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It binds to actin and promotes cell migration including the mobilisation, migration, and differentiation of stem/progenitor cells that form new blood vessels and regenerate tissue

oriens interneurons, induction of LTP by theta-burst stimulation paired with postsynaptic depolarization was not affected at all by NMDAR blockade but prevented by blockers of group I/II metabotropic glutamate receptors (mGluR) or selective mGluR1a antagonists (Perez et al., 2+ influx needed for triggering LTP

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The human pilot study on BPC-157 found that it was tolerated well in doses of up to 20mg when given intravenously, and no adverse side effects were seen [14]

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