Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/31737
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18034/20233 (89%)
Visitors : 23690324      Online Users : 614
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
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/31737


    Title: 2-Adamantanamine produces prolonged spinal block in rats
    Authors: Chen, Yu-Wen
    Chen, Chia-Ming
    Liu, Kuo-Sheng
    Wang, Jhi-Joung
    Hung, Ching-Hsia
    Contributors: Chi Mei Med Ctr, Dept Med Res
    China Med Univ, Dept Phys Therapy, Coll Hlth Care
    China Med Univ, Grad Inst Rehabil Sci, Coll Hlth Care
    Chi Mei Med Ctr, Dept Anesthesiol
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Natl Cheng Kung Univ, Dept Phys Therapy, Coll Med
    Natl Cheng Kung Univ, Coll Med, Inst Allied Hlth Sci
    Keywords: Intrathecal injection
    2-adamantanamine
    Mepivacairie
    Nociception
    Proprioception
    Motor function
    Date: 2017-06-13
    Issue Date: 2018-11-30 15:54:48 (UTC+8)
    Publisher: Elsevier Ireland Ltd
    Abstract: We aimed to investigate the local anesthetic effect of 2-adamantanamine in spinal anesthesia. The dose-response curves were constructed after intrathecally injecting the rats with five doses of 2-adamantanamine and a common local anesthetic mepivacaine. The quality and duration of 2-adamantanamine at producing spinal nociceptive, proprioceptive and motor block were compared with that of mepivacaine. We revealed that 2-adamantanamine provoked spinal nociceptive, proprioceptive and motor block dose-dependently. On the 50% effective dose (ED50) basis, the rank of potency was mepivacaine > 2-adamantanamine at producing spinal nociceptive, proprioceptive and motor block (p < 0.05 for the differences). 2-Adamantanamine, but not mepivacaine produced more nociceptive block than motor block (p < 0.05). At the equianesthetic doses (ED75, ED50, and ED25), the nociceptive block duration caused by 2-adamantanamine was greater than that caused by mepivacaine (p < 0.01 for the differences). These preclinical data showed that 2-adamantanamine is less potent than mepivacaine, while 2-adamantanamine provokes greater duration of spinal nociceptive block than mepivacaine. Furthermore, 2-adamantanamine demonstrates a more nociceptive-selective action over motor block. (C) 2017 Elsevier B.V. All rights reserved.
    Relation: Neuroscience Letters, v.653, pp.168-172
    Appears in Collections:[Dept. of Pharmacy] Periodical Articles

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML1296View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


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