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Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats

Prophylactic pharmacotherapy for health care in patients with high risk of cardiac arrest (CA) is an elusive and less explored strategy. Melatonin has possibilities used as a daily nutraceutical to trigger the cellular adaptation. We sought to find the effects of long-term daily prophylactic supplem...

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Autores principales: Hu, Yanan, Zhao, Xuyan, Jiang, Ge, Jin, Mingxin, Jiang, Wei, Han, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654502/
https://www.ncbi.nlm.nih.gov/pubmed/37973931
http://dx.doi.org/10.1038/s41598-023-47424-x
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author Hu, Yanan
Zhao, Xuyan
Jiang, Ge
Jin, Mingxin
Jiang, Wei
Han, Fei
author_facet Hu, Yanan
Zhao, Xuyan
Jiang, Ge
Jin, Mingxin
Jiang, Wei
Han, Fei
author_sort Hu, Yanan
collection PubMed
description Prophylactic pharmacotherapy for health care in patients with high risk of cardiac arrest (CA) is an elusive and less explored strategy. Melatonin has possibilities used as a daily nutraceutical to trigger the cellular adaptation. We sought to find the effects of long-term daily prophylactic supplement with melatonin on the victim of CA. Rats were divided into sham, CA, and melatonin + CA (Mel + CA) groups. The rats in the Mel + CA group received daily IP injection of melatonin 100 mg/kg for 14 days. CA was induced by 8 min asphyxia and followed by manual cardiopulmonary resuscitation. The endpoint was 24 h after resuscitation. Survival, neurological outcome, and hippocampal mitochondrial integrity, dynamics and function were assessed. Survival was significantly higher in the Mel + CA group than the CA group (81 vs. 42%, P = 0.04). Compared to the CA group, neurological damage in the CA1 region and the level of cytochrome c, cleaved caspase-3 and caspase-9 in the Mel + CA group were decreased (P < 0.05). Mitochondrial function and integrity were protected in the Mel + CA group compared to the CA group, according to the results of mitochondrial swelling, ΔΨm, ROS production, oxygen consumption rate, and respiratory control rate (P < 0.05). Melatonin increased SIRT3 and downregulated acetylated CypD. The mitochondrial dynamics and autophagy were improved in the Mel + CA group (P < 0.05). Long-term daily prophylactic supplement with melatonin buy the time from brain injury after CA.
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spelling pubmed-106545022023-11-16 Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats Hu, Yanan Zhao, Xuyan Jiang, Ge Jin, Mingxin Jiang, Wei Han, Fei Sci Rep Article Prophylactic pharmacotherapy for health care in patients with high risk of cardiac arrest (CA) is an elusive and less explored strategy. Melatonin has possibilities used as a daily nutraceutical to trigger the cellular adaptation. We sought to find the effects of long-term daily prophylactic supplement with melatonin on the victim of CA. Rats were divided into sham, CA, and melatonin + CA (Mel + CA) groups. The rats in the Mel + CA group received daily IP injection of melatonin 100 mg/kg for 14 days. CA was induced by 8 min asphyxia and followed by manual cardiopulmonary resuscitation. The endpoint was 24 h after resuscitation. Survival, neurological outcome, and hippocampal mitochondrial integrity, dynamics and function were assessed. Survival was significantly higher in the Mel + CA group than the CA group (81 vs. 42%, P = 0.04). Compared to the CA group, neurological damage in the CA1 region and the level of cytochrome c, cleaved caspase-3 and caspase-9 in the Mel + CA group were decreased (P < 0.05). Mitochondrial function and integrity were protected in the Mel + CA group compared to the CA group, according to the results of mitochondrial swelling, ΔΨm, ROS production, oxygen consumption rate, and respiratory control rate (P < 0.05). Melatonin increased SIRT3 and downregulated acetylated CypD. The mitochondrial dynamics and autophagy were improved in the Mel + CA group (P < 0.05). Long-term daily prophylactic supplement with melatonin buy the time from brain injury after CA. Nature Publishing Group UK 2023-11-16 /pmc/articles/PMC10654502/ /pubmed/37973931 http://dx.doi.org/10.1038/s41598-023-47424-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hu, Yanan
Zhao, Xuyan
Jiang, Ge
Jin, Mingxin
Jiang, Wei
Han, Fei
Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title_full Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title_fullStr Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title_full_unstemmed Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title_short Prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
title_sort prophylactic supplement with melatonin prevented the brain injury after cardiac arrest in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654502/
https://www.ncbi.nlm.nih.gov/pubmed/37973931
http://dx.doi.org/10.1038/s41598-023-47424-x
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