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Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats

Alterations in the renal vasculature during fetal programming can cause disturbances in renal structure and function that persist into adulthood. Calcitriol can affect cellular differentiation and proliferation, and promote endothelial cell maintenance, each of which is a key event in nephrogenesis....

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Autores principales: Deluque, Amanda L., de Almeida, Lucas F., Francescato, Heloísa D. C., da Silva, Cleonice G. A., Costa, Roberto S., Antunes-Rodrigues, José, Coimbra, Terezila M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016013/
https://www.ncbi.nlm.nih.gov/pubmed/32118008
http://dx.doi.org/10.3389/fmed.2020.00023
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author Deluque, Amanda L.
de Almeida, Lucas F.
Francescato, Heloísa D. C.
da Silva, Cleonice G. A.
Costa, Roberto S.
Antunes-Rodrigues, José
Coimbra, Terezila M.
author_facet Deluque, Amanda L.
de Almeida, Lucas F.
Francescato, Heloísa D. C.
da Silva, Cleonice G. A.
Costa, Roberto S.
Antunes-Rodrigues, José
Coimbra, Terezila M.
author_sort Deluque, Amanda L.
collection PubMed
description Alterations in the renal vasculature during fetal programming can cause disturbances in renal structure and function that persist into adulthood. Calcitriol can affect cellular differentiation and proliferation, and promote endothelial cell maintenance, each of which is a key event in nephrogenesis. Calcitriol is a negative endocrine regulator of the renin gene. Rats exposed to renin-angiotensin system (RAS) antagonists during lactation have been shown to develop renal disorders, which demonstrated that the RAS may play an important role in mammalian kidney development. We evaluated the effects of calcitriol administration on losartan [angiotensin II receptor antagonist (ANGII), AT(1)]-induced changes in renal differentiation in rats during lactation. Rats treated with losartan showed alterations in renal function and structure that persisted into adulthood. These disruptions included hydronephrosis, papillary atrophy, endothelial dysfunction, and aberrant endothelial structure. These changes were mitigated by treatment with calcitriol. The results of our study showed that animals exposed to AT(1) blockade during lactation exhibited altered renal microvasculature differentiation in adulthood that was attenuated by treatment with calcitriol.
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spelling pubmed-70160132020-02-28 Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats Deluque, Amanda L. de Almeida, Lucas F. Francescato, Heloísa D. C. da Silva, Cleonice G. A. Costa, Roberto S. Antunes-Rodrigues, José Coimbra, Terezila M. Front Med (Lausanne) Medicine Alterations in the renal vasculature during fetal programming can cause disturbances in renal structure and function that persist into adulthood. Calcitriol can affect cellular differentiation and proliferation, and promote endothelial cell maintenance, each of which is a key event in nephrogenesis. Calcitriol is a negative endocrine regulator of the renin gene. Rats exposed to renin-angiotensin system (RAS) antagonists during lactation have been shown to develop renal disorders, which demonstrated that the RAS may play an important role in mammalian kidney development. We evaluated the effects of calcitriol administration on losartan [angiotensin II receptor antagonist (ANGII), AT(1)]-induced changes in renal differentiation in rats during lactation. Rats treated with losartan showed alterations in renal function and structure that persisted into adulthood. These disruptions included hydronephrosis, papillary atrophy, endothelial dysfunction, and aberrant endothelial structure. These changes were mitigated by treatment with calcitriol. The results of our study showed that animals exposed to AT(1) blockade during lactation exhibited altered renal microvasculature differentiation in adulthood that was attenuated by treatment with calcitriol. Frontiers Media S.A. 2020-02-06 /pmc/articles/PMC7016013/ /pubmed/32118008 http://dx.doi.org/10.3389/fmed.2020.00023 Text en Copyright © 2020 Deluque, de Almeida, Francescato, da Silva, Costa, Antunes-Rodrigues and Coimbra. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Deluque, Amanda L.
de Almeida, Lucas F.
Francescato, Heloísa D. C.
da Silva, Cleonice G. A.
Costa, Roberto S.
Antunes-Rodrigues, José
Coimbra, Terezila M.
Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title_full Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title_fullStr Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title_full_unstemmed Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title_short Effect of Calcitriol on the Renal Microvasculature Differentiation Disturbances Induced by AT(1) Blockade During Nephrogenesis in Rats
title_sort effect of calcitriol on the renal microvasculature differentiation disturbances induced by at(1) blockade during nephrogenesis in rats
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016013/
https://www.ncbi.nlm.nih.gov/pubmed/32118008
http://dx.doi.org/10.3389/fmed.2020.00023
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