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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 395 (1982), S. 212-219 
    ISSN: 1432-2013
    Keywords: SITS ; Probenecid ; Phloretin ; Acetazolamide ; Lactate ; Renal tubule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The transport ofd-lactate across the epithelium of the late proximal convolution was investigated by two methods: 1. by measuring the zero net flux transtubular concentration difference (Δc tt,45s) and the permeability (P) ofd-lactate and calculating from both the transtubular active transport rate (J lac act ). 2. By measuring the 3.5 s efflux ofd-lactate from the tubular lumen, while blood was flowing through the capillaries. The 3.5 s efflux comprises two components, one going through the brush border (J lac bb ) and one going the paracellular pathway (J lac paracell =P lac·c lac lumen). Both,J lac act andJ lac bb ofd-lactate gave the sameK m 1.9 and 1.7 mmol/l and the same maximal transport rate 3.2 and 2.9 pmol cm−1 s−1. TheK i ofl-lactate tested againstJ lac act andJ lac bb ofd-lactate was also the same: 1.1 and 1.0 mmol/l. These data indicate that under our experimental conditions only the flux through the brush border seems to be rate limiting and thatd-lactate uses the same transport system asl-lactate. When Na+ was omitted from the perfusatesJ lac act disappeared completely, whileJ lac bb was reduced by 64%. These data reflect the Na+ dependence of thed-lactate transport through the brush border. Variation of intra-and extracellular pH by raisingpCO2, omitting HCO 3 − from the perfusates or adding acetazolamide had no effect on the transport ofd-lactate when α-ketoglutarate was used as fuel. However, when acetate was used as fuel, intracellular acidosis brought the reducedJ lac act back to the values obtained with α-ketoglutarate as fuel. It is suggested that this is an effect on a contraluminal transport step. Probenecid (5 mmol/l) and phloretin (0.25 mmol/l) inhibitedJ lac act significantly.J lac bb , however, was only inhibited by probenecid when acetate was used as fuel. These data indicate that both compounds act on thed-lactate exit at the contraluminal cell side, but that probenecid acts in addition at the luminal cell side. SITS (1 mmol/l) augmentedJ lac bb when acetate was used as fuel and is similar to the effect of lowering intracellular pH as described above. The SH reagents mersalyl (1.0 mmol/l) and maleolylglycine (1 mmol/l) did not influenceJ lac bb .
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 395 (1982), S. 220-226 
    ISSN: 1432-2013
    Keywords: Na+-dependent transport ; d-Lactate transport ; Small fatty acids ; 3-Hydroxybutyrate ; Acetoacetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The 3.5 s efflux ofd-lactate (1 mmol/l) injected in the lumen of the late proximal convolution as well as the zero net flux transtubular concentration difference ofd-lactate, which is a measure of its active transtubular transport rate, were determined. The inhibitory potency of small fatty acids and their analogs added to the perfusate in a concentration of 10 mmol/l on both, the 3.5 s efflux and in most cases also the 45 s transtubular concentration difference ofd-lactate was measured. It was found that 1. small fatty acids from acetate to octanoate inhibit 3.5s efflux ofd-lactate, the largest inhibition being exerted by propionate and butyrate. With increasing chain length the inhibitory potency decreased and disappeared with decanoate. 2. Considering the acetate-, propionate- and butyrate analogs, introduction of an electron attracting group such as Cl, Br, I, CN, SH, N3 on C atom 2 increased the inhibitory potency, compared to the unsubstituted fatty acid. An OH on C2 increased or did not change the inhibition while an OH on C atom 3 reduced or blunted the inhibition. A keto-group, as it is present in glyoxylate prevented inhibition, but pyruvate inhibited to the same extent as lactate, and acetoacetate was even more inhibitory than 3-hydroxybutyrate. Cl substitution on C3 preserved the strong inhibitory potency, while 4-Cl butyrate, was only sparsely inhibitory. A NH 3 + group at any position precludes inhibition. 3. As seen with Cl or OH substituted propionate and butyrate the inhibitory potency increased with decreasingpK a of the compounds. 4. Increasing the chain length by a CH3 as from acetate to propionate, from glycolate to lactate and also from glyoxylate to pyruvate increased the inhibitory potency. 5. When tested against the 3.5 s efflux ofl-lactate, the same inhibitory pattern was seen as withd-lactate. 6. The transport of chloroacetate, glycolate and acetoacetate, which were available in a radio-labeled form of high specific activity, was measured directly in 3.5 s efflux studies. It was Na+-dependent and could be inhibited by 10 mmol/ll-lactate. Glyoxylate, on the other hand, which did not inhibitd-lactate transport, did also not show a Na+-dependent,l-lactate inhibitable efflux from the tubular lumen. The data indicate that a variety of short chain fatty acids and their analogs are transported by the same Na+-dependent transport system in the brush border which transportsl- andd-lactate. The specificity is determined by the molecule size, hydrophobicity of one part of the molecule, the electron attracting abilities of substitutes on C-atom 2 or 3 and the charge distribution on the molecule.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 395 (1982), S. 227-231 
