科研成果详情

题名Epinephrine reversed high-concentration bupivacaine- induced inhibition of calcium channels and transient outward potassium current channels, but not on sodium channel in ventricular myocytes of rats
作者
发表日期2015-04-30
发表期刊BMC ANESTHESIOLOGY   影响因子和分区
语种英语
原始文献类型Article
关键词Bupivacaine Epinephrine Cardiac toxicity
其他关键词INDUCED ASYSTOLE ; RESUSCITATION ; HEART ; CARDIOMYOCYTES ; DEPRESSION ; TOXICITY ; OVERDOSE ; BLOCK ; K+
摘要Background: Epinephrine is a first-line drug for cardiopulmonary resuscitation, but its efficacy in the treatment of bupivacaine-induced cardiac toxicity is still in question. We hypothesized that epinephrine can reverse cardiac inhibition of bupivacaine by modulating ion flows through the ventricular myocyte membrane channels of rats. The aim of this study was to observe and report the effects of epinephrine on high-concentration bupivacaine-induced inhibition of sodium (I-Na), L-type calcium (ICa-L), and transient outward potassium (I-to) currents in the ventricular myocytes of rats. Methods: The ventricular myocytes were isolated from Sprague-Dawley rats (250-300 g) by acute enzymatic dissociation. The whole-cell patch clamp technique was used to record the ion channel currents in single ventricular myocytes both before and after administration of medications. Result: Administration of bupivacaine 100 mu mol/L significantly reduced I-Na, (P < 0.05). However, administration of bupivacaine 100 mu mol/L in conjunction with epinephrine 0.15 mu g/ml had no effect in restoring I-Na to its previous state. Similarly, a sharp decline of ICa-L and Ito was observed after administration of bupivacaine 100 mu mol/L (P < 0.05). In contrast to I-Na, ICa-L and I-to were significantly improved after the administration of the aforementioned combination of bupivacaine and epinephrine (P < 0.05). Conclusion: Epinephrine can reverse high-concentration bupivacaine induced inhibition of ICa-L and Ito, but not INa. Thus, epinephrine's effectiveness in reversal of bupivacaine-induced cardiac toxicity secondary to sodium channel inhibition may be limited.
资助项目natural science foundation of Zhejiang province, ChinaNatural Science Foundation of Zhejiang Province [LY13H090008]
出版者BIOMED CENTRAL LTD
出版地LONDON
ISSN1471-2253
卷号15期号:1页码:66
DOI10.1186/s12871-015-0049-1
页数8
WOS类目Anesthesiology
WOS研究方向Anesthesiology
WOS记录号WOS:000354161900001
收录类别SCIE ; PUBMED ; SCOPUS
URL查看原文
PubMed ID25924894
PMC记录号PMC4422592
SCOPUSEID2-s2.0-84928814685
通讯作者地址[Xu, Xuzhong]The First Affiliated Hospital of Wenzhou Medical University,Department of Anesthesiology,2 Fuxue Road,Zhejiang,325000,China
Scopus学科分类Anesthesiology and Pain Medicine
引用统计
被引频次:2[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/12719
专题附属第一医院_麻醉科
公共卫生学院_环境安全与健康风险评估研究院
通讯作者Xu, Xuzhong
作者单位
1.The First Affiliated Hospital of Wenzhou Medical University,Department of Anesthesiology,2 Fuxue Road,Zhejiang,325000,China;
2.Wenzhou Medical University,Environment and health institute,Zhejiang,China
第一作者单位附属第一医院;  第一临床医学院(信息与工程学院)、附属第一医院;  麻醉科
通讯作者单位附属第一医院;  第一临床医学院(信息与工程学院)、附属第一医院;  麻醉科
第一作者的第一单位附属第一医院
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Liu, Fuli,Wu, Bingjing,Du, Yongjun,et al. Epinephrine reversed high-concentration bupivacaine- induced inhibition of calcium channels and transient outward potassium current channels, but not on sodium channel in ventricular myocytes of rats[J]. BMC ANESTHESIOLOGY,2015,15(1):66.
APA Liu, Fuli., Wu, Bingjing., Du, Yongjun., Wu, Yiquan., Chen, Hongfei., ... & Xu, Xuzhong. (2015). Epinephrine reversed high-concentration bupivacaine- induced inhibition of calcium channels and transient outward potassium current channels, but not on sodium channel in ventricular myocytes of rats. BMC ANESTHESIOLOGY, 15(1), 66.
MLA Liu, Fuli,et al."Epinephrine reversed high-concentration bupivacaine- induced inhibition of calcium channels and transient outward potassium current channels, but not on sodium channel in ventricular myocytes of rats".BMC ANESTHESIOLOGY 15.1(2015):66.

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