The rate of kidney protein turnover in humans is not known. To this aim, we have measured kidney protein synthesis and degradation in postabsorptive humans using the arterio-venous catheterization technique combined with 14 C-leucine, 15 N-leucine, and 3 H-phenylalanine tracer infusions. These measurements were compared with those obtained across the splanchnic bed, the legs ( Ϸ muscle) and in the whole body. In the kidneys, protein balance was negative, as the rate of leucine release from protein degradation (16.8 Ϯ 5.1 mol/min и 1.73 m 2 ) was greater ( P Ͻ 0.02) than its uptake into protein synthesis (11.6 Ϯ 5.1 mol/min и 1.73 m 2 ). Splanchnic net protein balance was Ϸ 0 since leucine from protein degradation (32.1 Ϯ 9.9 mol/min и 1.73 m 2 ) and leucine into protein synthesis (30.8 Ϯ 11.5 mol/min и 1.73 m 2 ) were not different. In the legs, degradation exceeded synthesis (27.4 Ϯ 6.6 vs. 20.3 Ϯ 6.5 mol/min и 1.73 m 2 , P Ͻ 0.02). The kidneys extracted ␣ -ketoisocaproic acid, accounting for Ϸ 70% of net splanchnic ␣ -ketoisocaproic acid release. The contributions by the kidneys to whole-body leucine rate of appearance, utilization for protein synthesis, and oxidation were Ϸ 11%, Ϸ 10%, and Ϸ 26%, respectively; those by the splanchnic area Ϸ 22%, Ϸ 27%, and Ϸ 18%; those from estimated total skeletal muscle Ϸ 37%, Ϸ 34%, and Ϸ 48%. Estimated fractional protein synthetic rates were Ϸ 42%/d in the kidneys, Ϸ 12% in the splanchnic area, and Ϸ 1.5% in muscle. This study reports the first estimates of kidney protein synthesis and degradation in humans, also in comparison with those measured in the splanchnic area, the legs, and the whole-body.