Tissue and whole-body extracellular, red blood cell and albumin spaces in the rainbow trout as a function of time: a reappraisal of the volume of the secondary circulation

1998 ◽  
Vol 201 (9) ◽  
pp. 1381-1391 ◽  
Author(s):  
P G Buschnell ◽  
D J Conklin ◽  
D W Duff ◽  
K R Olson

[58Co]EDTA, [51Cr]RBC and [125I]albumin spaces in the whole body and 28 tissue samples were examined at timed intervals over 16 h in rainbow trout Oncorhynchus mykiss. [58Co]EDTA space (which approximates extracellular fluid volume; ECF) in fins, skin, gallbladder and eye are reported for the first time. After a 16 h equilibration, ECF volume was large (376-726 microl g-1 wet tissue mass) in kidney, swimbladder, skin and fins, moderate (219-313 microl g-1 wet tissue mass) in stomach, skull, spleen, liver, intestine, gills, eye and cecum, and small (53-181 microl g-1 wet tissue mass) in red muscle, fat, brain, gallbladder and white muscle. Whole-body ECF was 387+/-10.6 microl g-1 (mean +/- s.e.m.; N=11). [51Cr]RBC space relative to [58Co]EDTA space was large in spleen, liver, intestine and gill, and low in skin, fins, stomach and skull. Whole-body [51Cr]RBC space was 9.9+/-0.6 microl g-1 body mass (N=17). Blood volume calculated from [51Cr]RBC space at 16 h and a dorsal aortic hematocrit of 24.5 % was 40.4 microl g-1 body mass. Whole-body [125I]albumin space at 16 h was 118.0+/-7.4 microl g-1 body mass (N=6), which resulted in an estimated blood volume of 156. 6 microl g-1 body mass, nearly four times that estimated from the [51Cr]RBC space. Tissue hematocrits, calculated from [125I]albumin and [51Cr]RBC spaces, were significantly lower than dorsal aortic hematocrit in all tissues except spleen, kidney and liver. [58Co]EDTA and [51Cr]RBC spaces reached equilibrium in nearly all tissues within 1 h, whereas [125I]albumin continued to accumulate in many tissues up 24 h. The disparity between [125I]albumin distribution kinetics compared with the kinetics of [58Co]EDTA and [51Cr]RBC distribution, as well as the accumulation of [125I]albumin in tissues not known to have a secondary circulation, indicates that [125I]albumin is a poor marker of plasma volume in trout and that previous studies based on [125I]albumin clearance from the plasma have overestimated both the volume and the turnover rate of the secondary system. Revised estimates of secondary circulation volume, based on [58Co]EDTA distribution rate, indicate that it is no more than 10-20 % of the volume of the primary circulation. <P>

2006 ◽  
Vol 291 (3) ◽  
pp. R711-R718 ◽  
Author(s):  
Erik Sandblom ◽  
Michael Axelsson

Central venous blood pressure (Pven) increases in response to hypoxia in rainbow trout ( Oncorhynchus mykiss), but details on the control mechanisms of the venous vasculature during hypoxia have not been studied in fish. Basic cardiovascular variables including Pven, dorsal aortic blood pressure, cardiac output, and heart rate were monitored in vivo during normoxia and moderate hypoxia (PWO2 = ∼9 kPa), where PWO2 is water oxygen partial pressure. Venous capacitance curves for normoxia and hypoxia were constructed at 80–100, 90–110, and 100–120% of total blood volume by transiently (8 s) occluding the ventral aorta and measure Pven during circulatory arrest to estimate the mean circulatory filling pressure (MCFP). This allowed for estimates of hypoxia-induced changes in unstressed blood volume (USBV) and venous compliance. MCFP increased due to a decreased USBV at all blood volumes during hypoxia. These venous responses were blocked by α-adrenoceptor blockade with prazosin (1 mg/kg body mass). MCFP still increased during hypoxia after pretreatment with the adrenergic nerve-blocking agent bretylium (10 mg/kg body mass), but the decrease in USBV only persisted at 80–100% blood volume, whereas vascular capacitance decreased significantly at 90–110% blood volume. In all treatments, hypoxia typically reduced heart rate while cardiac output was maintained through a compensatory increase in stroke volume. Despite the markedly reduced response in venous capacitance after adrenergic blockade, Pven always increased in response to hypoxia. This study reveals that venous capacitance in rainbow trout is actively modulated in response to hypoxia by an α-adrenergic mechanism with both humoral and neural components.


