MOMENT ANALYSIS OF DRUG DISPOSITION IN KIDNEY .2. URINE PH-DEPENDENT TUBULAR SECRETION OF TETRAETHYLAMMONIUM IN THE ISOLATED PERFUSED RAT-KIDNEY

被引:14
作者
KAMIYA, A
TANIGAWARA, Y
SAITO, Y
HAYASHI, Y
AIBA, T
INUI, K
HORI, R
机构
[1] Department of Pharmacy, Kyoto University Hospital
关键词
D O I
10.1002/jps.2600790809
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Effects of urine pH on the renal tubular secretion of an organic cation (tetraethylammonium, TEA) and an organic anion (p‐aminohippurate, PAH) were investigated using the isolated erythrocyte‐perfused rat kidney. The method was based on a multiple indicator dilution experiment and noncompartmental moment analysis. Treatment with sodium bicarbonate and sodium dihydrogen phosphate increased and decreased urine pH, respectively, but affected neither the condition of the perfused kidney nor the renal handling of albumin and inulin. In TEA studies, the increase of urine pH prolonged the mean residence time in renal epithelial cells (T̄cell) and reduced the apparent secretion intrinsic clearance, but did not influence the volume of distribution in the kidney (Vddrug). The decrease of urine pH did not affect these kinetic parameters. By contrast, PAH secretion was constant against the change of urine pH. Since any change in the basolateral membrane transport is reflected in Vddrug, the net transport from blood to cells can be regarded as similar under these treatments. On the other hand, the prolonged T̄cell of TEA with the increased urine pH suggested a slow transport from cells to lumen across the brush‐border membranes. The present results coincide with the hypothetical mechanism that organic cations are secreted via an active transport system, coupled to the countertransport of H+ into cells. In conclusion, the present method is useful to separately evaluate the transmembrane transport across both sides of the renal epithelial cells in a morphologically intact kidney. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:692 / 697
页数:6
相关论文
共 42 条
[1]   MICROINJECTION STUDY OF P-AMINOHIPPURATE EXCRETION BY RAT KIDNEYS [J].
BAINES, AD ;
GOTTSCHA.CW ;
LASSITER, WE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1968, 214 (04) :703-&
[2]   MEAN RESIDENCE TIME IN THE BODY VERSUS MEAN RESIDENCE TIME IN THE CENTRAL COMPARTMENT [J].
BENET, LZ .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1985, 13 (05) :555-558
[3]   PHARMACOLOGICAL ROLE OF THE KIDNEY [J].
BRATER, DC .
DRUGS, 1980, 19 (01) :31-48
[4]   SOME CONSIDERATIONS ON THE ESTIMATION OF STEADY-STATE APPARENT VOLUME OF DISTRIBUTION AND THE RELATIONSHIPS BETWEEN VOLUME TERMS [J].
COLLIER, PS .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1983, 11 (01) :93-105
[5]   BRUSH-BORDER TEA TRANSPORT IN INTACT PROXIMAL TUBULES AND ISOLATED MEMBRANE-VESICLES [J].
DANTZLER, WH ;
BROKL, OH ;
WRIGHT, SH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (02) :F290-F297
[6]   NON-COMPARTMENTAL VS COMPARTMENTAL ANALYSIS - SOME BASES FOR CHOICE [J].
DISTEFANO, JJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 243 (01) :R1-R6
[7]  
Folin O, 1919, J BIOL CHEM, V38, P81
[8]   MOVEMENT OF PARA-AMINOHIPPURATE BETWEEN LUMEN AND CELLS OF RENAL TUBULE [J].
FOULKES, EC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1977, 232 (05) :F424-F428
[9]  
FOULKES EC, 1987, AM J PHYSIOL, V252, pF1042
[10]   CIMETIDINE TRANSPORT IN ISOLATED LUMINAL MEMBRANE-VESICLES FROM RABBIT KIDNEY [J].
GISCLON, L ;
WONG, FM ;
GIACOMINI, KM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (01) :F141-F150