    ISSN: 1432-2013
    Keywords: d-Lactate ; Benzoate ; Cinnamate ; Nicotinic acid ; Pyrazinoate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The 3.5 s efflux ofd-lactate (1 mmol/l) injected in the lumen of the late proximal convolution was measured. This efflux can be divided into a Na+-dependent, saturable component flowing through the brush border and a Na+-independent non-saturable component flowing through the paracellular pathway. The inhibitory potency of benzoate and its analogs, of phenyl-substituted acetate-, propionate-and butyrate analogs, of cinnamate and analogs, of heterocyclic monocarboxylic acids and related compounds added to the perfusate in a concentration of 10 mmol/l was measured. It was found that 1. benzoate added in a concentration of 10 mmol/l to the luminal perfusate inhibits transport ofd-lactate, and the meta- and para-substituted analogs of benzoate inhibit in a fashion predicted by Hammett's theory. Side groups which withdraw electrons from the COOH group inhibit while substitutes who deliver electrons toward the reaction center do not. 2. Replacement of a hydrogen atom by a phenyl ring at the C2 atom of acetate, glycolate and glyoxylate does not change the inhibitory pattern of these substances ond-lactate transport. Replacement of a hydrogen atom on the C2 atom of propionate and lactate reduces the ability of these molecules to inhibitd-lactate transport. But replacement of a hydrogen atom at the C3 atom of propionate, pyruvate and lactate abolishes the inhibitory potency. Similarly the inhibitory potency decreases from butyrate 〉 2-phenylbutyrate 〉 3-phenylbutyrate 〉 4 phenylbutyrate. The latter two are actually no longer inhibitory. 3. Trans-cinnamate, cis-cinnamate (3-phenyl trans or cis acrylic acid) and 3-phenylpropiolate are also not inhibitory. But introduction of an electron attracting CN group on C2 atom of cinnamate evokes inhibitory potency. 4. The heterocyclic compounds nicotinic acid and pyrazinoic acid exert strong inhibition ond-lactate transport, while picolinic acid and isonicotinic acid exert only moderate inhibition. Nicotinic and pyrazinoic acid show also a secretory component in their transport behaviour. 5. If the COOH group of benzoate is replaced by a SO3H group (benzenesulfonic acid) or if a second ring is induced (1 or 2 naphthoic acid) the inhibitory potency is lost. 6. Amongst other organic anions which do not inhibitd-lactate transport are paraaminohippurate, urate, and taurocholate. The data indicate that a main determinant of the specificity of the Na+-dependent aliphatic aromatic monocarboxylic acid reabsorption system in the renal brush border is the electron density at the reaction center, i.e. the free carboxylic group. Furthermore, the size of the molecule and its hydrophobicity at one cell pole is limiting for its ability to react with the carrier.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 404 (1985), S. 293-299 
    ISSN: 1432-2013
    Keywords: Epithelial transport ; Contraluminal cell membrane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In order to study the specificity for the contraluminal sulfate transport system the inhibitory potency of sulfate esters and sulfonate compounds on the35SO 4 2− influx from the interstitium into cortical tubular cells in situ has been determined. The following was found: 1. From 10 sulfate monoesters tested 9 inhibited contraluminal sulfate influx with an app.K i between 0.6 and 6 mmol/l; the two sulfate diesters tested, however, did not. 2. Out of 8 aliphatic sulfonate compounds only three, having a NH- or OH-group in a suitable position, exerted a moderate inhibition (app.K i ca. 2–6 mmol/l). 3. Amongst 14 benzene sulfonates tested only 2 compounds (5-nitrobenzene-sulfonate and 2-hydroxy-5-nitrobenzenesulfonate) inhibited with aK i〈5 mmol/l. 4. Out of 10 naphthalene sulfonates tested 8 inhibited with aK i〈5; the highest inhibition was seen with the NH-containing 8-anilinonaphthalene-1-sulfonate (ANS), but no inhibition with 2 compounds containing an amino group. 5. From the polycyclic sulfonates pyrene-3-sulfonate and anthracene-1-sulfonate inhibited with aK i of approximately 2 mmol/l, while no inhibition was seen with anthracene-2-sulfonate. 6. Out of 4 amino-sulfonates tested benzene-1-amino-sulfonate and a similar benzyl-analog inhibited with aK i of 1 mmol/l and smaller; cyclohexyl-1-amino-sulfonate (cyclamate), however, inhibited only slightly (app.K i of 6 mmol/l). The data indicate that sulfate monoesters are well accepted by the contraluminal sulfate transport system. The affinity of sulfonate compounds to this system depends on neighbouring OH-groups −NH-groups, meta-positioned electronegative groups or a hydrophobic moiety in an appropriate position.