1996 ◽  
Vol 19 (7) ◽  
pp. 411-414 ◽  
Author(s):  
F. Lopot ◽  
P. Kotyk ◽  
J. Bláha ◽  
J. Forejt

A continuous blood volume monitoring (CBVM) device (Inline Diagnostics, Riverdale, USA) was used to study response to prescribed ultrafiltration during haemodialysis (HD) in 66 stabilised HD patients. Fifty percent of patients showed the expected linear decrease in BV right from the beginning of HD (group 1), 32% exhibited no decrease at all (group 2), while eighteen percent formed the transient group 3 which showed a plateau of varying length after which a decrease occurred. The correct setting of dry weight was verified through evaluation of the ratio of extracellular fluid volume to total body water (VEC/TBW) in 26 patients by means of whole body multifrequency impedometry MFI (Xitron Tech., San Diego, USA) and through measurement of the Vena Cava Inferior diameter (VCID) pre and post HD (in 6 and 5 patients from groups 1 and 3 and from group 2, respectively). The mean VEC/TBW in groups 1 and 3 was 0.56 pre and 0.51 post HD as compared to 0.583 and 0.551 in group 2. VCID decreased on average by 14.1% in groups 1 and 3 but remained stable in group 2. Both findings thus confirmed inadequately high estimation of dry weight. Since CBVM is extremely easy to perform it can be used as a method of choice in detecting inadequately high prescribed dry weight. The status of the cardiovascular system must always be considered before final judgement is made.


1991 ◽  
Vol 48 (4) ◽  
pp. 583-590 ◽  
Author(s):  
Paul W. Webb

Routine swimming encompasses all volitional motions of fish. It is usually assumed to be quasi-steady, i.e. routine swimming is mechanically equivalent to steady swimming. Routine swimming of rainbow trout, Oncorhynchus mykiss, was dominated by unsteady motions of linear and centripetal (angular) acceleration. Constant-speed swimming was rare. Mean speeds and acceleration rates were small. Tail-beat frequencies were nevertheless strongly correlated with mean swimming speed, but increased more rapidly with increasing speed in routine swimming than in steady swimming. Tail-beat amplitudes and propulsive wavelengths were similar to values seen in steady swimming. The composition of routine swimming and analysis of the force balance showed that routine swimming was not quasi-steady. Therefore, forces and rates of working should be estimated from a complete description of whole-body deformation. This is impractical. Drag dominated resistance in routine swimming, such that average thrust (= resistance) may be computed from mean speed and/or averaged kinematic variables for the trailing edge with a correction factor of approximately 3. Analysis of routine swimming may permit comparisons among a wider range of vertebrates than possible with commonly used methods.


1994 ◽  
Vol 51 (2) ◽  
pp. 372-380 ◽  
Author(s):  
M. G. Rankin ◽  
D. G. Dixon

The 144-h LC50 (95% fiducial limits) of arsenite for 4.5-g rainbow trout (Oncorhynchus mykiss) was 18.5 (17.9–19.1) mg∙L−1. In a pair-fed growth study which exposed trout to 0.0, 0.76, 2.48, or 9.64 mg arsenite∙L−1 over 17 wk, growth was significantly reduced (by 55%) only at 9.64 mg∙L−1. The reduction was attributable to both reduced appetite (primarily) and direct metabolic impact (marginally). Fish at 9.64 mg∙L−1 suffered 10% mortality, usually associated with necrotic erosion of the mandibular and olfactory regions of the head. All fish exposed to 9.64 mg∙L−1 showed inflammation of the gallbladder wall, a lesion absent at lower exposure concentrations. There were no arsenite impacts on hepato- and splenosomatic index, hematocrit, hemoglobin, total plasma lipid, cholesterol, and protein or brain concentrations of norepinephrine, dopamine, and serotonin. Exposure to 0.0, 0.76, 2.48, and 9.64 mg arsenite∙L−1 for 26 wk resulted in mean (SE) equilibrium whole-body As concentrations of 0.3 (0.02), 0.2 (0.02), 0.4 (0.10), and 1.7 (0.40) μg As∙g wet weight−1, respectively, No depuration below these concentrations occurred during a 12-d period in arsenite-free water. The threshold of chronic toxicity was estimated to be 4.9 mg∙L−1.


