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C de Rouffignac

Publications and source records attributed to C de Rouffignac.

99 records · Page 6Linked to original sources

Micropuncture study of water, electrolytes, and urea movements along the loops of henle in psammomys.

The mechanism by which the osmotic pressure increases in tubular fluid along the descending limb of the loop of Henle was examined in Psammomys undergoing salt diuresis. In two series of experiments, micropuncture samples were collected either from proximal and distal convolutions at the surface of the cortex, or from loops of Henle and collecting ducts at the surface of the extrarenal part of the papilla. Inulin-(3)H, urea-(14)C, Na(+), and K(+) concentrations, as well as osmotic pressure, were determined in all micropuncture samples.Net movements of water along the descending and ascending limbs of the loop could not be deduced by comparing inulin data obtained from convoluted tubules and from loops of Henle, since there appeared to be a large difference in the filtration rate of the superficial glomeruli (9 nl/min) and the deep ones (21.4 nl/min) under the conditions of these experiments. The results indicate that no large net movement of water occurred along the loop since a) only 23% of the filtrate was reabsorbed along the loop of Henle (including pars recta) of superficial nephrons despite the fact that all these loops reached markedly hypertonic regions; b) there was no positive correlation between (F/P)(In) in early distal samples and the simultaneous osmotic pressure of the urine; c) when (F/P)(In) and (F/P)(Osm) in loop samples were correlated, the increase in inulin concentration accounted only for 15% of the increase in osmotic pressure. Therefore, 85% of the concentrating process taking place along the descending limb must have resulted from net addition of solutes; this was directly supported by Na(+) and K(+) measurements in the loop samples, which showed that, at the tip of the loops, the Na(+) and K(+) flow rates were correlated to the osmotic pressure. Moreover, since the load of Na(+) urea flow rate in superficial early distal tubules was constant and independent of the urinary osmotic pressure, it is suggested that a medullary recycling of both ions occurred between ascending and descending limbs.Urea-(14)C concentration in the loop samples indicates a net addition of urea into the descending limb; the mean and K(+) delivered to the distal superficial tubules was 4.18 times its filtration rate, suggesting a recycling of urea from collecting ducts to Henle's loops. The permeability properties of the wall of the thin descending limb are discussed in relation to the obtained results.

Animals↗

Desensitization to vasopressin action in the rat kidney medulla: studies on isolated nephron segments.

Because of the prominent role of the renal medulla in the elaboration of concentrated urine and the possible differential regulation of the various nephron segments, desensitization to vasopressin (AVP) was studied on freshly isolated rat medullary thick ascending limbs (MTALs) and outer medullary collecting ducts (MCDs). Desensitization was induced through intramuscular injections of 1-deamino-8-D-arginine-vasopressin (dDAVP, 2 micrograms/day for 3 days), the last of which was performed 1 h before kidney removal. The cellular response to AVP was studied by measuring cAMP accumulation in micro-dissected nephron segments. In the MTAL, we observed a marked (around 80%) and selective desensitization to AVP, the response to either glucagon or human calcitonin remaining unaltered. In the MCD, significant desensitization was observed in the presence of 1 nM AVP in the assay medium, and was no longer significant when the AVP concentration was increased to supramaximal levels (10-1,000 nM). These experiments thus reveal a clear dissociation between MTAL and MCD with regards to dDAVP-induced desensitization and extend previous observations made on target segments in the renal cortex.

Animals↗

Transepithelial Ca2+ and Mg2+ transport in the cortical thick ascending limb of Henle's loop of the mouse is a voltage-dependent process.

The mechanisms responsible for transepithelial Ca2+ and Mg2+ in transport in the isolated perfused cortical thick ascending limb (cTAL) of Henle's loop of the mouse nephron were investigated by measuring transepithelial voltages (PDte) and transepithelial ion net fluxes (JNa, JCl, JK, JCa, JMg) by electron microprobe analysis. In the presence of furosemide (10(-4) mol.l-1, lumen) and diphenylamine-2-carboxylate (DPC, 10(-4) mol.l-1, bath), known inhibitors of NaCl reabsorption in the TAL, Ca2+ and Mg2+ reabsorption was completely inhibited. In the presence of furosemide, JCa fell from 0.75 +/- 0.07 to -0.08 +/- 0.09 pmol.min-1.mm-1 (n = 5), and JMg from 0.47 +/- 0.04 to -0.01 +/- 0.11 pmol.min-1.mm-1 (n = 5). In the presence of DPC, JCa fell from 0.57 +/- 0.08 to -0.07 +/- 0.11 pmol.min-1.mm-1 (n = 5), and JMg from 0.16 +/- 0.02 to -0.11 +/- 0.07 pmol.min-1.mm-1 (n = 5). With furosemide, inhibition of Ca2+ and Mg2+ transport was paralleled by a 93% inhibition of NaCl reabsorption, while in the presence of DPC there was a 60% reduction of NaCl reabsorption. These effects were fully reversed after removal of the inhibitors from the lumen or bath solutions. In the absence of active NaCl transport, a lumen-to-bath directed-NaCl gradient (lumen: 150 mM NaCl + furosemide, bath: 50 mM NaCl + 200 mM mannitol) generated a negative transepithelial dilution potential of -13.8 +/- 1.1 mV (n = 8) which induced a significant Ca2+ and Mg2+ secretion into the tubular lumen of -0.59 +/- 0.06 and -0.43 +/- 0.05 pmol.min-1.mm-1 (n = 8), respectively. A bath-to-lumen-directed NaCl gradient, on the other hand, (lumen: 50 mM NaCl + furosemide, bath: 150 mM NaCl) generated a positive transepithelial dilution potential of +15.9 +/- 0.6 mV (n = 7), inducing a significant Ca2+ and Mg2+ reabsorption of 0.62 +/- 0.08 and 0.38 +/- 0.07 pmol.min-1.mm-1 (n = 7), respectively. Linear regression analysis of individual Ca2+ and Mg2+ net flux data versus voltage indicated that JCa and JMg were highly correlated to PDte. In conclusion, these data indicate that transepithelial Ca2+ and Mg2+ reabsorption in the mouse cTAL is predominantly a passive process, driven by the lumen-positive PDte.

Absorption↗