INHIBITION OF NA+-GLUCOSE COTRANSPORT IN KIDNEY CORTICAL-CELLS BY CADMIUM AND COPPER - PROTECTION BY ZINC

被引:17
作者
BLUMENTHAL, S
LEWAND, D
SOCHANIK, A
KREZOSKI, S
PETERING, DH
机构
[1] UNIV WISCONSIN, DEPT CHEM, MILWAUKEE, WI 53201 USA
[2] MED COLL WISCONSIN, MILWAUKEE, WI 53226 USA
[3] VET ADM MED CTR, DEPT NEPHROL, MILWAUKEE, WI 53295 USA
关键词
D O I
10.1006/taap.1994.1242
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Properties of the inhibition of Na+-glucose cotransport by Cd2+ in mouse kidney cortical cells have been determined. In no case was any inhibition observed before 3 hr. The extent of inhibition was dependent upon both the concentration of Cd2+ and the length of exposure. Kinetic studies showed that metallothionein mRNA induction by Cd2+ was initiated within 1 hr after incubation with Cd2+ began and peaked by 3-6 hr. Metallothionein protein increased more slowly, beginning at 3 hr and continuing for at least 9 hr. The protein had both Cd2+ and Zn2+ bound to it throughout this period. Nevertheless, a pool of nonmetallothionein Cd2+ appeared after 3 hr, coinciding with the onset of inhibition of Na+-glucose cotransport, and increased over the next 9 hr. Pretreatment of cells with Zn2+ protected them from the effects of Cd2+ on Na+-glucose cotransport. It delayed the onset of inhibition of transport as well as the extent of inhibition. Detailed analysis of the distribution of Cd2+ and Zn2+ in the soluble fraction of these cells showed that the concentration of non-metallothionein bound Cd2+ was not suppressed by the presence of Zn-metallothionein after the onset of exposure to Cd2+ Incubation of cells with larger concentration of Zn2+ and Cu2+ also inhibited Na+-glucose cotransport. (C) 1994 Academic Press, Inc.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 31 条
[1]  
ADAMS RG, 1969, Q J MED, V38, P425
[2]  
Ausubel FM., 1988, CURRENT PROTOCOLS MO
[3]   AMPLIFICATION OF THE METALLOTHIONEIN-I GENE IN CADMIUM-RESISTANT MOUSE CELLS [J].
BEACH, LR ;
PALMITER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (04) :2110-2114
[4]   RENAL FUNCTION IN WILSONS DISEASE [J].
BEARN, AG ;
YU, TF ;
GUTMAN, AB .
JOURNAL OF CLINICAL INVESTIGATION, 1957, 36 (07) :1107-1114
[5]   CADMIUM INHIBITS GLUCOSE-UPTAKE IN PRIMARY CULTURES OF MOUSE CORTICAL TUBULE CELLS [J].
BLUMENTHAL, SS ;
LEWAND, DL ;
BUDAY, MA ;
KLEINMAN, JG ;
KREZOSKI, SK ;
PETERING, DH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (06) :F1625-F1633
[6]   THE PHYSIOLOGICAL-FUNCTION OF METALLOTHIONEIN [J].
BRADY, FO .
TRENDS IN BIOCHEMICAL SCIENCES, 1982, 7 (04) :143-145
[7]   OXIDATIVE STRESS-INDUCED BY A COPPER THIOSEMICARBAZONE COMPLEX [J].
BYRNES, RW ;
MOHAN, M ;
ANTHOLINE, WE ;
XU, RX ;
PETERING, DH .
BIOCHEMISTRY, 1990, 29 (30) :7046-7053
[8]   INTERACTIONS OF 1,10-PHENANTHROLINE AND ITS COPPER COMPLEX WITH EHRLICH CELLS [J].
BYRNES, RW ;
ANTHOLINE, WE ;
PETERING, DH .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 12 (06) :457-469
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]   INVIVO AND EXVIVO DISPLACEMENT OF ZINC FROM METALLOTHIONEIN BY CADMIUM AND BY MERCURY [J].
DAY, FA ;
FUNK, AE ;
BRADY, FO .
CHEMICO-BIOLOGICAL INTERACTIONS, 1984, 50 (02) :159-174