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massive intestinal resection leading to short bowel, and functional incapability of the post-anastomotic remained intestine, all together indicate most improvement achieved by BPC 157 regimens, per-orally, parenterally and locally (10, 11, 35, 42, 43)

A 2011 study found BPC-157 accelerated healing of colitis in rats and reduced inflammatory markers, with effects comparable to or exceeding standard anti-inflammatory treatments

GHK-Cu has a substantially larger research base

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Sikiric et al., 2020b), along with suggested significance of NO-synthase and the basal formation of NO in stomach mucosa, greater than that seen in other tissues (Whittle et al., 1992), BPC 157 exhibits a general, effective competing with both L-arginine analogs (i.e., L-NAME) and L-arginine (Sikiric et al., 2014)