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 |
ISSN | 1471-2253 |
卷号 | 15期号:1页码:66 |
DOI | 10.1186/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 ID | 25924894 |
PMC记录号 | PMC4422592 |
SCOPUSEID | 2-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 | |
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 |
推荐引用方式 GB/T 7714 | 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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