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Biomedical subjects

K A Shoshenko

Publications and source records attributed to K A Shoshenko.

At least 37 records · Page 2Linked to original sources

[Blood supply in the arterial and venous bed of submaxillary muscle of frogs].

The velocity and morphometric parameters of blood flow in arterial and venous bifurcations of the trunks with diameter less than 85 microns in the frog m. submaxillaris were somewhat different as the angles of the braches II, the length of the vessels, and the bifurcation coefficient were greater in arterial part than in the venous bed. Due to this, the velocity in the arterioles was higher than in veins. According to the Pouiseulus equation, the pressure difference between arterioles and veins was 8.5 torr. About 44% of this difference was due to arterial vessels, about 36%--to the capillaries, pre- and post-capillaries, and about 20%--to the veins.

Animals↗

[Architectonics of the arterial bed and blood flow in the lungs of frogs].

In morphometric studies of arteriolar branching of the frog lung with determination of the blood flow rate and its distribution, the diameter of the trunk was shown to lay between 16 and 350 mcm. The law of variation (in connection with the diameter range) and the specific features of interrelationship between some structural characteristics of the vascular branching were revealed. Analysis of the data obtained in vivo showed that the morphofunctional characteristics of the arteriolar branches in the frog lung corresponded to the theoretical "minimum work" model.

Animals↗

[Blood flow distribution in the branches of frog mesentery arterial microvessels].

The blood flow distribution in 49 arterial branchings of the mesentery (R. temporaria) was investigated (D of the trunk = 25.7 + 0.0 mum). Linear rate was measured by the impulse digital chronometry of the intervals of the erythrocyte transit time. The geometric characteristics of the branching was determined in vivo, on photographs. An asymmetric structure of the investigated branching was shown; branch 1 had the inner initial cross-section which was 2.2 times greater than that of branch 2 and lesser turning angles (29 and 59 degrees). The blood flow in branch 1 was three times greater than the blood flow in branch 2; this was due to its greater inner initial cross-section and a higher linear rate. According to calculations, the blood flow resistance of the branch-turn was insignificant in the general blood flow resistance of branches; therefore the turning angle of the branches could not serve as an important regulator of the volume of the blood flowing in them. An experimentally revealed association between the blood flow in the branches, their radius and their turning angles is well described by equations of the "optimal" model of the vessel branching.

Animals↗

[Development of the mitochondrial apparatus and blood supply of skeletal muscle fibers during ontogenesis of domestic fowl].

The diameter, length, and numerical density of capillaries, diameter of muscle fibers, size and numerical density of their profiles, and relative volume of mitochondria in them were determined in the chicken red oxidative gastrocnemius and white glycolytic pectoral muscle during development from day 10 of embryogenesis to six month of postnatal life. The bulk blood flow was measured in these muscles by hydrogen clearance during postembryonic development. During embryogenesis, the fibers of gastrocnemius muscle develop and grow at a higher rate, while during postembryonic development, those of the pectoral muscle develop faster. The density of mitochondrial profiles increases during embryogenesis and decreases after hatching, while their mean size increases, especially in the oxidative fibers, but it somewhat decreases in 6-month old chicks. Redistribution of mitochondria by the fiber section during development takes place in both muscles: they are localized predominantly in the center in 18-day embryos and in the periphery, especially in the gastrocnemius fibers, in 6-month old fowl. At hatching, the lengths of capillaries are similar in both muscles, but as chicks grow, the proportion of longer (more than 600 microm) capillaries in the pectoral muscle sharply increases, while their density and bulk blood flow decrease. Ratios were determined between structural parameters of the capillary bed and mitochondria, on the one hand, and oxygen consumption (ml/min per 1 mm fiber and 100 g muscle mass), on the other.

Animals↗

[Cardiac minute volume and its pattern in Rana ridibunda frogs].

In frogs with an average body mass 56 g, the minute volume of the heart is equal to 4.5 ml/min X 100 g, which is approximately an order lower than in mammals with the same body mass. Pulmonary fraction constitutes 52% of the minute volume of the heart. The main bulk of systemic fraction of the minute volume of the heart (78%) passes to locomotor system and skin, whereas 19% of this volume are adressed to vegetative organs. This pattern of distribution significantly differs from that in mammals with a similar body mass, in which the vegetative and locomotor fractions are approximately equal. Differentiation in muscular blood supply was noted--there is a threefold difference in the volume of blood flow between gastrocnemius and submandibular muscles.

Animals↗

[Regional blood flow distribution in waking rats under elevated external temperature].

The heart output (HO) was estimated by means of the 133 Xe clearance in the rat tail, the rat being placed either in a narrow hole or a spacious box. In the hole, the HO rose from 24 to 36 ml/(min.100 g), in the box the HO portions of skeletal muscles and bones were by 3.8 and 2.0 times lower; in the hole, their reduction was insignificant; the lung radioactivity rose from 4 to 20% (the hole) and to 42% (the box) which suggests a considerable increase in the blood flow through arterial-venous anastomoses.

Animals↗