Monophosphoryl lipid A reduces both arrhythmia severity and infarct size in a rat model of ischaemia

被引:11
作者
Song, W [1 ]
Furman, BL [1 ]
Parratt, JR [1 ]
机构
[1] Univ Strathclyde, Dept Physiol & Pharmacol, Glasgow G1 1XW, Lanark, Scotland
关键词
monophosphoryl lipid A; myocardial ischaemia; ventricular arrhythmias; infarct size; ischaemic preconditioning;
D O I
10.1016/S0014-2999(98)00126-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A non-toxic derivative of the active lipid A component of the endotoxin molecule (monophosphoryl lipid A) when given to rats in a dose of 5 mg kg(-1) by intraperitoneal injection 24 h prior to anaesthesia and coronary artery occlusion, markedly decreased the severity of ischaemia-reduced ventricular arrhythmias (ventricular fibrillation reduced from 60 to 21%; P < 0.05) and reduced myocardial infarct size (from 35.8 +/- 1.6% of the area at risk to 22.7 +/- 2.0%; P < 0.05). It did not modify blood pressure or heart rate either before or during the period of ischaemia. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:285 / 287
页数:3
相关论文
共 12 条
[1]   Myocardial protection after monophosphoryl lipid A: Studies of delayed anti-ischaemic properties in rabbit heart [J].
Baxter, GF ;
Goodwin, RW ;
Wright, MJ ;
Kerac, M ;
Heads, RJ ;
Yellon, DM .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 117 (08) :1685-1692
[2]   INTERLEUKIN-1 PRETREATMENT DECREASES ISCHEMIA REPERFUSION INJURY [J].
BROWN, JM ;
WHITE, CW ;
TERADA, LS ;
GROSSO, MA ;
SHANLEY, PF ;
MULVIN, DW ;
BANERJEE, A ;
WHITMAN, GJR ;
HARKEN, AH ;
REPINE, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5026-5030
[3]   ENDOTOXIN PRETREATMENT INCREASES ENDOGENOUS MYOCARDIAL CATALASE ACTIVITY AND DECREASES ISCHEMIA REPERFUSION INJURY OF ISOLATED RAT HEARTS [J].
BROWN, JM ;
GROSSO, MA ;
TERADA, LS ;
WHITMAN, GJR ;
BANERJEE, A ;
WHITE, CW ;
HARKEN, AH ;
REPINE, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) :2516-2520
[4]   CORONARY-ARTERY LIGATION IN ANESTHETIZED RATS AS A METHOD FOR THE PRODUCTION OF EXPERIMENTAL DYSRHYTHMIAS AND FOR THE DETERMINATION OF INFARCT SIZE [J].
CLARK, C ;
FOREMAN, MI ;
KANE, KA ;
MCDONALD, FM ;
PARRATT, JR .
JOURNAL OF PHARMACOLOGICAL METHODS, 1980, 3 (04) :357-368
[5]   INTERLEUKIN-1 AND ITS BIOLOGICALLY RELATED CYTOKINES [J].
DINARELLO, CA .
ADVANCES IN IMMUNOLOGY, 1989, 44 :153-205
[6]  
NELSON DW, 1991, SURGERY, V110, P365
[7]   DELAYED PROTECTION OF THE HEART AGAINST ISCHEMIA [J].
PARRATT, JR ;
SZEKERES, L .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1995, 16 (10) :351-355
[8]   Cardioprotection with ischemic preconditioning and MLA: Role of adenosine-regulating enzymes? [J].
Przyklenk, K ;
Zhao, L ;
Kloner, RA ;
Elliott, GT .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (03) :H1004-H1014
[9]  
WU S, 1994, BRIT J PHARMACOL, V113, P1083
[10]  
WU S, 1996, BRIT J PHARMACOL, V118, P2157