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Responsiveness of afferent renal nerve units in renovascular hypertension in rats

Previous data suggest that renal afferent nerve activity is increased in hypertension exerting sympathoexcitatory effects. Hence, we wanted to test the hypothesis that in renovascular hypertension, the activity of dorsal root ganglion (DRG) neurons with afferent projections from the kidneys is augme...

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Autores principales: Rodionova, Kristina, Hilgers, Karl F., Rafii-Tabrizi, Salman, Doellner, Johannes, Cordasic, Nada, Linz, Peter, Karl, Anna-Lena, Ott, Christian, Schmieder, Roland E., Schiffer, Mario, Amann, Kerstin, Veelken, Roland, Ditting, Tilmann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433106/
https://www.ncbi.nlm.nih.gov/pubmed/34232378
http://dx.doi.org/10.1007/s00424-021-02591-6
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author Rodionova, Kristina
Hilgers, Karl F.
Rafii-Tabrizi, Salman
Doellner, Johannes
Cordasic, Nada
Linz, Peter
Karl, Anna-Lena
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Ditting, Tilmann
author_facet Rodionova, Kristina
Hilgers, Karl F.
Rafii-Tabrizi, Salman
Doellner, Johannes
Cordasic, Nada
Linz, Peter
Karl, Anna-Lena
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Ditting, Tilmann
author_sort Rodionova, Kristina
collection PubMed
description Previous data suggest that renal afferent nerve activity is increased in hypertension exerting sympathoexcitatory effects. Hence, we wanted to test the hypothesis that in renovascular hypertension, the activity of dorsal root ganglion (DRG) neurons with afferent projections from the kidneys is augmented depending on the degree of intrarenal inflammation. For comparison, a nonhypertensive model of mesangioproliferative nephritis was investigated. Renovascular hypertension (2-kidney, 1-clip [2K1C]) was induced by unilateral clipping of the left renal artery and mesangioproliferative glomerulonephritis (anti-Thy1.1) by IV injection of a 1.75-mg/kg BW OX-7 antibody. Neuronal labeling (dicarbocyanine dye [DiI]) in all rats allowed identification of renal afferent dorsal root ganglion (DRG) neurons. A current clamp was used to characterize neurons as tonic (sustained action potential [AP] firing) or phasic (1–4 AP) upon stimulation by current injection. All kidneys were investigated using standard morphological techniques. DRG neurons exhibited less often tonic response if in vivo axonal input from clipped kidneys was received (30.4% vs. 61.2% control, p < 0.05). However, if the nerves to the left clipped kidneys were cut 7 days prior to investigation, the number of tonic renal neurons completely recovered to well above control levels. Interestingly, electrophysiological properties of neurons that had in vivo axons from the right non-clipped kidneys were not distinguishable from controls. Renal DRG neurons from nephritic rats also showed less often tonic activity upon current injection (43.4% vs. 64.8% control, p < 0.05). Putative sympathoexcitatory and impaired sympathoinhibitory renal afferent nerve fibers probably contribute to increased sympathetic activity in 2K1C hypertension. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00424-021-02591-6.
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spelling pubmed-84331062021-09-24 Responsiveness of afferent renal nerve units in renovascular hypertension in rats Rodionova, Kristina Hilgers, Karl F. Rafii-Tabrizi, Salman Doellner, Johannes Cordasic, Nada Linz, Peter Karl, Anna-Lena Ott, Christian Schmieder, Roland E. Schiffer, Mario Amann, Kerstin Veelken, Roland Ditting, Tilmann Pflugers Arch Integrative Physiology Previous data suggest that renal afferent nerve activity is increased in hypertension exerting sympathoexcitatory effects. Hence, we wanted to test the hypothesis that in renovascular hypertension, the activity of dorsal root ganglion (DRG) neurons with afferent projections from the kidneys is augmented depending on the degree of intrarenal inflammation. For comparison, a nonhypertensive model of mesangioproliferative nephritis was investigated. Renovascular hypertension (2-kidney, 1-clip [2K1C]) was induced by unilateral clipping of the left renal artery and mesangioproliferative glomerulonephritis (anti-Thy1.1) by IV injection of a 1.75-mg/kg BW OX-7 antibody. Neuronal labeling (dicarbocyanine dye [DiI]) in all rats allowed identification of renal afferent dorsal root ganglion (DRG) neurons. A current clamp was used to characterize neurons as tonic (sustained action potential [AP] firing) or phasic (1–4 AP) upon stimulation by current injection. All kidneys were investigated using standard morphological techniques. DRG neurons exhibited less often tonic response if in vivo axonal input from clipped kidneys was received (30.4% vs. 61.2% control, p < 0.05). However, if the nerves to the left clipped kidneys were cut 7 days prior to investigation, the number of tonic renal neurons completely recovered to well above control levels. Interestingly, electrophysiological properties of neurons that had in vivo axons from the right non-clipped kidneys were not distinguishable from controls. Renal DRG neurons from nephritic rats also showed less often tonic activity upon current injection (43.4% vs. 64.8% control, p < 0.05). Putative sympathoexcitatory and impaired sympathoinhibitory renal afferent nerve fibers probably contribute to increased sympathetic activity in 2K1C hypertension. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00424-021-02591-6. Springer Berlin Heidelberg 2021-07-07 2021 /pmc/articles/PMC8433106/ /pubmed/34232378 http://dx.doi.org/10.1007/s00424-021-02591-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Integrative Physiology
Rodionova, Kristina
Hilgers, Karl F.
Rafii-Tabrizi, Salman
Doellner, Johannes
Cordasic, Nada
Linz, Peter
Karl, Anna-Lena
Ott, Christian
Schmieder, Roland E.
Schiffer, Mario
Amann, Kerstin
Veelken, Roland
Ditting, Tilmann
Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title_full Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title_fullStr Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title_full_unstemmed Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title_short Responsiveness of afferent renal nerve units in renovascular hypertension in rats
title_sort responsiveness of afferent renal nerve units in renovascular hypertension in rats
topic Integrative Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433106/
https://www.ncbi.nlm.nih.gov/pubmed/34232378
http://dx.doi.org/10.1007/s00424-021-02591-6
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