Abstract
Evidence for the secretion of weak organic acids was first obtained for the indicator dye, phenol red, by Marshall and Vickers in 1923 [104]. They observed that when administered parenterally, phenol red is rapidly and quantitatively excreted in the urine. Since some 60% of this substance is bound to plasma albumin and, hence, cannot be filtered through the glomerular capillaries, the authors concluded that the high rate of excretion of phenol red must be due to mechanisms other than glomerular filtration. The authors noticed further that when the plasma concentration of phenol red was raised, the rate of excretion tended to level off. So they guessed that there must be a tubular secretion mechanism which becomes saturated at moderate plasma concentrations.
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References
Anagnostopoulos T (1977) Electrophysiological study of the antiluminal membrane in the proximal tubule of Necturus. J Physiol (London) 267: 89–111
Anagnostopoulos T, Pianelles G (1979) Organic anion permeation at the proximal tubule of Necturus. Pfliigers Arch 381: 231–239
Aubert L, Motais R (1975) Molecular features of organic anion permeability in ox red blood cells. J Physiol (London) 246: 159–179
Baines AD, Gottschalk CW, Lassiter WE (1968) Microinjection study of p-aminohippurate excretion by rat kidneys. Am J Physiol 214: 703–709
Barác-Nieto M, Cohen J J (1968) Nonesterified fatty add uptake by the dog kidney: effect of probenecid and chlorothiazide. Am J Physiol 215: 98–107
Barác-Nieto M (1971) Renal uptake of para-aminohippuric acid. In vitro effects of palmitate and 1-caritine. Biochim Biophys Acta 233: 446–452
Barany EH (1972) Inhibition by hippurate and probenecid of in vitro uptake of iodipamide and o-iodohippurate. A composite uptake system for iodipamide in choroid plexus, kidney cortex and anterior uvea of several species. Acta Physiol Scand 86: 12–27
Barany EH (1973) The liver like anion transport system in rabbit kidney, uvea and choroid plexus. I. Selectivity of some inhibitors, direction of transport, possible physiological sub-strates. Acta Physiol Scand 88: 412–429
Barany EH (1973) The liver like anion transport system in rabbit kidney, uvea and choroid plexus. H. Efficiency of acidic drugs and other inhibitors. Acta Physiol Scand 88: 491–504
Barany EH (1974) Selectivity of probenecid congeners for different organic acid transport systems in rabbit renal cortex. Acta Pharmacol Toxicol 35: 309–316
Bass NH, Lundborg P (1973) Postnatal-development of mechanisms for elimination of organic acids from brain and cerebrospinal fluid system of rat. Rapid efflux of 3H-para-amino-hippuric acid following intrathecal infusion. Brain Res 56: 285–298
Becker B (1961) The transport of organic anions by the rabbit eye. I. In vitro iodopyracet accumulation by ciliary body iris preparation. Am J Ophthalmol 50: 862–867
Berndt WO (1967) Probenecid binding by cortical slices and homogenates. Proc Soc Exp Biol Med 126: 123–126
Berner W, Kinne R (1976) Transport of p-aminohippuric acid by plasma membrane vesicles isolated from rat kidney cortex. Pfliigers Arch 361: 269–277
Bito LZ (1976) Inhibition of renal prostaglandine metabolism and excretion by probenecid, bromeresol green and indomethacin. Prostaglandins 12: 639–649
Bito LZ, Davson H, Salvador EV (1976) Inhibition of in vitro concentrative prostaglandin accumulation by prostaglandins, prostaglandin analogues and by some inhibitors of organic anion transport. J Physiol (London) 256: 257–271
Bito LZ, Baroody RA (1978) Comparison of renal prostaglandin and p-aminohippuric acid transport processes. Am J Physiol 234: F80–F88
Bowman HM, Hirsch GH, Hook IB (1973) Effect of medium pH on p-aminohippurate accumulation by slices of rat renal cortex. Experientia 29: 955–956
