Effects of Arachidonic Acid Supplementation on Acute Anabolic Signaling and Chronic Functional Performance and Body Composition Adaptations

PLoS One. 2016 May 16;11(5):e0155153. doi: 10.1371/journal.pone.0155153. eCollection 2016.

Abstract

Background: The primary purpose of this investigation was to examine the effects of arachidonic acid (ARA) supplementation on functional performance and body composition in trained males. In addition, we performed a secondary study looking at molecular responses of ARA supplementation following an acute exercise bout in rodents.

Methods: Thirty strength-trained males (age: 20.4 ± 2.1 yrs) were randomly divided into two groups: ARA or placebo (i.e. CTL). Then, both groups underwent an 8-week, 3-day per week, non-periodized training protocol. Quadriceps muscle thickness, whole-body composition scan (DEXA), muscle strength, and power were assessed at baseline and post-test. In the rodent model, male Wistar rats (~250 g, ~8 weeks old) were pre-fed with either ARA or water (CTL) for 8 days and were fed the final dose of ARA prior to being acutely strength trained via electrical stimulation on unilateral plantar flexions. A mixed muscle sample was removed from the exercised and non-exercised leg 3 hours post-exercise.

Results: Lean body mass (2.9%, p<0.0005), upper-body strength (8.7%, p<0.0001), and peak power (12.7%, p<0.0001) increased only in the ARA group. For the animal trial, GSK-β (Ser9) phosphorylation (p<0.001) independent of exercise and AMPK phosphorylation after exercise (p-AMPK less in ARA, p = 0.041) were different in ARA-fed versus CTL rats.

Conclusions: Our findings suggest that ARA supplementation can positively augment strength-training induced adaptations in resistance-trained males. However, chronic studies at the molecular level are required to further elucidate how ARA combined with strength training affect muscle adaptation.

MeSH terms

  • Adaptation, Physiological / drug effects*
  • Adolescent
  • Adult
  • Animal Feed
  • Animals
  • Arachidonic Acids / pharmacology*
  • Body Composition / drug effects*
  • Body Composition / genetics
  • Dietary Supplements*
  • Energy Metabolism / drug effects*
  • Energy Metabolism / genetics
  • Gene Expression Regulation / drug effects
  • Humans
  • Male
  • Models, Animal
  • Muscle Development / drug effects
  • Muscle Development / genetics
  • Muscle Strength / drug effects
  • Musculoskeletal Physiological Phenomena / drug effects*
  • Phosphoproteins / metabolism
  • Physical Conditioning, Animal
  • Protein Biosynthesis
  • Proteomics / methods
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Resistance Training
  • Signal Transduction / drug effects*
  • TOR Serine-Threonine Kinases / metabolism
  • Young Adult

Substances

  • Arachidonic Acids
  • Phosphoproteins
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases

Grants and funding

This study was funded in part by Molecular Nutrition TM. The funder provided support by paying the reagents for the muscle samples analysis. Molecular Nutrition TM did not have any additional roles in the study conception, data collection and analysis, input on the decision to publish or mannuscript preparation. All the other costs other than aforementioned were supported by Molecular and Applied Sciences Laboratory (Auburn University) and Human Performance Laboratory (University of Tampa).