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.