Bratton C, Marshall EK (1939) A new coupling component for sulfanilamide determination. J Biol Chem 128: 537–550
Bueht H (1949) On the tubular excretion of thiosulfate and creatine under the influence of carinamide. Scand J Clin Lab Invest 1: 270–276
Buffa P, Peters RA (1949) Formation of citrate in vivo induced by fluoroacetate poisoning. Nature (London) 163: 914
Burg MB, Orloff J (1969) p-aminohippurate uptake and exchange by separated renal tubules. Am J Physiol 217: 1064–1068
Cabantchik ZT, Rothstein A (1972) The nature of the membrane sites controlling the anion permeability of human red blood cells as determined by studies with disulfonic stilbene derivatives. J Membr Biol 10: 311–330
Carrasquer G, Wilczewski TW (1971) Effect of ureteral stop flow on PAH in lumen and cortex homogenate in the rat kidney. Proc Soc Exp Biol Med 137: 284–291
Chung ST, Park YS, Hong SK (1970) Effects of cations on transport of weak acids in rabbit kidney slices. Am J Physiol 219: 30–33
Cohen J J, Randall EW (1964) Alkalosis and renal p-aminohippurate transport in dog: relation to lactate uptake. Am J Physiol 206: 383–390
Cook DL, Lawler CA, Calvin LD, Green DM (1952) Mechanism of bile formation. Am J Physiol 171: 62–74
Copenhaver JH, Forster RP (1958) Displacement characteristics of intracellularly accumulated p-aminohippurate in a mammalian renal transport system in vitro. Am J Physiol 195: 327–330
Copenhaver JH, Davis JR (1965) Effect of hydrogen concentration on transport characteristics of p-aminohippurate by rabbit kidney slices. Proc Soc Exp Biol Med 119: 611–614
Cortney MA, Mylle M, Lassiter WE, Gottschalk CW (1965) Renal tubular transport of water, solute and PAH in rats loaded with saline. Am J Physiol 209: 1199–1205
Coulson R, Bowman RH (1974) Excretion and degradation of exogenous adenosine 3’,5’- monophosphate by isolated perfused rat kidney. Life Sci 14: 545–556
Cousin JL, Motais R, Sola H (1975) Transmembrane exchange of chloride with bicarbonate in mammlian red blood cells: evidence for a sulphonamide sensitive “carrier”. J Physiol (London) 253: 385–399
Cross RJ, Taggart JV (1950) Renal tubular transport: accumulation of PAH by rabbit kidney slices. Am J Physiol 161: 181–191
Dantzler WH (1969) Effects of K+, Na+ and ouabain on urate and PAH uptake by snake and chicken kidney slices. Am J Physiol 217: 1510–1519
Dantzler WH (1974) K+-effects on PAH transport and membrane permeabilities in isolated snake renal tubules. Am J Physiol 227: 1361–1370
Dantzler WH, Bentley SK (1975) High K+-effects on PAH transport and permeabilities in isolated snake renal tubules. Am J Physiol 229: 191–199
Dantzler WH, Bentley SK (1976) Low Na+-effects on PAH transport and permeabilities in isolated snake renal tubules. Am J Physiol 230: 256–262
Dantzler WH, Bentley SK (1980) Bath and lumen effects of SITS on PAH transport by isolated perfused renal tubules. Am J Physiol 238: F16–F25
Davson H, Pollay M (1963) Influence of various drugs on the transport of 1311 and PAH across the cerebrospinal fluid blood barrier. J Physiol (London) 167: 239–246
Deetjen P, Sonnenberg H (1965) Der tubuläre Transport von p-Aminohippursäure. Pflügers Arch 285: 35–44
Despopoulos A (1956) In vitro effects of acetate ion on renal metabolism of p-aminohippurate. Am J Physiol 184: 393–399
Despopoulos A (1965) A definition of substrate specifity in renal transport of organic anions. J Theoret Biol 8: 163–192
Duggan DE (1966) The accumulation of chlorothiazide and related saluretic agents by iso-lated renal tubules. J Pharmacol Exp Ther 152: 122–129
Duggan DE, Hocke KF, White SD, Noll RM, Stevenson CR (1977) The effects of probenecid upon the individual components of indomethacin elimination. J Pharmacol Exp Ther 201: 463–511
