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[4] This inquiry largely examined the variations in levels of substance P, beta-endorphin, and corticosteronekey biomarkers relevant for decoding the stress response and the potential regulatory actions of DSIP

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Our analysis indicates that pathways related to energy metabolism (e.g., fatty acid metabolism, mitochondrial electron transport chain, TCA cycle) and amino acid metabolism (e.g., branched-chain amino acids, phenylalanine, tyrosine, and tryptophan) were particularly affected

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