1990 ◽  
Vol 47 (11) ◽  
pp. 2228-2234 ◽  
Author(s):  
S. M. McGeachy ◽  
D. G. Dixon

The effects of water temperature (5 or 15 °C) on the toxicity of arsenate to rainbow trout were examined over an 11-wk period. The fish were exposed to nominal arsenate concentrations set as fixed proportions of the 144-h LC50s for arsenate at their respective temperature (5 °C: 0, 1.5, 18, and 36 mg∙L−1; 15 °C: 0, 1.5, 9, and 18 mg∙L−1). Arsenate toxicity was assessed in terms of mortality, total arsenic concentration, wet weight, condition factor, liver and muscle glycogen levels, hepato- and splenosomatic indices, and histopathology. Contrary to the previously reported relationship between acute toxicity and temperature, trout were more tolerant of chronic exposure to arsenate at 15 °C than at 5 °C. While the high-exposure concentration (5 °C, 36 mg∙L−1; 15 °C, 18 mg∙L−1) fish at both temperatures attained the same internal arsenic concentration (2 to 3 μg∙g−1), up to 50% of those fish tested at 5 °C died. The whole-body arsenic concentrations in moribund trout were found to vary between 4 and 6 μg∙g−1, suggesting that a critical arsenic body-concentration is reached before death or toxicant insult occur.


2004 ◽  
Vol 61 (4) ◽  
pp. 618-626 ◽  
Author(s):  
Katherine A Sloman ◽  
Graham R Scott ◽  
D Gordon McDonald ◽  
Chris M Wood

Competition for social status can result in physiological differences between individuals, including differences in ionoregulatory ability. Subordinate rainbow trout (Oncorhynchus mykiss) had two-fold higher uptake rates of sodium across the gill and two-fold higher whole-body sodium efflux rates than the dominant fish with which they were paired. Sodium efflux was then divided into branchial and renal components, both of which were higher in subordinates. Branchial sodium efflux accounted for 95%–98% of sodium loss. Plasma sodium concentrations were more variable, although not significantly different, in subordinate fish, suggesting that the increased loss of sodium in these trout is compensated for by an increase in uptake rates. Urine flow rates and plasma cortisol concentrations were higher in subordinate fish, but there was no difference in glomerular filtration rate between dominants and subordinates. Renal sodium reabsorption was significantly reduced in subordinates. In summary, the ionoregulation of subordinate individuals was altered, most likely occurring as a result of stress-induced changes in gill permeability, resulting in a higher throughput of water and increased branchial sodium efflux. These changes in ionoregulatory ability have many physiological implications, including the increased susceptibility of subordinates to ionoregulatory challenges and an increased metabolic cost of ionoregulation.


1997 ◽  
Vol 75 (11) ◽  
pp. 1916-1922 ◽  
Author(s):  
Grant E. Brown ◽  
R. Jan F. Smith

We investigated, under laboratory conditions, the presence of chemical alarm signals in juvenile rainbow trout (Oncorhynchus mykiss). In an initial experiment, we exposed trout to a whole-body extract from conspecifics or a distilled-water control. When exposed to whole-body extract, trout significantly (i) decreased time spent swimming, (ii) increased time taken to resume foraging, and (iii) decreased the number of food items eaten. These data indicate a significant chemically mediated antipredator response. A second experiment was conducted to determine (i) if this is a generalized response to injured fish or a specific response to injured conspecifics, and (ii) if the chemical signal is localized in the skin. We exposed juvenile trout to one of three chemical stimuli: (1) trout skin extract, (2) trout body extract, or (3) swordtail (Xiphophorus helleri) skin extract. Significant antipredator responses were observed in trout exposed to conspecific skin extract, but responses of those exposed to conspecific body extract or swordtail skin extract did not differ from those of distilled-water controls. These data strongly suggest that juvenile rainbow trout possess a chemical alarm signal, localized in the skin, that elicits antipredator behaviour when detected.by conspecifics.


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