Cargando…
Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT
Background: Vagus nerve stimulation (VNS) has gained great importance as a promising therapy for a myriad of diseases. Of particular interest is the therapy of cardiovascular diseases, such as heart failure or atrial fibrillation using selective cardiac VNS. However, there is still a lack of organ-s...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511100/ https://www.ncbi.nlm.nih.gov/pubmed/36172280 http://dx.doi.org/10.3389/fcell.2022.968870 |
_version_ | 1784797589293498368 |
---|---|
author | Kronsteiner, Bettina Zopf, Lydia M. Heimel, Patrick Oberoi, Gunpreet Kramer, Anne M. Slezak, Paul Weninger, Wolfgang J. Podesser, Bruno K. Kiss, Attila Moscato, Francesco |
author_facet | Kronsteiner, Bettina Zopf, Lydia M. Heimel, Patrick Oberoi, Gunpreet Kramer, Anne M. Slezak, Paul Weninger, Wolfgang J. Podesser, Bruno K. Kiss, Attila Moscato, Francesco |
author_sort | Kronsteiner, Bettina |
collection | PubMed |
description | Background: Vagus nerve stimulation (VNS) has gained great importance as a promising therapy for a myriad of diseases. Of particular interest is the therapy of cardiovascular diseases, such as heart failure or atrial fibrillation using selective cardiac VNS. However, there is still a lack of organ-specific anatomical knowledge about the fascicular anatomy and topography of the cardiac branch (CB), which diminishes the therapeutic possibilities for selective cardiac neuromodulation. Here, we established a topographical and anatomical map of the superior cardiac VN in two animal species to dissect cervical and cardiac VN morphology. Methods: Autonomic nerves including superior CBs were harvested from domestic pigs and New Zeeland rabbits followed by imaging with microcomputed tomography (µCT) and 3D rendering. The data were analyzed in terms of relevant topographical and anatomical parameters. Results: Our data showed that cardiac vagal fascicles remained separated from other VN fascicles up to 22.19 mm (IQR 14.02–41.30 mm) in pigs and 7.68 mm (IQR 4.06–12.77 mm) in rabbits from the CB point and then started merging with other fascicles. Exchanges of nerve fascicles between sympathetic trunk (ST) and VN were observed in 3 out of 11 nerves, which might cause additional unwanted effects in unselective VNS. Our 3D rendered digital model of the cardiac fascicles was generated showing that CB first remained on the medial side where it branched off the VN, as also shown in the µCT data of 11 pig nerves, and then migrated towards the ventromedial site the further it was traced cranially. Conclusion: Our data provided an anatomical map of the cardiac vagal branches including cervical VN and ST for future approaches of selective cardiac neurostimulation, indicating the best position of selective cardiac VNS just above the CB point. |
format | Online Article Text |
id | pubmed-9511100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95111002022-09-27 Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT Kronsteiner, Bettina Zopf, Lydia M. Heimel, Patrick Oberoi, Gunpreet Kramer, Anne M. Slezak, Paul Weninger, Wolfgang J. Podesser, Bruno K. Kiss, Attila Moscato, Francesco Front Cell Dev Biol Cell and Developmental Biology Background: Vagus nerve stimulation (VNS) has gained great importance as a promising therapy for a myriad of diseases. Of particular interest is the therapy of cardiovascular diseases, such as heart failure or atrial fibrillation using selective cardiac VNS. However, there is still a lack of organ-specific anatomical knowledge about the fascicular anatomy and topography of the cardiac branch (CB), which diminishes the therapeutic possibilities for selective cardiac neuromodulation. Here, we established a topographical and anatomical map of the superior cardiac VN in two animal species to dissect cervical and cardiac VN morphology. Methods: Autonomic nerves including superior CBs were harvested from domestic pigs and New Zeeland rabbits followed by imaging with microcomputed tomography (µCT) and 3D rendering. The data were analyzed in terms of relevant topographical and anatomical parameters. Results: Our data showed that cardiac vagal fascicles remained separated from other VN fascicles up to 22.19 mm (IQR 14.02–41.30 mm) in pigs and 7.68 mm (IQR 4.06–12.77 mm) in rabbits from the CB point and then started merging with other fascicles. Exchanges of nerve fascicles between sympathetic trunk (ST) and VN were observed in 3 out of 11 nerves, which might cause additional unwanted effects in unselective VNS. Our 3D rendered digital model of the cardiac fascicles was generated showing that CB first remained on the medial side where it branched off the VN, as also shown in the µCT data of 11 pig nerves, and then migrated towards the ventromedial site the further it was traced cranially. Conclusion: Our data provided an anatomical map of the cardiac vagal branches including cervical VN and ST for future approaches of selective cardiac neurostimulation, indicating the best position of selective cardiac VNS just above the CB point. Frontiers Media S.A. 2022-09-12 /pmc/articles/PMC9511100/ /pubmed/36172280 http://dx.doi.org/10.3389/fcell.2022.968870 Text en Copyright © 2022 Kronsteiner, Zopf, Heimel, Oberoi, Kramer, Slezak, Weninger, Podesser, Kiss and Moscato. 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 | Cell and Developmental Biology Kronsteiner, Bettina Zopf, Lydia M. Heimel, Patrick Oberoi, Gunpreet Kramer, Anne M. Slezak, Paul Weninger, Wolfgang J. Podesser, Bruno K. Kiss, Attila Moscato, Francesco Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title | Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title_full | Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title_fullStr | Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title_full_unstemmed | Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title_short | Mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using MicroCT |
title_sort | mapping the functional anatomy and topography of the cardiac autonomic innervation for selective cardiac neuromodulation using microct |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9511100/ https://www.ncbi.nlm.nih.gov/pubmed/36172280 http://dx.doi.org/10.3389/fcell.2022.968870 |
work_keys_str_mv | AT kronsteinerbettina mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT zopflydiam mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT heimelpatrick mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT oberoigunpreet mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT kramerannem mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT slezakpaul mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT weningerwolfgangj mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT podesserbrunok mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT kissattila mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct AT moscatofrancesco mappingthefunctionalanatomyandtopographyofthecardiacautonomicinnervationforselectivecardiacneuromodulationusingmicroct |