Animal study demonstrates that heat-treated soy protein isolate reduces amino acid bioavailability and impairs social novelty in mice, suggesting disrupted tryptophan metabolism.
High-temperature (HT) treatments above 100 °C are important in food processing; however, their effects on the nutritional value of moist heat-treated proteins are less understood. Therefore, this study examined the impact of HT at 121 °C on soy protein isolate (SPI) in water. After 20 min of HT treatment, most amino acid levels in SPI decreased significantly, despite minimal nitrogen loss. HT also increased insoluble protein and larger soluble peptides after in vitro digestion. Mice administered HT-treated SPI showed lower serum levels of free amino acids, thereby reducing bioavailability. Long-term feeding with a 20% protein diet based on HT-treated SPI impaired social novelty recognition and decreased peripheral serotonin levels, while anxiety-like behavior, object close-range exploration, sociability, and serum tryptophan (Trp) remained unaffected. These findings indicate that HT treatment not only reduces the nutritional value of SPI but may also generate Maillard-type compounds or modified peptides that interfere with Trp metabolism and social behavior.
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Asai et al. (2026) studied this question.
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