Ecker JL, Hook JB (1974) Analysis of factors influencing in vitro developmental pattern of para-aminohippurate transport by rabbit kidney. Biochim Biophys Acta 339: 210–217
Ecker JL, Hook JB (1974) Accumulation of para-aminohippuric acid by separated renal tubules from newborn and adult rabbits. J Pharmacol Exp Ther 190: 352–357
Ehrenspeck G, Brodsky WA (1976) Effect of 4-acetamido-4’-isothiocyano-2,2’-disulfonie stilbene on ion transport in turtle bladders, Biochim Biophys Acta 419: 555–558
Essig A, Taggart JY (1960) Competitive inhibition of renal transport of p-aminohippurate by other monosubstituted hippurates. Am J Physiol 199: 509–512
Essig A (1961) Competitive inhibition of renal transport of p-aminohippurate by analogous of chlorothiazides. Am J Physiol 201: 303–308
Eveloff J, Morishige WK, Hong SK (1976) The binding of phenol red to rabbit renal cortex. Biochim Biophys Acta 448: 167–180
Eveloff J, Kinne R, Kinter WB (1979) p-Aminohippurate acid transport into brush border vesicles isolated from flounder kidney. Am J Physiol 237: F291–F298
Farah A, Frazer M, Stoffel M (1963) Studies on the run out of p-aminohippuric acid from renal slices. J Pharmacol Exp Ther 139: 120–128
Fishman RA (1964) Active transport and the blood brain barrier to penicillin and related organic acids. Trans Am Neurol Assoc 89: 51–55
Forster RP, Sperber I, Taggart JV (1954) Transport of phenolsulphonphthalein dyes in isolated tubules of the flounder and in kidney slices of the dog fish. Competitive phenomena. J Cell Comp Physiol 44: 315–318
Forster RP, Hong SK (1958) In vitro transport of dyes by isolated renal tubules of the flounder as disclosed by direct visualization. Intracellular accumulation and transcellular movement. J Cell Comp Physiol 51: 259–272
Forster RP (1967) Renal transport mechanisms. Fed Proc 26: 1008–1019
Foulkes EC, Miller BJ (1959) Transport of p-aminohippurate from cell to lumen in kidney tubule. Am J Physiol 196: 83–85
Foulkes EC, Miller BF (1959) Steps in PAH transport by kidney slices. Am J Physiol 196: 86–92
Foulkes EC, Miller BF (1961) The role of potassium in the renal transport of p-aminohippurate. In: Kleinzeller A, Kotyk A (eds) Membrane transport and metabolism. Academic Press, London New York, pp 559–565
Foulkes EC (1977) Movement of p-aminohippurate between lumen and cells of renal tubule. Am J Physiol 232: F424–F428
Frömter E (1979) Untersuchungen zum Wirkungsmechanismus von Acetazolamide and SITS auf den Bicarbonattransport im proximalen Tubulus der Niere. In: Krück K (ed) Diuretica Symposion. Diucomb Veranstaltungs-Service, Düsseldorf
Gatley S, Shervatt HSA (1977) The synthesis of hippurate from benzoate and glycine by rat liver mitochondria. Submitochondrial localisation and kinetics. Biochem J 166: 39–47
Gerencser GA, Park YS, Hong SK (1973) Sodium influence upon transport kinetics of p-aminohippurate in rabbit kidney slices. Proc Soc Exp Biol Med 144: 440–444
Gerencser GA, Hong SK (1975) Roles of sodium and potassium ions on p-aminohippurate transport in rabbit kidney slices. Biochim Biophys Acta 406: 108–119
Gerencser GA, Chaizetzeree C, Hong SK (1977) Acetate influence upon the transport kinetics of p-aminohippurate at 37 C in rabbit kidney slices. Proc Soc Exp Biol Med 154: 397–400
Gertz KH (1963) Transtubuläre Natriumchloridflüsse und Permeabilität für Nichtelektrolyte im proximalen und distalen Konvolut der Rattenniere. Pflügers Arch 276: 336–356
Girndt J, Malyusz M, Rumpf KW, Neubaur J, Scheller F (1974) Metabolism of p-aminohippurate and its relevance in man. Nephron 13: 138–144
Giorgi G, Segre G (1969) Effect of various drugs on the intestinal absorption of PAH in rabbits. Eur J Pharmacol 6: 183–193
