The continuing thrust of our research effort is to understand the biochemistry, physiology and nutrition of iron and other trace elements, particulary copper, zinc and manganese. Trace element requirements, homeostasis, and ultimate functions have been meticulously reviewed. However, the detailed events at the cell membrane and within cells which determine the availability of the elements to their respective enzymes and/or tissues has not been documented. We seek to elucidate the specific mechanisms involved in the absorption, storage, utilization and excretion of trace metals from mammalian systems. Our goal is to explain iron and other trace element metabolism in terms of the solution chemistry of the metal ions, their interaction, and the biochemistry of specific metal binding and transporting proteins and low-molecular weight ligands. Our commitment is to apply this knowledge both to the detection and prevention of pathological and nutritional disorders of trace element metabolism. There are four main aspects of our continuing studies: 1. To define the mechanism of interaction among trace elements during dietary assimilation. 2. To study the effect of low-molecular weight ligands on the mechanism of transmembrane transport of iron and other trace metals. Particular attention will be given to the ability of these chelating agents to """"""""steer"""""""" trace elements to specific tissues. 3. To determine the potential interrelationships of copper and ascorbic acid in the regulation and control of iron metabolism. 4. To study the biological mechanisms whereby ferric (III) iron may be reduced to ferrous (II) iron under aerobic conditions. 5. To continue our collaborative studies on the nutrition of iron and copper fortification of school lunch programs in Durango, Mexico.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM012386-18
Application #
3150823
Study Section
Nutrition Study Section (NTN)
Project Start
1977-05-01
Project End
1986-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
18
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Arts and Sciences
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Saltman, P D; Strause, L G (1993) The role of trace minerals in osteoporosis. J Am Coll Nutr 12:384-9
Bakan, D A; Saltman, P; Theriault, Y et al. (1991) Kinetics and mechanisms of reduction of Cu(II) and Fe(III) complexes by soybean leghemoglobin alpha. Biochim Biophys Acta 1079:182-96
Powell, S; Saltman, P; Uretzky, G et al. (1990) The effect of zinc on reperfusion arrhythmias in the isolated perfused rat heart. Free Radic Biol Med 8:33-46
Gelvan, D; Saltman, P (1990) Different cellular targets for Cu- and Fe-catalyzed oxidation observed using a Cu-compatible thiobarbituric acid assay. Biochim Biophys Acta 1035:353-60
Saltman, P (1989) Oxidative stress: a radical view. Semin Hematol 26:249-56
O'Connor, D T; Strause, L; Saltman, P et al. (1987) Serum zinc is unaffected by effective captopril treatment of hypertension. J Clin Hypertens 3:405-8
Reid, L S; Gray, H B; Dalvit, C et al. (1987) Electron transfer from cytochrome b5 to iron and copper complexes. Biochemistry 26:7102-7
Dyke, B; Hegenauer, J; Saltman, P et al. (1987) Isolation and characterization of a new zinc-binding protein from albacore tuna plasma. Biochemistry 26:3228-34
Strause, L; Saltman, P; Glowacki, J (1987) The effect of deficiencies of manganese and copper on osteoinduction and on resorption of bone particles in rats. Calcif Tissue Int 41:145-50
Hegetschweiler, K; Saltman, P; Dalvit, C et al. (1987) Kinetics and mechanisms of the oxidation of myoglobin by Fe(III) and Cu(II) complexes. Biochim Biophys Acta 912:384-97

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