Morphometric and flow indicator studies of the teleost heart

1975 ◽  
Vol 53 (6) ◽  
pp. 691-698 ◽  
Author(s):  
James N. Cameron

The structure of the heart of four species of Alaskan fishes (Thymallus arcticus, Esox lucius, Lota lota, and Catostomus catostomus) was examined in varying detail. The ventricle constitutes 0.07 to 0.09% of the body weight, 26 to 35% of which consists of an outer, cortical layer, and the balance a spongy, trabeculated inner layer. Blood supply to the cortex comes exclusively from the coronary artery, whereas the inner layer is supplied by venous (deoxygenated) blood from the ventricular lumen. Flow indicator studies implied that the cortical layer receives about half as much blood per unit weight as the inner layer, but probably receives about the same amount of oxygen, since arterial blood contains roughly twice as much oxygen as does venous blood. Calculations of the probable limits for oxygen uptake of the ventricle are made on the basis of data in this study and in the literature.

2004 ◽  
Vol 96 (2) ◽  
pp. 428-437 ◽  
Author(s):  
Gabriel Laszlo

The measurement of cardiac output was first proposed by Fick, who published his equation in 1870. Fick's calculation called for the measurement of the contents of oxygen or CO2 in pulmonary arterial and systemic arterial blood. These values could not be determined directly in human subjects until the acceptance of cardiac catheterization as a clinical procedure in 1940. In the meanwhile, several attempts were made to perfect respiratory methods for the indirect determination of blood-gas contents by respiratory techniques that yielded estimates of the mixed venous and pulmonary capillary gas pressures. The immediate uptake of nonresident gases can be used in a similar way to calculate cardiac output, with the added advantage that they are absent from the mixed venous blood. The fact that these procedures are safe and relatively nonintrusive makes them attractive to physiologists, pharmacologists, and sports scientists as well as to clinicians concerned with the physiopathology of the heart and lung. This paper outlines the development of these techniques, with a discussion of some of the ways in which they stimulated research into the transport of gases in the body through the alveolar membrane.


From the fact that no carbonic acid gas is given out by venous blood when that fluid is subjected to the action of the air-pump, former experimentalists had inferred that this blood contains no carbonic acid. The author of the present paper contends that this is an erroneous inference; first, by showing that serum, which had been made to absorb a considerable quantity of this gas, does not yield it upon the removal of the atmospheric pressure; and next, by adducing several experiments in proof of the strong attraction exerted on carbonic acid both by hydrogen and by oxygen gases, which were found to absorb it readily through the medium of moistened membrane. By means of a peculiar apparatus, consisting of a double-necked bottle, to which a set of bent tubes were adapted, he ascertained that venous blood, agitated with pure hydrogen gas, and allowed to remain for an hour in contact with it, imparts to that gas a considerable quantity of carbonic acid. The same result had, indeed, been obtained, in a former experiment, by the simple application of heat to venous blood confined under hydrogen gas; but on account of the possible chemical agency of heat, the inference drawn from that experiment is less conclusive than from experiments in which the air-pump alone is employed. The author found that, in like manner, atmospheric air, by remaining, for a sufficient time, in contact with venous blood, on the application of the air-pump, acquires carbonic acid. The hypothesis that the carbon of the blood attracts the oxygen of the air into the fluid, and there combines with it, and that the carbonic acid thus formed is afterwards exhaled, appears to be inconsistent with the fact that all acids, and carbonic acid more especially, impart to the blood a black colour; whereas the immediate effect of exposing venous blood to atmospheric air, or to oxygen gas, is a change of colour from a dark to a bright scarlet, implying its conversion from the venous to the arterial character: hence the author infers that the acid is not formed during the experiment in question, but already exists in the venous blood, and is extracted from it by the atmospheric air. Similar experiments made with oxygen gas, in place of atmospheric air, were attended with the like results, but in a more striking degree and tend therefore to corroborate the views entertained by the author of the theory of respiration. According to these views, it is neither in the lungs, nor generally in the course of the circulation, but only during its passage through the capillary system of vessels, that the blood undergoes the change from arterial to venous; a change consisting in the formation of carbonic acid, by the addition of particles of carbon derived from the solid textures of the body, and which had combined with the oxygen supplied by the arterial blood: and it is by this combination that heat is evolved, as well as a dark colour imparted to the blood. The author ascribes, however, the bright red colour of arterial blood, not to the action of oxygen, which is of itself completely inert as a colouring agent, but to that of the saline ingredients naturally contained in healthy blood. On arriving at the lungs, the first change induced on the blood is effected by the oxygen of the atmospheric air, and consists in the removal of the carbonic acid, which had been the source of the dark colour of the venous blood; and the second consists in the attraction by the blood of a portion of oxygen, which it absorbs from the air, and which takes the place of the carbonic acid. The peculiar texture of the lungs, and the elevation of temperature in warm-blooded animals, concur in promoting the rapid production of these changes.