Greger R, Lang F, Puls F, Deetjen P (1976) Urate interaction with plasma proteins and erythrocytes. Pflügers Arch 352: 121–133
Greger R, Lang F, Oberleithner H, Deetjen P (1978) Handling of oxalate by the rat kidney. Pflügers Arch 374: 243–248
Grantham JJ, Irwin RL (1973) Fluid secretion in isolated proximal straight renal tubules. J Clin Invest 52: 2441–2450
Grantham J J, Qualizza PB, Irwin RL (1974) Net fluid secretion in proximal straight renal tubules in vitro: role of PAH. Am J Physiol 226: 191–197
Grantham J J (1976) Fluid secretion in the nephron. Relation to renal failure. Physiol Rev 56: 248–258
Häberle DA (1975) Influence of glomerular filtration rate on the rate of para-aminohippurate secretion by the rat kidney. Micropuncture and clearance studies. Kidney Int 7: 385–396
Häberle DA, Ruhland G, Lausser A, Moore L, Neiss A (1978) Influence of glomerular filtration rate on renal PAH secretion rate in the rat kidney. Dependency of PAH extraction on renal filtration fraction. Pflügers Arch 375: 131–139
Haberle DA, Deetjen P, Wunderlich P: unpublished
Haberle DA, Hennings H, Rembold H: unpublished
Hewitt WR, Clark RL, Hook JB (1976) Investigations on metabolic modulation of p-amino- hippurate accumulation by rabbit renal cortical slices. J Pharmacol Exp Ther 199: 498–509
Hirsch GH, Hook JB (1970) Maturation of renal organic acid transport. Substrate stimulation by penicillin and p-aminohippurate (PAH). J Pharmacol Exp Ther 171: 103–108
Hirsch GH, Pakuts A (1974) Development of p-aminohippurate transport and oxygen-consumption in rabbit kidneys. Biochem Pharmacol 23: 2323–2325
Holloway LS, Cassin S (1972) In vitro uptake of PAH-3H by choroid plexus from dogs of various ages. Am J Physiol 223: 507–509
Holohan PD, Pessah NI, Ross CR (1975) Binding of N 1-methylnicotinamide and para-amino- hippuric acid to a particular fraction from the dog kidney. J Pharmacol Exp Ther 195: 22–33
Holohan PD, Pessah NI, Ross CR (1979) Reconstitution of N 1-methylnicotinamide and p-aminohippuricacid transport in phospholipid vesicles with a protein fraction isolated from dog kidney membranes. Mol Pharmacol 16: 343–356
Hong SK, Park YS (1971) Transport of bromcresol green in the rabbit kidney slice. Am J Physiol 221: 1779–1784
Hong SK, Goldringer JM, Song YK, Koshier FJ, Lee SH (1978) Effect of SITS on organic anion transport in the rabbit kidney cortical slices, Am J Physiol 234: F302–F307
Hook JB, Williamson HE, Hirsch GH (1970) Functional maturation of renal PAH transport in the dog. Can J Physiol Pharmacol 48: 169–175
Hoshi T, Sudo K, Suzuki Y (1976) Characteristics of changes in the intracellular potential associated with transport of neutral, dibasic and acidic amino acids in Triturus proximal tubule. Biochim Biophys Acta 448: 492–504
Irish JM, Dantzler WH (1976) PAH transport and fluid reabsorption by isolated perfused frog proximal tubules. Am J Physiol 230: 1509–1516
Irish JM (1979) Secretion of prostaglandin E2 by rabbit proximal tubules. Am J Physiol 237: F268–F273
Kikuta Y, Hayashi H, Saito Y (1979) Effects of changes in sodium electrochemical potential gradient on p-aminohippurate transport in newt kidney. Biochim Biophys Acta 556: 354–365
Kim J, Hong SK (1962) Urinary and biliary excretion of various phenol red derivatives in the anaesthetized dog. Am J Physiol 202: 174–178
Kim JK, Hook JB (1972) On the mechanism of acetate enhancement of renal para-amino-hippurate transport. Biochim Biophys Acta 290: 368–375
Kinsella JL, Holohan PD, Pessah NI, Ross CR (1979) Transport of organic ions in renal cortical luminal and antiluminal membrane vesicles. J Pharmacol Exp Ther 209: 443–451
Kinter WB (1975) Structure and function of renal tubules isolated from fish kidneys. Fortschr Zool 23: 223–231