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  • 15
    ISSN: 1432-2013
    Keywords: Basolateral cell membrane ; Methylsuccinate-transport ; 2-Oxolutarate-transport ; Citrate-transport ; Lithium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The transport of dicarboxylic acids in the proximal convolution was investigated by measuring: a) the zero net flux transtubular concentration difference ofdl-methyl-succinate, b) its 2-s influx from the interstitium into tubular cells, and c) its 3.5-s efflux from the tubular lumen. With the first method a luminal concentration exceeding the peritubular concentration was observed, thus indicating a net active transtubular secretion of this slowly metabolized substance. All transport steps, luminal and contraluminal, as well as the overall transport, were Na+-dependent and inhibited by lithium (apparentK i ≈ 1.8 mmol/l). The overall transport of methylsuccinate, as well as the contraluminal influx into proximal tubular cells, could be inhibited by paraaminohippurate and H2-DIDS with an apparentK i of ≈ 1.8 mmol/l, by taurocholate with an apparentK i ≈ 3.` mmol/l and by pyruvate with an apparentK i ≈ 5 mmol/l, but not by sulfate, thiosulfate,l-lactate, oxalate and urate. As judged from the inhibition of contraluminal methylsuccinate influx by 48 dicarboxylic acids (aliphatic and aromatic), a specificity pattern was observed similar to that of inhibition of luminal efflux of 2-oxoglutarate [22]: a preference of dicarboxylates in the transconfiguration with a chain length of 4–5 carbons; little change in the inhibitory potency with CH3 −, OH−, SH−and O=, but strong reduction with a NH 3 + in the 2 position; only a small reduction of inhibitory potency with 2,3 disubstituted SH and OH analogs; preference of the dicarboxylic benzene in the 1,4 position and of the diacetyl benzene in the 1,2 position. The data indicate a Na+-dependent dicarboxylic transport system at the contraluminal cell side of the proximal tubule which is very similar to the luminal transport system for dicarboxylic acids.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 402 (1984), S. 264-271 
    ISSN: 1432-2013
    Keywords: Epithelial transport ; Contraluminal cell membrane ; Anion exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In order to study contraluminal sulfate transport the influx rate of35SO 4 2− from the interstitium into cortical tubular cells has been determined. Preloading of the rat with sulfate augmented contraluminal35SO 4 2− influx; preperfusion with sulfate-free solutions diminished it. The contraluminal35SO 4 2− influx in sulfate-loaded animals followed two parameter kinetics (K m 1.4 mmol/l,J max 1.2 pmol·s−1·cm−1). The contraluminal35SO 4 2− influx (starting concentration 10 μmol/l) did not change when the K+ concentration was varied between 4 and 40 mmol/l and the Ca2+ concentration from zero to 3 mmol/l. Omission of Na+ from the perfusates augmented contraluminal35SO 4 2− influx markedly. The increase is larger at pH 6 than at pH 7.4. Changes of pH affect contraluminal35SO 4 2− influx only when the solutions are Na+- and K+-free. Under these conditions the35SO 4 2− influx decreased when the ambient pH was raised from pH 6.0 to pH 8.0. Thiosulfate, selenate, molybdate, oxalate, phosphate, arsenate, and bicarbonate exerted competitive inhibition, while formate, 2-oxoglutarate and paraaminohippurate showed a biphasic response: inhibition at 50 mmol/l, no inhibition at 150 mmol/l. Chloride and bicarbonate inhibited35SO 4 2− influx at 10 μmol/l35SO 4 2− , but augmented sulfate influx at 5 mmol/l35SO 4 2− concentration in rats not preloaded with sulfate. The data indicate the presence of a contraluminal sulfate transport system which is shared by a variety of inorganic and organic anions. The biphasic behaviour of some anions suggests parallel pathways leading to a cis-inhibition at small and trans-stimulation at high anion concentrations. Na+ and H+ may be cotransported or interact with the transport system at a modifier site.
