Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/27729
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18281/20508 (89%)
Visitors : 19502262      Online Users : 1045
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/27729


    题名: Cutaneous Analgesia and Systemic Toxicity of Carbetapentane and Caramiphen in Rats
    作者: Hung, Ching-Hsia
    Chu, Chin-Chen
    Chen, Yu-Chung
    Liu, Kuo-Sheng
    Chen, Yu-Wen
    Wang, Jhi-Joung
    贡献者: 藥學系
    关键词: Spinal-Anesthesia
    Isobolographic Analysis
    Inguinal Herniorrhaphy
    Antitussive Activity
    Bupivacaine
    Oxybuprocaine
    Dextrorphan
    Pain
    3-Methoxymorphinan
    Dextromethorphan
    日期: 2012
    上传时间: 2014-03-24 15:23:01 (UTC+8)
    出版者: Lippincott Williams & Wilkins
    摘要: Background: Caramiphen produces spinal anesthesia; caramiphen and carbetapentane have never been tested as infiltrative cutaneous analgesic. The aim of this study was to compare cutaneous analgesia of caramiphen and carbetapentane with bupivacaine and evaluated their central nervous system and cardiovascular toxicity.Methods: After the blockade of cutaneous trunci muscle reflex with subcutaneous drug injections in rats, we evaluated the local anesthetic effect of carbetapentane and caramiphen on infiltrative cutaneous analgesia. After continuous intravenous infusion of equipotent doses of bupivacaine, carbetapentane, caramiphen, and saline, we observed mean arterial blood pressure and heart rate and monitored the onset time of seizure, apnea, and impending death.Results: Carbetapentane and caramiphen acted like bupivacaine and elicited cutaneous analgesia in a dose-related fashion. On a 50% effective dose (ED50) basis, the ranks of potencies were bupivacaine (1.78 [1.52-2.07]) > carbetapentane (2.53 [2.38-2.77]) 9 caramiphen (3.60 [3.41-3.99]) (P < 0.01). At equianalgesic doses (ED25, ED50, ED75), the duration caused by carbetapentane or caramiphen was similar to that caused by bupivacaine. Under equipotent doses, the infusion time of carbetapentane or caramiphen required to cause seizure, apnea, and impending death was longer than that of bupivacaine (P < 0.05). The decline in mean arterial blood pressure and heart rate was slower with carbetapentane or caramiphen when compared with bupivacaine (P < 0.01 for the differences) at equipotent doses.Conclusions: Carbetapentane and caramiphen were similar to bupivacaine at producing durations of cutaneous analgesia but were less likely than bupivacaine to induce central nervous system and cardiovascular systemic toxicity.
    關聯: Regional Anesthesia And Pain Medicine, 37(1), 34-39
    显示于类别:[Dept. of Pharmacy] Periodical Articles

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML2075检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback