AI Article Synopsis

  • Fatigue following chemotherapy is a major issue for cancer patients, and recent studies link the BDNF Val66Met gene variant to its severity.
  • In a study with transgenic mice, researchers injected 5-fluorouracil (5FU) to model chemotherapy effects and measured fatigue through voluntary wheel running activity.
  • Findings indicated that while Val66Met mice showed less severe fatigue in the first week post-treatment, middle-aged mice experienced greater fatigue in the second week, suggesting the BDNF variant may have a protective effect against chemotherapy-induced fatigue.

Article Abstract

Fatigue is a persistent and debilitating symptom following cancer treatments such as chemotherapy. Recent clinical studies have suggested a common single-nucleotide polymorphism of brain-derived neurotrophic factor (BDNF), Val66Met (rs6265), may be related to the severity of fatigue following cancer treatment. In this study, we tested transgenic mice homozygous for the human Val66Met BDNF gene and wild-type controls. We injected three doses of 5-fluorouracil (5FU) as a model of chemotherapy treatment, and we used changes in voluntary wheel running activity (VWRA) as a measure of fatigue-like behavior. Prior to 5FU injection, we found that during the baseline wheel-running period, the Val66Met mice lost more weight than WT controls. We next administered 5FU and saw a robust fatigue-like phenotype that lasted about 2 weeks. During the first week, the fatigue-like phenotype was less severe in the Val66Met mice and unrelated to the age of the mice. In contrast, during the second week after 5FU treatment, the fatigue-like phenotype was unrelated to the BDNF genotype but was more severe in middle aged mice compared to young mice. We conclude that the BDNF polymorphism may play a direct, protective role against chemotherapy-induced fatigue.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087735PMC
http://dx.doi.org/10.3389/fnbeh.2022.880969DOI Listing

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