دورية أكاديمية

Effects of microRNA-208a on inflammation and oxidative stress in ketamine-induced cardiotoxicity through Notch/NF-κB signal pathways by CHD9.

التفاصيل البيبلوغرافية
العنوان: Effects of microRNA-208a on inflammation and oxidative stress in ketamine-induced cardiotoxicity through Notch/NF-κB signal pathways by CHD9.
المؤلفون: Yuan H; Department of Pain Medicine, Nantong Hospital of Traditional Chinese Medicine, Nantong 226001, China 543038275@qq.com yuanhongjie81@foxmail.com., Du S; Department of Pain Medicine, Nantong Hospital of Traditional Chinese Medicine, Nantong 226001, China.; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Deng Y; Department of Pain Medicine, Nantong Hospital of Traditional Chinese Medicine, Nantong 226001, China.; Department of Anesthesiology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China 543038275@qq.com yuanhongjie81@foxmail.com., Xu X; Department of Pain Medicine, Nantong Hospital of Traditional Chinese Medicine, Nantong 226001, China., Zhang Q; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Wang M; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Wang P; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Su Y; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Liang X; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., Sun Y; Department of Anesthesiology, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen 518055, China., An Z; Department of Pain Medicine ,Affiliated Hospital of Shaanxi University of Traditional Chinese Medicine, Xianyang 712000, China.
المصدر: Bioscience reports [Biosci Rep] 2019 May 17; Vol. 39 (5). Date of Electronic Publication: 2019 May 17 (Print Publication: 2019).
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Portland Press on behalf of the Biochemical Society Country of Publication: England NLM ID: 8102797 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 1573-4935 (Electronic) Linking ISSN: 01448463 NLM ISO Abbreviation: Biosci Rep Subsets: MEDLINE
أسماء مطبوعة: Publication: London : Portland Press on behalf of the Biochemical Society
Original Publication: London : The Biochemical Society, c1981-
مواضيع طبية MeSH: Cardiotoxicity/*genetics , Inflammation/*genetics , MicroRNAs/*genetics , NF-kappa B/*genetics , Oxidative Stress/*genetics , Receptors, Notch/*genetics , Trans-Activators/*genetics, Animals ; Cell Line ; Heart/physiopathology ; Ketamine/pharmacology ; Rats ; Rats, Sprague-Dawley ; Signal Transduction/genetics
مستخلص: Background: MicroRNA can regulate gene expression, and participate in multiple vital activities, such as inflammation, oxidative stress epigenetic modification, cell proliferation, and apoptosis. It plays an important role in the genesis and development of cardiovascular disease. Objective: To assess the role of microRNA-208a in ketamine-induced cardiotoxicity. Methods: All rats were randomly selected into two groups: sham and model groups. After fixed, all rats in the model group was intraperitoneally (IP) injected with 100 mg/kg of ketamine. Heart samples were stained with HE assay. Total RNAs from serum were used to hybridize with the SurePrint G3 Rat Whole Genome GE 8×60 K Microarray G4858A platform. Results: In the rat model with ketamine-induced cardiotoxicity, microRNA-208a expression was increased. Then, over-expression of microRNA-208a increased inflammation and oxidative stress in vitro model. However, down-regulation of microRNA-208a decreased inflammation and oxidative stress in vitro model. Over-expression of microRNA-208a suppressed CHD9 and Notch1, and induced p65 protein expression in vitro model. Overexpression of CHD9 reduced the effects of microRNA-208a on inflammation and oxidative stress in heart cell through Notch/p65 signal pathways. Notch1 activation reduced the effects of microRNA-208a on inflammation and oxidative stress in heart cell through p65 signal pathways. Conclusion: MicroRNA-208a may be a potential biomarker for ketamine-induced cardiotoxicity through inflammation and oxidative stress by Notch/NF-κB signal pathways by CHD9.
(© 2019 The Author(s).)
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فهرسة مساهمة: Keywords: CHD9; Notch; cardiotoxicity; ketamine; microRNA-208a; p65
المشرفين على المادة: 0 (MicroRNAs)
0 (NF-kappa B)
0 (Receptors, Notch)
0 (Trans-Activators)
690G0D6V8H (Ketamine)
EC 3.6.4.12 (CHD9 protein, rat)
تواريخ الأحداث: Date Created: 20190330 Date Completed: 20200610 Latest Revision: 20220301
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC6522736
DOI: 10.1042/BSR20182381
PMID: 30923228
قاعدة البيانات: MEDLINE
الوصف
تدمد:1573-4935
DOI:10.1042/BSR20182381