Organ and tissue-specific properties of the microcirculatory bed of the heart

The auricular and ventricular microcirculatory bed has been studied in persons of mature age, not suffering from any cardio-vascular diseases during their life. As a whole, 48 objects have been studied. The microcirculatory bed has been revealed in sections of the cardiac wall 70-100 mcm thick using silver nitrate impregnation after V. V. Kuprianov. Organ- and tissue-specific properties of the vascular microcirculatory bed are revealed in interrelations of the vessels and the structural elements of the cardiac wall (myocardium, and connective tissue structures), in position of nuclei of the endothelial cells of the capillary wall and in places of the capillary branchings. Principle differences in structure of the auricular and ventricular microcirculatory bed are demonstrated. The notion the organ- and tissue-specific properties of the microcirculatory bed vessels is discussed.     

Study of the microcirculatory bed by a method of demonstrating lactate dehydrogenase]

The method of detection of lactate dehydrogenase with some modification was used to study the microcirculatory bed in total preparations of serous membranes and plane sections of organs of any square surface. The employment of non-fixed material, the short time (from 15 to 60 min) necessary to obtain preparations of any size and simultaneous determination of the localization and the degree of the activity of the enzyme--are, to the authors opinion, undoubtful advantages of the given method, which can be an addition to the well-known impregnation method of determination of the microcirculatory bed.     

The microcirculatory bed of the human heart

Using a complex approach in studying microcirculatory bed of the human heart, possibilities of scanning electron microscopy of corrosive preparations, those of silver nitrate impregnation after V. V. Kuprianov are demonstrated. The silver nitrate impregnation makes it possible to study the wall structure of the microcirculatory pathways, to analyse arrangement of nuclei in the endothelial and muscle cells of the microcirculatory links, to reveal together with the vessels the surrounding tissues. Scanograms of the corrosive preparations of the arterioles demonstrate "circulatory strips", that are absent in the venular part. The relief of the luminal casts of the microcirculatory bed vessels in the human heart is presented as impresses of nuclei of the endothelial and smooth muscle cells. Peculiarities in form and distribution of these nuclei in various links of the microbed are demonstrated.     

Morphology of the wall of some main arteries normally and in limited motor activity]

Effects of different periods of hypokinesia upon the structure of the main arteries wall and the microcirculatory bed of the aorta adventitia were studied in rabbits by histological methods. It was shown that hypokinesia lasting more than 4 weeks resulted in the atrophy of the medical sheath and dystrophy of the elastic framework in the wall of main arteries. In the microcirculatory bed of the aorta adventitia there occurred blood stagnation, the integrity of the microvessels wall (mainly capillaries, postcapillaries and venules) was broken. The degree of the above morphological changes depends on duration of hypokinesia.     

Comparative evaluation of the adaptive mechanisms of the microcirculatory bed during dehydration

In total preparations of the white rat small intestine mesentery, impregnated with silver nitrate, as well as under conditions of vital microscopical observations at certain stages of alimentary experimental dehydration, analogous changes in the microcirculatory bed links have been demonstrated. Comparison of quantitative parameters in decreasing diameters of the microvessels, specific for dehydrated preparations has shown a great importance of these changes in the impregnated preparations at the expense of tissue condensation at their histological treatment. The advantages of a complex application of both methods for estimating dynamics of vascular, intervascular and extravascular changes are proved.     

The vascular terminal network device in the anterior stomach wall

The microcirculatory bed of the anterior stomach wall has been studied in man, dog, rabbit, guinea pig and rat, starting from the fact that in the modern gastro-duodenal surgery the various sectors of this stomach part have a special importance. The stomach microvascular network has been rendered manifest by microcorrosion preparations and by intravascular injections with coloured tracers (China Ink-gelatin, silver nitrate, methylene blue). Examinations under biocular magnifying glass and microscope of the histological slides, as well as of the block-transparentized ones in tetraline, have facilitated the microvascular morphometry as well as the calculation of some hemodynamic indices of blood flow evaluation in a limited territory of the anterior stomach wall. The obtained data can be of use when evaluating the microcirculation of the stomach parietal territories in selective vagotomies, anastomoses, plasties, resections and other operations of the stomach.     

