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A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria
The kidneys facilitate energy conservation through reabsorption of nutrients including glucose. Almost all of the filtered blood glucose is reabsorbed by the kidneys. Loss of glucose in urine (glycosuria) is offset by an increase in endogenous glucose production to maintain normal energy supply in t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542134/ https://www.ncbi.nlm.nih.gov/pubmed/37790458 http://dx.doi.org/10.1101/2023.09.01.555894 |
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author | Faniyan, Tumininu S. Zhang, Xinyi Morgan, Donald A. Robles, Jorge Bathina, Siresha Brookes, Paul S. Rahmouni, Kamal Perry, Rachel J. Chhabra, Kavaljit H. |
author_facet | Faniyan, Tumininu S. Zhang, Xinyi Morgan, Donald A. Robles, Jorge Bathina, Siresha Brookes, Paul S. Rahmouni, Kamal Perry, Rachel J. Chhabra, Kavaljit H. |
author_sort | Faniyan, Tumininu S. |
collection | PubMed |
description | The kidneys facilitate energy conservation through reabsorption of nutrients including glucose. Almost all of the filtered blood glucose is reabsorbed by the kidneys. Loss of glucose in urine (glycosuria) is offset by an increase in endogenous glucose production to maintain normal energy supply in the body. How the body senses this glucose loss and consequently enhances glucose production is unclear. Using renal Glut2 knockout mice, we demonstrate that elevated glycosuria activates the hypothalamic-pituitary-adrenal axis, which in turn drives endogenous glucose production. This phenotype was attenuated by selective afferent renal denervation, indicating the involvement of the afferent nerves in promoting the compensatory increase in glucose production. In addition, through plasma proteomics analyses we observed that acute phase proteins - which are usually involved in body’s defense mechanisms against a threat – were the top candidates which were either upregulated or downregulated in renal Glut2 KO mice. Overall, afferent renal nerves contribute to promoting endogenous glucose production in response to elevated glycosuria and loss of glucose in urine is sensed as a biological threat in mice. These findings may be useful in improving efficiency of drugs like SGLT2 inhibitors that are intended to treat hyperglycemia by enhancing glycosuria, but are met with a compensatory increase in endogenous glucose production. |
format | Online Article Text |
id | pubmed-10542134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105421342023-10-03 A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria Faniyan, Tumininu S. Zhang, Xinyi Morgan, Donald A. Robles, Jorge Bathina, Siresha Brookes, Paul S. Rahmouni, Kamal Perry, Rachel J. Chhabra, Kavaljit H. bioRxiv Article The kidneys facilitate energy conservation through reabsorption of nutrients including glucose. Almost all of the filtered blood glucose is reabsorbed by the kidneys. Loss of glucose in urine (glycosuria) is offset by an increase in endogenous glucose production to maintain normal energy supply in the body. How the body senses this glucose loss and consequently enhances glucose production is unclear. Using renal Glut2 knockout mice, we demonstrate that elevated glycosuria activates the hypothalamic-pituitary-adrenal axis, which in turn drives endogenous glucose production. This phenotype was attenuated by selective afferent renal denervation, indicating the involvement of the afferent nerves in promoting the compensatory increase in glucose production. In addition, through plasma proteomics analyses we observed that acute phase proteins - which are usually involved in body’s defense mechanisms against a threat – were the top candidates which were either upregulated or downregulated in renal Glut2 KO mice. Overall, afferent renal nerves contribute to promoting endogenous glucose production in response to elevated glycosuria and loss of glucose in urine is sensed as a biological threat in mice. These findings may be useful in improving efficiency of drugs like SGLT2 inhibitors that are intended to treat hyperglycemia by enhancing glycosuria, but are met with a compensatory increase in endogenous glucose production. Cold Spring Harbor Laboratory 2023-09-05 /pmc/articles/PMC10542134/ /pubmed/37790458 http://dx.doi.org/10.1101/2023.09.01.555894 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Faniyan, Tumininu S. Zhang, Xinyi Morgan, Donald A. Robles, Jorge Bathina, Siresha Brookes, Paul S. Rahmouni, Kamal Perry, Rachel J. Chhabra, Kavaljit H. A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title | A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title_full | A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title_fullStr | A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title_full_unstemmed | A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title_short | A kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
title_sort | kidney-hypothalamus axis promotes compensatory glucose production in response to glycosuria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542134/ https://www.ncbi.nlm.nih.gov/pubmed/37790458 http://dx.doi.org/10.1101/2023.09.01.555894 |
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