Stable gastric pentadecapeptide BPC 157 heals rat colovesical fistula.
Grgic. Tihomir T; Grgic. Dora D; Drmic. Domagoj D; Sever. Anita Zenko AZ; Petrovic. Igor I; Sucic. Mario M; Kokot. Antonio A; Klicek. Robert R; Sever. Marko M; Seiwerth. Sven S; Sikiric. Predrag P
Key Findings
- Oral BPC‑157 at 10 µg/kg daily healed colovesical fistulas in rats.
- Intraperitoneal BPC‑157 at 10 µg/kg or even 10 ng/kg also produced rapid, complete healing.
- Treated rats showed no fecal leakage, reduced adhesions, and no intestinal obstruction, unlike controls.
Practical Outcomes
- For biohackers interested in gut repair, this study suggests that very low doses of BPC‑157 might support healing of severe intestinal lesions. However, the data are from rats, so human dosing would need careful scaling and safety testing. Until human trials confirm these effects, any self‑experiment should proceed with caution and preferably under medical supervision.
Summary
In a rat study, the peptide BPC‑157 (a stable 15‑amino‑acid stomach peptide) was given either in the drinking water or by injection after surgically creating a connection between the colon and bladder. Both low‑dose oral (10 µg per kg body weight) and very low‑dose injection (10 µg or even 10 ng per kg) quickly repaired the holes, stopped leakage, and prevented scar tissue and blockages. The treated rats healed fully, while untreated rats kept having leaks and complications.
Abstract
To establish the effects of BPC 157 on the healing of rat colovesical fistulas, Wistar Albino male rats were randomly assigned to different groups. BPC 157, a stable gastric pentadecapeptide, has been used in clinical applications-specifically, in ulcerative colitis-and was successful in treating both external and internal fistulas. BPC 157 was provided daily, perorally, in drinking water (10µg/kg, 12ml/rat/day) until sacrifice or, alternatively, 10µg/kg or 10ng/kg intraperitoneally, with the first application at 30min after surgery and the last at 24h before sacrifice. Controls simultaneously received an equivolume of saline (5.0ml/kg ip) or water only (12ml/rat/day). Assessment (i.e., colon and vesical defects, fistula leaking, fecaluria and defecation through the fistula, adhesions and intestinal obstruction as healing processes) took place on days 7, 14 and 28. Control colovesical fistulas regularly exhibited poor healing, with both of the defects persisting; continuous fistula leakage; fecaluria and defecation through the fistula; advanced adhesion formation; and intestinal obstruction. By contrast, BPC 157 given perorally or intraperitoneally and in µg- and ng-regimens rapidly improved the whole presentation, with both colon and vesical defects simultaneously ameliorated and eventually healed. The maximal instilled volume was continuously raised until it reached the values of healthy rats, there were no signs of fecaluria and no defecation through the fistula, there was counteraction of advanced adhesion formation or there was an intestinal obstruction. In conclusion, BPC 157 effects appear to be suited to inducing full healing of colocutaneous fistulas in rats.
Study Information
pubmed
2016
2016-02-11T00:00:00.000Z
10.1016/j.ejphar.2016.02.038
21
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