2015 ◽  
Vol 11 (10) ◽  
pp. 20150592 ◽  
Author(s):  
John Davenport ◽  
T. Todd Jones ◽  
Thierry M. Work ◽  
George H. Balazs

Counter-current heat exchangers associated with appendages of endotherms feature bundles of closely applied arteriovenous vessels. The accepted paradigm is that heat from warm arterial blood travelling into the appendage crosses into cool venous blood returning to the body. High core temperature is maintained, but the appendage functions at low temperature. Leatherback turtles have elevated core temperatures in cold seawater and arteriovenous plexuses at the roots of all four limbs. We demonstrate that plexuses of the hindlimbs are situated wholly within the hip musculature, and that, at the distal ends of the plexuses, most blood vessels supply or drain the hip muscles, with little distal vascular supply to, or drainage from the limb blades. Venous blood entering a plexus will therefore be drained from active locomotory muscles that are overlaid by thick blubber when the adults are foraging in cold temperate waters. Plexuses maintain high limb muscle temperature and avoid excessive loss of heat to the core, the reverse of the accepted paradigm. Plexuses protect the core from overheating generated by muscular thermogenesis during nesting.


1956 ◽  
Vol 184 (3) ◽  
pp. 441-444 ◽  
Author(s):  
John A. Benson ◽  
Philip R. Lee ◽  
John F. Scholer ◽  
Kwang S. Kim ◽  
Jesse L. Bollman

The content of either D2O or Na24 has been measured in the intestinal lymph, portal venous blood, and femoral arterial blood of unanesthetized hydrated rats after administration of the isotope into the stomach, duodenum, or peripheral or portal vein. Little, if any, water or sodium ion is delivered to the body by a lymphatic pathway after absorption from the small intestine. At least 99% is carried in portal venous blood. The amount of isotope found in intestinal lymph was proportional to lymph volume whatever the route of administration, and derived mainly from the arterial blood. Even during absorption of water or sodium ion from the small intestine the arterial circulation is the principal source of the water and sodium of the lymph.


Author(s):  
R. C. Newell ◽  
H. R. Northcroft

The rate of cirral beat of Balanus balanoides is related to the logarithm of the body weight as an exponential function. In any one animal, there is little effect of temperature on cirral activity between 7·5° and 10° C. Between 10° and 20° C, however, there is a rapid increase in cirral beat with temperature followed by a fall at temperatures above 20° C.Balanus balanoides exhibits a fast, medium and zero rate of oxygen consumption. These rates of oxygen consumption correspond with (a) normal cirral beating, (b) ‘testing’ activity with no cirral movement, and (c) with the closure of the mantle cavity. Both of the possible levels of oxygen uptake are related to the logarithm of the body weight in a logarithmic fashion over the temperature range 7·5°–22·5° C. Temperature affects the two rates of oxygen consumption differently. In the slower rate (rate B) there is an increase in the rate of oxygen consumption between 7·5° and 14° C but there is no significant increase in the rate of oxygen consumption between 14° and 22·5 C°.


1956 ◽  
Vol 186 (2) ◽  
pp. 203-206 ◽  
Author(s):  
H. O. Kunkel ◽  
John F. Spalding ◽  
Glovanni de Franciscis ◽  
Mary F. Futrell

Study of the relationship of cytochrome oxidase activity of certain tissues to the body weight has been extended to include three species of large animals. In the comparison of rats, sheep, swine and cattle, the cytochrome oxidase activity of skeletal muscle (principally of the gracilis) was found to be roughly an inverse function of body weight. A logarithmic regression of –0.239 was calculated. Although the cytochrome oxidase activity per unit weight of liver in the sheep, swine and cattle series does not reflect the variation in body mass, the regression of the logarithm of total liver cytochrome oxidase activity on the logarithm of body weight was calculated to be 0.674. The data support the concept that the summated total measurable cytochrome oxidase activity is very nearly proportional to body weight to the 3/4 power and, hence, to basal metabolism.


