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Norton explains that the same intervention yields opposite outcomes depending on baseline oxidative status. In young people, even moderate doses of antioxidants can blunt hypertrophy and strength gains, as shown by multiple prior studies. In the new elderly study, the antioxidant group not only gained more muscle and strength but also had greater improvements in oxidative status and inflammatory markers. He also alludes to parallel findings with anti-inflammatories: high-dose ibuprofen (>800 mg/day) hinders gains in young, but in elderly, acetaminophen (and likely other anti-inflammatories) appear beneficial. This aligns with the concept that aging shifts the body's internal milieu upward on the U-shaped curve, making interventions that lower inflammation and oxidation advantageous. He emphasizes that broad recommendations should wait until the body of evidence matures, but the mechanism is now supported by human outcome data.
Skeletal muscle remodeling relies on a hormetic range of reactive oxygen species and inflammatory mediators as signaling molecules. In young healthy muscle, baseline levels are already within this optimal range—adding antioxidants or anti-inflammatories suppresses necessary anabolic signaling below the threshold. In sarcopenic elderly, chronic low-grade inflammation (inflammaging) and elevated oxidative stress push the system above the optimal window, inhibiting anabolic pathways. Vitamin C and E act as antioxidants, reducing reactive species and inflammatory cytokines back into the beneficial range, thereby restoring the signaling environment for muscle protein synthesis and strength development.
If you take elderly people who have come out of that range because they have higher levels of inflammation and oxidative stress and you give them antioxidants, they get more shifted towards that optimal range and they get better results.

