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The **sodium-dependent vitamin C transporters** SVCT1 (SLC23A1) and SVCT2 (SLC23A2) are primary ascorbate transporters in mammals, regulating cellular uptake and distribution of vitamin C. SVCT1 is predominantly expressed in epithelial tissues (notably kidney, mediating renal reabsorption of ascorbate), while SVCT2 is widely expressed in non-epithelial tissues including the brain. These hydrophobic membrane proteins belong to the nucleobase-ascorbate transporter (NAT) family and operate via a sodium-dependent symport mechanism, coupling the movement of ascorbate against its concentration gradient to the inward flow of sodium ions generated by the Na+/K+ ATPase. They are critical for maintaining the high intracellular concentrations of ascorbate required for antioxidant defense, modulation of oxidative stress, and overall physiological health. Loss of function of SVCT transporters is incompatible with survival in model organisms, and their dysfunction may contribute to neurological, cardiovascular, and other diseases associated with vitamin C deficiency[3][4][7].
Sodium gradient-driven co-transport of ascorbate across cell membranes Coupling inward movement of ascorbate with sodium ions
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