Morphologic mechanisms of blood flow regulation in the hemomicrocirculatory system of the human heart during ontogenesis

Hearts of 220 human corpses, who had not any cardiovascular system disease during their life, have been distributed into age groups, beginning from fetuses up to old age. By means of injection, silver nitrate impregnation and scanning electron microscopy methods, applied to corrosive preparations, morphological mechanisms of the blood stream regulation in the hemomicrocirculatory bed of the human heart have been revealed in ontogenesis. The first group of the regulation mechanisms includes proper mechanisms inherent in the links of the microbed: spatial orientation of microvessels, precapillary sphincters, anastomoses between these vessels, sequence in arrangement of the endothelial cell nuclei, length, diameter and number of links in the microcirculatory bed. The second group embraces those mechanisms, that depend on structure of the myocardial wall, influencing the microcirculatory bed.     

Comparative morphometry of vessels of the microcirculatory bed of the cat pericardium in impregnated preparations and during in vivo microscopy

In impregnated (with silver nitrate) preparations of the cat pericardium and in photonegative pericardial microvessels photographed in vital experiments, diameters of the main vascular groups in the microcirculatory bed (arterioles, precapillaries, capillaries, postcapillaries and venules) were comparatively estimated. When impregnated, the vascular diameter decreases; the degree of the changes is not equal and depends on the wall structure. Therefore, when studying impregnated preparations, it is necessary to introduce the correction coefficients in order to make the data obtained comparable with the vital ones.     

The system of bony canals as the basis for the angioarchitectonics of bones]

The spatial interrelationships of osteon canals were studied in corrosion preparations with the help of rastral electron microscopy. The structure of microvessels, their belonging to a definite link of the microcirculatory bed, the interaction of vessels and their position with respect to the osseous matrix were studied in bone sections impregnated with silver nitrate after V. V. Kuprijanov. Haversian canals in the compact substance of the bone are longitudinally oriented, can duplicate and form a single system of canals. The neighbouring canals of osteons might be bound by means of Volkmann's canals. The investigation of the Haversian canals in serial sections has shown that the diameter of the same canals of osteons can change at different levels, the diameter of the osteons themselves remaining unchanged. This seems to speak of uneven development of osteons in their different parts. In the Haversian canal there are one-two or occasionally three vessels having all three links of the morphocirculatory bed. The course and ramification of the vessel are identical to the shape of the osteon canal which includes them. The vessels are closely connected with the bony matrix by means of connective tissue bundles directed from the canal wall to the vessel wall. These bundles appear to serve as a peculiar anchor or amortizing apparatus and its elasticity might be a factor of a change of the shape and direction of the canal vessels in the bone development process.     

Morphometric findings in the microcirculatory bed of the sigmoid serosa during the fetal period in man

During fetal life, formation and arrangement of the microcirculatory bed in the serous membrane of the sigmoid colon correspond to the growth and functioning of the latter at different stages of ontogenesis. Two periods in the development of the microcirculatory bed of the serous membrane of the sigmoid colon are revealed: the first period coincides with the first half of the fetal development when capillary growth is considerable, i.e. with the growth of metabolic part in the microcirculatory bed; the second period coincides with the second half of the fetal development when intensified growth of the sigmoid portion of the large intenstine and its transport sections in the microcirculatory bed (arterioles, precapillaries, postcapillaries, venules) are observed.     

Formation of the microcirculatory bed of the muscle coat of the wall of the sigmoid colon during human fetal development]

During intrauterine life microcirculatory bed of the muscular coat is forming and developing in accordance with its differentiation, growth and functional changes at various steps of its ontogenesis. This step-like differentiation in the parts composing the microcirculatory bed and the whole microcirculatory network of longitudinal and circulatory layers of the muscular coat is genetically connected with differentiation taking place in the wall of the sigmoid colon during the developmental period studied and, in the end, reflects morphological maturation of the sigmoid colon at different stages of its individual ontogenesis.     

