Naloxone pro-drug rescues morphine induced respiratory depression in Sprague-Dawley rats

被引:3
作者
Wallisch, Michael [1 ]
El Rody, Nehad M. [1 ]
Huang, Baohua [2 ]
Koop, Dennis R. [1 ]
Baker, James R., Jr. [2 ]
Olsen, George D. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Sch Med, Portland, OR 97239 USA
[2] Univ Michigan, Michigan Nanotechnol Inst Med & Biol Sci, Ann Arbor, MI 48109 USA
关键词
Morphine; Naloxone; Respiratory depression; Delivery vehicle; GUINEA-PIG; METHADONE; BUPRENORPHINE; ACTIVATION; EXPOSURE; REVERSAL; PLASMA;
D O I
10.1016/j.resp.2011.10.009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Respiratory depression is the main obstacle for the safe administration of morphine for acute pain after injury. Due to this complication, new delivery methods are needed to insure that safe and effective doses of opioid analgesics are administered during emergencies. A depot formulation containing a naloxone pro-drug was designed to release the antidote when morphine causes dangerous hypoxic conditions in the blood. The aim of this work was to test the naloxone release in vivo in response to a severe overdose of morphine in the Sprague-Dawley rat model. Non-invasive two-chamber plethysmography was used to monitor and record respiration and to test the capability of the naloxone pro-drug to respond to and rescue morphine-induced respiratory depression in the animal. We show that the pro-drug formulation can both prevent and reverse severe morphine induced respiratory depression. The animal model demonstrates that co-administration of the naloxone pro-drug reliably antagonizes profound respiratory depressive effects of morphine. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 60
页数:9
相关论文
共 22 条
[1]   VENTILATION AND OXYGEN-CONSUMPTION IN THE GUINEA-PIG [J].
BLAKE, CI ;
BANCHERO, N .
RESPIRATION PHYSIOLOGY, 1985, 61 (03) :347-355
[2]   Flunitrazepam variably alters morphine, buprenorphine, and methadone lethality in the rat [J].
Borron, SW ;
Monier, C ;
Risède, P ;
Baud, FJ .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2002, 21 (11) :599-605
[3]   Characteristics and comparative severity of respiratory response to toxic doses of fentanyl, methadone, morphine, and buprenorphine in rats [J].
Chevillard, Lucie ;
Megarbane, Bruno ;
Risede, Patricia ;
Baud, Frederic J. .
TOXICOLOGY LETTERS, 2009, 191 (2-3) :327-340
[4]   Incidence, Reversal, and Prevention of Opioid-induced Respiratory Depression [J].
Dahan, Albert ;
Aarts, Leon ;
Smith, Terry W. .
ANESTHESIOLOGY, 2010, 112 (01) :226-238
[5]   Synthesis and biological evaluation of 2′-carbamate-linked and 2′-carbonate-linked prodrugs of paclitaxel:: Selective activation by the tumor-associated protease plasmin [J].
de Groot, FMH ;
van Berkom, LWA ;
Scheeren, HW .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (16) :3093-3102
[6]   Noninvasive measurement of midexpiratory flow indicates bronchoconstriction in allergic rats [J].
Glaab, T ;
Hoymann, HG ;
Hohlfeld, JM ;
Korolewitz, R ;
Hecht, M ;
Alarie, Y ;
Tschernig, T ;
Braun, A ;
Krug, N ;
Fabel, H .
JOURNAL OF APPLIED PHYSIOLOGY, 2002, 93 (04) :1208-1214
[7]   Mu opioid receptor antagonists: Recent developments [J].
Goodman, Allan J. ;
Le Bourdonnec, Bertrand ;
Dolle, Roland E. .
CHEMMEDCHEM, 2007, 2 (11) :1552-1570
[8]   Human plasma-mediated hypoxic activation of indolequinone-based naloxone pro-drugs [J].
Huang, Baohua ;
Tang, Shengzhuang ;
Desai, Ankur ;
Cheng, Xue-min ;
Kotlyar, Alina ;
Van Der Spek, Abraham ;
Thomas, Thommey P. ;
Baker, James R., Jr. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (17) :5016-5020
[9]   THE EVALUATION OF ANALGESIC POTENCY OF DRUGS USING THERMAL STIMULATION IN THE RAT [J].
JACKSON, H .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1952, 7 (02) :196-203
[10]   EFFECT OF NALOXONE ON THE MORPHINE CONCENTRATION IN THE CENTRAL-NERVOUS-SYSTEM AND PLASMA IN RATS [J].
MIYAMOTO, Y ;
MORITA, N ;
NAKAMURA, N ;
YAMANISHI, T ;
KISHIOKA, S ;
YAMAMOTO, H .
JAPANESE JOURNAL OF PHARMACOLOGY, 1993, 63 (02) :235-240