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BPC-157

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

Quick Stats
Studies 196
Trials 1
Score 2
2022 pubmed 7 citations

The anti-nociceptive effect of BPC-157 on the incisional pain model in rats.

Jung. Young-Hoon YH; Kim. Haekyu H; Kim. Hyaejin H; Kim. Eunsoo E; Baik. Jiseok J; Kang. Hyunjong H

Key Findings

  • BPC‑157 (10‑40 µg/kg) raised the pain‑threshold at 2 hours after surgery, similar to morphine, but the benefit disappeared by day 7.
  • A higher threshold persisted at day 4 for the BPC‑157 groups, indicating a modest mid‑term effect.
  • In the formalin test, BPC‑157 reduced early (phase 1) flinching but had no impact on the later (phase 2) inflammatory pain phase.

Practical Outcomes

  • BPC‑157 might provide a short‑lived boost in post‑operative pain relief, but it isn’t a strong or lasting analgesic. For biohackers looking to manage acute surgical pain, it’s not a substitute for proven analgesics like NSAIDs or opioids, and dosing in humans remains untested.

Summary

In rats, the peptide BPC‑157 lowered pain right after a skin incision, but the effect was brief and faded after a few days. It helped with the first burst of pain but didn’t reduce the later, inflammation‑driven pain that morphine can affect.

Abstract

The pentadecapeptide BPC-157 has been shown to have anti-inflammatory and wound healing effects on multiple target tissues and organs. Peptides have potent anti-inflammatory effects on periodontal tissues in rats with periodontitis. Few studies have investigated the effect of BPC-157 on pain after dental procedures or oral surgeries. The purpose of the present study was to investigate the antinociceptive effects of BPC-157 on postoperative incisional pain in rats. Sprague-Dawley rats were randomly divided into five groups: control (saline with the same volume), BPC10 (10 µg/kg of BPC-157), BPC20 (20 µg/kg of BPC-157), BPC40 (40 µg/kg of BPC-157), and morphine (5 mg/kg of morphine). A 1-cm longitudinal incision was made through the skin, fascia, and muscle of the plantar aspect of the hind paw in isoflurane-anesthetised rats. Withdrawal responses were measured using von Frey filaments at 0, 2, 6 h and 4, 7 d after incision. The formalin test was also performed to differentiate its anti-nociceptive effect from an inflammatory reaction or central sensitization. Pain behavior was quantified periodically in phases 1 and 2 by counting the number of flinches in the ipsilateral paw after injection with 30 µL of 5% formalin. The threshold of mechanical allodynia was significantly increased in the BPC10, BPC20, BPC40 and morphine groups compared with that in the control group at 2 h. These increasing thresholds then returned to the levels of the control group. The BPC-157 group showed a much higher threshold at 4 days after incision than the control group. The thresholds of the BPC groups, except the morphine group, were normalized 7 days after incision.The flinching numbers of the BPC10, BPC20, BPC40 and morphine groups were significantly decreased in phase 1, but there was no decrease in the BPC-157 groups except the morphine group in phase 2. BPC-157 was effective only for a short period after incision. It was also effective during phase 1 but not during phase 2, as determined by the formalin test. BPC-157 might have a short antinociceptive effect, even though it has anti-inflammatory and wound healing effects.

Study Information

Provider

pubmed

Year

2022

Date

2022-03-25T00:00:00.000Z

DOI

10.17245/jdapm.2022.22.2.97

Citations

7

References

37