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Biomedical subjects

J Cardinal

Publications and source records attributed to J Cardinal.

61 records · Page 4Linked to original sources
PubMed1980

Proximal tubular response to variations in extracellular sodium concentration.

In vitro microperfusion was used to study the effect of low and high extracellular sodium concentrations on the transport capacity of the proximal convoluted tubule (PCT). Tubules from rabbit kidney were perfused with luminal and peritubular solutions containing 80, 115, 190, and 225 mM sodium. Control solutions contained 150 mM sodium. No ionic substitution was made and the proximal convoluted tubules were studied under hypo- or hypertonic conditions after a 20-min equilibration period. Sodium concentration was measured at 80, 150, and 225 mM sodium in the perfused and collected fluids and no significant difference was observed. Net sodium transport (JNa) remained relatively constant between 115 and 150 mM sodium. It decreased progressively at high sodium concentrations. Depression in JNa was also observed at 80 mM sodium. Fractional sodium reabsorption increased to 125.0% of control at 115 mM sodium and decreased to 69.4 and 40.1% at 190 and 225 mM sodium, respectively. At 80 mM, the results were not different from control. These findings indicate that at concentrations of 115-225 mM sodium the proximal convoluted tubule has the intrinsic capacity to regulate sodium transport.

Animals↗
PubMed1979

Carotid sinus reflex and norepinephrine release following acute volume depletion in dogs.

Norepinephrine (NE) release and pressor response to sympathetic stimulation were studied in dogs under furosemide-induced acute volume depletion. The rise in blood pressure observed following carotid clamping proved similar before and after acute salt and water depletion in the first group of animals and NE rose comparably in these two conditions. Similar results were obtained in a second group of dogs that received an angiotensin II converting enzyme inhibitor (CEI). This study shows that contrary to isotonic saline loading, acute salt and water depletion cause a progressive increase in NE plasma levels. Moreover, these results clearly demonstrate that the decrease in sympatho--adrenergic response and the predominant role played by the renin--aniotensin system during chronic salt depletion are not observed in acute conditions.

Animals↗
PubMed1978

Effect of potassium on proximal tubular function.

In order to study the effect of potassium on the renal tubule, proximal convoluted tubules were dissected from rabbit kidneys and perfused in vitro. Omitting potassium from both the perfusate and bath caused the rate of fluid absorption and the transtubular potential difference to fall to zero. This effect was due to the absence of potassium in the bathing medium since no change was observed when potassium was omitted from the perfusate only. With 0.5 and 1.0 meq/liter of potassium in the bath, there was still a significant decrease from control in both the potential difference and the rate of fluid absorption. With 2.5 meq/liter of potassium in the bath, the results did not differ from control. In further studies, tubules were perfused with 10 meq/liter of potassium in both perfusate and bath. There was no change in the potential difference of fluid absorption. These results are consistent with the view that active transtubular transport of sodium is linked to the influx of potassium into the cell at the peritubular membrane and that this is probably mediated by sodium-potassium-ATPase. Our results also suggest that the variations of potassium concentration in the physiological range do not affect proximal tubular function.

Absorption↗
PubMed1975

Lack of relationship of potential difference to fluid absorption in the proximal renal tubule.

Fluid absorption by isolated perfused rabbit proximal convoluted tubules is accompanied by an electrical potential difference (PD), negative in the lumen, when the tubule is bathed by rabbit serum and perfused with an ultrafitrate of that serum. In contrast the PD is positive when the perfusate composition approximates that of fluid in the late proximal tubule in vivo, which lacks glucose, amino acids and bicarbonate. The principal purpose of the present studies was to investigate the characteristics of fluid absorption under these conditions. Proximal convoluted tubules were dissected from rabbit kidneys and perfused in vitro. When the PD was positive, the mean net fluid absorption was 81 nl mm minus 1 min minus 1. The positive PD is caused by a chloride concentration difference across the tubule epithelium (higher in the lumen than in the bath). Elimination of the chloride concentration difference by replacing the bicarbonate in the bath as well as in the perfusate with chloride caused the PD to fall to zero without a significant change in the rate of fluid absorption. Therefore, neither the positive PD nor the chloride concentration difference is significantly related to the fluid absorption. Ouabain inhibited fluid absorption under all of the above conditions, making it likely that the fluid absorption is due to active sodium transport. Although the results are consistent with the generally accepted view that active sodium transport is a major driving force for fluid absorption, the mechanism of anion (chloride) transport is uncertain owing to the lack of correlation between fluid absorption and the transepithelial PD.

Absorption↗