Role of Brain-Derived Neurotrophic Factor for the Treatment of Glaucoma and Retinitis Pigmentosa

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Metal complexes increase uptake of Zn and Cu by plants: implications for uptake and deficiency studies in chelator-buffered solutions

The uptake of trace metals by plants is commonly assumed to depend on the free metal-ion activity, rather than on the total concentration of dissolved metal. Although this free-ion hypothesis has proved to be useful for the interpretation and prediction of metal uptake, several exceptions have been reported where metal complexes also affected metal uptake by plants. In this study, we measured uptake of Zn and Cu by spinach (Spinacia oleracea L.) and tomato (Lycopersicon esculentum L.) in chelator-buffered or resin (Chelex)-buffered solutions, under Zn-deficient and non-deficient conditions. Several ligands, with differing dissociation rates, were used in the chelator-buffered solutions. At the same free-ion activity, Cu and Zn uptake was less in Chelex-buffered than in chelator-buffered solutions. In the chelator-buffered solution, uptake of Cu and Zn at same free-ion activity and same total concentration followed the order: NTA > HEDTA > EDTA > CDTA, i.e., the same order as the dissociation rate. These differences in metal uptake were also reflected in the deficiency symptoms and plant yield in the experiments where Zn deficiency was imposed. The critical Zn2+ activity for Zn deficiency varied by one order of magnitude depending on the buffer, and followed the order HEDTA < CDTA < resin-buffered (no soluble ligand). These results suggest that, when present, aqueous complexes can increase metal uptake by plants because uptake is rate-limited by diffusion of the free ion to the root or cell surface. Thus, the critical free-ion activity in chelator-buffered solutions depends on the type and concentration of the ligand employed. © 2006 Springer Science+Business Media B.V.F. Degryse, E. Smolders, D. R. Parke

Cadmium uptake by durum wheat in presence of citrate

The aim of this study was to determine the mechanisms underlying the uptake of Cd by durum wheat (Triticum turgidum L. ssp. durum cv. “acalou”) in the presence of citrate under hydroponic conditions. Wheat seedlings were exposed for 3 h to simplified nutrient solutions initially containing 35 nM of free Cd with or without citrate. Uptake experiments with citrate alone were also performed. Solutions were radio labelled with 109Cd or citrate-14C. The depletion of Cd and citrate in the exposure solution was followed, and at the end of the exposure Cd and citrate were quantified in all compartments of the experimental system (root surface, inner roots and aerial parts). The apparent rates of internalization of Cd (r Cd) and citrate (r cit) were estimated from the ratio of the uptake flux to the contents adsorbed at the root surface. About two times more Cd was taken up in the presence of citrate. Assuming that citrate and Cd-citrate complexes were taken up at the same rate, a direct uptake of intact complexes could not account for the higher uptake of Cd in presence of citrate. In addition, Cd was internalized at the same rate in the absence or presence of citrate (r Cd = 3.62 h−1), whereas the internalization rate constants of Cd and citrate were different (r Cd ≈ 8 r cit). This strengthens the idea that a direct uptake of non-dissociated Cd-citrate complexes probably did not account for the higher Cd uptake in presence of citrate. A dissociation of Cd-citrate complexes within the diffusion layer or at the root surface and the subsequent additional supply of free Cd were more likely to explain the higher Cd uptake in presence of citrate