Kinter WB (1959) Renal tubular transport of diodrast and PAH in Necturus. Evidence for simultaneous reabsorption and secretion. Am J Physiol 196: 1141–1149
Kippen J, Klinenberg JR (1978) Effects of renal fuels on uptake of PAH and uric acid by separated renal tubules of the rabbit. Am J Physiol 235: F137–F141
Klahr S, Robson AM, Guggenheim SJ, Tateishi S, Bourgoignie JJ, Hwang KH (1970) Ammonium induced alterations in PAH uptake and cation composition of kidney slices. Am J Physiol 219: 994–1000
Kliger AS, Eastman ST, Zachek M, Kullick M, Preuss H (1977) Effect of renal fuels on p-aminohippurate transport in rat renal cortical fragments. Metabolism 26: 979–988
Knauf PA, Rothstein A (1971) Chemical modification of membranes. I. Effect of sulfhydryl and amino reactive reagents on anion and cation permeability of the human red blood cell. J Gen Physiol 58: 190–210
Knoefel PK, Huang KC, Despopoulos A (1959) Conjugation and excretion of the amino and acetamido benzoic acid. Am J Physiol 196: 1224–1230
KoishiT (1959) Studies on renal tubular transport. 1. Accumulation of p-aminohippurate by kidney slices. Jpn J Pharmacol 8: 101–123
Koshier FJ, Stokols MF, Goldringer JM, Acara M, Hong SK (1980) Effect of DIDS on renal tubular transport. Am J Physiol 238: F99–F106
Lee KSh, Hong SK (1960) Binding of some sulphonphthalein dyes to plasma protein of various species. Yonsei Med J 1: 22–24
Maddy AH (1964) Fluorescent labelling of the plasma membrane. Biochim Biophys Acta 88: 390–399
Malyusz M, Girndt J, Malyusz G, Ochwadt B (1972) Metabolism of para-aminohippurate in kidney of normal rats and rats with experimental Goldblatt-hypertension. Pfliigers Arch 333: 156–165
Marshall EK, Vickers JL (1923) The mechanism of the elimination of phenolsulphonphtha- lein by the kidney; a proof of secretion by the convoluted tubules. Bull Johns Hopkins Hosp 34: 1–7
Masoni A, Payan P (1974) Urea, inulin and para-aminohippuric acid (PAH) excretion by gills of eel, anguilla-anguilla-L. Comp Biochem 47: 1241–1244
Maude DL (1970) Effects of substrate and inhibitors of the tricarboxylic acid cycle on pro-ximal tubular fluid transport in vitro. Biochim Biophys Acta 215: 216–219
Maxild J, Mueller JV (1969) Metabolic studies on renal transport of p-aminohippurate in vitro. Biochim Biophys Acta 184: 614–624
Maxild J (1971) Role of fatty acid metabolism on renal transport of para-aminohippurate in vitro. Biochim Biophys Acta 233: 434–445
Maxild J (1973) Energy requirements for active transport of p-aminohippurate in renal cortical slices. Arch Int Physiol Biochim 81: 501–521
May DG, Weiner IM (1970) Bidirectional transport of m-hydroxybenzoate in proximal tubules of the dog. Am J Physiol 218: 430–436
McDonough A, Hong SK (1976) Na+-K+-ATPase and PAH transport in the renal cortex. Fed Proc 35: 848 Abstr
Meijer AJ, Dam K van (1974) The metabolic significance of anion transport in mitochondria. Biochim Biophys Acta 346: 213–244
Motáis R, Cousin JL (1976) The inhibitor effect of probenecid and structural analogues on organic anions and chloride permeabilities in ox erythrocytes. Biochim Biophys Acta 419: 309–313
Mudge GH, Taggart JV (1950) Effect of acetate on the renal excretion of p-aminohippurate in the dog. Am J Physiol 161: 191–197
Mudge GH, Berndt WO, Valtin H (1973) Tubular transport of urea, glucose, phosphate, uric acid, sulfate and thiosulfate. In: Qrloff J, Berliner R (eds) Handbook of physiology, Sect VIII. Am Physiol Soc, Washington, pp 587–652
Not used
Murdaugh HV, Eliott B (1969) Effect of glycine excess on para-aminohippurate uptake by the kidney. Proc Soc Exp Biol Med 130: 1181–1182
Nechay BR, Pardee LM (1965) Inhibition of N’-methylnicotinamide secretion by ouabain in the chicken kidney. J Pharmacol Exp Ther 147: 270–276
