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BPC-157

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

Quick Stats
Studies 196
Trials 1
Score 2
2023 pubmed 6 citations

From Selye's and Szabo's Cysteamine-Duodenal Ulcer in Rats to Dopamine in the Stomach: Therapy Significance and Possibilities.

Sikiric. Predrag P; Boban Blagaic. Alenka A; Krezic. Ivan I; Zizek. Helena H; Kalogjera. Luka L; Smoday. Ivan Maria IM; Vukovic. Vlasta V; Oroz. Katarina K; Chiddenton. Helen Marie HM; Buric. Sara S; Antunovic. Marko M; Gojkovic. Slaven S; Strbe. Sanja S; Skocic. Milena M; Sikiric. Suncana S; Milavic. Marija M; Beketic Oreskovic. Lidija L; Kokot. Antonio A; Koprivanac. Antun A; Dobric. Ivan I; Sever. Marko M; Staresinic. Mario M; Batelja Vuletic. Lovorka L; Skrtic. Anita A; Seiwerth. Sven S

Key Findings

  • Dopamine agonists tend to protect against and heal gastric ulcers, while dopamine antagonists can cause ulcers but might pre‑condition tissue against bigger injuries.
  • BPC‑157 is highlighted as a stable peptide that could mediate the beneficial dopamine effects on the gut.
  • The authors suggest that targeting dopamine pathways could be a strategy for treating lower gastrointestinal issues.

Practical Outcomes

  • For biohackers, the review hints that BPC‑157 might support gut healing via dopamine mechanisms, but it provides no concrete dosing or protocol. Until more direct human studies appear, the information is mostly theoretical and not ready for immediate self‑experimentation.

Summary

The paper reviews how dopamine and dopamine‑acting drugs affect stomach ulcer healing and mentions that the peptide BPC‑157 might work as a bridge in this dopamine‑gut connection. It mainly discusses theory and past animal studies, not new human data or dosing instructions.

Abstract

We reviewed gastric ulcer healing by dopamine considering several distinctive duodenal key points. Selye and Szabo describe the cysteamine-induced duodenal ulcer in rats as a duodenal stress ulcer in patients. Szabo's cysteamine duodenal ulcer as the dopamine duodenal healing and cysteamine as a dopamine antagonist signifies the dopamine agonists anti-ulcer effect and dopamine antagonists ulcerogenic effect. From these viewpoints, we focused on dopamine and gastric ulcer healing. We mentioned antecedent studies on the dopamine presence in the stomach and gastric juice. Then we reviewed, in the timeline, therapy significance arising from the anti-ulcer potency of the various dopamine agonists, which is highly prevailing over the quite persistent beneficial evidence arising from the various dopamine antagonists. Meanwhile, the beneficial effects of several peptides (i.e., amylin, cholecystokinin, leptin, and stable gastric pentadecapeptide BPC 157, suggested as an acting mediator of the dopamine brain-gut axis) were included in the dopamine gastric ulcer story. We attempt to resolve dopamine agonists/antagonists issue with the dopamine significance in the stress (cysteamine as a prototype of the duodenal stress ulcer), and cytoprotection (cysteamine in small dose as a prototype of the cytoprotective agents; cysteamine duodenal ulcer in gastrectomized rats). Thereby, along with dopamine agonists' beneficial effects, in special circumstances, dopamine antagonists having their own ulcerogenic effect may act as "mild stress (or)" or "small irritant" counteracting subsequent strong alcohol or stress procedure-induced severe lesions in this particular tissue. Finally, in the conclusion, as a new improvement in further therapy, we emphasized the advantages of the dopamine agents' application in lower gastrointestinal tract therapy.

Study Information

Provider

pubmed

Year

2023

Date

2023-12-07T00:00:00.000Z

DOI

10.3390/ph16121699

Citations

6

References

116