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 413 (1988), S. 134-146 
    ISSN: 1432-2013
    Keywords: Organic anion transport ; Sulfate transport ; Dicarboxylate transport ; Phenolate transport ; Salicylate transport ; Cinnamate transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In order to study the specificities of the contraluminal anion transport systems, the inhibitory potency of substituted benzene analogs on influx of [3H]PAH, [14C]succinate, and [35S]sulfate from the interstitium into cortical tubular cells has been determined in situ: (1) Contraluminal [3H]PAH influx is moderately inhibited by benzene-carboxylate and benzene-sulfonate, and strongly by benzene-dicarboxylates,-disulfonates and carboxy-benzene-sulfonates, if the substituents are located at positions 1 and 3 or 1 and 4. The affinity of the PAH transporter to polysubstituted benzoates increases with increasing hydrophobicity, decreasing electron density at the carboxyl group and decreasing pKa. Similar dependencies are observed for phenols. Benzaldehydes which do not carry an ionic negative charge are accepted by the PAH-transporter, if they possess a second partially charged aldehyde or NO2-group. (2) Contraluminal [14C]succinate influx is inhibited by benzene 1,3- or 1,4-dicarboxylates,-disulfonates and 1,3-or 1,4-carboxybenzene-sulfonates. Monosubstituted benzoates do not interact with the dicarboxylate transporter, but NO2-polysubstituted benzoates do. Phenol itself and 2-substituted phenol interact weakly possibly due to oligomer formation. (3) The contraluminal sulfate transporter interacts only with compounds which show a negative group accumulation such as 3,5-dinitro- or 3,5-dichloro-substituted salicylates. The data are consistent with three separate anion transport systems in the contraluminal membrane: The PAH transporter interacts with hydrophobic molecules carrying one or two negative charges (−COO−, −SO 3 − ) or two or more than two partial negative charges (−OH, −CHO, −SO2NH2, −NO2). The dicarboxylate transporter requires two electronegative ionic charges (−COO−, −SO 3 − ) at 5–9 Å distance or one ionic and several partial charges (−Cl, −NO2) at a favourable distance. The sulfate transporter interacts with molecules which have neighbouring electronegative charge accumulation.
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 375 (1978), S. 97-103 
    ISSN: 1432-2013
    Keywords: Renal tubule ; Phosphate transport ; Paracellular shunt ; Calcium ; Ca2+ ionophore A 23187
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Proximal inorganic phosphate (P i ) transport was evaluated using the standing droplet method with simultaneous microperfusion of the peritubular blood capillaries. In chronic parathyroidectomized (PTX) rats addition of 3 μM of the Ca2+ ionophore A 23187 to the luminal perfusate had no effect on the P i transport, although the isotonic fluid reabsorption was reduced by 20%. When the Ca2+ concentration in the perfusates was raised from 1.5 mM to 3.0 mM the reabsorption did not change significantly. But when Ca2+ was omitted from the perfusates the P i reabsorption dropped by 19%, and when 2 mM EDTA were added to the perfusates P i transport decreased by 35%. The influx of P i from the interstitial space and from the cell into the phosphate-free luminal perfusate did not change, when the perfusates were Ca2+-free, but it increased by 23% in the presence of 2 mM EDTA. The data indicate that 1. a rise in intracellular Ca2+ above normal is not a factor which modifies “basal” P i transport i.e. when P i transport is independent of the action of parathyroid hormone. 2. A reduction of extracellular Ca2+ concentration from normal toward zero reduces P i transport without changing the paracellular leak permeability for P i . 3. With EDTA the paracellular leak permeability for P i is increased, thus causing an even greater reduction in net P i transport than with Ca2+-free solutions alone.