Nikoforov AA, Bresler VM (1977) Double dependence of organic acid transport in proximal tubules of surviving frog kidney on sodium ions. II. Relationship between counterflows of fluorescein and sodium ions across cell layers. Biochim Biophys Acta 468: 100–113
Oldendorf WH (1973) Carrier mediated blood brain barrier transport of short chain mono-carboxylic organic acids. Am J Physiol 224: 1450–1453
Pakarinen A, Runeberg L (1969) Effects of phenolsulphonpthalein and probenecid on the uptake and utilization of citrate and a-ketoglutarate by kidney in vitro. Biochem Pharmacol 18: 2439–2452
Pakarinen A (1970) Palmitate uptake and oxydation by kidney cortex slices. - Effects of probenecid, p-aminohippurate,and phenolsulfonphthalein. Biochem Pharmacol 19: 2707–2718
Pappenheimer JR, Heisey SR, Jordan EF (1961) Active transport of Diodrast and phenol- sulfonpththalein from cerebrospinal fluid to blood. Am J Physiol 200: 1–10
Park YS, Yoo HS, Hong SK (1971) Kinetic studies on transport of organic anions in rabbit kidney slices. Am J Physiol 220: 95–99
Park YS, Solomon S (1977) pH, temperature dependence of organic acid transport in rat kidney slices. Am J Physiol 233: F382–F387
Pegg DG, Hewitt WR, Hook JB (1975) Substrate stimulation of p-aminohippuric acid transport — effect on uptake and run out. Proc Soc Exp Biol Med 149: 546–549
Pegg DG, Hook JB (1977) Glutathione S-transferases: An evaluation of their role in renal organic anion transport. J Pharmacol Exp Ther 200: 65–74
Podevin RA, Boumendil-Podevin EF (1975) Inhibition by cyclic AMP and dibutyryl cyclic AMP of transport of organic acids in the kidney cortex. Biochim Biophys Acta 375: 106–114
Podevin RA, Boumendil-Podevin EF (1977) Monovalent cation and ouabain effects on PAH uptake by rabbit kidney slices. Am J Physiol 232: F239–F247
Podevin RA, Boumendil-Podevin EF, Bujoli-Riche J, Pirol CL(1980) Effects of probenecid on transport and metabolism of cyclic AMP by isolated rabbit renal tubules. Biochim Biophys Acta 629: 135–142
Pollay M, Davson H (1963) The passage of certain substances out of the cerebrospinal fluid. Brain 86: 137–150
Preuss HG, Massry SG, Mäher JF, Gilliece M, Schreiner GS (1966) Effects of uremic sera on renal tubular p-aminohippurate transport. Nephron 3: 265–273
Preuss HG, Weiss FR, Vavatsimanos O, Vertuno LL, Schreiner GE (1973) Acid-base effects on renal organic cation transport. Proc Soc Exp Biol Med 142: 356–358
Preuss HG, Byrne D, Shim PS (1976) Effect of para-aminohippurate on renal glutamine metabolism in the rat. J Pharmacol Exp Hier 197: 199–205
Rasmussen F (1969) Active mammary excretion of N 4-acetylated p-aminohippuric acid. Acta Vet Scand 10: 193–199
Rennick BR (1977) Renal tubular transport of prostaglandins: Inhibition by probenecid and indomethacin. Am J Physiol 233: F133–F137
Riggs TR, Christensen HN (1951) Metabolic conjugations of p-aminobenzoic adic in the rat. J Biol Chem 193: 675–681
Robinson JR (1957) The recovery of kidney slices from anoxia in different media. J Physiol (London) 136: 585–594
Robinson JWL, Mirkovitch V, Sepulveda FV (1977) A comparison of the effects of ouabain and ethaerynic acid on the dog kidney in vivo and in vitro. Pflügers Arch 371: 9–18
Roch-Ramel F, Peters G (1978) Urinary excretion of uric acid in nonhuman mammalian species. In: Kelley WN, Weiner IM (eds) Handbook of experimental pharmacology, vol 51, Uric acid. Springer, Berlin Heidelberg New York, pp 211–255
Roch-Ramel F (1980) Renal tubular transport of urate in mammals. Renal Pathophysiology. Recent Adv 281: 139–143
Rollhäuser A (1957) Histologische und cytologische Untersuchungen über den Mechanismus der tubulären Farbstoffausscheidung der Rattenniere. Z Zellforsch 46: 52–66
