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These observations suggest that the actions of DSIP on substance P, beta-endorphin, and corticosterone are indicative of a wider array of biochemical modifications, proposing that DSIP may trigger a cascade of molecular events that may facilitate its stress-modulatory functions

The oral route delivers BPC-157 through the GI tract, which is where the original peptide sequence was identified and where its gastroprotective properties are most mechanistically direct

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24 h) significantly increases the viability of Sprague-Dawley rat Achilles tendon fibroblasts cultured under oxidative stress induced by 0.1 mM H 2 O 2 [1]