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Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls

We have previously shown that in urethane-anaesthetized rats, intravenous injection of the angiotensin II (Ang II) AT(1) receptor antagonist losartan reversed the pressor effect of the cannabinoid CB(1) receptor agonist CP55940 given in the paraventricular nucleus of hypothalamus (PVN). The aim of o...

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Autores principales: Mińczuk, Krzysztof, Schlicker, Eberhard, Malinowska, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101384/
https://www.ncbi.nlm.nih.gov/pubmed/35563848
http://dx.doi.org/10.3390/cells11091542
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author Mińczuk, Krzysztof
Schlicker, Eberhard
Malinowska, Barbara
author_facet Mińczuk, Krzysztof
Schlicker, Eberhard
Malinowska, Barbara
author_sort Mińczuk, Krzysztof
collection PubMed
description We have previously shown that in urethane-anaesthetized rats, intravenous injection of the angiotensin II (Ang II) AT(1) receptor antagonist losartan reversed the pressor effect of the cannabinoid CB(1) receptor agonist CP55940 given in the paraventricular nucleus of hypothalamus (PVN). The aim of our study was to determine the potential interactions in the PVN between CB(1) receptors and AT(1) and AT(2) receptors for Ang II and Mas receptors for Ang 1–7 in blood pressure regulation in conscious spontaneously hypertensive (SHR) and normotensive Wistar Kyoto (WKY) rats. The pressor effects of Ang II, Ang 1–7 and CP55940 microinjected into the PVN were stronger in SHRs than in WKYs. Increases in blood pressure in response to Ang II were strongly inhibited by antagonists of AT(1) (losartan), AT(2) (PD123319) and CB(1) (AM251) receptors, to Ang 1–7 by a Mas antagonist (A-779) and AM251 and to CP55940 by losartan, PD123319 and A-779. Higher (AT(1) and CB(1)) and lower (AT(2) and Mas) receptor expression in the PVN of SHR compared to WKY may partially explain the above differences. In conclusion, blood pressure control in the PVN depends on the mutual interaction of CB(1), AT(1), AT(2) and Mas receptors in conscious spontaneously hypertensive rats and their normotensive controls.
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spelling pubmed-91013842022-05-14 Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls Mińczuk, Krzysztof Schlicker, Eberhard Malinowska, Barbara Cells Article We have previously shown that in urethane-anaesthetized rats, intravenous injection of the angiotensin II (Ang II) AT(1) receptor antagonist losartan reversed the pressor effect of the cannabinoid CB(1) receptor agonist CP55940 given in the paraventricular nucleus of hypothalamus (PVN). The aim of our study was to determine the potential interactions in the PVN between CB(1) receptors and AT(1) and AT(2) receptors for Ang II and Mas receptors for Ang 1–7 in blood pressure regulation in conscious spontaneously hypertensive (SHR) and normotensive Wistar Kyoto (WKY) rats. The pressor effects of Ang II, Ang 1–7 and CP55940 microinjected into the PVN were stronger in SHRs than in WKYs. Increases in blood pressure in response to Ang II were strongly inhibited by antagonists of AT(1) (losartan), AT(2) (PD123319) and CB(1) (AM251) receptors, to Ang 1–7 by a Mas antagonist (A-779) and AM251 and to CP55940 by losartan, PD123319 and A-779. Higher (AT(1) and CB(1)) and lower (AT(2) and Mas) receptor expression in the PVN of SHR compared to WKY may partially explain the above differences. In conclusion, blood pressure control in the PVN depends on the mutual interaction of CB(1), AT(1), AT(2) and Mas receptors in conscious spontaneously hypertensive rats and their normotensive controls. MDPI 2022-05-04 /pmc/articles/PMC9101384/ /pubmed/35563848 http://dx.doi.org/10.3390/cells11091542 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mińczuk, Krzysztof
Schlicker, Eberhard
Malinowska, Barbara
Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title_full Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title_fullStr Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title_full_unstemmed Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title_short Cross-Talk between CB(1), AT(1), AT(2) and Mas Receptors Responsible for Blood Pressure Control in the Paraventricular Nucleus of Hypothalamus in Conscious Spontaneously Hypertensive Rats and Their Normotensive Controls
title_sort cross-talk between cb(1), at(1), at(2) and mas receptors responsible for blood pressure control in the paraventricular nucleus of hypothalamus in conscious spontaneously hypertensive rats and their normotensive controls
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101384/
https://www.ncbi.nlm.nih.gov/pubmed/35563848
http://dx.doi.org/10.3390/cells11091542
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