High-Intensity Exercise Training Alters the Effect of <i>N</i>-Acetylcysteine on Exercise-Related Muscle Ionic Shifts in Men

• Main Authors: Anders K. Lemminger (Author), Matteo Fiorenza (Author), Kasper Eibye (Author), Jens Bangsbo (Author), Morten Hostrup (Author)
• Format: Book
• Published: MDPI AG, 2022-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.3390/antiox12010053; 2076-3921
• Keywords: ROS; oxygen species; scavengers; NAC; high-intensity training; potassium; Therapeutics. Pharmacology; RM1-950
• Source: Antioxidants, Vol 12, Iss 1, p 53 (2022)

This study investigated whether high-intensity exercise training alters the effect of <i>N</i>-acetylcysteine (a precursor of antioxidant glutathione) on exercise-related muscle ionic shifts. We assigned 20 recreationally-active men to 6 weeks of high-intensity exercise training, comprising three weekly sessions of 4-10 × 20-s all-out bouts interspersed by 2 min recovery (SET, n = 10), or habitual lifestyle maintenance (n = 10). Before and after SET, we measured ionic shifts across the working muscle, using leg arteriovenous balance technique, during one-legged knee-extensor exercise to exhaustion with and without <i>N</i>-acetylcysteine infusion. Furthermore, we sampled vastus lateralis muscle biopsies for analyses of metabolites, mitochondrial respiratory function, and proteins regulating ion transport and antioxidant defense. SET lowered exercise-related H⁺, K⁺, lactate⁻, and Na⁺ shifts and enhanced exercise performance by ≈45%. While <i>N</i>-acetylcysteine did not affect exercise-related ionic shifts before SET, it lowered H⁺, HCO₃⁻, and Na⁺ shifts after SET. SET enhanced muscle mitochondrial respiratory capacity and augmented the abundance of Na⁺/K⁺-ATPase subunits (α₁ and β₁), ATP-sensitive K⁺ channel subunit (Kir6.2), and monocarboxylate transporter-1, as well as superoxide dismutase-2 and glutathione peroxidase-1. Collectively, these findings demonstrate that high-intensity exercise training not only induces multiple adaptations that enhance the ability to counter exercise-related ionic shifts but also potentiates the effect of <i>N</i>-acetylcysteine on ionic shifts during exercise.