Development of the microcirculatory bed of the human tongue in the prenatal period

Morphofunctional regularities of formation and development of the blood microcirculatory bed in the human tongue have been studied in the prenatal period of morphogenesis. 119 human embryos and fetuses at the age of 5 weeks--9 months have been investigated. A complex of methods have been used: common histological (hematoxylin--eosin, after van Gieson and Mallory), injection of the lingual vessels with 20% suspension of Indian ink--gelatin, transmissive electron microscopy. General regularities of organogenesis, stages of the blood microcirculatory bed development and peculiarities of the process on formation of the primary protocapillary lingual blood bed are revealed. Regularities in structure of the terminal vascular constructions are studied for each structural element of the organ--mucosal membrane, muscles, glands, lingual tonsil. For these elements at the ultrastructural level certain features of the organic specificity in the structure of the blood microcirculatory bed links are determined.     

Vascularization of the myenteric plexus in the small intestine of pigeons]

By means of light and electron microscopy vascularization of the myenteric plexus has been studied in the pigeon small intestine. Ganglia of the plexus, their cell composition, ultrastructure of neurons have been described. Links of the microcirculatory bed of the intramural ganglia are characterized, interrelations of capillaries with neurons are described, quantitative estimation of microhemovessels, surrounding the microcirculatory bed of the myenteric plexus in the intestinal wall in birds and mammalia.     

Morphofunctional features of different divisions of the microcirculatory bed of jejunal villi in the white rat

By means of injecting the vessels with vegetative peroxidase, scanning electron microscopy of corrosive preparations, biomicroscopy, transmissive electron microscopy and in serial semithin sections, spatial organization of the blood microcirculatory bed of the villus in the white rat jejunum has been studied and identification of various microvascular segments has been made. Increasing dimentions of the villus result only in multiplication of the outflow and inflow pathways of blood, while the number of the marginal capillary-distributers remains unchanged--one along each lateral part of the villus. The cause of this regularity should be sought in certain requirements to orientation of transport processes in the villose stroma and, first of all, in the conditions of the hemato-lymphatic transference at adaptation.     

Microcirculatory bed of the heart during peripheral arteriovenous shunting

In the experiment performed on 108 test and 28 control dogs, by means of injection and histological methods, the effect of arteriovenous fistula on the cardiac microcirculatory bed has been studied. The arteriovenous blood shunting results in plethora and stasis in the cardiac microcirculatory bed, in dilatation of all its links, in aggregation and adhesion of the blood formed elements, in increased permeability of microvessels, in diapedesis of erythrocytes and in myocardial edema, in winding microvessels, in development of the venoarterial reaction, in hypertrophy of myocytes, recalibration and sclerosis of the microvascular walls.     

Ultrastructure of blood capillaries in vascular plexuses of the lateral ventricles of the human brain

Ultrastructure of the wall of the microcirculatory bed links in the lateral ventricles of the human brain has been studied, as well as their interrelations with neural elements and ependyma. Together with typical morphological structural signs, certain peculiarities are revealed, characterizing organic specificity. Elements, performing function of the blood-brain barrier are determined: epithelium (ependyma), basal membranes, interstitium. A well developed afferent and efferent nervous apparatus of the vascular plexus, evidently, actively participates in regulation of the microcirculatory blood bed and in formation of liquor.     

Immunofluorescent Labelling of K-Papovavirus Antigens in Glycol Methacrylate Embedded Material: A Method for Studying Infected Cell Populations by Fluorescence Microscopy and Histological Staining of Adjacent Sections