Rosenblatt SG, Patak RV, Lifschitz MD (1978) Organic acid secretory pathway and urinary excretion of prostaglandin E in the dog. Am J Physiol 235: F473–F479
Ross CR, Pessah NI, Farah A (1968) Studies of uptake and run out of p-aminohippurate and N-methylnicotinamide in dog renal slices. J Pharmacol Exp Ther 160: 381–386
Ross CR, Weiner IM (1972) Adenine nucleotides and PAH transport in slices of renal cortex: effects of DNP and CN-. Am J Physiol 222: 356–359
Rothstein A, Cabantchik ZI, Baishin M, Juliano R (1975) Enhancement of anion permeability in lecithin vesicles by hydrophobic proteins extracted from red blood cell membranes. Biochem Biophys Res Commun 64: 144–150
Rothstein A, Cabantchik ZI, Knauf P (1976) Mechanism of anion transport in red blood cells: role of membrane proteins. Fed Proc 35: 3–10
Rothstein A (1979) Role of protein channels in anion transport across the red cell mem-brane. In: Quagliariello E, Palmieri F, Papa S, Klingenberg M (eds) Function and molecular aspects of biomembrane transport, vol 3. Elsevier North Holland Biomed Press, Amsterdam, pp 15–24
Schachter D, Freinkel N (1951) Self-depression of TmPAH dog at high plasma levels and its reversibility by acetate. Am J Physiol 167: 531–538
Schachter DJ, Manis J, Taggart JV (1955) Renal synthesis, degradation and active transport of aliphatic acylamino acids. Relationship to p-aminohippurate transport. Am J Physiol 182: 537–544
Schanker LS, Johnson JM, Jeffrey JJ (1964) Rapid passage of organic anions into human red cells. Am J Physiol 207: 503–508
Schneider W (1970) Konzentrationsabhängigkeit des PAH-Flusses in Froschhaut und Krötenblase. Pflügers Arch 319: R97
Sheikh M, Malier J (1970) The kinetic parameters of renal transport of p-aminohippurate in vitro. Bioehim Biophys Acta 196: 305–319
Sheikh MI (1972) Renal handling of phenol red. I. A comparative study on accumulation of phenol red and para-aminohippurate in rabbit kidney tubules in vitro. J Physiol (London) 227: 565–590
Sheikh MI (1976) Renal handling of phenol red. II. The mechanism of substituted phenol- sulfonphthalein (PSP) dye transport in rabbit kidney tubules in vitro. J Physiol (London) 256: 175–195
Sheikh MI, Stahl M (1977) Characteristics of accumulation of probenecid by rabbit kidney cortical slices. Am J Physiol 232: F513–F523
Sheikh MI, Miller JV (1980) Renal handling of phenol red. IV. Tubular localisation in rabbit and rat kidney in vivo. Am J Physiol 238: F159–F165
Smith HW (1951) The kidney. Oxford University Press, New York
Spencer AM, Sack J, Hong SK (1979) Relationship between PAH transport and Na+-K+- ATPase activity in the rabbit kidney. Am J Physiol 236: F126–F130
Sperber I (1954) Competitive inhibition and specificity of renal tubular transport mechanisms. Arch Int Pharmacodyn 97: 221–231
Steele TH, Rieselbach RE (1976) The renal handling of urate and other organic anions. In: Brenner B, Rector FC (eds) The kidney, vol I. WB Saunders, Philadelphia London Toronto, pp 442–476
Stopp M, Bräunlich H (1980) In vitro analysis of drug induced stimulation of renal tubular p-aminohippurate (PAH) transport in rats. Biochem Pharmacol 29: 983–986
Taggart JV, Silverman L, Trayner EM (1953) Influence of renal electrolyte composition on the tubular excretion of PAH. Am J Physiol 173: 345–350
Tanner GA, Kinter WB (1966) Reabsorption and secretion of PAH and Diodrast in Necturus kidney. Am J Physiol 210: 221–231
Tanner GA, Isenberg MT (1970) Secretion of p-aminohippurate by rat kidney proximal tubules. Am J Physiol 219: 889–892
Tanner GA, Carmines PK, Kinter WB (1979) Excretion of phenol red by Necturus kidney. Am J Physiol 236: F442–F447
Trimble ME (1979) Transport and metabolism of octanoate by the perfused rat kidney. Am J Physiol 237: F210–F217
