AI Article Synopsis

  • This pilot study investigates how resistance training (RT) affects kynurenine (KYN) metabolism and physical function in breast cancer survivors (BCSs).
  • Thirty-six BCSs participated in a 12-week program, with improvements in strength (25-35%) noted in the RT group, while both RT and a control group saw similar enhancements in fatigue and quality of life (fatigue decreased by 36%).
  • The findings indicate that RT not only improves physical function but may also influence KYN metabolism, shown by a decrease in KYN and an increase in PGC-1α, suggesting a potential mechanism for combating fatigue and physical challenges in BCSs.

Article Abstract

This pilot examines whether resistance training (RT) can induce changes in kynurenine (KYN) metabolism, which may contribute to improved physical function in breast cancer survivors (BCSs). Thirty-six BCSs (63.2 ± 1.1 years) underwent assessments of physical function and visual analog scale (100 cm) fatigue and quality of life before and after 12 weeks of RT (N = 22) or non-exercise control (CBCT©: Cognitively Based Compassion Training, N = 10). Blood was collected before and after interventions for assessment of KYN, kynurenic acid (KYNA), and peroxisome proliferator-activated receptor γ co-activator 1α (PGC-1α). At baseline, the women were moderately fatigued (mean score: 46 cm) and at risk of poor functional mobility. A group*time interaction was observed for all measures of strength with improvements (~25−35%) following RT (p’s < 0.01), but not CBCT. Time effects were observed for fatigue (−36%) and quality of life (5%) (p’s < 0.01), where both groups improved in a similar manner. A group*time interaction was observed for KYN (p = 0.02) and PGC-1α (p < 0.05), with KYN decreasing and PGC-1α increasing following RT and the opposite following CBCT. These changes resulted in KYN/KYNA decreasing 34% post-RT, but increasing 21% following CBCT. These data support RT as a therapeutic intervention to counteract the long-term side effect of fatigue and physical dysfunction in BCSs. Additionally, the results suggest that this effect may be mediated through the activation of PGC-1α leading to alterations in KYN metabolism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225420PMC
http://dx.doi.org/10.3390/jfmk7020045DOI Listing

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