PROTECTIVE MECHANISM OF SODIUM MOLYBDATE AGAINST THE ACUTE TOXICITY OF CADMIUM IN RATS .2. PREVENTION OF CYTOPLASMIC ACIDIFICATION

被引:7
作者
KOIZUMI, T [1 ]
YOKOTA, T [1 ]
FUKUCHI, M [1 ]
TATSUMOTO, H [1 ]
YAMANE, Y [1 ]
机构
[1] CHIBA UNIV,FAC ENGN,DEPT HUMAN ENVIRONM CHEM,CHIBA 260,JAPAN
关键词
CADMIUM; MOLYBDENUM; INTRACELLULAR PH; NA+/H+ EXCHANGER; CELLULAR ACIDIFICATION; FREE CYTOSOLIC CALCIUM;
D O I
10.1007/BF00124071
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In order to clarify the protective mechanism of sodium molybdate against the acute toxicity of cadmium chloride in rat, the effect of in vivo sodium molybdate pretreatment on the cytotoxic action of cadmium in isolated hepatocytes was studied. The cytosolic pH of hepatocytes isolated from untreated rats immediately decreased with incubation in either neutral Hank's balanced salt solution (HBS), pH 7.4, containing 5-mu-M cadmium chloride minimum or acidic HBS (pH 7.1, 6.8, 6.5, and 6.2). The presence of 5-mu-M cadmium in HBS adjusted to pH 7.1 aggravated cytosolic acidification induced by the acidic medium alone. Cell viability of hepatocytes incubated in HBS at pH 6.2 was significantly reduced as compared to that of control cells in HBS at pH 7.4, but the presence of cadmium in the acidic HBS had no aggravating action against such a toxic action of the acidic medium although cellular uptake of the metal in the medium increased, as compared to that in HBS at pH 7.4. Molybdenum pretreatment alleviated cytoplasmic acidification induced by the treatment with HBS at pH 7.4 or 7.1 containing cadmium or by extracellular acid load without cadmium. This pretreatment also prevented the loss of cell viability induced by the treatment with HBS at pH 6.2 but could not attenuate that when cadmium was present in the medium. These facts suggest that molybdenum pretreatment alleviated the acute toxicity of cadmium in rat by preventing cytoplasmic acidification caused by the harmful metal.
引用
收藏
页码:357 / 369
页数:13
相关论文
共 38 条
[1]  
ANKE M, 1977, 3RD TRAC EL MET MAN, P230
[2]  
BABCOCK DF, 1983, J BIOL CHEM, V258, P6380
[3]   OPTICAL MEASUREMENTS OF INTRACELLULAR PH IN SINGLE LLC-PK1 CELLS - DEMONSTRATION OF CL-HCO3 EXCHANGE [J].
CHAILLET, JR ;
AMSLER, K ;
BORON, WF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (02) :522-526
[4]  
COHEN HJ, 1971, J BIOL CHEM, V246, P359
[5]  
DERENZO EC, 1953, J AM CHEM SOC, V75, P753, DOI 10.1021/ja01099a515
[6]   TIME COURSE OF CADMIUM-INDUCED ULTRASTRUCTURAL-CHANGES IN RAT-LIVER [J].
DUDLEY, RE ;
SVOBODA, DJ ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1984, 76 (01) :150-160
[7]   THE REGULATION OF THE INTRACELLULAR PH IN CELLS FROM VERTEBRATES [J].
FRELIN, C ;
VIGNE, P ;
LADOUX, A ;
LAZDUNSKI, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (01) :3-14
[8]  
FURGUSON WS, 1943, J AGR SCI, V33, P44
[9]   CHEMICAL MODIFICATION OF THE NA+-H+ EXCHANGER OF THYMIC LYMPHOCYTES - INHIBITION BY N-ETHYLMALEIMIDE [J].
GRINSTEIN, S ;
COHEN, S ;
ROTHSTEIN, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 812 (01) :213-222
[10]   NA+/H+ EXCHANGE AND GROWTH FACTOR-INDUCED CYTOSOLIC PH CHANGES - ROLE IN CELLULAR PROLIFERATION [J].
GRINSTEIN, S ;
ROTIN, D ;
MASON, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 988 (01) :73-97