Abstract
The aim of this work was to determine the influence of chronic prenatal hypoxia on remodeling of gap junctions in cardiomyocytes in rat ventricular myocardium at different stages of postnatal ontogeny. Chronic prenatal hypoxia to decline total and mean individual profile length of the gap junction per 100 μm intercalated disk in comparison with the norm, at 30 th day was decrease the amount of gap junctions per 100 μm intercalated disc in comparison of control level and caused predominantly violation build large gap junctions.
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