Trypsin and protease V (pronase) were studied for their ability to enhance immuno-fluorescent labelling of papovavirus antigens in glycol methacrylate embedded sections of organs infected with murine K-papovavirus. Treatment of Bouin's fixed sections with 0.4% trypsin for 30 minutes resulted in specific immunofluorescent staining equal to that seen in frozen sections and produced little if any loss of histological detail. Treatment with protease V resulted in less brilliant fluorescence and less satisfactory tissue preservation. Studies were then conducted to determine the fixative which would produce brightest specific fluorescent antibody staining of papovavirus-infected cells while providing clearest definition of intranuclear inclusions and best morphological detail in histologically stained adjacent sections. Brightest immunofluorescence staining was accomplished on material fixed in 96% ethanol/1% glacial acetic acid or Bouin's solution. These fixatives also gave clear definition of intranuclear inclusions with histological stains and provided excellent morphological detail. Phosphate buffered paraformaldehyde/picric acid and 3.7% formalin gave less satisfactory fluorescence and obscured intranuclear inclusions in histological preparations. Sections fixed in 4% paraformaldehyde, 4% paraformaldehyde/1% glutaraldehyde, and 0.5 M p-toluenesulfonic acid were negative for specific fluorescence. Glycol methacrylate, used with proper fixation and trypsin pretreatment of sections, provides a useful embedding medium for immunofluorescent identification of virus-infected cells, and the 1.0-2.0 μm sections routinely obtainable with GMA permit study of individual infected cells by fluorescent antibody and histological staining of adjacent sections.     

Immunofluorescent labelling of K-papovavirus antigens in glycol methacrylate embedded material: a method for studying infected cell populations by fluorescence microscopy and histological staining of adjacent sections

Trypsin and protease V (pronase) were studied for their ability to enhance immunofluorescent labelling of papovavirus antigens in glycol methacrylate embedded sections of organs infected with murine K-papovavirus. Treatment of Bouin's fixed sections with 0.4% trypsin for 30 minutes resulted in specific immunofluorescent staining equal to that seen in frozen sections and produced little if any loss of histological detail. Treatment with protease V resulted in less brilliant fluorescence and less satisfactory tissue preservation. Studies were then conducted to determine the fluorescence and less satisfactory tissue preservation. Studies were then conducted to determine the fixative which would produce brightest specific fluorescent antibody staining of papovavirus-infected cells while providing clearest definition of intranuclear inclusions and best morphological detail in histologically stained adjacent sections. Brightest immunofluorescence staining was accomplished on material fixed in 96% ethanol/1% glacial acetic acid or Bouin's solution. These fixatives also gave clear definition of intranuclear inclusions with histological stains and provided excellent morphological detail. Phosphate buffered paraformaldehyde/picric acid and 3.7% formalin gave less satisfactory fluorescence and obscured intranuclear inclusions in histological preparations. Sections fixed in 4% paraformaldehyde, 4% paraformaldehyde/1% glutaraldehyde, and 0.5 M p-toluenesulfonic acid were negative for specific fluorescence. Glycol methacrylate, used with proper fixation and trypsin pretreatment of sections, provides a useful embedding medium for immunofluorescent identification of virus-infected cells, and the 1.0-2.0 micron sections routinely obtainable with GMA permit study of individual infected cells by fluorescent antibody and histological staining of adjacent sections.     

Organizational features and morphometric characteristics of the hemomicrocirculatory bed of the human brain dura mater

By means of silver nitrate impregnation and hematoxylin -- eosin staining the microcirculatory bed of the human brain dura mater (the second half of the mature age) has been investigated. Owing to the analysis of the morphometrical data of module organization of the hemomicrocirculatory bed, an objective quantitative characteristics of its peculiarities in various layers and areas of the dura mater is presented. In three layers of the dura mater in the fornix and skull basis area, falx cerebri and tentorium cerebelli venular links predominate. Most of all morphometrical parameters of the venular vessels increase in the internal layer of the dura mater in the skull basis area. Conditions of functioning for the human brain dura mater are reflected in its blood bed, its specificity manifesting at the microcirculatory level.     

Effects of Mounting Media on Fading of Toluidine Blue and Pyronin G Staining in Epoxy Sections

Available mounting media cause fading of histological preparations over time. A study was designed to find the most suitable medium for durable mounting of Araldite embedded semithin sections of rabbit cerebral cortex stained with toluidine blue and pyronin G. Among four synthetic mounting media tested, only DePeX prevented fading of the sections during the first month. All mounting media tested helped preserve staining intensity after one month, since the fading rate after one year is only about half that in sections prepared without mounting medium. The average optical density of sections after one year was higher in preparations mounted with DePeX than in sections treated with the other mounting techniques tested in this study. After one year, the average optical density of sections mounted with DePeX had decreased approximately 20%.