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Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats

BACKGROUND: The renal tissue renin-angiotensin system is known to be activated by salt loading in salt-sensitive rats; however, the response in other organs remains unclear. METHOD: Spontaneously hypertensive rats were subjected to normal tap water or transient high-salt-concentration water from 6 t...

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Autores principales: Ryuzaki, Masaki, Miyashita, Kazutoshi, Sato, Masaaki, Inoue, Hiroyuki, Fujii, Kentaro, Hagiwara, Aika, Uto, Asuka, Endo, Sho, Oshida, Takuma, Kinouchi, Kenichiro, Itoh, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654260/
https://www.ncbi.nlm.nih.gov/pubmed/34285148
http://dx.doi.org/10.1097/HJH.0000000000002974
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author Ryuzaki, Masaki
Miyashita, Kazutoshi
Sato, Masaaki
Inoue, Hiroyuki
Fujii, Kentaro
Hagiwara, Aika
Uto, Asuka
Endo, Sho
Oshida, Takuma
Kinouchi, Kenichiro
Itoh, Hiroshi
author_facet Ryuzaki, Masaki
Miyashita, Kazutoshi
Sato, Masaaki
Inoue, Hiroyuki
Fujii, Kentaro
Hagiwara, Aika
Uto, Asuka
Endo, Sho
Oshida, Takuma
Kinouchi, Kenichiro
Itoh, Hiroshi
author_sort Ryuzaki, Masaki
collection PubMed
description BACKGROUND: The renal tissue renin-angiotensin system is known to be activated by salt loading in salt-sensitive rats; however, the response in other organs remains unclear. METHOD: Spontaneously hypertensive rats were subjected to normal tap water or transient high-salt-concentration water from 6 to 14 weeks of age and were thereafter given normal tap water. From 18 to 20 weeks of age, rats given water with a high salt concentration were treated with an angiotensin II type 1 receptor blocker, valsartan. RESULTS: Sustained blood pressure elevation by transient salt loading coincided with a persistent decrease in the fecal sodium content and sustained excess of the circulating volume in spontaneously hypertensive rats. Administration of valsartan sustainably reduced the blood pressure and normalized the fecal sodium levels. Notably, transient salt loading persistently induced the intestinal tissue renin-angiotensin system and enhanced sodium transporter expression exclusively in the small intestine of salt-sensitive rats, suggesting the potential connection of intestinal sodium absorption to salt sensitivity. CONCLUSION: These results reveal the previously unappreciated contribution of the intestinal tissue renin-angiotensin system to sodium homeostasis and blood pressure regulation in the pathophysiology of salt-sensitive hypertension.
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spelling pubmed-86542602021-12-15 Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats Ryuzaki, Masaki Miyashita, Kazutoshi Sato, Masaaki Inoue, Hiroyuki Fujii, Kentaro Hagiwara, Aika Uto, Asuka Endo, Sho Oshida, Takuma Kinouchi, Kenichiro Itoh, Hiroshi J Hypertens Original Articles BACKGROUND: The renal tissue renin-angiotensin system is known to be activated by salt loading in salt-sensitive rats; however, the response in other organs remains unclear. METHOD: Spontaneously hypertensive rats were subjected to normal tap water or transient high-salt-concentration water from 6 to 14 weeks of age and were thereafter given normal tap water. From 18 to 20 weeks of age, rats given water with a high salt concentration were treated with an angiotensin II type 1 receptor blocker, valsartan. RESULTS: Sustained blood pressure elevation by transient salt loading coincided with a persistent decrease in the fecal sodium content and sustained excess of the circulating volume in spontaneously hypertensive rats. Administration of valsartan sustainably reduced the blood pressure and normalized the fecal sodium levels. Notably, transient salt loading persistently induced the intestinal tissue renin-angiotensin system and enhanced sodium transporter expression exclusively in the small intestine of salt-sensitive rats, suggesting the potential connection of intestinal sodium absorption to salt sensitivity. CONCLUSION: These results reveal the previously unappreciated contribution of the intestinal tissue renin-angiotensin system to sodium homeostasis and blood pressure regulation in the pathophysiology of salt-sensitive hypertension. Lippincott Williams & Wilkins 2022-01 2021-07-19 /pmc/articles/PMC8654260/ /pubmed/34285148 http://dx.doi.org/10.1097/HJH.0000000000002974 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles
Ryuzaki, Masaki
Miyashita, Kazutoshi
Sato, Masaaki
Inoue, Hiroyuki
Fujii, Kentaro
Hagiwara, Aika
Uto, Asuka
Endo, Sho
Oshida, Takuma
Kinouchi, Kenichiro
Itoh, Hiroshi
Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title_full Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title_fullStr Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title_full_unstemmed Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title_short Activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
title_sort activation of the intestinal tissue renin-angiotensin system by transient sodium loading in salt-sensitive rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654260/
https://www.ncbi.nlm.nih.gov/pubmed/34285148
http://dx.doi.org/10.1097/HJH.0000000000002974
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