1963 ◽  
Vol 18 (5) ◽  
pp. 970-974 ◽  
Author(s):  
G. Malcolm Brown ◽  
Robert E. Semple ◽  
C. S. Lennox ◽  
G. S. Bird ◽  
C. W. Baugh

Skin, muscle, and rectal temperatures, and O2 consumption of Eskimos and Caucasians have been compared during an acute cold exposure involving immersion of one hand and forearm in a 5 C water bath. The Eskimos consumed less O2, maintained their rectal temperatures at a higher level, and gave up less heat from the muscles of the limbs. Though the Eskimos had significantly more adipose tissue, average skin temperatures were the same in the two groups. The pattern of temperatures noted now and the previously observed higher blood flow in the hand and forearm of Eskimos point to increased cooling of arterial blood by returning venous blood in the extremities with resultant preservation of heat in the body core. Submitted on August 6, 1962


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Dilmurodjon Eshmuminov ◽  
Dustin Becker ◽  
Max L. Hefti ◽  
Matteo Mueller ◽  
Catherine Hagedorn ◽  
...  

AbstractLong-term perfusion of liver grafts outside of the body may enable repair of poor-quality livers that are currently declined for transplantation, mitigating the global shortage of donor livers. In current ex vivo liver perfusion protocols, hyperoxic blood (arterial blood) is commonly delivered in the portal vein (PV). We perfused porcine livers for one week and investigated the effect of and mechanisms behind hyperoxia in the PV on hepatic arterial resistance. Applying PV hyperoxia in porcine livers (n = 5, arterial PV group), we observed an increased need for vasodilator Nitroprussiat (285 ± 162 ml/week) to maintain the reference hepatic artery flow of 0.25 l/min during ex vivo perfusion. With physiologic oxygenation (venous blood) in the PV the need for vasodilator could be reduced to 41 ± 34 ml/week (p = 0.011; n = 5, venous PV group). This phenomenon has not been reported previously, owing to the fact that such experiments are not feasible practically in vivo. We investigated the mechanism of the variation in HA resistance in response to blood oxygen saturation with a focus on the release of vasoactive substances, such as Endothelin 1 (ET-1) and nitric oxide (NO), at the protein and mRNA levels. However, no difference was found between groups for ET-1 and NO release. We propose direct oxygen sensing of endothelial cells and/or increased NO break down rate with hyperoxia as possible explanations for enhanced HA resistance.


2015 ◽  
Vol 21 (4) ◽  
pp. 421-427
Author(s):  
Romeu Rodrigues de Souza ◽  
Sarah Martins dos Santos ◽  
Laura Beatriz Mesiano Maifrino ◽  
Eliane Florencio Gama ◽  
Erico Chagas Caperuto ◽  
...  

Abstract The objective of the present study was to follow the structural modifications of the aortic wall in middle-aged rats submitted to a resistance training protocol for a period of four months. Three groups of 8 animals per group were considered: middle-aged group (MA), old control group (OC) and old trained group (OT). Training consisted in to climb a 1.1-m vertical (80° incline) ladder with weights tied to their tail. Aortic wall structural modifications were studied through light and electron microscopy and morphometry. The mean arterial blood pressure at rest was similar in the three experimental groups (p = .07). At the beginning of the experiment, the OC and OT groups had similar repetition maximums, ranging from 1.6-fold to 1.9-fold the body weight. At the end of the experiment, the repetition maximum of the OT group was 5-fold greater than the body weight (p = .03). The LV weight was 15% larger in the OT group than in the MA group and 12% larger than in the OC group (p = .02). The LV wall thickness of the OT group was significantly larger than that of both, the MA group and the OC group (p = .03). The LV internal diameter in the OT group was significantly smaller than that observed in the MA and OC groups (p = .02). Resistance training diminished the alterations associated with aging improving aortic wall structure by reducing the thickness, normalising the elastic material, the collagen and the smooth muscle cells. Resistance training seems to be a potential treatment for reducing the deleterious effects of aging on the aortic wall.


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