Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P41181 (collecting duct)
 5,183 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. Cortical collecting ducts were dissected from slices of rabbit kidney, then perfused in vitro.2. Transtubular electrical potentials were measured before and after abrupt changes in peritubular fluid pH.3. Variation in peritubular fluid pH, induced either by alteration in HCO(3) (-) concentration or in H(2)PO(4) (-)/HPO(4) (2-) ratio, produced biphasic responses in potential. Thus, reduction in pH caused an immediate fall, and then a prolonged and marked rise, in transtubular potential. The converse occurred on raising the pH.4. Variation in luminal fluid pH between pH 4.85 and pH 7.35 did not alter this pattern of response.5. In contrast to the above, reduction of peritubular fluid pH by elevation of P(CO2) produced either no effect or a decrease in transtubular potential.6. The transtubular potential of the cortical collecting duct appears to be a function of the pH gradient across some as yet unidentified part of the wall of the duct.
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PMID:Peritubular pH and transtubular potentials in isolated perfused cortical collecting ducts of rabbit kidney. 501 64

A mathematical model of the outer medullary collecting duct (OMCD) has been developed, consisting of alpha-intercalated cells and a paracellular pathway, and which includes Na(+), K(+), Cl(-), HCO(3)(-), CO(2), H(2)CO(3), phosphate, ammonia, and urea. Proton secretion across the luminal cell membrane is mediated by both H(+)-ATPase and H-K-ATPase, with fluxes through the H-K-ATPase given by a previously developed kinetic model (Weinstein AM. Am J Physiol Renal Physiol 274: F856-F867, 1998). The flux across each ATPase is substantial, and variation in abundance of either pump can be used to control OMCD proton secretion. In comparison with the H(+)-ATPase, flux through the H-K-ATPase is relatively insensitive to changes in lumen pH, so as luminal acidification proceeds, proton secretion shifts toward this pathway. Peritubular HCO(3)(-) exit is via a conductive pathway and via the Cl(-)/HCO(3)(-) exchanger, AE1. To represent AE1, a kinetic model has been developed based on transport studies obtained at 38 degrees C in red blood cells. (Gasbjerg PK, Knauf PA, and Brahm J. J Gen Physiol 108: 565-575, 1996; Knauf PA, Gasbjerg PK, and Brahm J. J Gen Physiol 108: 577-589, 1996). Model calculations indicate that if all of the chloride entry via AE1 recycles across a peritubular chloride channel and if this channel is anything other than highly selective for chloride, then it should conduct a substantial fraction of the bicarbonate exit. Since both luminal membrane proton pumps are sensitive to small changes in cytosolic pH, variation in density of either AE1 or peritubular anion conductance can modulate OMCD proton secretory rate. With respect to the OMCD in situ, available buffer is predicted to be abundant, including delivered HCO(3)(-) and HPO(4)(2-), as well as peritubular NH(3). Thus, buffer availability is unlikely to exert a regulatory role in total proton secretion by this tubule segment.
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PMID:A mathematical model of the outer medullary collecting duct of the rat. 1089 85