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Biomedical subjects

K Rakusan

Publications and source records attributed to K Rakusan.

At least 91 records · Page 5Linked to original sources

A model for intracellular energy transport.

A model for oxygen transfer to cells from capillaries is considered in which mitochondria are either clustered at the cell periphery around capillaries or homogeneously distributed through the cytosol. The capillary Po2 required to supply cells utilizing oxygen at the same rate is much less when mitochondria cluster around capillaries. Two alternative mechanisms are considered for distributing energy from peripheral mitochondria to the rest of the cell; i.e., diffusion of ATP or creatine phosphate with enough creatine kinase to ensure equilibrium between the approximately P carriers. The latter has clear advantages and would appear to be adequate to supply a fairly large mitochondria-free cell core (e.g., 24-micrometer diameter) with very little change in ADP levels or in the free energy of ATP hydrolysis at maximum work rates. Thus, a viable alternative to the traditional Krogh model is presented which takes into account the inhomogeneity of the diffusion pathway as a result of mitochondrial clustering.

Animals↗

Use of tibial length to quantify cardiac hypertrophy: application in the aging rat.

Fluctuations in body weight as occur with aging make body weight an unreliable reference for normalizing heart weight. We compared heart weight normalized by tibial length, which remains constant after maturity, with that normalized by body weight in 5- to 28-mo-old male Wistar rats. When normalized by tibial length or body weight, relative to the 5-mo heart, the senescent left ventricle undergoes 17 vs. 38% hypertrophy, respectively, and the right ventricle undergoes 0 vs. 28% hypertrophy, respectively. Histological measurements in the 25- compared with the 5-mo-old left ventricles reveal 6% larger myocyte diameters and 12% larger cellular cross-sectional areas, indicating about 15% hypertrophy; this value agrees more closely with the estimates based on tibial length than with those based on body weight. To allow prediction of left ventricular weight in a living rat, a regression equation using body weight, age, and tibial length was derived. This enabled us to perform a longitudinal aging study that verified that the above results were not biased by selective survival. Thus, in conditions in which body weight changes, cardiac hypertrophy can be more accurately quantified by relating heart weight to tibial length than to body weight. This approach may have applicability for assessing relative sizes of other organs as well.

Aging↗

The effect of growth and aging on functional capillary supply of the rat heart.

The functional capillary supply of the rat heart was studied in 4-5, 12 and 24 month old animals, respectively. The subepicardial capillaries were visualized by cinemicrophotography of the beating heart in open-chest rats. The intercapillary distances under both normoxemic and hypoxemic conditions were directly measured from focused film frames. The difference between normoxemic and hypoxemic values yielded the degree of capillary recruitment. If one treats all the animals as a single group, then the intercapillary distance decreases under hypoxemic conditions from 17.1 to 16.2 microns which represents an additional recruitment of approximately 11% of capillaries. The degree of recruitment, however, is more pronounced in the youngest age group which is also characterized by shorter intercapillary distances, i.e., higher capillarization than the remaining two age groups (p less than .01). On the other hand, no significant differences between the hearts from one and two year old animals has been found. These results are discussed and compared with those based on morphometric measurements as well as with previous "in vivo" data obtained from the younger age groups.

Aging↗

[Cardiomegaly due to iron deficiency in the rat (author's transl)].

The effects of chronic iron deficiency were studied in new born rats. Hemoglobin concentrations were significantly depressed throughout the experimental period when compared with those of control animals. At third postnatal month, there was a 56% increase of absolute heart weight and a 230% increase of relative heart weight. Heart weight increased much more than myocytes dimensions. This finding may be interpreted as characteristic of a double process of hypertrophy and hyperplasia. Both cell hypertrophy and multiplication were responsible for the observed hypertrophy of the heart. Number of capillaries/mm2 was unchanged, but both mean capillary diameter and total surface of capillary wall increased progressively during the period of anemia. The adaptation to myocardial hypoxia may be, in this experiment situation, localized at the capillary level rather than at the mitochondria. At cell level, we did not note any particular modification of the ultrastructure and particularly no degenerative change. No mitochondrial lesions were found even in severe anemics (blood hemoglobin below 3.2 g/100 ml).

Anemia, Hypochromic↗

Normal and hypertrophic growth of the rat heart: changes in cell dimensions and number.

The length and width of enzymatically isolated individual rat cardiac myocytes were concurrently measured during normal and stimulated cardiac growth. In normal rats weighing between 75 and 750 g the length and width increased by 64 and 68% while their ratio remained constant (ca. 5.3). The cell volume, calculated on the basis of a cylindrical model, increased almost 5 times. The rates of increase in the volume of an average myocyte and in left ventricular mass were found to be similar, indicating that normal myocardial growth could be explained by hypertrophy of existing myocytes and no proliferation would be required. In cardiomegaly induced by aortic constriction in the adult rat, an increase in cell volume was observed while no significant changes in the length-to-width ratios could be detected. The cell volumes of the hypertrophic hearts corresponded to those observed in hearts of similar weight obtained from larger normal rats and the stimulated cardiac growth could also be explained solely by hypertrophy of existing cells.

Animals↗

Blood flow in rats during hemorrhagic shock: differences between surviving and dying animals.

Cardiac output distribution was measured during hemorrhage and hemorrhagic shock in unanaesthetized rats. In comparison to control animals, a varying degree of decreased blood flow was found in the skin, kidneys, splanchnic bed, and carcass. Bronchial and hepatic arterial blood flows were within normal limits for the entire experiment. Whereas the coronary blood flow fluctuated between values higher and lower than normal, the cerebral blood flow values were normal or decreased. When survivors were compared to dying rats, differences were foun in the early and late stages of shock. Initially, the carcass flow in survivors was higher, while the splanchnic flow was lower, than in dying rats. This redistribution of cardiac output may be responsible for an increased venous return and improved chances for survival. At the late stages of shock, survivors had significantly higher bronchial and hepatic arterial blood flow.

Animals↗

Hemoglobin values and organ weights in fast and slow growing rats at the time of weaning.

Three experimental groups of newborn rats were formed according to the number of animals suckled by one dam: fast growing animals (4 per litter), normally growing animals (8 per litter) and slow growing animals (16 per litter). All the animals were killed on the 21st day of life and the following data were collected: hemoglobin and hematocrit values, body weight and the weights of heart, kidney, liver and spleen. The results were statistically analyzed according to experimental group and also in relation to body weight with all rats treated as a single group. Hemoglobin concentration was highest in the smallest animals, gradually declining towards the lowest values around the normal body weight with a subsequent increase in the heaviest animals. The relationship between the organ weights and body weight followed an allometric formula. The slopes of the lines alpha were close to 1 in case of the heart, kidney and liver, indicating the growth of these organs proportional to the growth of the total body. The spleen grows faster than the total body in this experimental situation (alpha = 1.6).

Animals↗

Iron supplementation in suckling rats: its effect on the heart.

The present study attempted to determine the significance of the "anemia" which normally occurs in infants. We compared various parameters in suckling rats whose hemoglobin concentration had been artificially raised by gastric tube feeding of iron with those of control animals. The 20-day-old experimental animals showed significant increases in the weights of the liver (10%) aan spleen (40%). They had also developed a statistically significant 8% increase in heart weight, accompanied by a smaller myocardial fiber size and, thus, higher fiber density. The association in these young animals of higher than normal hemoglobin levels with smaller hearts and myocardial fibers suggests that the normally developing "anemia" of infancy may well serve an important physiological function: to stimulate myocardial growth.

Anemia↗