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A broader mechanistic review by Seiwerth and colleagues in Current Pharmaceutical Design laid out how BPC-157 seems to borrow the same angiogenic and growth-factor pathways the body uses to heal the gut, and apply them to tendon, ligament, muscle, and bone (Seiwerth et al., 2018)

Ultra-accelerated injury repair dramatically speeds healing of muscle tears, tendinitis, sprains and ligament damage, slashing post-surgery and post-training recovery times Digestive system healing (leaky gut) brutal cytoprotective properties repair stomach and intestinal walls, making it a key ally against leaky gut syndrome, gastric reflux, ulcers and IBD (Crohn's, colitis) Joint and bone health promotes bone healing, bone density and cartilage health in worn joints, going far beyond soft-tissue repair Nervous system and organ protection helps protect the liver against toxins (including alcohol) and promotes neuroprotection, balancing neurotransmitters and modulating brain inflammation Gastric-origin advantage derived from gastric juice, it carries innate cytoprotective properties that simultaneously protect the stomach lining while healing the rest of the body Technical sheet

However, rigorous clinical trials specifically testing BPC-157 for eczema in humans are not yet available

Because KPV offers the anti-inflammatory properties of alpha-MSH without being pigment-inducing, it is a good candidate for wound healing without changing the characteristics of the skin

[DOI] [PubMed] [Google Scholar] Miller LG

Later, the same group confirmed HDAC inhibition by SFN in vivo , using the adenomatous polyposis coli multiple intestinal neoplasia mouse model that had ingested 443 mg SFN/kg (about 6 mol SFN/d) for 70 d, and observed the re-expression of p21 and bax genes that triggered cell-cycle arrest and apoptosis in transformed cells and microadenomas, thereby suppressing polyp formation compared with controls ( Reference Myzak, Dashwood and Orner 54 )