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Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure

AIM: We have reported earlier that a high salt intake triggered an aestivation‐like natriuretic‐ureotelic body water conservation response that lowered muscle mass and increased blood pressure. Here, we tested the hypothesis that a similar adaptive water conservation response occurs in experimental...

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Autores principales: Kovarik, Johannes J., Morisawa, Norihiko, Wild, Johannes, Marton, Adriana, Takase‐Minegishi, Kaoru, Minegishi, Shintaro, Daub, Steffen, Sands, Jeff M., Klein, Janet D., Bailey, James L., Kovalik, Jean‐Paul, Rauh, Manfred, Karbach, Susanne, Hilgers, Karl F., Luft, Friedrich, Nishiyama, Akira, Nakano, Daisuke, Kitada, Kento, Titze, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244025/
https://www.ncbi.nlm.nih.gov/pubmed/33590667
http://dx.doi.org/10.1111/apha.13629
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author Kovarik, Johannes J.
Morisawa, Norihiko
Wild, Johannes
Marton, Adriana
Takase‐Minegishi, Kaoru
Minegishi, Shintaro
Daub, Steffen
Sands, Jeff M.
Klein, Janet D.
Bailey, James L.
Kovalik, Jean‐Paul
Rauh, Manfred
Karbach, Susanne
Hilgers, Karl F.
Luft, Friedrich
Nishiyama, Akira
Nakano, Daisuke
Kitada, Kento
Titze, Jens
author_facet Kovarik, Johannes J.
Morisawa, Norihiko
Wild, Johannes
Marton, Adriana
Takase‐Minegishi, Kaoru
Minegishi, Shintaro
Daub, Steffen
Sands, Jeff M.
Klein, Janet D.
Bailey, James L.
Kovalik, Jean‐Paul
Rauh, Manfred
Karbach, Susanne
Hilgers, Karl F.
Luft, Friedrich
Nishiyama, Akira
Nakano, Daisuke
Kitada, Kento
Titze, Jens
author_sort Kovarik, Johannes J.
collection PubMed
description AIM: We have reported earlier that a high salt intake triggered an aestivation‐like natriuretic‐ureotelic body water conservation response that lowered muscle mass and increased blood pressure. Here, we tested the hypothesis that a similar adaptive water conservation response occurs in experimental chronic renal failure. METHODS: In four subsequent experiments in Sprague Dawley rats, we used surgical 5/6 renal mass reduction (5/6 Nx) to induce chronic renal failure. We studied solute and water excretion in 24‐hour metabolic cage experiments, chronic blood pressure by radiotelemetry, chronic metabolic adjustment in liver and skeletal muscle by metabolomics and selected enzyme activity measurements, body Na(+), K(+) and water by dry ashing, and acute transepidermal water loss in conjunction with skin blood flow and intra‐arterial blood pressure. RESULTS: 5/6 Nx rats were polyuric, because their kidneys could not sufficiently concentrate the urine. Physiological adaptation to this renal water loss included mobilization of nitrogen and energy from muscle for organic osmolyte production, elevated norepinephrine and copeptin levels with reduced skin blood flow, which by means of compensation reduced their transepidermal water loss. This complex physiologic‐metabolic adjustment across multiple organs allowed the rats to stabilize their body water content despite persisting renal water loss, albeit at the expense of hypertension and catabolic mobilization of muscle protein. CONCLUSION: Physiological adaptation to body water loss, termed aestivation, is an evolutionary conserved survival strategy and an under‐studied research area in medical physiology, which besides hypertension and muscle mass loss in chronic renal failure may explain many otherwise unexplainable phenomena in medicine.
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spelling pubmed-82440252021-07-02 Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure Kovarik, Johannes J. Morisawa, Norihiko Wild, Johannes Marton, Adriana Takase‐Minegishi, Kaoru Minegishi, Shintaro Daub, Steffen Sands, Jeff M. Klein, Janet D. Bailey, James L. Kovalik, Jean‐Paul Rauh, Manfred Karbach, Susanne Hilgers, Karl F. Luft, Friedrich Nishiyama, Akira Nakano, Daisuke Kitada, Kento Titze, Jens Acta Physiol (Oxf) Cardivascular Physiology AIM: We have reported earlier that a high salt intake triggered an aestivation‐like natriuretic‐ureotelic body water conservation response that lowered muscle mass and increased blood pressure. Here, we tested the hypothesis that a similar adaptive water conservation response occurs in experimental chronic renal failure. METHODS: In four subsequent experiments in Sprague Dawley rats, we used surgical 5/6 renal mass reduction (5/6 Nx) to induce chronic renal failure. We studied solute and water excretion in 24‐hour metabolic cage experiments, chronic blood pressure by radiotelemetry, chronic metabolic adjustment in liver and skeletal muscle by metabolomics and selected enzyme activity measurements, body Na(+), K(+) and water by dry ashing, and acute transepidermal water loss in conjunction with skin blood flow and intra‐arterial blood pressure. RESULTS: 5/6 Nx rats were polyuric, because their kidneys could not sufficiently concentrate the urine. Physiological adaptation to this renal water loss included mobilization of nitrogen and energy from muscle for organic osmolyte production, elevated norepinephrine and copeptin levels with reduced skin blood flow, which by means of compensation reduced their transepidermal water loss. This complex physiologic‐metabolic adjustment across multiple organs allowed the rats to stabilize their body water content despite persisting renal water loss, albeit at the expense of hypertension and catabolic mobilization of muscle protein. CONCLUSION: Physiological adaptation to body water loss, termed aestivation, is an evolutionary conserved survival strategy and an under‐studied research area in medical physiology, which besides hypertension and muscle mass loss in chronic renal failure may explain many otherwise unexplainable phenomena in medicine. John Wiley and Sons Inc. 2021-03-07 2021-05 /pmc/articles/PMC8244025/ /pubmed/33590667 http://dx.doi.org/10.1111/apha.13629 Text en © 2021 The Authors. Acta Physiologica published by John Wiley & Sons Ltd on behalf of Scandinavian Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cardivascular Physiology
Kovarik, Johannes J.
Morisawa, Norihiko
Wild, Johannes
Marton, Adriana
Takase‐Minegishi, Kaoru
Minegishi, Shintaro
Daub, Steffen
Sands, Jeff M.
Klein, Janet D.
Bailey, James L.
Kovalik, Jean‐Paul
Rauh, Manfred
Karbach, Susanne
Hilgers, Karl F.
Luft, Friedrich
Nishiyama, Akira
Nakano, Daisuke
Kitada, Kento
Titze, Jens
Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title_full Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title_fullStr Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title_full_unstemmed Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title_short Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
title_sort adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure
topic Cardivascular Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244025/
https://www.ncbi.nlm.nih.gov/pubmed/33590667
http://dx.doi.org/10.1111/apha.13629
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