Copper transport

被引:234
作者
Linder, MC [1 ]
Wooten, L
Cerveza, P
Cotton, S
Shulze, R
Lomeli, N
机构
[1] Calif State Univ Fullerton, Dept Chem & Biochem, Fullerton, CA 92834 USA
[2] Calif State Univ Fullerton, Inst Mol Biol & Nutr, Fullerton, CA 92834 USA
关键词
copper transport; ceruloplasmin; albumin; transcuprein; milk; turnover; lactation; mammary gland; humans;
D O I
10.1093/ajcn/67.5.965S
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
In adult humans, the net absorption of dietary copper is approximate to 1 mg/d. Dietary copper joins some 4-5 mg of endogenous copper flowing into the gastrointestinal tract through various digestive juices. Most of this copper returns to the circulation and to the tissues (including liver) that formed them. Much lower amounts of copper flow into and out of other major parts of the body (including heart, skeletal muscle, and brain). Newly absorbed copper is transported to body tissues in two phases, borne primarily by plasma protein carriers (albumin, transcuprein, and ceruloplasmin). In the first phase, copper goes from the intestine to the liver and kidney; in the second phase, copper usually goes from the liver land perhaps also the kidney) to other organs. Ceruloplasmin plays a role in this second phase. Alternatively, liver copper can also exit via the bile, and in a form that is less easily reabsorbed. Copper is also present in and transported by other body fluids, including those bathing the brain and central nervous system and surrounding the fetus in the amniotic sac. Ceruloplasmin is present in these fluids and may also be involved in copper transport there. The concentrations of copper and ceruloplasmin in milk vary with lactational stage. Parallel changes occur in ceruloplasmin messenger RNA expression in the mammary gland las determined in pigs). Copper in milk ceruloplasmin appears to be particularly available for absorption, at least in rats.
引用
收藏
页码:965S / 971S
页数:7
相关论文
共 44 条
[1]   COPPER UPTAKE AND INTRACELLULAR-DISTRIBUTION DURING RETINOIC ACID-INDUCED DIFFERENTIATION OF HL-60 CELLS [J].
BAE, B ;
PERCIVAL, SS .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1994, 5 (09) :457-461
[2]   COPPER DISTRIBUTION AMONG SERUM-PROTEINS IN PEDIATRIC LIVER DISORDERS AND MALIGNANCIES [J].
BARROW, L ;
TANNER, MS .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1988, 18 (06) :555-560
[3]  
BRESLOW E, 1964, J BIOL CHEM, V239, P3252
[4]   THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J].
BULL, PC ;
THOMAS, GR ;
ROMMENS, JM ;
FORBES, JR ;
COX, DW .
NATURE GENETICS, 1993, 5 (04) :327-337
[5]  
CAMPBELL CH, 1981, BIOCHIM BIOPHYS ACTA, V678, P27
[6]   COPPER AND CERULOPLASMIN ACTIVITY IN HUMAN AMNIOTIC-FLUID [J].
CHAN, WY ;
RICHICHI, J ;
GRIESMANN, GE ;
CUSHING, W ;
KLING, OR ;
RENNERT, OM .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1980, 138 (03) :257-259
[7]  
DARWISH HM, 1984, AM J PHYSIOL, V246, pG72
[8]   CHARACTERIZATION OF A PARTICULATE PATHWAY FOR COPPER IN K562 CELLS [J].
DAVIDSON, LA ;
MCORMOND, SL ;
HARRIS, ED .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1994, 1221 (01) :1-6
[9]   KINETICS OF COPPER-METABOLISM IN RATS - A COMPARTMENTAL MODEL [J].
DUNN, MA ;
GREEN, MH ;
LEACH, RM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (01) :E115-E125
[10]  
ETTINGER MJ, 1986, FASEB J, V45, P2800