease involving sympathetic nervous system dysregulation.
format Online
Article
Text
id pubmed-9887112
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98871122023-02-01 Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla Kulkarni, Soumya S. Mischel, Nicholas A. Mueller, Patrick J. Front Physiol Physiology The rostral ventrolateral medulla (RVLM) is an important brain region involved in both resting and reflex regulation of the sympathetic nervous system. Anatomical evidence suggests that as a bilateral structure, each RVLM innervates sympathetic preganglionic neurons on both sides of the spinal cord. However, the functional importance of ipsilateral versus contralateral projections from the RVLM is lacking. Similarly, during hypotension, the RVLM is believed to rely primarily on withdrawal of tonic gamma aminobutyric acid (GABA) inhibition to increase sympathetic outflow but whether GABA withdrawal mediates increased activity of functionally different sympathetic nerves is unknown. We sought to test the hypothesis that activation of the ipsilateral versus contralateral RVLM produces differential increases in splanchnic versus adrenal sympathetic nerve activities, as representative examples of functionally different sympathetic nerves. We also tested whether GABA withdrawal is responsible for hypotension-induced increases in splanchnic and adrenal sympathetic nerve activity. To test our hypothesis, we measured splanchnic and adrenal sympathetic nerve activity simultaneously in Inactin-anesthetized, male Sprague-Dawley rats during ipsilateral or contralateral glutamatergic activation of the RVLM. We also produced hypotension (sodium nitroprusside, i.v.) before and after bilateral blockade of GABA(A) receptors in the RVLM (bicuculline, 5 mM 90 nL). Glutamate (100 mM, 30 nL) injected into the ipsilateral or contralateral RVLM produced equivalent increases in splanchnic sympathetic nerve activity, but increased adrenal sympathetic nerve activity by more than double with ipsilateral injections versus contralateral injections (p < 0.05; n = 6). In response to hypotension, increases in adrenal sympathetic nerve activity were similar after bicuculline (p > 0.05), but splanchnic sympathetic nerve activity responses were eliminated (p < 0.05; n = 5). These results provide the first functional evidence that the RVLM has predominantly ipsilateral innervation of adrenal nerves. In addition, baroreflex-mediated increases in splanchnic but not adrenal sympathetic nerve activity are mediated by GABA(A) receptors in the RVLM. Our studies provide a deeper understanding of neural control of sympathetic regulation and insight towards novel treatments for cardiovascular disease involving sympathetic nervous system dysregulation. Frontiers Media S.A. 2023-01-17 /pmc/articles/PMC9887112/ /pubmed/36733693 http://dx.doi.org/10.3389/fphys.2022.1099513 Text en Copyright © 2023 Kulkarni, Mischel and Mueller. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Kulkarni, Soumya S.
Mischel, Nicholas A.
Mueller, Patrick J.
Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title_full Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title_fullStr Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title_full_unstemmed Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title_short Revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
title_sort revisiting differential control of sympathetic outflow by the rostral ventrolateral medulla
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887112/
https://www.ncbi.nlm.nih.gov/pubmed/36733693
http://dx.doi.org/10.3389/fphys.2022.1099513
work_keys_str_mv AT kulkarnisoumyas revisitingdifferentialcontrolofsympatheticoutflowbytherostralventrolateralmedulla
AT mischelnicholasa revisitingdifferentialcontrolofsympatheticoutflowbytherostralventrolateralmedulla
AT muellerpatrickj revisitingdifferentialcontrolofsympatheticoutflowbytherostralventrolateralmedulla