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Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience
Stress-induced conditions are associated with impaired cerebral blood flow (CBF) and increased risk of dementia and stroke. However, these conditions do not develop in resilient humans and animals. Here the effects of predator stress (PS, cat urine scent, ten days) on CBF and mechanisms of CBF regul...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738343/ https://www.ncbi.nlm.nih.gov/pubmed/36499055 http://dx.doi.org/10.3390/ijms232314729 |
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author | Kondashevskaya, Marina V. Downey, H. Fred Tseilikman, Vadim E. Alexandrin, Valery V. Artem’yeva, Kseniya A. Aleksankina, Valentina V. Tseilikman, Olga B. Pashkov, Anton A. Goryacheva, Anna V. Ivleva, Irina S. Karpenko, Marina N. Shatilov, Vladislav A. Manukhina, Eugenia B. |
author_facet | Kondashevskaya, Marina V. Downey, H. Fred Tseilikman, Vadim E. Alexandrin, Valery V. Artem’yeva, Kseniya A. Aleksankina, Valentina V. Tseilikman, Olga B. Pashkov, Anton A. Goryacheva, Anna V. Ivleva, Irina S. Karpenko, Marina N. Shatilov, Vladislav A. Manukhina, Eugenia B. |
author_sort | Kondashevskaya, Marina V. |
collection | PubMed |
description | Stress-induced conditions are associated with impaired cerebral blood flow (CBF) and increased risk of dementia and stroke. However, these conditions do not develop in resilient humans and animals. Here the effects of predator stress (PS, cat urine scent, ten days) on CBF and mechanisms of CBF regulation were compared in PS-susceptible (PSs) and PS-resilient (PSr) rats. Fourteen days post-stress, the rats were segregated into PSs and PSr groups based on a behavior-related anxiety index (AI). CBF and its endothelium-dependent changes were measured in the parietal cortex by laser Doppler flowmetry. The major findings are: (1) PS susceptibility was associated with reduced basal CBF and endothelial dysfunction. In PSr rats, the basal CBF was higher, and endothelial dysfunction was attenuated. (2) CBF was inversely correlated with the AI of PS-exposed rats. (3) Endothelial dysfunction was associated with a decrease in eNOS mRNA in PSs rats compared to the PSr and control rats. (4) Brain dopamine was reduced in PSs rats and increased in PSr rats. (5) Plasma corticosterone of PSs was reduced compared to PSr and control rats. (6) A hypercoagulation state was present in PSs rats but not in PSr rats. Thus, potential stress resilience mechanisms that are protective for CBF were identified. |
format | Online Article Text |
id | pubmed-9738343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97383432022-12-11 Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience Kondashevskaya, Marina V. Downey, H. Fred Tseilikman, Vadim E. Alexandrin, Valery V. Artem’yeva, Kseniya A. Aleksankina, Valentina V. Tseilikman, Olga B. Pashkov, Anton A. Goryacheva, Anna V. Ivleva, Irina S. Karpenko, Marina N. Shatilov, Vladislav A. Manukhina, Eugenia B. Int J Mol Sci Article Stress-induced conditions are associated with impaired cerebral blood flow (CBF) and increased risk of dementia and stroke. However, these conditions do not develop in resilient humans and animals. Here the effects of predator stress (PS, cat urine scent, ten days) on CBF and mechanisms of CBF regulation were compared in PS-susceptible (PSs) and PS-resilient (PSr) rats. Fourteen days post-stress, the rats were segregated into PSs and PSr groups based on a behavior-related anxiety index (AI). CBF and its endothelium-dependent changes were measured in the parietal cortex by laser Doppler flowmetry. The major findings are: (1) PS susceptibility was associated with reduced basal CBF and endothelial dysfunction. In PSr rats, the basal CBF was higher, and endothelial dysfunction was attenuated. (2) CBF was inversely correlated with the AI of PS-exposed rats. (3) Endothelial dysfunction was associated with a decrease in eNOS mRNA in PSs rats compared to the PSr and control rats. (4) Brain dopamine was reduced in PSs rats and increased in PSr rats. (5) Plasma corticosterone of PSs was reduced compared to PSr and control rats. (6) A hypercoagulation state was present in PSs rats but not in PSr rats. Thus, potential stress resilience mechanisms that are protective for CBF were identified. MDPI 2022-11-25 /pmc/articles/PMC9738343/ /pubmed/36499055 http://dx.doi.org/10.3390/ijms232314729 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 Kondashevskaya, Marina V. Downey, H. Fred Tseilikman, Vadim E. Alexandrin, Valery V. Artem’yeva, Kseniya A. Aleksankina, Valentina V. Tseilikman, Olga B. Pashkov, Anton A. Goryacheva, Anna V. Ivleva, Irina S. Karpenko, Marina N. Shatilov, Vladislav A. Manukhina, Eugenia B. Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title | Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title_full | Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title_fullStr | Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title_full_unstemmed | Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title_short | Cerebral Blood Flow in Predator Stress-Resilient and -Susceptible Rats and Mechanisms of Resilience |
title_sort | cerebral blood flow in predator stress-resilient and -susceptible rats and mechanisms of resilience |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738343/ https://www.ncbi.nlm.nih.gov/pubmed/36499055 http://dx.doi.org/10.3390/ijms232314729 |
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