Red Cell and plasma sodium and potassium changes in the San Diego pocket mouse during hibernation

1965 ◽  
Vol 65 (3) ◽  
pp. 415-418 ◽  
Author(s):  
William DeW. Andrus ◽  
Stuart E. Starr ◽  
Richard R. Strathmann
1961 ◽  
Vol 39 (1) ◽  
pp. 1-8 ◽  
Author(s):  
John R. Beaton

Further observations on metabolic alterations in fasted rats cooled under ice to rectal temperatures approximating 15 °C are reported. In the hypothermic rats, metabolism of injected lactic acid does not appear to be impaired. There is however: increased concentration of inorganic phosphorus in blood but not in liver; increased concentration of glutathione in liver but not in blood; increased plasma chloride concentration; decreased red cell potassium concentration; increased red cell water content; decreased plasma water content. Hypothermia, under these conditions, did not alter concentrations of liver acid-extractable glycogen, red cell sodium, plasma sodium, plasma potassium, nor serum calcium. Administration of urea in saline prior to cooling elevated plasma sodium and potassium concentrations in hypothermic rats. These observations are discussed in relation to previously reported effects of hypothermia on carbohydrate metabolite levels.


1962 ◽  
Vol 40 (1) ◽  
pp. 113-122 ◽  
Author(s):  
G. S. Kanter

The handling of sodium and potassium by the renal tubules at various levels of hypothermia was studied. Fourteen dogs were anesthetized with 30 mg/kg sodium pentobarbital. After suitable control clearance measurements, the rectal temperature was lowered progressively by ice-packing to about 25 °C while renal clearances were continuously measured. Artificial respiration was not used. No change in plasma sodium was detected but plasma potassium fell significantly from a control value of 4.1 ± 0.09 meq/1. at 38 °C to 3.4 ± 0.12 meq/1. at 25 °C. Urine sodium concentration fell during exposure to cold while potassium concentration increased slightly. In spite of the marked fall in glomerular nitration rate (69.0 ± 3.1 ml/minute control to 17.0 ± 3.6 ml/minute at 25 °C) the final urine flow at 25 °C was slightly greater than that of control. The clearance ratios (in percentage) increased significantly, reflecting the marked decrease in tubular reabsorption: water, 0.49 ± 0.05 at 38 °C to 2.02 ± 0.25 at 25 °C; sodium, 0.47 ± 0.12 to 1.13 ± 0.27; potassium, 18.0 ± 2.6 to 54.0 ± 12.0. The difference in clearance ratio alterations is a reflection of the dissimilar effect of hypothermia on particular renal regulations.


1976 ◽  
Vol 52 (2) ◽  
pp. 216-226 ◽  
Author(s):  
David S. Campion ◽  
Robert Olsen ◽  
Sydney H. Dromgoole ◽  
James B. Peter

1963 ◽  
Vol 25 (4) ◽  
pp. 457-464 ◽  
Author(s):  
W. N. HOLMES ◽  
D. G. BUTLER

SUMMARY The effects were studied of cortisol, corticosterone and aldosterone on the concentrations of sodium and potassium in muscle and blood plasma and on water content of muscle in the fresh-water rainbow trout (Salmo gairdneri). These steroids appeared to cause a loss in plasma sodium throughout the 96 hr. experimental period. An initial rise in muscle sodium was observed during the first 24 hr. after commencement of the treatments. The subsequent decline in muscle sodium was interrupted by a transient rise followed by a continuing decline. The effect of these hormones on the potassium concentrations in plasma was variable, although there was a significant rise in the potassium concentration in muscle during the period of decline in sodium concentration. The significance of these results in relation to the possible enhanced adrenocortical activity of the trout during adaptation to a marine environment is discussed.


1973 ◽  
Vol 21 (4) ◽  
pp. 515 ◽  
Author(s):  
MR Hughes ◽  
JG Blackman

This is the first report of salt gland secretion in cranes (Gruidae). The sodium and potassium concentrations of the plasma, tears, salt gland secretion, and urine of the brolga were determined. Tear sodium was equal to plasma sodium; tear plasma was four times as concentrated as plasma potassium. These values were normal for tears. The salt gland secretion sodium concentration (about 300 m-equivll) was lower than that reported for other NaC1-injected birds. This may be due to the diet, small gland size, or to insufficient stress. The salt gland secretion to plasma ratios were the same for sodium and potassium. This is unusual. The urine had a lower sodium concentration than the plasma.


