Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model
Background: Circadian rhythms have a considerable impact on the daily physiology of the heart, and their disruption causes pathology. Several studies have revealed that circadian disruption impaired cardiac remodeling after myocardial infarction (MI); however, the underlying brain-heart mechanisms r...
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Frontiers Media S.A.
2021-03-01
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Series: | Frontiers in Cardiovascular Medicine |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fcvm.2021.668387/full |
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doaj-9e63f36b6d264a91a1a5ff762f8c894c |
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record_format |
Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yuhong Wang Yuhong Wang Yuhong Wang Yuhong Wang Wanli Jiang Hu Chen Hu Chen Hu Chen Hu Chen Huixin Zhou Huixin Zhou Huixin Zhou Huixin Zhou Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Zihan Liu Zihan Liu Zihan Liu Zihan Liu Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Yuyang Zhou Yuyang Zhou Yuyang Zhou Yuyang Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Lilei Yu Lilei Yu Lilei Yu Lilei Yu Hong Jiang Hong Jiang Hong Jiang Hong Jiang |
spellingShingle |
Yuhong Wang Yuhong Wang Yuhong Wang Yuhong Wang Wanli Jiang Hu Chen Hu Chen Hu Chen Hu Chen Huixin Zhou Huixin Zhou Huixin Zhou Huixin Zhou Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Zihan Liu Zihan Liu Zihan Liu Zihan Liu Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Yuyang Zhou Yuyang Zhou Yuyang Zhou Yuyang Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Lilei Yu Lilei Yu Lilei Yu Lilei Yu Hong Jiang Hong Jiang Hong Jiang Hong Jiang Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model Frontiers in Cardiovascular Medicine sympathetic nervous system autonomic nervous system cardiac dysfunction circadian disruption sympathetic ganglionic blockade |
author_facet |
Yuhong Wang Yuhong Wang Yuhong Wang Yuhong Wang Wanli Jiang Hu Chen Hu Chen Hu Chen Hu Chen Huixin Zhou Huixin Zhou Huixin Zhou Huixin Zhou Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Zihan Liu Zihan Liu Zihan Liu Zihan Liu Zhihao Liu Zhihao Liu Zhihao Liu Zhihao Liu Yuyang Zhou Yuyang Zhou Yuyang Zhou Yuyang Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Xiaoya Zhou Lilei Yu Lilei Yu Lilei Yu Lilei Yu Hong Jiang Hong Jiang Hong Jiang Hong Jiang |
author_sort |
Yuhong Wang |
title |
Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model |
title_short |
Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model |
title_full |
Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model |
title_fullStr |
Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model |
title_full_unstemmed |
Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption Model |
title_sort |
sympathetic nervous system mediates cardiac remodeling after myocardial infarction in a circadian disruption model |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cardiovascular Medicine |
issn |
2297-055X |
publishDate |
2021-03-01 |
description |
Background: Circadian rhythms have a considerable impact on the daily physiology of the heart, and their disruption causes pathology. Several studies have revealed that circadian disruption impaired cardiac remodeling after myocardial infarction (MI); however, the underlying brain-heart mechanisms remain unknown. We aim to discuss whether circadian disruption facilitates cardiac remodeling after MI by activating sympathetic nervous system.Methods: Rats were randomly divided into three groups: Sham group (Sham), MI group (MI), and MI+ circadian disruption group (MI+Dis); rats were treated with pseudorabies virus (PRV) injections for trans-synaptic retrograde tracing; rats were randomly divided into two groups: MI+ circadian disruption + Empty Vector+ clozapine N-oxide (CNO) (Empty Vector), and MI+ circadian disruption + hM4D(Gi)+ CNO [hM4D(Gi)].Results: Circadian disruption significantly facilitated cardiac remodeling after