Tune BM, Fernholt M (1973) Relationship between cephaloridine and para-aminohippurate transport in kidney. Am J Physiol 225: 1114–1117
Tune BM, Wu KY, Kepson RL (1977) Inhibition of transport and prevention of toxicity of cephaloridine in the kidney. Dose-responsiveness of the rabbit and guinea pig to probenecid. J Pharmacol Exp Ther 202: 466–473
Tune BM, Burg MB, Pattlak CS (1969) Characteristics of p-aminohippurate transport in proximal renal tubules. Am J Physiol 217: 1057–1063
Ullrich KJ, Rumrich G, Klöss S (1974) Specifity and sodium dependence of the active sugar transport in the proximal convolution of the rat kidney. Pflügers Arch 351: 35–48
Ullrich KJ, Rumrich G, Klöss S (1974) Sodium dependence of the amino acid transport in the proximal convolution of the rat kidney. Pflügers Arch 351: 49–60
Ullrich KJ (1976) Renal tubular mechanisms of organic solute transport. Kidney Int 9: 134–148
Ullrich KJ, Capasso G, Rumrich G, Papavassiliou F, Klöss S (1977) Coupling between the proximal tubular transport processes: Studies with ouabain, SITS and HCO3-free solutions. Pflügers Arch 368: 245–252
Ullrich KJ (1979) Renal transport of organic solutes. In: Giebisch G, Tosteson DC, Ussing HH (eds) Membrane transport in biology, vol IVA, Transport organs. Springer, Berlin Heidelberg New York, pp 413–448
Vogel G, Kröger W (1965) Das Tm-PAH der Niere als Na+-abhängige Größe. Pflügers Arch 286: 317–322
Vogel G (1965) The importance of Na+ for the renal transport of glucose and p-aminohip- puric acid. Arch Exp Pathol Pharmacol 250: 287–295
Vogel G, Kröger W (1966) Die Bedeutung des Transportes, der Konzentration und der Darbietungsrichtung von Na+ für den tubulären Glucose- und PAH-Transport. Pflügers Arch 288: 342–358
Vogel G, Stöckert I (1966) Die Bedeutung des Anions für den renalen tubulären Transport von Na+ und die Transporte von Glucose und PAH. Pflügers Arch 292: 309–315
Wedeen RP, Weiner B (1969) Extraction of hippuran- I and 3H-PAH from red blood cells and plasma in the rat. Am J Physiol 217: 838–844
Wedeen RP, Weiner B (1974) Distribution of p-aminohippuric acid in rat kidney slices. 3. Effect of inhibitors. Am J Physiol 226: 953–961
Wedeen RP, Vygas BT (1978) Phlorhizin stimulation of p-aminohippurate uptake in rat kidney cortex slices, Kidney Int 14: 158–168
Weiner IM (1971) Excretion of drugs by the kidney. In: Eichlar O, Farah A, Harken H, Welch AD (eds) Handbook of experimental pharmacology, New Ser, vol 28, part I. Springer, Berlin Heidelberg New York, pp 328–353
Weiner IM (1973) Transport of weak acids and bases. In: Qrloff J, Berliner RW (eds) Handbook of physiology, Sect 8, Renal physiology. Am Soc Physiol, Washington, pp 521–554
Weinman EJ, Frankfurt SJ, Ince A, Samson S (1978) Renal tubular transport of organic acids. Studies with oxalate and para-aminohippurate in the rat. J Clin Invest 61: 801–806
Weiss FR, Preuss HG (1970) Influence of extracellular and intracellular factors on hippurate uptake by rat kidney cortex: acid base effects. Proc Soc Exp Biol Med 135: 30–32
Welch K (1962) Concentration of thiocyanate by the choroid plexus of the rabbit in vitro. Proc Soc Exp Biol Med 109: 953–954
Wright EM (1974) Active transport of iodide and other anions across the choroid plexus. J Physiol (London) 240: 535–566
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© 1981 Springer-Verlag Berlin Heidelberg
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Häberle, D.A. (1981). Characteristics of p-Aminohippurate Transport in the Mammalian Kidney. In: Greger, R., Lang, F., Silbernagl, S. (eds) Renal Transport of Organic Substances. Proceedings in Life Sciences. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68147-9_14
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