4-hydroxynonenal, a novel indicator of lipid peroxidation for
reperfusion injury of the myocardium.
Blasig, Ingolf E., Tilman Grune, Katrin Sch[diaeresis]onheit, Elvira
Rohde, Manuela Jakstadt, Reiner F. Haseloff, Werner G. Siems.
Institut f[umlaut]ur Molekulare Pharmakologie, Forschungsverbund
Berlin; Klinik f[umlaut]ur Physikalische Medizin und Rehabilitation,
Humboldt Universit[umlaut]at Berlin; Herzog-Julius-Hospital, Bad
Harzburg; Germany.
APStracts 2:0065H, 1995.
4-Hydroxynonenal (HNE) has been proposed as an important marker of
radical induced lipid peroxidation (LPO) during postischemic
reperfusion injury of the myocardium. Therefore, the liberation of
HNE into the effluent of isolated perfused rat hearts was
investigated. For the first time, the formation of the aldehyde is
demonstrated in myocardium. During control perfusion, 1.28+0.33 pmol
HNE.min-1.mg protein-1 were formed by the hearts of 18 month old WKY
rats and 2.74+1.12 pmol.min-1.mg protein-1 by those of 18 month old
sponta neously hypertensive (SHR) rats, respectively. In the WKY
group, HNE release increased to 3.35+1.13 pmol.min-1.mg protein-1 2
min after the onset of reperfusion following 30 min of total and
global ischemia, compared to the preischemic control period
(p<0.05). In the SHR group, HNE liberation was higher during
reperfusion (8.66+1.33 pmol.min-1.mg protein-1, maximum at 2 min
reperfusion) compared to both the respective preischemic control and
the respective reperfusion interval of the WKY group (p<0.05 each).
The SHR rats showed signs of congestive cardiac failure of a
decompensated hypertrophy in comparison to the normoten sive WKY
rats. Moreover, the SHR rat hearts exhibited a lower release of
adenine nucleotide degradation products (adenine, inosine,
hypoxanthine plus uric acid: 48.1+10.2 nmol.30 min-1.mg protein-1;
p<0.05) and a diminished functional recovery (left ventricular
developed pressure, 32+16 mmHg; p<0.05) during 30 min of
reperfusion, compared to the WKY group (77.9+14.4 nmol.30 min-1.mg
protein-1; 90+21 mmHg). The results suggest that products of radical
-induced LPO are generated and released from the reperfusion-injured
failing myocardium in relation to the degree of functional
deterioration. To evaluate this injury, 4-hydroxynonenal is a potent
indicator .
Received 11 August 1994; accepted in final form 15 February 1995.
APS Manuscript Number H715-4.
Article publication pending Am. J. Physiol. (Heart Circ. Physiology).
ISSN 1080-4757 Copyright 1995 The American Physiological Society.
Published in APStracts on 10 March 1995.