Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats
Introduction: It has been demonstrated HOE-642 ameliorates ischemic contracture, prevents post-resuscitation diastolic dysfunction, and favors the earlier return of contractile function. This study is the first report to explore the optimal dose of HOE-642 in protecting the neuronal mitochondrial fu...
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doaj-8310f71383eb4c8ba92b479e2ffabaea2021-05-20T07:36:57ZengElsevierBiomedicine & Pharmacotherapy0753-33222019-02-01110818824Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in ratsLanying Wei0Wenshuai Zhao1Yanan Hu2Xifan Wang3Xintong Liu4Pengjiao Zhang5Fei Han6Department of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaDepartment of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaDepartment of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaDepartment of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaDepartment of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaDepartment of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaCorresponding author at: Department of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, 150 Haping Road, Harbin, Heilongjiang, 150081, China.; Department of Anesthesiology, The Third Affiliated Hospital, Harbin Medical University, Harbin, 150081, Heilongjiang, ChinaIntroduction: It has been demonstrated HOE-642 ameliorates ischemic contracture, prevents post-resuscitation diastolic dysfunction, and favors the earlier return of contractile function. This study is the first report to explore the optimal dose of HOE-642 in protecting the neuronal mitochondrial function after cardiac arrest. Methods: Cardiac arrest was induced by 8 min asphyxia in rats. There were Sham (S), Normothermic (NORM), and Hypothermic (HYPO) groups. The NORM or HYPO groups consist of four subgroups: NORM/HYPO + HOE-642 0, 1, 3, and 5 mg/kg. Survival and NDS were evaluated after 24 h of resuscitation. ΔΨm, mitochondrial swelling, ROS production, and mitochondrial complex IIV activity of the hippocampus were detected. Results: Survival in the HYPO + 1 mg group was the best and significantly higher than in the NORM + 0 mg and NORM + 1 mg groups. NDS in the HYPO + 0 mg, HYPO + 1 mg, and HYPO + 3 mg groups was significantly lower than in the NORM + 0 mg group. ΔΨm in the NORM + 1 mg (n = 5) group was significantly higher than in the NORM + 0 mg (n = 8), NORM + 3 mg (n = 5), and NORM + 5 mg (n = 5) groups. The ROS production in the NORM + 1 mg and NORM + 3 mg groups were significantly lower than in the NORM + 0 mg and NORM + 5 mg groups. Complex I and III activities in the HYPO + 1 mg (n = 5) group were significantly higher than in the HYPO + 3 mg (n = 5), and HYPO + 5 mg (n = 5) groups. Complex II and IV activities in the NORM + 3 mg and HYPO + 3 mg groups were significantly higher than in the NORM + 0 mg, NORM + 1 mg, and HYPO + 0 mg (n = 4)groups. Conclusions: HOE-642 1 or 3 mg/kg showed benefits compared to HOE-642 5 mg/kg used when initiating resuscitation. When combined with hypothermia after cardiac arrest, HOE-642 1 or 3 mg/kg improved survival and neurological function compared with hypothermia or HOE-642 alone, however, HOE-642 5 mg/kg plus hypothermia did not.http://www.sciencedirect.com/science/article/pii/S0753332218378922CPRCardiac arrestHOE-642Ischemia-reperfusionMitochondria |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lanying Wei Wenshuai Zhao Yanan Hu Xifan Wang Xintong Liu Pengjiao Zhang Fei Han |
spellingShingle |
Lanying Wei Wenshuai Zhao Yanan Hu Xifan Wang Xintong Liu Pengjiao Zhang Fei Han Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats Biomedicine & Pharmacotherapy CPR Cardiac arrest HOE-642 Ischemia-reperfusion Mitochondria |
author_facet |
Lanying Wei Wenshuai Zhao Yanan Hu Xifan Wang Xintong Liu Pengjiao Zhang Fei Han |
author_sort |
Lanying Wei |
title |
Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
title_short |
Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
title_full |
Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
title_fullStr |
Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
title_full_unstemmed |
Exploration of the optimal dose of HOE-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
title_sort |
exploration of the optimal dose of hoe-642 for the protection of neuronal mitochondrial function after cardiac arrest in rats |
publisher |
Elsevier |
series |
Biomedicine & Pharmacotherapy |
issn |
0753-3322 |
publishDate |
2019-02-01 |
description |
Introduction: It has been demonstrated HOE-642 ameliorates ischemic contracture, prevents post-resuscitation diastolic dysfunction, and favors the earlier return of contractile function. This study is the first report to explore the optimal dose of HOE-642 in protecting the neuronal mitochondrial function after cardiac arrest. Methods: Cardiac arrest was induced by 8 min asphyxia in rats. There were Sham (S), Normothermic (NORM), and Hypothermic (HYPO) groups. The NORM or HYPO groups consist of four subgroups: NORM/HYPO + HOE-642 0, 1, 3, and 5 mg/kg. Survival and NDS were evaluated after 24 h of resuscitation. ΔΨm, mitochondrial swelling, ROS production, and mitochondrial complex IIV activity of the hippocampus were detected. Results: Survival in the HYPO + 1 mg group was the best and significantly higher than in the NORM + 0 mg and NORM + 1 mg groups. NDS in the HYPO + 0 mg, HYPO + 1 mg, and HYPO + 3 mg groups was significantly lower than in the NORM + 0 mg group. ΔΨm in the NORM + 1 mg (n = 5) group was significantly higher than in the NORM + 0 mg (n = 8), NORM + 3 mg (n = 5), and NORM + 5 mg (n = 5) groups. The ROS production in the NORM + 1 mg and NORM + 3 mg groups were significantly lower than in the NORM + 0 mg and NORM + 5 mg groups. Complex I and III activities in the HYPO + 1 mg (n = 5) group were significantly higher than in the HYPO + 3 mg (n = 5), and HYPO + 5 mg (n = 5) groups. Complex II and IV activities in the NORM + 3 mg and HYPO + 3 mg groups were significantly higher than in the NORM + 0 mg, NORM + 1 mg, and HYPO + 0 mg (n = 4)groups. Conclusions: HOE-642 1 or 3 mg/kg showed benefits compared to HOE-642 5 mg/kg used when initiating resuscitation. When combined with hypothermia after cardiac arrest, HOE-642 1 or 3 mg/kg improved survival and neurological function compared with hypothermia or HOE-642 alone, however, HOE-642 5 mg/kg plus hypothermia did not. |
topic |
CPR Cardiac arrest HOE-642 Ischemia-reperfusion Mitochondria |
url |
http://www.sciencedirect.com/science/article/pii/S0753332218378922 |
work_keys_str_mv |
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