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Platinized graphene fiber electrodes uncover direct spleen-vagus communication

Neural interfacing nerve fascicles along the splenic neurovascular plexus (SNVP) is needed to better understand the spleen physiology, and for selective neuromodulation of this major organ. However, their small size and anatomical location have proven to be a significant challenge. Here, we use a re...

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Autores principales: Gonzalez-Gonzalez, Maria A., Bendale, Geetanjali S., Wang, Kezhong, Wallace, Gordon G., Romero-Ortega, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448843/
https://www.ncbi.nlm.nih.gov/pubmed/34535751
http://dx.doi.org/10.1038/s42003-021-02628-7
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author Gonzalez-Gonzalez, Maria A.
Bendale, Geetanjali S.
Wang, Kezhong
Wallace, Gordon G.
Romero-Ortega, Mario
author_facet Gonzalez-Gonzalez, Maria A.
Bendale, Geetanjali S.
Wang, Kezhong
Wallace, Gordon G.
Romero-Ortega, Mario
author_sort Gonzalez-Gonzalez, Maria A.
collection PubMed
description Neural interfacing nerve fascicles along the splenic neurovascular plexus (SNVP) is needed to better understand the spleen physiology, and for selective neuromodulation of this major organ. However, their small size and anatomical location have proven to be a significant challenge. Here, we use a reduced liquid crystalline graphene oxide (rGO) fiber coated with platinum (Pt) as a super-flexible suture-like electrode to interface multiple SNVP. The Pt-rGO fibers work as a handover knot electrodes over the small SNVP, allowing sensitive recording from four splenic nerve terminal branches (SN 1–4), to uncover differential activity and axon composition among them. Here, the asymmetric defasciculation of the SN branches is revealed by electron microscopy, and the functional compartmentalization in spleen innervation is evidenced in response to hypoxia and pharmacological modulation of mean arterial pressure. We demonstrate that electrical stimulation of cervical and sub-diaphragmatic vagus nerve (VN), evokes activity in a subset of SN terminal branches, providing evidence for a direct VN control over the spleen. This notion is supported by adenoviral tract-tracing of SN branches, revealing an unconventional direct brain-spleen projection. High-performance Pt-rGO fiber electrodes, may be used for the fine neural modulation of other small neurovascular plexus at the point of entry of major organs as a bioelectronic medical alternative.
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spelling pubmed-84488432021-10-05 Platinized graphene fiber electrodes uncover direct spleen-vagus communication Gonzalez-Gonzalez, Maria A. Bendale, Geetanjali S. Wang, Kezhong Wallace, Gordon G. Romero-Ortega, Mario Commun Biol Article Neural interfacing nerve fascicles along the splenic neurovascular plexus (SNVP) is needed to better understand the spleen physiology, and for selective neuromodulation of this major organ. However, their small size and anatomical location have proven to be a significant challenge. Here, we use a reduced liquid crystalline graphene oxide (rGO) fiber coated with platinum (Pt) as a super-flexible suture-like electrode to interface multiple SNVP. The Pt-rGO fibers work as a handover knot electrodes over the small SNVP, allowing sensitive recording from four splenic nerve terminal branches (SN 1–4), to uncover differential activity and axon composition among them. Here, the asymmetric defasciculation of the SN branches is revealed by electron microscopy, and the functional compartmentalization in spleen innervation is evidenced in response to hypoxia and pharmacological modulation of mean arterial pressure. We demonstrate that electrical stimulation of cervical and sub-diaphragmatic vagus nerve (VN), evokes activity in a subset of SN terminal branches, providing evidence for a direct VN control over the spleen. This notion is supported by adenoviral tract-tracing of SN branches, revealing an unconventional direct brain-spleen projection. High-performance Pt-rGO fiber electrodes, may be used for the fine neural modulation of other small neurovascular plexus at the point of entry of major organs as a bioelectronic medical alternative. Nature Publishing Group UK 2021-09-17 /pmc/articles/PMC8448843/ /pubmed/34535751 http://dx.doi.org/10.1038/s42003-021-02628-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gonzalez-Gonzalez, Maria A.
Bendale, Geetanjali S.
Wang, Kezhong
Wallace, Gordon G.
Romero-Ortega, Mario
Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title_full Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title_fullStr Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title_full_unstemmed Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title_short Platinized graphene fiber electrodes uncover direct spleen-vagus communication
title_sort platinized graphene fiber electrodes uncover direct spleen-vagus communication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448843/
https://www.ncbi.nlm.nih.gov/pubmed/34535751
http://dx.doi.org/10.1038/s42003-021-02628-7
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