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Updated: Aug 21, 2026
![Radiosynthesis of 1-(2-[18F]Fluoroethyl)-L-Tryptophan using a One-pot, Two-step Protocol](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F63025.jpg&w=3840&q=50)
Radiosynthesis of 1-(2-[18F]Fluoroethyl)-L-Tryptophan using a One-pot, Two-step Protocol
Published on: September 21, 2021
Kinetic Profiling of Tryptophan and Its Metabolites from Sheep Whey and Soy Protein Isolate in Rats: Toward
Haoyan Zhu1,2, Xinwei Tian1, Lulu Wang2
1Shaanxi Engineering Laboratory for Food Green Processing and Safety Control, and Shaanxi Key Laboratory for Hazard Factors Assessment in Processing and Storage of Agricultural Products, College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an710119, China.
Abstract:
Tryptophan (Trp) is essential for homeostasis, but direct intake may cause risks. This study compared metabolic kinetics between free Trp and protein-bound Trp from soy protein isolate (SPI) and sheep whey protein (SWP). A novel UPLC-TQ/MS assay was built to quantify Trp and its metabolites simultaneously: 5-hydroxytryptophan (5-HTP), kynurenic acid (Kyna), indole-3-acetic acid (IAA), and indole-3-propionic acid (IPA). Pharmacokinetic profiling showed free Trp peaked rapidly in rats. Tissue distribution exhibited distinct enrichment: Trp in heart and adipose, 5-HTP in kidney and epididymal fat, Kyna in kidney and brown fat, and IAA/IPA in brain. Relative to free Trp, SPI and SWP delayed metabolite release and boosted microbial Trp conversion to IAA and IPA. SPI activated the 5-hydroxytryptamine pathway, raising plasma 5-HTP and fecal IAA; SWP favored the kynurenine pathway, elevating plasma Kyna and fecal IPA. These findings highlight differential outcomes of free versus protein-bound Trp supplementation.
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