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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2005 pubmed 91 citations

Effect of antibacterial cathelicidin peptide CAP18/LL-37 on sepsis in neonatal rats.

Fukumoto. Koji K; Nagaoka. Isao I; Yamataka. Atsuyuki A; Kobayashi. Hiroyuki H; Yanai. Toshihiro T; Kato. Yoshifumi Y; Miyano. Takeshi T

Key Findings

  • LL‑37 given together with LPS reduced mortality in neonatal rats
  • Low doses of LL‑37 given 2 h after LPS lowered death rates, while high doses increased mortality
  • High preventive doses of LL‑37 eliminated deaths and lowered CRP levels

Practical Outcomes

  • LL‑37 shows promise for sepsis prevention, but the benefit is dose‑dependent and high post‑infection doses can be harmful. The results are from a rat model, so they aren’t directly applicable to humans yet. Biohackers should view this as early safety/efficacy data and wait for human studies before considering any self‑experimentation.

Summary

In newborn rats with a sepsis-like infection, the natural antimicrobial peptide LL‑37 helped some animals survive, especially when given at the same time as the infection or in low amounts later. However, giving too much LL‑37 after the infection actually made things worse, and the study was done only in rat pups, not people.

Abstract

Cathelicidins are a family of antibacterial peptides. Human cathelicidin LL-37 inhibits the binding of endotoxin lipopolysaccharide (LPS) to CD14-positive cells and could ameliorate sepsis. The aim of this study was to observe the effect of LL-37 on sepsis in neonatal rats. Intraperitoneal injection (IPI) of LPS was used to create sepsis in suckling rats. Group 1 rats were given LPS with LL-37, group 2 rats were given LL-37 2 h after LPS, and group 3 rats were given LPS without LL-37. Control group rats were given isovolemic normal saline by IPI. Rats given LL-37 IPI were divided into seven subgroups. Following IPI, an overall assessment score (OAS) and rectal temperature (RT) were assessed hourly. Serum C-reactive protein (CRP) was also assessed at death or at sacrifice 10 h after IPI. All rats in group 3 died. For rats receiving lower doses of LL-37 in groups 1 and 2, mortality was decreased. No deaths occurred among those receiving higher doses of LL-37 in group 1; however, mortality increased in group 2. In group 1, OAS and RT deteriorated initially for those receiving lower doses of LL-37, then improved. OAS and RT did not deteriorate throughout the study in rats given higher doses of LL-37. In group 2 rats given higher doses of LL-37, OAS and RT were not significantly different from rats in group 3. CRP was significantly decreased in group 1 compared with group 3, and decreased in group 2 for lower doses only. We conclude that LL-37 may prevent sepsis and be useful in lower doses for treating sepsis. However, LL-37 appears to have adverse effects when used at higher doses for treating sepsis.

Study Information

Provider

pubmed

Year

2005

DOI

10.1007/s00383-004-1256-x

Citations

91

References

21