Aluminum exposure and metabolism

被引:115
作者
Greger, JL [1 ]
Sutherland, JE [1 ]
机构
[1] UNIV WISCONSIN, CTR ENVIRONM TOXICOL, MADISON, WI 53706 USA
关键词
aluminum; exposure; diet; pharmaceuticals; metabolism; absorption; citrate; calcium; iron; transferrin; tissue turnover; urine; bile; toxicity;
D O I
10.3109/10408369709006422
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Aluminum (Al) is a nonessential, toxic metal to which humans are frequently exposed. Oral exposure to aluminum occurs through ingestion of aluminum-containing pharmaceuticals and to a lesser extent foods and water. Parenteral exposure to aluminum can occur via contaminated total parenteral nutrition (TPN), intravenous (iv) solutions, or contaminated dialysates. Inhalation exposure may be important in some occupational settings. The gut is the most effective organ in preventing tissue aluminum accumulation after oral exposure. Typically gastrointestinal absorption of aluminum from diets is <1%. Although the mechanisms of aluminum absorption have not been elucidated, both passive and active transcellular processes and paracellular transport are believed to occur. Aluminum and calcium may share some absorptive pathways. Aluminum absorption is also affected by the speciation of aluminum and a variety of other substances, including citrate, in the gut milieu. Not all absorbed or parenterally delivered aluminum is excreted in urine. Low glomerular filtration of aluminum reflects that most aluminum in plasma is nonfilterable because of complexation to proteins, predominantly transferrin. The importance of biliary secretion of aluminum is debatable and the mechanism(s) is poorly understood and appears to be saturable by fairly low oral doses of aluminum.
引用
收藏
页码:439 / 474
页数:36
相关论文
共 295 条
[11]   PLASMA AND URINE ALUMINUM CONCENTRATIONS IN HEALTHY-SUBJECTS AFTER ADMINISTRATION OF SUCRALFATE [J].
ALLAIN, P ;
MAURAS, Y ;
KRARI, N ;
DUCHIER, J ;
COURNOT, A ;
LARCHEVEQUE, J .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 29 (04) :391-395
[12]   DISSIMILAR ALUMINUM AND GALLIUM PERMEATION OF THE BLOOD-BRAIN-BARRIER DEMONSTRATED BY INVIVO MICRODIALYSIS [J].
ALLEN, DD ;
YOKEL, RA .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) :903-908
[13]   IRON STATUS AFFECTS ALUMINUM UPTAKE AND TRANSPORT BY CACO-2 CELLS [J].
ALVAREZHERNANDEZ, X ;
MADIGOSKY, SR ;
STEWART, B ;
GLASS, J .
JOURNAL OF NUTRITION, 1994, 124 (09) :1574-1580
[14]   BIOACCUMULATION OF WATER-SOLUBLE ALUMINUM-CHLORIDE IN THE HIPPOCAMPUS AFTER TRANSDERMAL UPTAKE IN MICE [J].
ANANE, R ;
BONINI, M ;
GRAFEILLE, JM ;
CREPPY, EE .
ARCHIVES OF TOXICOLOGY, 1995, 69 (08) :568-571
[15]  
ANDERSEN JR, 1987, TRACE ELEM MED, V4, P42
[16]   TRANSFERRIN RECEPTOR DISTRIBUTION AND REGULATION IN THE RAT SMALL-INTESTINE - EFFECT OF IRON STORES AND ERYTHROPOIESIS [J].
ANDERSON, GJ ;
POWELL, LW ;
HALLIDAY, JW .
GASTROENTEROLOGY, 1990, 98 (03) :576-585
[17]   EARLY DEPOSITION OF ALUMINUM IN BONE IN DIABETIC-PATIENTS ON HEMODIALYSIS [J].
ANDRESS, DL ;
KOPP, JB ;
MALONEY, NA ;
COBURN, JW ;
SHERRARD, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (06) :292-296
[18]  
ANGHILERI LJ, 1994, ANN CLIN LAB SCI, V24, P22
[19]  
ARVANITAKIS C, 1988, CLIN NEPHROL, V29, P235
[20]  
BAKIR AA, 1989, CLIN NEPHROL, V31, P40