1958 ◽  
Vol 36 (3) ◽  
pp. 333-338 ◽  
Author(s):  
F. A. Sréter ◽  
Sydney M. Friedman

After running a distance of 100 meters in 7 minutes, untrained rats showed a rise in plasma potassium and a fall in plasma sodium as measured in tail vein samples. These changes are in accord with in vitro observations of the effects of exercise on isolated muscle preparations and similarly are taken to indicate a gain of sodium and a loss of potassium by the exercised muscles in the whole animal. Within 10 minutes of completion of the exercise, plasma sodium concentration was restored to normal while potassium was restored within 20 minutes. Exercise was accompanied by a fall in haematocrit, which remained low for up to 40 minutes. A period of 2 months of preliminary training modified the response to exercise. In these trained animals, a fall in sodium concentration occurred as before but the rise in potassium concentration was less in degree and the haematocrit did not change. It is suggested that the rate of increase of plasma potassium is an index of muscle efficiency while the height of plasma potassium is correlated with the fatigue limit of exercise.


1979 ◽  
Vol 82 (1) ◽  
pp. 159-170 ◽  
Author(s):  
T. MILLER ◽  
S. D. BRADSHAW

SUMMARY Concentrations of corticosteroids and aldosterone have been measured in the plasma and related to the maximum cortisol binding capacity, to the concentration of sodium and potassium of the plasma and to the condition of the animals, in a natural population of the quokka (Setonix brachyurus, Quoy & Gaimard) on Rottnest Island, Western Australia. A marked population in one area has been repetitively sampled at approximately 6 week intervals over a period of 2 years. Animals were found to be in significantly better condition during the hot–dry season. Their plasma concentrations of corticosteroids, 1·09 ± 0·11 (s.e.m.) and 1·47 ± 0·14 μg/100 ml and their plasma sodium concentrations, 147 ± 0·87 and 142 ± 1·17 mequiv./l, for the hot–dry and cold–wet seasons respectively, were both significantly different (P < 0·05). Plasma concentrations of aldosterone were 8·40 ± 0·57 and 7·06 ± 0·53 ng/100 ml for the hot–dry and cold–wet seasons. The level of aldosterone fell to levels comparable to those found in salt-replete laboratory animals only during the month of July. In the laboratory, salt deprivation resulted in a significant rise in the concentration of plasma aldosterone, 2·33 ± 0·57 (s.e.m.) ng/100 ml when salt-replete and 16·95 ± 2·74 ng/ 100 ml when salt-deprived (P< 0·001). Total plasma corticosteroid levels were unaffected by changes in the sodium content of the diet. Injections of ACTH at a rate of 2 i.u./kg caused a significant rise in the levels of plasma corticosteroids which were essentially identical in both high- and low-condition animals. Body temperature fell to a significantly lower level in low-condition animals held in cages after injection of ACTH. These results indicate that the seasonal mortality of the quokka on Rottnest Island does not result from any breakdown in adrenal function, despite a substantial decline in the condition of the animals.


1964 ◽  
Vol 31 (1) ◽  
pp. 39-44 ◽  
Author(s):  
J. S. TINDAL ◽  
A. YOKOYAMA

SUMMARY Nine male goats were castrated at 6 weeks of age, and four of them were hypophysectomized at 7–8 months of age. Hypophysectomy resulted in a decreased rate of growth compared with the controls. Packed cell volume and blood sugar levels were slightly lower in the hypophysectomized group, but plasma sodium and potassium levels were normal. During a 48 hr. starvation period, the level of plasma non-esterified fatty acids rose steadily in the control group. The hypophysectomized group showed a rapid rise until the 19th hr. of starvation, a rapid decline until the 24th hr., and a slight rise until the end of the starvation period.


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