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The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model

As some of the renin–angiotensin–aldosterone system (RAAS)-dependent mechanisms underlying the cognitive performance modulation could include oxidative balance alterations, in this study we aimed to describe some of the potential interactions between RAAS modulators (Losartan and Ramipril) and oxida...

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Autores principales: Ababei, Daniela-Carmen, Balmus, Ioana-Miruna, Bild, Walther, Ciobica, Alin Stelian, Lefter, Radu Marian, Rusu, Răzvan-Nicolae, Stanciu, Gabriela Dumitrita, Cojocaru, Sabina, Hancianu, Monica, Bild, Veronica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452197/
https://www.ncbi.nlm.nih.gov/pubmed/37626567
http://dx.doi.org/10.3390/brainsci13081211
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author Ababei, Daniela-Carmen
Balmus, Ioana-Miruna
Bild, Walther
Ciobica, Alin Stelian
Lefter, Radu Marian
Rusu, Răzvan-Nicolae
Stanciu, Gabriela Dumitrita
Cojocaru, Sabina
Hancianu, Monica
Bild, Veronica
author_facet Ababei, Daniela-Carmen
Balmus, Ioana-Miruna
Bild, Walther
Ciobica, Alin Stelian
Lefter, Radu Marian
Rusu, Răzvan-Nicolae
Stanciu, Gabriela Dumitrita
Cojocaru, Sabina
Hancianu, Monica
Bild, Veronica
author_sort Ababei, Daniela-Carmen
collection PubMed
description As some of the renin–angiotensin–aldosterone system (RAAS)-dependent mechanisms underlying the cognitive performance modulation could include oxidative balance alterations, in this study we aimed to describe some of the potential interactions between RAAS modulators (Losartan and Ramipril) and oxidative stress in a typical model of memory impairment. In this study, 48 white male Swiss mice were divided into six groups and received RAAS modulators (oral administration Ramipril 4 mg/kg, Losartan 20 mg/kg) and a muscarinic receptors inhibitor (intraperitoneal injection scopolamine, 0.5 mg/kg) for 8 consecutive days. Then, 24 h after the last administration, the animals were euthanized and whole blood and brain tissues were collected. Biological samples were then processed, and biochemical analysis was carried out to assess superoxide dismutase and glutathione activities and malondialdehyde concentrations. In the present experimental conditions, we showed that RAAS modulation via the angiotensin-converting enzyme inhibition (Ramipril) and via the angiotensin II receptor blockage (Losartan) chronic treatments could lead to oxidative stress modulation in a non-selective muscarinic receptors blocker (scopolamine) animal model. Our results showed that Losartan could exhibit a significant systemic antioxidant potential partly preventing the negative oxidative effects of scopolamine and a brain antioxidant potential, mainly by inhibiting the oxidative-stress-mediated cellular damage and apoptosis. Ramipril could also minimize the oxidative-mediated damage to the lipid components of brain tissue resulting from scopolamine administration. Both blood serum and brain changes in oxidative stress status were observed following 8-day treatments with Ramipril, Losartan, scopolamine, and combinations. While the serum oxidative stress modulation observed in this study could suggest the potential effect of RAAS modulation and scopolamine administration on the circulatory system, blood vessels endothelia, and arterial tension modulation, the observed brain tissues oxidative stress modulation could lead to important information on the complex interaction between renin–angiotensin and cholinergic systems.
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spelling pubmed-104521972023-08-26 The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model Ababei, Daniela-Carmen Balmus, Ioana-Miruna Bild, Walther Ciobica, Alin Stelian Lefter, Radu Marian Rusu, Răzvan-Nicolae Stanciu, Gabriela Dumitrita Cojocaru, Sabina Hancianu, Monica Bild, Veronica Brain Sci Article As some of the renin–angiotensin–aldosterone system (RAAS)-dependent mechanisms underlying the cognitive performance modulation could include oxidative balance alterations, in this study we aimed to describe some of the potential interactions between RAAS modulators (Losartan and Ramipril) and oxidative stress in a typical model of memory impairment. In this study, 48 white male Swiss mice were divided into six groups and received RAAS modulators (oral administration Ramipril 4 mg/kg, Losartan 20 mg/kg) and a muscarinic receptors inhibitor (intraperitoneal injection scopolamine, 0.5 mg/kg) for 8 consecutive days. Then, 24 h after the last administration, the animals were euthanized and whole blood and brain tissues were collected. Biological samples were then processed, and biochemical analysis was carried out to assess superoxide dismutase and glutathione activities and malondialdehyde concentrations. In the present experimental conditions, we showed that RAAS modulation via the angiotensin-converting enzyme inhibition (Ramipril) and via the angiotensin II receptor blockage (Losartan) chronic treatments could lead to oxidative stress modulation in a non-selective muscarinic receptors blocker (scopolamine) animal model. Our results showed that Losartan could exhibit a significant systemic antioxidant potential partly preventing the negative oxidative effects of scopolamine and a brain antioxidant potential, mainly by inhibiting the oxidative-stress-mediated cellular damage and apoptosis. Ramipril could also minimize the oxidative-mediated damage to the lipid components of brain tissue resulting from scopolamine administration. Both blood serum and brain changes in oxidative stress status were observed following 8-day treatments with Ramipril, Losartan, scopolamine, and combinations. While the serum oxidative stress modulation observed in this study could suggest the potential effect of RAAS modulation and scopolamine administration on the circulatory system, blood vessels endothelia, and arterial tension modulation, the observed brain tissues oxidative stress modulation could lead to important information on the complex interaction between renin–angiotensin and cholinergic systems. MDPI 2023-08-16 /pmc/articles/PMC10452197/ /pubmed/37626567 http://dx.doi.org/10.3390/brainsci13081211 Text en © 2023 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
Ababei, Daniela-Carmen
Balmus, Ioana-Miruna
Bild, Walther
Ciobica, Alin Stelian
Lefter, Radu Marian
Rusu, Răzvan-Nicolae
Stanciu, Gabriela Dumitrita
Cojocaru, Sabina
Hancianu, Monica
Bild, Veronica
The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title_full The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title_fullStr The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title_full_unstemmed The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title_short The Impact of Some Modulators of the Renin–Angiotensin System on the Scopolamine-Induced Memory Loss Mice Model
title_sort impact of some modulators of the renin–angiotensin system on the scopolamine-induced memory loss mice model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452197/
https://www.ncbi.nlm.nih.gov/pubmed/37626567
http://dx.doi.org/10.3390/brainsci13081211
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