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  • 19
    ISSN: 1432-2013
    Keywords: Proximal Kidney Tubule ; Mercurials ; SH Reagents ; Site Group Reagents ; Transtubular Transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of site group reagents were tested on the following transport processes of the proximal convolution. Isotonic Na+ absorption, evaluated by the shrinking droplet procedure, histidine and glucose transport, evaluated by measuring the respective transtubular concentration difference at zero substance and water net flux. The test substances were applied either by continuous microperfusion of the peritubular capillaries or by luminal perfusion prior to the transport tests or by addition to the luminal test solution. The SH reagents (0.2 mM) N-ethylmaleimide,p-chloromercuribenzoate (pCMB) 3,6-bis-(acetatomercurimethyl)dioxane and Mersalyl (Salyrgane) caused 50% inhibition of the isotonic Na+ absorption in approximately 1.5 min when applied to the capillary perfusate. The same effect was reached in 2–3 min by 0.2 mMp-chloromercuriphenylsulfonate, benzamido-4-iodo-acetylstilbene-2,5-disulfonate and 2,2′-dihydroperoxy-2,2′-dibutylperoxide. However, the large molecular SH reagentspCMB-dextran T10 and benzoxanthene-3,4-dicarboxylic-N-iodoacetyloligoprolyl-2-aminoethylimid, did not inhibit the isotonic Na+ absorption. If an inhibitory effect was observed on the Na+ transport its onset was faster, when the substance was applied from the blood site than when it was given from the tubular lumen. Because SH reagents inhibit the isotonic Na transport faster when applied from the blood side, and because SH reagents with MW up to 690 are inhibitory whereas larger ones with MW over 1700 are not, it seems that they exert their inhibitory action on SH groups located a) predominantly on the blood side and b) deep within the membrane and not at the surface. Histidine- and glucose transport was inhibited only when the sodium transport was inhibited considerably. The oxygen consumption of teased kidney slices is not inhibited by 0.2 mMpCMB or Mersalyl within 10 min, but it is inhibited considerably by 1 mM of these substances in the same period of incubation time. The COOH reagents N,N′-carbonyl-diimidazole and N-ethyl-N′-(3-dimethyl-aminopropyl)carbodiimid (10 mM) and the NH2 reagents 4-acetamido-4′-isothiocyanatostilbene-2,2′-disulfonic acid, 2 Na+ (SITS) (1 mM) as well as danslychloride (applied from the lumen at 5 mM in paraffin oil) did not inhibit the isotonic Na+ absorption.
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 372 (1977), S. 269-274 
    ISSN: 1432-2013
    Keywords: Renal tubule ; Phosphate transport ; Parathyroidectomy ; Parathyroid hormone ; Phosphate diet
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The standing droplet method was applied in combination with microperfusion of the peritubular blood capillaries to determine the build up of transtubular concentration differences of phosphate (Pi) in proximal convoluted tubules. As revealed in experiments with chronic parathyroidectomized (PTX) rats, the time dependent decrease of the intraluminal Pi concentration, or increase of transtubular Pi concentration difference ( $$\Delta {\text{c}}_{{\text{P}}_i }$$ ), changes along the proximal convolution in a ratio 4:2:1 in the first quarter: second plus third quarter: fourth quarter. In acute (〉2 h) PTX rats $$\Delta {\text{c}}_{{\text{P}}_i }$$ decreased by 31% in the first and by 41% in the fourth quarter of the convolution when parathyroid hormone (PTH; 5 U initially and 12 U/h continuously) was infused. In chronic (〉2 days) PTX rats the correspondent values of 17% and 29% were significantly smaller. When the rats were kept for 7–11 weeks on a low phosphate diet (〈0,15% P in the dry matter) their Pi transport was in the range of that of the PTX rats. PTH infusion, however, diminished the P i reabsorption rate in the fourth quarter of the convolution only, but not that in the early parts of the convolution. On the contrary, rats kept for the same time on a high phosphate diet (2%) showed all along the proximal convolution one by one third of the phosphate transport rate of animals on a low phosphate diet. Acute parathyroidectomy of the high P diet rats led to 51% increase in P i transport. The data show that 1. the phosphate transport decreases as a function of proximal convolution length, 2. PTH exerts a considerable inhibitory effect on P i transport only in acute PTX rats, while the effect in chronic PTX rats is rather small, 3. the P content of the diet inversely correlates with the P i transport. 4. further with low P diet the PTH inhibits P i transport in late, but not in early segments of the proximal convolution.
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