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In doing so, it promotes retention of metallothionein-bound copper in the enterocyte that will then be excreted in the feces when the enterocyte is shed.11 It is on this basis that zinc was postulated to reduce intestinal copper absorption and became a modality of treatment for Wilsons

Fibroblast Migration and Collagen Synthesis Fibroblasts are responsible for laying down collagen during tissue repair

This selective action represents sophisticated biological intelligence, promoting healthy tissue growth while suppressing diseased cell proliferation

Angiogenesis and VEGF Signalling Research indicates BPC-157 may upregulate vascular endothelial growth factor (VEGF) pathways in experimental models, contributing to: Capillary formation Accelerated wound closure Improved microvascular repair Reference: Hsieh et al., 2017 Angiogenic mechanisms in BPC 157-treated tissues PubMed: 3

PL BioScience has advanced an oral BPC-157 formulation (designated PL-10) to Phase II clinical trials for inflammatory bowel disease representing the most clinically advanced human development of oral BPC-157 to date.3 Human peer-reviewed results from these trials are pending, but the preclinical rationale is strong