Effects of the antimicrobial peptide LL-37 and hyperthermic preconditioning in septic rats.
Torossian. Alexander A; Gurschi. Eugeniu E; Bals. Robert R; Vassiliou. Timon T; Wulf. Hinnerk F HF; Bauhofer. Artur A
Key Findings
- Therapeutic LL‑37 (0.5 mg/kg) after sepsis increased 120‑hour survival to ~70% versus 30% in untreated rats
- Prophylactic LL‑37 before sepsis gave modest benefit (55% survival)
- Combining LL‑37 therapy with hyperthermic preconditioning (41 °C for 1 h) yielded the highest survival (90%) and reduced pro‑inflammatory cytokines
Practical Outcomes
- While the data suggest LL‑37 could be a powerful immune‑modulating agent, the study is limited to rats and uses a dose and heat protocol not yet tested in humans. Biohackers should view this as a proof‑of‑concept rather than a ready‑to‑use supplement, and await human safety and dosing studies before considering any self‑experimentation.
Summary
In a rat study, giving the antimicrobial peptide LL‑37 after a severe abdominal infection boosted survival from 30% to about 70%, and giving it together with a short, high‑heat treatment (41 °C for an hour) raised survival even higher to 90%. The heat treatment alone didn’t help, but the combo lowered harmful inflammation markers. These results are promising but still early and done in animals, so they don’t translate directly into a safe, ready‑to‑use protocol for people.
Abstract
The authors tested the effects of LL-37 prophylaxis or therapy on the outcome after intraabdominal sepsis and examined whether hyperthermic preconditioning plus LL-37 therapy augments host immune response and improves survival. A rat model of peritoneal contamination and infection (PCI) with human stool was used to simulate clinical conditions. In trial 1, the authors compared (1) PCI, (2) LL-37 prophylaxis (0.5 mg/kg, 12 h before PCI), and (3) LL-37 therapy (0.5 mg/kg, 1 h after PCI). In trial 2, the authors compared (1) PCI, (2) LL-37 therapy, (3) hyperthermic preconditioning (41 degrees C for 1 h, 24 h before PCI), and (4) LL-37 therapy and hyperthermic preconditioning. The primary endpoint was mortality at 120 h. In trial 2, secondary endpoints were systemic levels of tumor necrosis factor alpha, interleukin 6, macrophage inflammatory protein 2, and heat shock protein 70; leukocyte counts; and neutrophil granulocyte phagocytosis. In trial 1, 30% of the control group compared with 70% of the LL-37 therapy group survived, but 55% after LL-37 prophylaxis survived (P = 0.038). In trial 2, 38% of the controls, 67% of the LL-37 therapy, 59% of the hyperthermic preconditioned, and 90% of the hyperthermic preconditioned plus LL-37 therapy group survived (P = 0.01). LL-37 therapy plus hyperthermic preconditioning reduced proinflammatory cytokine concentrations after sepsis; specifically compared with controls, macrophage inflammatory protein-2 and interleukin-6 levels were 1.5 +/- 1.5 versus 11 +/- 6 pg/ml (P = 0.028) and 13 +/- 8 versus 86 +/- 31 pg/ml, (P = 0.015), respectively. In this model of intraabdominal sepsis, LL-37 therapy improved outcome. Hyperthermic preconditioning per se was not successful, but in combination with LL-37 therapy, the survival rate after sepsis was increased and the proinflammatory cytokine response was downgraded.
Study Information
pubmed
2007
2007-09-01T00:00:00.000Z
10.1097/01.anes.0000278906.86815.eb
19
33