Abstract | BACKGROUND: Previous work on endothelial dysfunction in post-MI heart failure has shown conflicting results. AIM: To analyze gender related alterations in NO-, PGI(2)- and EDHF-dependent endothelial function in the thoracic aorta 7 and 42 days after myocardial infarction (MI). METHODS AND RESULTS: MI was induced by coronary artery ligation in female and male Sprague-Dawley rats. There was no gender related difference in infarct-size or in the impairment of fractional shortening of the left ventricle 42 days after coronary ligation. Neither acetylcholine-induced (Ach) vasodilation nor basal PGI(2) production in the aorta was modified by coronary ligation. Interestingly, 7 days after MI, basal NO production was impaired and the EDHF component of Ach-induced vasodilation was up-regulated, in both male and female rats. However, 42 days post-MI, basal NO was only impaired in male rats, while EDHF was only up-regulated in female rats. CONCLUSION: MI induced impairment of functional activity of basal NO production and adaptive up-regulation of the EDHF component of Ach-induced relaxation. The above alterations in endothelial function in the aorta were gender-specific at 42 days but not 7 days after MI. Some of the previously reported discrepancies in the development of endothelial dysfunction in the post-MI period may be gender related differences.
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Authors | Gabor Csanyi, Michael Bauer, Wolfgang Dietl, Magdalena Lomnicka, Tatiana Stepuro, Bruno K Podesser, Stefan Chlopicki |
Journal | European journal of heart failure
(Eur J Heart Fail)
Vol. 8
Issue 8
Pg. 769-76
(Dec 2006)
ISSN: 1388-9842 [Print] England |
PMID | 17101291
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biological Factors
- Potassium Channels
- endothelium-dependent hyperpolarization factor
- Nitric Oxide
- Cytochrome P-450 Enzyme System
- Epoprostenol
- Prostaglandin-Endoperoxide Synthases
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Topics |
- Animals
- Aorta
(metabolism)
- Biological Factors
(metabolism)
- Cytochrome P-450 Enzyme System
(metabolism)
- Endothelium
(metabolism)
- Epoprostenol
(metabolism)
- Female
- Male
- Myocardial Infarction
(metabolism, physiopathology, surgery)
- Nitric Oxide
(metabolism)
- Potassium Channels
(metabolism)
- Prostaglandin-Endoperoxide Synthases
(metabolism)
- Rats
- Rats, Sprague-Dawley
- Up-Regulation
- Ventricular Remodeling
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