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BPC-157

Body Protection Compound-157, PL-14736, Pentadecapeptide BPC 157

Quick Stats
Studies 196
Trials 1
Score 3
2009 pubmed

Antiinflammatory effect of BPC 157 on experimental periodontitis in rats.

Keremi. B B; Lohinai. Z Z; Komora. P P; Duhaj. S S; Borsi. K K; Jobbagy-Ovari. G G; Kallo. K K; Szekely. A D AD; Fazekas. A A; Dobo-Nagy. C C; Sikiric. P P; Varga. G G

Key Findings

  • BPC‑157 did not affect gingival blood flow in healthy tissue
  • In rats with ligature‑induced periodontitis, BPC‑157 reduced plasma extravasation and histological signs of inflammation
  • Systemic BPC‑157 treatment markedly decreased alveolar bone loss in the disease model

Practical Outcomes

  • The result hints that BPC‑157 could someday be used to combat gum inflammation and bone loss, but the data are limited to rats and no human dosing or safety info is available. Enthusiasts should treat this as early‑stage evidence and wait for clinical trials before adding it to a personal protocol.

Summary

In a rat study, daily injections of the peptide BPC‑157 for 12 days didn’t change normal gum blood flow, but it dramatically cut inflammation, fluid leakage, and bone loss caused by experimentally induced gum disease. This suggests the peptide has strong anti‑inflammatory effects in the mouth, at least in animals.

Abstract

The pentadecapeptide BPC 157 has been shown to have anti-inflammatory and wound healing effects on multiple target tissues and organs. The purpose of the present study was to investigate the effect of BPC 157 on inflammation and bone resorption in experimental periodontitis in rats. First the acute effect of BPC was tested on gingival blood flow by laser doppler flowmetry. Then periodontitis was produced by a silk ligature placed around the lower left first molar. Rats were treated with BPC 157 (once daily for 12 days) or vehicle. At day 13, the gingivomucosal tissues encircling the molars were removed on both sides. Inflammation was assessed by Evans blue plasma extravasation technique and by histology. Alveolar bone loss was analyzed by microCT. BPC 157 had no effect on gingivomucosal blood flow. Twelve day ligature caused a significantly increased Evans blue extravasation in the gingivomucosal tissue, histological signs of inflammation, and alveolar bone destruction. BPC 157 treatment significantly reduced both plasma extravasation, histological alterations and alveolar bone resorption. In conclusion, systemic application of BPC 157 does not alter blood circulation in healthy gingiva. Chronic application of the peptide has potent antiinflammatory effects on periodontal tissues in ligature induced periodontitis in rats. Taken together, this proof of concept study suggests that BPC 157 may represent a new peptide candidate in the treatment of periodontal disease.

Study Information

Provider

pubmed

Year

2009