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

      research-article
      1 , 2 , 3 , 4 , 1 , 1 , 5 , 1 , 6 , 4 , 7 , 7 , 7 , 1 , 8 , 4 , 9 , 10 , 3 , 3 , 1 , 11 , , 1 , 9 , 12 ,
      Acta Physiologica (Oxford, England)
      John Wiley and Sons Inc.
      aestivation, body sodium, body water, dehydration, double‐barrier concept, glucose‐alanine‐shuttle, glycine methylation, hepato‐renal, hypertension, kidney, liver, muscle mass loss, organic osmolytes, purine metabolism, skin, transamination, transepidermal water loss, urea cycle, urine concentration

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          Abstract

          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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          Most cited references107

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            Striking convergent evolution is found in the properties of the organic osmotic solute (osmolyte) systems observed in bacteria, plants, and animals. Polyhydric alcohols, free amino acids and their derivatives, and combinations of urea and methylamines are the three types of osmolyte systems found in all water-stressed organisms except the halobacteria. The selective advantages of the organic osmolyte systems are, first, a compatibility with macromolecular structure and function at high or variable (or both) osmolyte concentrations, and, second, greatly reduced needs for modifying proteins to function in concentrated intracellular solutions. Osmolyte compatibility is proposed to result from the absence of osmolyte interactions with substrates and cofactors, and the nonperturbing or favorable effects of osmolytes on macromolecular-solvent interactions.
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              Physiology and pathophysiology of carnosine.

              Carnosine (β-alanyl-l-histidine) was discovered in 1900 as an abundant non-protein nitrogen-containing compound of meat. The dipeptide is not only found in skeletal muscle, but also in other excitable tissues. Most animals, except humans, also possess a methylated variant of carnosine, either anserine or ophidine/balenine, collectively called the histidine-containing dipeptides. This review aims to decipher the physiological roles of carnosine, based on its biochemical properties. The latter include pH-buffering, metal-ion chelation, and antioxidant capacity as well as the capacity to protect against formation of advanced glycation and lipoxidation end-products. For these reasons, the therapeutic potential of carnosine supplementation has been tested in numerous diseases in which ischemic or oxidative stress are involved. For several pathologies, such as diabetes and its complications, ocular disease, aging, and neurological disorders, promising preclinical and clinical results have been obtained. Also the pathophysiological relevance of serum carnosinase, the enzyme actively degrading carnosine into l-histidine and β-alanine, is discussed. The carnosine system has evolved as a pluripotent solution to a number of homeostatic challenges. l-Histidine, and more specifically its imidazole moiety, appears to be the prime bioactive component, whereas β-alanine is mainly regulating the synthesis of the dipeptide. This paper summarizes a century of scientific exploration on the (patho)physiological role of carnosine and related compounds. However, far more experiments in the fields of physiology and related disciplines (biology, pharmacology, genetics, molecular biology, etc.) are required to gain a full understanding of the function and applications of this intriguing molecule.
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                Author and article information

                Contributors
                kento-k@med.kagawa-u.ac.jp
                jens.titze@duke-nus.edu.sg
                Journal
                Acta Physiol (Oxf)
                Acta Physiol (Oxf)
                10.1111/(ISSN)1748-1716
                APHA
                Acta Physiologica (Oxford, England)
                John Wiley and Sons Inc. (Hoboken )
                1748-1708
                1748-1716
                07 March 2021
                May 2021
                : 232
                : 1 ( doiID: 10.1111/apha.v232.1 )
                : e13629
                Affiliations
                [ 1 ] Programme in Cardiovascular and Metabolic Disorders Duke‐NUS Medical School Singapore Singapore
                [ 2 ] Clinical Division of Nephrology and Dialysis Department of Internal Medicine III Medical University of Vienna Vienna Austria
                [ 3 ] Department of Pharmacology Faculty of Medicine Kagawa University Kagawa Japan
                [ 4 ] Division for Cardiology 1 Centre for Cardiology Johannes Gutenberg‐University Mainz Mainz Germany
                [ 5 ] Department of Stem Cell and Immune Regulation Yokohama City University Graduate School of Medicine Yokohama Japan
                [ 6 ] Department of Medical Science and Cardiorenal Medicine Yokohama City University Graduate School of Medicine Yokohama Japan
                [ 7 ] Renal Division Department of Medicine Emory University Atlanta GA USA
                [ 8 ] Division of Paediatrics Research Laboratory Erlangen Germany
                [ 9 ] Division of Nephrology and Hypertension University Clinic Erlangen Erlangen Germany
                [ 10 ] Experimental and Clinical Research Center Max Delbrück Center for Molecular Medicine Berlin Germany
                [ 11 ] JSPS Overseas Research Fellow Japan Society for the Promotion of Science Tokyo Japan
                [ 12 ] Division of Nephrology Duke University School of Medicine Durham NC USA
                Author notes
                [*] [* ] Correspondence

                Kento Kitada and Jens Titze, Programme in Cardiovascular and Metabolic Disorders, Duke‐NUS Medical School, 8 College Road, Singapore 169856, Singapore.

                Email: jens.titze@ 123456duke-nus.edu.sg ; kento-k@ 123456med.kagawa-u.ac.jp

                Author information
                https://orcid.org/0000-0002-0206-082X
                https://orcid.org/0000-0002-1446-8101
                https://orcid.org/0000-0002-7702-1577
                https://orcid.org/0000-0001-9822-0607
                https://orcid.org/0000-0002-8635-1199
                https://orcid.org/0000-0001-8463-8404
                Article
                APHA13629
                10.1111/apha.13629
                8244025
                33590667
                caa79865-02d8-4bf4-998a-386f05f96745
                © 2021 The Authors. Acta Physiologica published by John Wiley & Sons Ltd on behalf of Scandinavian Physiological Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 February 2021
                : 13 September 2020
                : 11 February 2021
                Page count
                Figures: 5, Tables: 2, Pages: 19, Words: 12781
                Funding
                Funded by: Public Trust Cardiovascular Research Fund
                Funded by: Austrian Science Fund , open-funder-registry 10.13039/501100002428;
                Funded by: Mitsukoshi Health and Welfare Foundation
                Funded by: Astellas Foundation for Research on Metabolic Disorders , open-funder-registry 10.13039/501100007263;
                Funded by: Duke NUS
                Funded by: Japan Heart Foundation , open-funder-registry 10.13039/501100013642;
                Funded by: Renal Research Institute
                Funded by: Japan Society for the Promotion of Science , open-funder-registry 10.13039/501100001691;
                Award ID: 19K17889
                Funded by: Mochida Memorial Foundation for Medical and Pharmaceutical Research , open-funder-registry 10.13039/501100005865;
                Funded by: Uehara Memorial Foundation , open-funder-registry 10.13039/100008732;
                Funded by: DRL Forschung unter Weltraumbedingungen
                Award ID: 50WB2024
                Funded by: National Heart, Lung, and Blood Institute , open-funder-registry 10.13039/100000050;
                Award ID: RO1 HL118579
                Categories
                Regular Paper
                Cardivascular Physiology
                Custom metadata
                2.0
                May 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.2 mode:remove_FC converted:30.06.2021

                Anatomy & Physiology
                aestivation,body sodium,body water,dehydration,double‐barrier concept,glucose‐alanine‐shuttle,glycine methylation,hepato‐renal,hypertension,kidney,liver,muscle mass loss,organic osmolytes,purine metabolism,skin,transamination,transepidermal water loss,urea cycle,urine concentration

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