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Although collagen structure has been studied by polarized light microscopy since the early 19th century and continued since, modern studies and reviews failed to correlate the conclusions based on data obtained by the techniques with those of polarized light microscopy. Collagen I is intensely positively birefringent in respect to length of the fibres; the positive intrinsic birefringence indicates a quasi-crystalline alignment parallel to the fibre and molecule axis of the amino acid residues of the polypeptide chains. This would not have been compatible with a helical structure but has been achieved by similar tilt angles and opposite directions of the coiling and supercoiling. Birefringence characteristics of collagen are also affected by chemical treatments, extractions and staining procedures. Attachment of chemical groups to the anionic charges present on the surface of collagen molecules results in increased positive birefringence in the case of bipolar molecules attached to two or more anionic residues. Unipolar attachment to the same groups, or to the cationic groups of the associated proteoglycans, as well as sulfation or acetylation of hydroxyls of the protein and/or the carbohydrate, reduced or reversed the sign of birefringence. Increased birefringence caused by stretching cannot be due to intramolecular events and is caused by intermolecular changes. The same applies to changes in collagen during aging. Reticulin is a group of different substances which mostly contain collagen III. The pliability and deformability of this collagen is related to its weakly negative birefringence due to large side chains and presence of different and greater amounts of interstitial proteoglycans and other molecules. The so-called reticulin of healing wounds differs in its constitution from other reticulins but is also rich in intermolecular carbohydrate components.

Data are reported which show significant regional capillary differences in left ventricular endocardium and epicardium of normal rats and of rats with hyperthyroid-induced cardiac hypertrophy. The epicardial region of control rats has 38% more capillaries than the endocardial region. Control endocardial myocytes are 62% larger in cross-sectional area than epicardial myocytes. Hypertrophic hearts exhibit regional differences in capillary density similar to those in the normal hearts, but there is an overall reduction of 12 and 17.5% in capillary density in both regions. The average cross-sectional area of myocytes increases 34.5% in the epicardium and 22.5% in the endocardium.

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Quantitative light- and electron-microscopic data are reported for the endomyocardium and epimyocardium of the left ventricle in adult dogs. The endomyocardium has a markedly lower capillary density, and larger myocyte cross-sectional area, than the epimyocardium. The sarcolemmal-surface/cell-volume ratio is significantly less in endocardial myocytes. No regional differences were found with regard to capillary diameter, interstitial space volume, or volume percent occupied by blood vessels and myocytes. Likewise, there are no differences in proportions of cardiac cell volume occupied by myofibrils (57%), mitochondria (25%), nuclei (1.5%), T tubes (1.2%), and sarcoplasmic reticulum (2.0%). The ratios of surface areas of T tubes and SR to their respective volumes and to cell volumes do not vary with transmural location. The regional differences and similarities are discussed in relation to general problems of blood flow in the heart and cardiac hypertrophy.

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