Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor

Abstract Vasopressin (AVP) increases water permeability in the renal collecting duct through the regulation of aquaporin-2 (AQP2) trafficking. Several disorders, including hypertension and inappropriate antidiuretic hormone secretion (SIADH), are associated with abnormalities in water homeostasis. I...

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Autores principales: Marianna Ranieri, Annarita Di Mise, Mariangela Centrone, Mariagrazia D’Agostino, Stine Julie Tingskov, Maria Venneri, Tommaso Pellegrino, Graziana Difonzo, Francesco Caponio, Rikke Norregaard, Giovanna Valenti, Grazia Tamma
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:12cb165d760144b5a15b242e983724db2021-12-02T13:34:50ZOlive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor10.1038/s41598-021-83850-52045-2322https://doaj.org/article/12cb165d760144b5a15b242e983724db2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-83850-5https://doaj.org/toc/2045-2322Abstract Vasopressin (AVP) increases water permeability in the renal collecting duct through the regulation of aquaporin-2 (AQP2) trafficking. Several disorders, including hypertension and inappropriate antidiuretic hormone secretion (SIADH), are associated with abnormalities in water homeostasis. It has been shown that certain phytocompounds are beneficial to human health. Here, the effects of the Olive Leaf Extract (OLE) have been evaluated using in vitro and in vivo models. Confocal studies showed that OLE prevents the vasopressin induced AQP2 translocation to the plasma membrane in MCD4 cells and rat kidneys. Incubation with OLE decreases the AVP-dependent increase of the osmotic water permeability coefficient (Pf). To elucidate the possible effectors of OLE, intracellular calcium was evaluated. OLE increases the intracellular calcium through the activation of the Calcium Sensing Receptor (CaSR). NPS2143, a selective CaSR inhibitor, abolished the inhibitory effect of OLE on AVP-dependent water permeability. In vivo experiments revealed that treatment with OLE increases the expression of the CaSR mRNA and decreases AQP2 mRNA paralleled by an increase of the AQP2-targeting miRNA-137. Together, these findings suggest that OLE antagonizes vasopressin action through stimulation of the CaSR indicating that this extract may be beneficial to attenuate disorders characterized by abnormal CaSR signaling and affecting renal water reabsorption.Marianna RanieriAnnarita Di MiseMariangela CentroneMariagrazia D’AgostinoStine Julie TingskovMaria VenneriTommaso PellegrinoGraziana DifonzoFrancesco CaponioRikke NorregaardGiovanna ValentiGrazia TammaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Marianna Ranieri
Annarita Di Mise
Mariangela Centrone
Mariagrazia D’Agostino
Stine Julie Tingskov
Maria Venneri
Tommaso Pellegrino
Graziana Difonzo
Francesco Caponio
Rikke Norregaard
Giovanna Valenti
Grazia Tamma
Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
description Abstract Vasopressin (AVP) increases water permeability in the renal collecting duct through the regulation of aquaporin-2 (AQP2) trafficking. Several disorders, including hypertension and inappropriate antidiuretic hormone secretion (SIADH), are associated with abnormalities in water homeostasis. It has been shown that certain phytocompounds are beneficial to human health. Here, the effects of the Olive Leaf Extract (OLE) have been evaluated using in vitro and in vivo models. Confocal studies showed that OLE prevents the vasopressin induced AQP2 translocation to the plasma membrane in MCD4 cells and rat kidneys. Incubation with OLE decreases the AVP-dependent increase of the osmotic water permeability coefficient (Pf). To elucidate the possible effectors of OLE, intracellular calcium was evaluated. OLE increases the intracellular calcium through the activation of the Calcium Sensing Receptor (CaSR). NPS2143, a selective CaSR inhibitor, abolished the inhibitory effect of OLE on AVP-dependent water permeability. In vivo experiments revealed that treatment with OLE increases the expression of the CaSR mRNA and decreases AQP2 mRNA paralleled by an increase of the AQP2-targeting miRNA-137. Together, these findings suggest that OLE antagonizes vasopressin action through stimulation of the CaSR indicating that this extract may be beneficial to attenuate disorders characterized by abnormal CaSR signaling and affecting renal water reabsorption.
format article
author Marianna Ranieri
Annarita Di Mise
Mariangela Centrone
Mariagrazia D’Agostino
Stine Julie Tingskov
Maria Venneri
Tommaso Pellegrino
Graziana Difonzo
Francesco Caponio
Rikke Norregaard
Giovanna Valenti
Grazia Tamma
author_facet Marianna Ranieri
Annarita Di Mise
Mariangela Centrone
Mariagrazia D’Agostino
Stine Julie Tingskov
Maria Venneri
Tommaso Pellegrino
Graziana Difonzo
Francesco Caponio
Rikke Norregaard
Giovanna Valenti
Grazia Tamma
author_sort Marianna Ranieri
title Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
title_short Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
title_full Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
title_fullStr Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
title_full_unstemmed Olive Leaf Extract (OLE) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
title_sort olive leaf extract (ole) impaired vasopressin-induced aquaporin-2 trafficking through the activation of the calcium-sensing receptor
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/12cb165d760144b5a15b242e983724db
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