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BPC-157

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

Quick Stats
Studies 196
Trials 1
Score 4
2013 pubmed 57 citations

Mortal hyperkalemia disturbances in rats are NO-system related. The life saving effect of pentadecapeptide BPC 157.

Barisic. Ivan I; Balenovic. Diana D; Klicek. Robert R; Radic. Bozo B; Nikitovic. Bojana B; Drmic. Domagoj D; Udovicic. Mario M; Strinic. Dean D; Bardak. Darija D; Berkopic. Lidija L; Djuzel. Viktor V; Sever. Marko M; Cvjetko. Ivan I; Romic. Zeljko Z; Sindic. Aleksandra A; Bencic. Martina Lovric ML; Seiwerth. Sven S; Sikiric. Predrag P

Key Findings

  • BPC‑157 at ultra‑low doses (10 ng‑10 µg) fully prevented death from massive KCl (9 mEq/kg IP) in rats, restoring normal sinus rhythm within an hour.
  • The peptide was effective when administered 30 min before or as soon as 10 min after the potassium load, via intraperitoneal injection or oral gavage.
  • In HEK293 cells, BPC‑157 directly modulated potassium conductance, counteracting membrane depolarization caused by high extracellular potassium.

Practical Outcomes

  • For biohackers, BPC‑157 could be investigated as a rapid rescue agent for acute potassium overload or hyperkalemia, but human dosing and safety are untested. The data suggest a single low‑dose (microgram range) given orally or by injection might work within minutes. Until clinical trials confirm it, use only in experimental or veterinary contexts and consider it a hypothesis‑generating finding.

Summary

In rats, a tiny amount of the peptide BPC‑157 (10 ng‑10 µg) completely rescued animals from a lethal potassium overdose, fixing heart rhythm, blood pressure and muscle weakness. It worked whether given before the overdose or just minutes after, and it was effective both by injection and by mouth. In lab cells, BPC‑157 directly helped potassium channels stay normal, showing a possible direct anti‑hyperkalemia action.

Abstract

We demonstrate the full counteracting ability of stable gastric pentadecapeptide BPC 157 against KCl-overdose (intraperitoneal (i), intragastric (ii), in vitro (iii)), NO-system related. (i) We demonstrated potential (/kg) of: BPC 157 (10ng, 10μg ip, complete counteraction), l-arginine (100mg ip, attenuation) vs. L-NAME (5mg ip, deadly aggravation), given alone and/or combined, before or after intraperitoneal KCl-solution application (9mEq/kg). Therapy was confronted with promptly unrelenting hyperkalemia (>12mmol/L), arrhythmias (and muscular weakness, hypertension, low pressure in lower esophageal and pyloric sphincter) with an ultimate and a regularly inevitable lethal outcome within 30min. Previously, we established BPC 157-NO-system interaction; now, a huge life-saving potential. Given 30min before KCl, all BPC 157 regimens regained sinus rhythm, had less prolongation of QRS, and had no asystolic pause. BPC 157 therapy, given 10min after KCl-application, starts the rescue within 5-10min, completely restoring normal sinus rhythm at 1h. Likewise, other hyperkalemia-disturbances (muscular weakness, hypertension, low sphincteric pressure) were also counteracted. Accordingly with NO-system relation, deadly aggravation by L-NAME: l-arginine brings the values to the control levels while BPC 157 always completely nullified lesions, markedly below those of controls. Combined with l-arginine, BPC 157 exhibited no additive effect. (ii) Intragastric KCl-solution application (27mEq/kg) - (hyperkalemia 7mmol/L): severe stomach mucosal lesions, sphincter failure and peaked T waves were fully counteracted by intragastric BPC 157 (10ng, 10μg) application, given 30min before or 10min after KCl. (iii). In HEK293 cells, hyperkalemic conditions (18.6mM potassium concentrations), BPC 157 directly affects potassium conductance, counteracting the effect on membrane potential and depolarizations caused by hyperkalemic conditions.

Study Information

Provider

pubmed

Year

2013

Date

2013-01-14T00:00:00.000Z

DOI

10.1016/j.regpep.2012.12.007

Citations

57

References

42