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Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum

Piezo1 channel is a sensor for shear-stress in the vasculature. Piezo1 activation induces vasodilation, and its deficiency contributes to vascular disorders, such as hypertension. In this study, we aimed to determine whether Piezo1 channel has a functional role in the dilation of pudendal arteries a...

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Autores principales: Dela Justina, Vanessa, de Freitas, Raiany Alves, Arishe, Olufunke O., Giachini, Fernanda R., Webb, R. Clinton, Priviero, Fernanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950814/
https://www.ncbi.nlm.nih.gov/pubmed/36846322
http://dx.doi.org/10.3389/fphys.2023.998951
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author Dela Justina, Vanessa
de Freitas, Raiany Alves
Arishe, Olufunke O.
Giachini, Fernanda R.
Webb, R. Clinton
Priviero, Fernanda
author_facet Dela Justina, Vanessa
de Freitas, Raiany Alves
Arishe, Olufunke O.
Giachini, Fernanda R.
Webb, R. Clinton
Priviero, Fernanda
author_sort Dela Justina, Vanessa
collection PubMed
description Piezo1 channel is a sensor for shear-stress in the vasculature. Piezo1 activation induces vasodilation, and its deficiency contributes to vascular disorders, such as hypertension. In this study, we aimed to determine whether Piezo1 channel has a functional role in the dilation of pudendal arteries and corpus cavernosum (CC). For this, male Wistar rats were used, and the relaxation of the pudendal artery and CC was obtained using the Piezo1 activator, Yoda1, in the presence and absence of Dooku (Yoda1 antagonist), GsMTx4 (non-selective mechanosensory channel inhibitor) and L-NAME (nitric oxide synthase inhibitor). In the CC, Yoda1 was also tested in the presence of indomethacin (non-selective COX inhibitor) and tetraethylammonium (TEA, non-selective potassium channel inhibitor). The expression of Piezo1 was confirmed by Western blotting. Our data show that Piezo1 activation leads to the relaxation of the pudendal artery and CC as the chemical activator of Piezo1, Yoda1, relaxed the pudendal artery (47%) and CC (41%). This response was impaired by L-NAME and abolished by Dooku and GsMTx4 in the pudendal artery only. Indomethacin and TEA did not affect the relaxation induced by Yoda1 in the CC. Limited tools to explore this channel prevent further investigation of its underlying mechanisms of action. In conclusion, our data demonstrate that Piezo1 is expressed and induced the relaxation of the pudendal artery and CC. Further studies are necessary to determine its role in penile erection and if erectile dysfunction is associated with Piezo1 deficiency.
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spelling pubmed-99508142023-02-25 Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum Dela Justina, Vanessa de Freitas, Raiany Alves Arishe, Olufunke O. Giachini, Fernanda R. Webb, R. Clinton Priviero, Fernanda Front Physiol Physiology Piezo1 channel is a sensor for shear-stress in the vasculature. Piezo1 activation induces vasodilation, and its deficiency contributes to vascular disorders, such as hypertension. In this study, we aimed to determine whether Piezo1 channel has a functional role in the dilation of pudendal arteries and corpus cavernosum (CC). For this, male Wistar rats were used, and the relaxation of the pudendal artery and CC was obtained using the Piezo1 activator, Yoda1, in the presence and absence of Dooku (Yoda1 antagonist), GsMTx4 (non-selective mechanosensory channel inhibitor) and L-NAME (nitric oxide synthase inhibitor). In the CC, Yoda1 was also tested in the presence of indomethacin (non-selective COX inhibitor) and tetraethylammonium (TEA, non-selective potassium channel inhibitor). The expression of Piezo1 was confirmed by Western blotting. Our data show that Piezo1 activation leads to the relaxation of the pudendal artery and CC as the chemical activator of Piezo1, Yoda1, relaxed the pudendal artery (47%) and CC (41%). This response was impaired by L-NAME and abolished by Dooku and GsMTx4 in the pudendal artery only. Indomethacin and TEA did not affect the relaxation induced by Yoda1 in the CC. Limited tools to explore this channel prevent further investigation of its underlying mechanisms of action. In conclusion, our data demonstrate that Piezo1 is expressed and induced the relaxation of the pudendal artery and CC. Further studies are necessary to determine its role in penile erection and if erectile dysfunction is associated with Piezo1 deficiency. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950814/ /pubmed/36846322 http://dx.doi.org/10.3389/fphys.2023.998951 Text en Copyright © 2023 Dela Justina, de Freitas, Arishe, Giachini, Webb and Priviero. https://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 Physiology
Dela Justina, Vanessa
de Freitas, Raiany Alves
Arishe, Olufunke O.
Giachini, Fernanda R.
Webb, R. Clinton
Priviero, Fernanda
Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title_full Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title_fullStr Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title_full_unstemmed Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title_short Piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
title_sort piezo1 activation induces relaxation of the pudendal artery and corpus cavernosum
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950814/
https://www.ncbi.nlm.nih.gov/pubmed/36846322
http://dx.doi.org/10.3389/fphys.2023.998951
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