Schechter P J, Prakash N J
Am J Clin Nutr. 1979 May;32(5):1011-4. doi: 10.1093/ajcn/32.5.1011.
L-Histidine, 4 g/day in gelatin capsules, was administered orally to eight normal volunteers for 2 weeks in a double-blind, balanced, crossover study with 2 weeks of placebo treatment. Body weight, serum and urinary zinc and histidine concentrations, as well as subjective ratings of appetite, taste and smell perception, and food intake were monitored. L-Histidine therapy had no significant effect on appetite, taste and smell perception, food intake, or body weight. Similarly, no effects were observed on total serum zinc, albumin-bound zinc or alpha 2-macroglobulin-bound zinc concentrations, or on urinary histidine excretion. Serum histidine concentrations increased with therapy. Urinary zinc excretion was increased significantly after 1 week, but not after 2 weeks of L-histidine therapy. It can be concluded that oral L-histidine, at the dose used, has no value as an anorectic agent.
在一项双盲、平衡、交叉研究中,对8名正常志愿者进行了为期2周的口服L-组氨酸(以明胶胶囊形式,每日4克)治疗,并穿插2周的安慰剂治疗。监测了体重、血清和尿液中的锌及组氨酸浓度,以及食欲、味觉和嗅觉的主观评分和食物摄入量。L-组氨酸治疗对食欲、味觉和嗅觉、食物摄入量或体重均无显著影响。同样,对血清总锌、白蛋白结合锌或α2-巨球蛋白结合锌浓度,以及尿组氨酸排泄也未观察到影响。血清组氨酸浓度随治疗而升高。L-组氨酸治疗1周后尿锌排泄显著增加,但2周后未增加。可以得出结论,所用剂量的口服L-组氨酸作为一种食欲抑制剂没有价值。