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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 4
2015 pubmed

Exercise, but not acute sleep loss, increases salivary antimicrobial protein secretion.

Gillum. Trevor L TL; Kuennen. Matthew R MR; Castillo. Micaela N MN; Williams. Nicole L NL; Jordan-Patterson. Alex T AT

Key Findings

  • Acute sleep loss did not change baseline levels of salivary antimicrobial peptides (AMPs).
  • A single 45‑minute run at 75% VO2peak significantly increased the concentration and secretion rate of LL‑37, HNP1‑3, lactoferrin, and lysozyme.
  • The immune‑boosting effect of exercise was observed both immediately after and one hour post‑exercise, regardless of prior sleep deprivation.

Practical Outcomes

  • Incorporate a moderate‑intensity cardio session (≈45 min at 75% VO2max) into your routine to enhance oral and mucosal immunity, especially on nights when you can’t get enough sleep. This simple protocol can help maintain immune defenses and control inflammation without needing supplements.

Summary

A short 45‑minute run at about 75% of your max oxygen use boosts key antimicrobial proteins in saliva—like LL‑37, HNP1‑3, lactoferrin and lysozyme—whether you’ve slept well or missed a night. The rise in these proteins suggests stronger mucosal immunity and better inflammation control after exercise, even when you’re short on sleep.

Abstract

Sleep deficiencies may play a role in depressing immune parameters. Little is known about the impact of exercise after sleep deprivation on mucosal immunity. The purpose of this study was to quantify salivary antimicrobial proteins (AMPs) in response to sleep loss before and after exercise. Four men and 4 women (age: 22.8 ± 2; : 49.1 ± 7.1 ml · kg(-1) · min(-1)) completed 2 exercise trials consisting of 45 minutes of running at 75% VO2peak after a normal night of sleep (CON) and after a night without sleep (WS). Exercise trials were separated by 10 ± 3 days. Saliva was collected before, immediately after, and 1 hour after exercise. LL-37, HNP1-3, Lactoferrin (Lac), and Lysozyme (Lys) were measured. Sleep loss did not affect the concentration or secretion rate of AMPs before or in response to exercise. However, exercise increased the concentration from pre- to post-exercise of LL-37 (pre: 15.5 ± 8.7; post: 22.3 ± 16.2 ng · ml(-1)), HNP1-3 (pre: 2.2 ± 2.3; post: 3.3 ± 2.5 µg · ml(-1)), Lac (pre: 5,234 ± 4,202; post: 12,283 ± 10,995 ng · ml(-1)), and Lys (pre: 5,831 ± 4,465; post: 12,542 ± 10,755 ng · ml(-1)), p <= 0.05. The secretion rates were higher immediately after and 1 hour after exercise compared with before exercise for LL-37 (pre: 3.1 ± 2.1; post: 5.1 ± 3.7; +1: 6.9 ± 8.4 ng · min(-1)), HNP1-3 (pre: 0.38 ± 0.38; post: 0.80 ± 0.75; +1: 0.84 ± 0.67 µg · min(-1)), Lac (pre: 1,096 ± 829; post: 2,948 ± 2,923; +1: 2,464 ± 3,785 ng · min(-1)), and Lys (pre: 1,534 ± 1,790; post: 3,042 ± 2,773; +1: 1,916 ± 1,682 ng · min-(1)), p <= 0.05. These data suggest that the major constituents of the mucosal immune system are unaffected by acute sleep loss and by exercise after acute sleep loss. Exercise increased the concentration and secretion rate of each AMP suggesting enhanced immunity and control of inflammation, despite limited sleep.

Study Information

Provider

pubmed

Year

2015

DOI

10.1519/jsc.0000000000000828