题名 | Menaquinone-4 alleviates hypoxic-ischemic brain damage in neonatal rats by reducing mitochondrial dysfunction via Sirt1-PGC-1α-TFAM signaling pathway |
作者 | |
发表日期 | 2024-05-16 |
发表期刊 | International immunopharmacology 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Journal Article |
关键词 | Hypoxic-ischemic encephalopathy Menaquinone-4 Mitochondrial dysfunction Sirt1 |
其他关键词 | VITAMIN-K ; METABOLISM ; SIRT1 |
摘要 | Hypoxic-ischemic encephalopathy (HIE) is a major contributor to neonatal mortality and neurodevelopmental disorders, but currently there is no effective therapy drug for HIE. Mitochondrial dysfunction plays a pivotal role in hypoxic-ischemic brain damage(HIBD). Menaquinone-4 (MK-4), a subtype of vitamin K2 prevalent in the brain, has been shown to enhance mitochondrial function and exhibit protective effects against ischemia-reperfusion injury. However, the impact and underlying molecular mechanism of MK-4 in HIE have not been fully elucidated., In this study, we established the neonatal rats HIBD model in vivo and oxygen-glucose deprivation and reperfusion (OGD/R) of primary neurons in vitro to explore the neuroprotective effects of MK-4 on HI damage, and illuminate the potential mechanism., Our findings revealed that MK-4 ameliorated mitochondrial dysfunction, reduced oxidative stress, and prevented HI-induced neuronal apoptosis by activating the Sirt1-PGC-1α-TFAM signaling pathway through Sirt1 mediation. Importantly, these protective effects were partially reversed by EX-527, a Sirt1 inhibitor., Our study elucidated the potential therapeutic mechanism of MK-4 in neonatal HIE, suggesting its viability as an agent for enhancing recovery from HI-induced cerebral damage in newborns. Further exploration into MK-4 could lead to novel interventions for HIE therapy. |
资助项目 | National Natural Science Foundation of China[82271747];Wu Jieping Medical Foundation[320.6750.2023-24-2]; |
出版者 | Elsevier B.V. |
ISSN | 1567-5769 |
EISSN | 1878-1705 |
卷号 | 134 |
DOI | 10.1016/j.intimp.2024.112257 |
页数 | 14 |
WOS类目 | Immunology ; Pharmacology & Pharmacy |
WOS研究方向 | Immunology ; Pharmacology & Pharmacy |
WOS记录号 | WOS:001280520400001 |
收录类别 | PUBMED ; SCOPUS ; SCIE |
URL | 查看原文 |
PubMed ID | 38759366 |
SCOPUSEID | 2-s2.0-85193069967 |
通讯作者地址 | [Wang, Zhouguang]Department of Neonatology,The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,Wenzhou,China |
Scopus学科分类 | Immunology and Allergy;Immunology;Pharmacology |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/212905 |
专题 | 第二临床医学院、附属第二医院、育英儿童医院 药学院(分析测试中心) 附属第二医院 其他_附属慈溪医院(慈溪市人民医院) |
通讯作者 | Wang, Zhouguang; Lin, Zhenlang |
作者单位 | 1.Department of Neonatology,The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University,Zhejiang,Wenzhou,325027,China; 2.Key Laboratory of Perinatal Medicine of Wenzhou,Zhejiang,Wenzhou,325027,China; 3.Key Laboratory of Structural Malformations in Children of Zhejiang Province,Zhejiang,Wenzhou,325027,China; 4.National Key Laboratory of Macromolecular Drug Development and Manufacturing,School of Pharmaceutical Science,Wenzhou Medical University,Zhejiang,Wenzhou,325035,China; 5.Affiliated Cixi Hospital,Wenzhou Medical University,Zhejiang,Cixi,315300,China |
第一作者单位 | 第二临床医学院,附属第二医院、育英儿童医院; 附属第二医院 |
通讯作者单位 | 第二临床医学院,附属第二医院、育英儿童医院; 附属第二医院 |
第一作者的第一单位 | 第二临床医学院,附属第二医院、育英儿童医院 |
推荐引用方式 GB/T 7714 | Feng, Xiaoli,Zheng, Yihui,Mao, Niping,et al. Menaquinone-4 alleviates hypoxic-ischemic brain damage in neonatal rats by reducing mitochondrial dysfunction via Sirt1-PGC-1α-TFAM signaling pathway[J]. International immunopharmacology,2024,134. |
APA | Feng, Xiaoli., Zheng, Yihui., Mao, Niping., Shen, Ming., Chu, Liuxi., ... & Lin, Zhenlang. (2024). Menaquinone-4 alleviates hypoxic-ischemic brain damage in neonatal rats by reducing mitochondrial dysfunction via Sirt1-PGC-1α-TFAM signaling pathway. International immunopharmacology, 134. |
MLA | Feng, Xiaoli,et al."Menaquinone-4 alleviates hypoxic-ischemic brain damage in neonatal rats by reducing mitochondrial dysfunction via Sirt1-PGC-1α-TFAM signaling pathway".International immunopharmacology 134(2024). |
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