Gender Differences in Cardiac Ischemic Injury and Protection—Experimental Aspects
This review summarizes some available information on gender differences of myocardial injury with particular attention to experimental approach. It has been observed that significant gender differences exist already in normal heart. They involve among others cardiac growth, contractile function, cal...
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Veröffentlicht in: | Experimental biology and medicine (Maywood, N.J.) N.J.), 2009-09, Vol.234 (9), p.1011-1019 |
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Zusammenfassung: | This review summarizes some available information on gender differences of myocardial
injury with particular attention to experimental approach. It has been observed that
significant gender differences exist already in normal heart. They involve among
others cardiac growth, contractile function, calcium metabolism and function of
mitochondria. Differences, characteristic of the normal myocardium, generate the
logical presumption of the different reaction of the male and female heart to various
pathogenic factors. Most of the experimental studies confirm the clinical
observations: increased resistance of the female heart to ischemia/reperfusion injury
was shown in dogs, rats, mice and rabbits. Furthermore, gender differences in the
ischemic tolerance of the adult myocardium can be influenced by interventions (e.g.
hypoxia) imposed during the early phases of ontogenetic development. The already high
tolerance of the adult female heart can be increased by adaptation to chronic hypoxia
and ischemic preconditioning. It seems that the protective effect depends on age: it
was absent in young, highly tolerant heart but it appeared with the decrease of
natural resistance during aging. Both experimental and clinical studies have
indicated that female gender influences favorably also the remodeling and the
adaptive response to myocardial infarction. It follows from the data available that
male and female heart differs significantly in many parameters under both
physiological and pathological conditions. Detailed molecular and cellular mechanisms
of these differences are still unknown; they involve genomic and non-genomic effects
of sex steroid hormones, particularly the most frequently studied estrogens. The
cardiovascular system is, however, influenced not only by estrogens but also by other
sex hormones, e.g. androgens. Moreover, steroid hormone receptors do not act alone
but interact with a broad array of co-regulatory proteins to alter transcription. The
differences are so important that they deserve serious consideration in clinical
practice in search for proper diagnostic and therapeutic procedures. |
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ISSN: | 1535-3702 1535-3699 |
DOI: | 10.3181/0812-MR-362 |