MI with lower systolic function, larger left ventricular volume, and aggravated cardiac fibrosis. Cardiac sympathetic remodeling makers and serum norepinephrine levels were also significantly increased by circadian disruption. PRV virus-labeled neurons were identified in the superior cervical ganglion (SCG), paraventricular nucleus (PVN), and suprachiasmatic nucleus (SCN) regions. Ganglionic blockade via designer receptors exclusively activated by designer drugs (DREADD) technique suppressed the activity of sympathetic nervous system and significantly alleviated the disruption-related cardiac dysfunction.Conclusion: Circadian disruption adversely affected cardiac remodeling after MI possibly by activating sympathetic nervous system, and suppressing sympathetic activity can attenuate this disruption-related cardiac dysfunction. |
topic |
sympathetic nervous system autonomic nervous system cardiac dysfunction circadian disruption sympathetic ganglionic blockade |
url |
https://www.frontiersin.org/articles/10.3389/fcvm.2021.668387/full |
work_keys_str_mv |
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doaj-9e63f36b6d264a91a1a5ff762f8c894c2021-03-26T04:25:22ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2021-03-01810.3389/fcvm.2021.668387668387Sympathetic Nervous System Mediates Cardiac Remodeling After Myocardial Infarction in a Circadian Disruption ModelYuhong Wang0Yuhong Wang1Yuhong Wang2Yuhong Wang3Wanli Jiang4Hu Chen5Hu Chen6Hu Chen7Hu Chen8Huixin Zhou9Huixin Zhou10Huixin Zhou11Huixin Zhou12Zhihao Liu13Zhihao Liu14Zhihao Liu15Zhihao Liu16Zihan Liu17Zihan Liu18Zihan Liu19Zihan Liu20Zhihao Liu21Zhihao Liu22Zhihao Liu23Zhihao Liu24Yuyang Zhou25Yuyang Zhou26Yuyang Zhou27Yuyang Zhou28Xiaoya Zhou29Xiaoya Zhou30Xiaoya Zhou31Xiaoya Zhou32Lilei Yu33Lilei Yu34Lilei Yu35Lilei Yu36Hong Jiang37Hong Jiang38Hong Jiang39Hong Jiang40Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, ChinaCardiac Autonomic Nervous Research Center, Wuhan University, Wuhan, ChinaDepartment of Cardiology Cardiovascular Research Institute, Wuhan University, Wuhan, ChinaHubei Key Laboratory of Cardiology, Wuhan, ChinaBackground: Circadian rhythms have a considerable impact on the daily physiology of the heart, and their disruption causes pathology. Several studies have revealed that circadian disruption impaired cardiac remodeling after myocardial infarction (MI); however, the underlying brain-heart mechanisms remain unknown. We aim to discuss whether circadian disruption facilitates cardiac remodeling after MI by activating sympathetic nervous system.Methods: Rats were randomly divided into three groups: Sham group (Sham), MI group (MI), and MI+ circadian disruption group (MI+Dis); rats were treated with pseudorabies virus (PRV) injections for trans-synaptic retrograde tracing; rats were randomly divided into two groups: MI+ circadian disruption + Empty Vector+ clozapine N-oxide (CNO) (Empty Vector), and MI+ circadian disruption + hM4D(Gi)+ CNO [hM4D(Gi)].Results: Circadian disruption significantly facilitated cardiac remodeling after MI with lower systolic function, larger left ventricular volume, and aggravated cardiac fibrosis. Cardiac sympathetic remodeling makers and serum norepinephrine levels were also significantly increased by circadian disruption. PRV virus-labeled neurons were identified in the superior cervical ganglion (SCG), paraventricular nucleus (PVN), and suprachiasmatic nucleus (SCN) regions. Ganglionic blockade via designer receptors exclusively activated by designer drugs (DREADD) technique suppressed the activity of sympathetic nervous system and significantly alleviated the disruption-related cardiac dysfunction.Conclusion: Circadian disruption adversely affected cardiac remodeling after MI possibly by activating sympathetic nervous system, and suppressing sympathetic activity can attenuate this disruption-related cardiac dysfunction.https://www.frontiersin.org/articles/10.3389/fcvm.2021.668387/fullsympathetic nervous systemautonomic nervous systemcardiac dysfunctioncircadian disruptionsympathetic ganglionic blockade |