Renal Sodium- and Potassium-Activated Adenosine Triphosphatase Deficiency During Post-obstructive Diuresis in the Rat

1974 ◽  
Vol 52 (1) ◽  
pp. 105-113 ◽  
Author(s):  
D. R. Wilson ◽  
W. Knox ◽  
E. Hall ◽  
A. K. Sen

Renal function studies and tissue enzyme analysis were carried out in rats with bilateral ureteral ligation (24 h) and after relief of obstruction at intervals of 2 h, 24 h, 3 days, and 7 days. A persistent decrease in glomerular filtration rate and in tubular reabsorption of sodium, solute, and water was noted at each interval after relief of obstruction. Renal sodium- and potassium-activated adenosine triphosphatase (Na–K-ATPase) activity was unchanged in kidneys obstructed for 24 h, but enzyme activity was decreased in the outer medulla of the kidney and, less often, in the renal cortex, at each interval studied during the post-obstructive period. Magnesium-dependent adenosine triphosphatase (Mg-ATPase) activity was not changed in any of the groups. In the post-obstructive kidney (24 h, 3 days, and 7 days) there was a significant correlation between the decrease in outer medullary Na–K-ATPase activity and the changes in filtered sodium load, tubular reabsorption of sodium, and urine osmolality. A deficiency of renal Na–K-ATPase could be important in the pathogenesis of post-obstructive natriuresis and diuresis.

1975 ◽  
Vol 228 (6) ◽  
pp. 1745-1749 ◽  
Author(s):  
KA Fisher ◽  
LG Welt ◽  
JP Hayslett

Prevoius studies have suggested that the increase in specific activity of Na-K-ATPase in renal tissue during treatment with glucocorticoids occurred as a result of aconcurrent rise in net tubular reabsorption of sodium. Since recent data have indicated a specific effect of glucocortiocoids on epithelial cells, experiments were performed to determine whether enzyme activity and net sodium reabsorption could be dissociated.Evidence is provided demonstrating that base-line specific activity of Na-K-ATPase in rat renal cortex and outer medulla does not correlate directly with net sodium reabsorption since enzyme activity did not change after a chronic reduction in glomerularfiltration rate and the rate of sodium reabsorption. Further studies showed a markedrise in Na-K-ATPase after 4 days of treatment with methylprednisolone despite a fall in sodium absorption. These results suggest a direct effect of glucocorticoids onrenal Na-K-ATPase and illistrate the difficulty in assigning a transport role tothis enzyme from the correlation of specific activity with rates of net electrolyte transport.


1979 ◽  
Vol 236 (1) ◽  
pp. F9-F13
Author(s):  
C. S. Lo ◽  
T. N. Lo

Experiments were carried out to compare temporal changes in glomerular filtration rate (GFR), filtered Na+ load, and renal cortical (Na+ + K+)-adenosine triphosphatase (Na-K-ATPase) activity in the hypothyroid rat after administration of a single dose of triiodothyronine (T3) (50 microgram/100 g body wt). The cortex showed an increase in Na-K-ATPase at 24 h and progressive increases to a peak of 62% at 48 h. GFR and filtered Na+ load showed no changes at 24 and 48 h. At 72h, however, significant increases of 62 and 63% (per rat) were observed in GFR and filtered Na+ load, respectively. The results show that the early increase in Na-K-ATPase activity upon T3 treatment precedes the increases in GFR and filtered Na+ load, suggesting a direct effect of T3 on the regulation of Na-K-ATPase activity in the hypothyroid rat kidney cortex, rather than a secondary response to a primary increase in filtered Na+ load as proposed previously.


1977 ◽  
Vol 233 (2) ◽  
pp. F138-F144 ◽  
Author(s):  
N. B. Clark ◽  
R. F. Wideman

Renal excretion patterns of calcium, phosphate, sodium, and potassium were studied in parathyroidectomized (PTX) and parathyroid extract (PTE)-injected PTX starlings. Sturnus vulgaris. Anesthetized birds (Equi-Thesin or Dial) were infused intravenously with 2.5% mannitol containing [14C]inulin. PTX caused significant hypocalcemia, hyperphosphatemia, increased relative calcium clearance (CCa/CIn), and decreased relative clearances of phosphate and potassium, but did not change the clearance of sodium. Glomerular filtration rate (GFR=CIn) and urine flow remained unchanged up to 2 h after PTX. PTE administration 3 h after PTX returned serum calcium and phosphate values to control levels and caused a transient (10-min) increase in GFR. Following PTE, the relative clearances of phosphate, sodium- and potassium increased, while that of calcium decreased significantly relative to the PTX levels. PTE caused net tubular secretion of phosphate, decreased tubular reabsorption of sodium and potassium (sometimes potassium secretion), and a return of excretion of calcium to control levels. These studies indicate that the parathyroid role in calcium and phosphate homeostasis in starlings is predominantly on the kidney.


1975 ◽  
Vol 53 (1) ◽  
pp. 81-85 ◽  
Author(s):  
Mortimer Levy

Glucagon causes marked elevations of glomerular filtration rate (GFR) in dogs when administered intravenously (i.v.) in small doses. The associated natriuresis is thought to be entirely due to increments in the filtered sodium load. In this study, renal denervation, thyroparathyroidectomy, and blockade of cholinergic, α- and β-adrenergic, dopaminergic and histaminergic receptors did not prevent the usual glucagon-induced elevations of GFR or rate of sodium excretion (UNaV). This effect of glucagon was not mediated through the release of cyclic AMP, or by plasma compositional changes of Ca2+, K+, or amino acids. Pure porcine secretin, in doses of 5–10 μg/min delivered either i.v. or into the left renal artery did not alter GFR; clearance rate of p-aminohippurate (CPAH) or UNaV in either hydropenic or saline-loaded dogs. Nor did this polypeptide, structurally very similar to glucagon, abolish the effect of glucagon on GFR. It did, however, partially inhibit the glucagon-induced natriuresis, presumably by preventing a previously undetected glucagon action on tubular reabsorption of sodium.


Author(s):  
James Cronshaw ◽  
Jamison E. Gilder

Adenosine triphosphatase (ATPase) activity has been shown to be associated with numerous physiological processes in both plants and animal cells. Biochemical studies have shown that in higher plants ATPase activity is high in cell wall preparations and is associated with the plasma membrane, nuclei, mitochondria, chloroplasts and lysosomes. However, there have been only a few ATPase localization studies of higher plants at the electron microscope level. Poux (1967) demonstrated ATPase activity associated with most cellular organelles in the protoderm cells of Cucumis roots. Hall (1971) has demonstrated ATPase activity in root tip cells of Zea mays. There was high surface activity largely associated with the plasma membrane and plasmodesmata. ATPase activity was also demonstrated in mitochondria, dictyosomes, endoplasmic reticulum and plastids.


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