Romero-Haro A A, Figuerola J, Alonso-Alvarez C
Instituto de Investigación en Recursos Cinegéticos (IREC), CSIC-UCLM-JCCM, Ronda de Toledo 12, 13071Ciudad Real, 41092 Sevilla, Spain.
Estación Biológica de Doñana-CSIC, Sevilla, 28029 Madrid, Spain.
Integr Org Biol. 2023 Sep 23;5(1):obad034. doi: 10.1093/iob/obad034. eCollection 2023.
Telomeres are repetitive DNA sequences at the end of chromosomes that protect them from degradation. They have been the focus of intense research because short telomeres would predict accelerated ageing and reduced longevity in vertebrates. Oxidative stress is considered a physiological driver of the telomere shortening and, consequently, short lifespan. Among molecules fighting against oxidative stress, glutathione is involved in many antioxidant pathways. Literature supports that oxidative stress may trigger a compensatory "hormetic" response increasing glutathione levels and telomere length. Here, we tested the link between total glutathione concentration and telomere length in captive birds (zebra finches; ). Total glutathione levels were experimentally decreased during birds' growth using a specific inhibitor of glutathione synthesis (buthionine sulfoximine; BSO). We monitored the birds' reproductive performance in an outdoor aviary during the first month of life, and their longevity for almost 9 years. Among control individuals, erythrocyte glutathione levels during development positively predicted erythrocyte telomere length in adulthood. However, BSO-treated females, but not males, showed longer telomeres than control females in adulthood. This counterintuitive finding suggests that females mounted a compensatory response. Such compensation agrees with precedent findings in the same population where the BSO treatment increased growth and adult body mass in females but not males. BSO did not influence longevity or reproductive output in any sex. However, early glutathione levels and adult telomere length interactively predicted longevity only among control females. Those females with "naturally" low (non-manipulated) glutathione levels at the nestling age but capable of producing longer telomeres in adulthood seem to live longer. The results suggest that the capability to mount a hormetic response triggered by low early glutathione levels can improve fitness via telomere length. Overall, the results may indicate a sex-specific link between glutathione and telomere values. Telomerase activity and sexual steroids (estrogens) are good candidates to explain the sex-biased mechanism underlying the early-life impact of oxidative stress on adult telomere length.
端粒是染色体末端的重复DNA序列,可保护染色体不被降解。它们一直是深入研究的焦点,因为短端粒预示着脊椎动物衰老加速和寿命缩短。氧化应激被认为是端粒缩短进而导致寿命缩短的生理驱动因素。在对抗氧化应激的分子中,谷胱甘肽参与许多抗氧化途径。文献表明,氧化应激可能引发一种补偿性的“应激效应”反应,增加谷胱甘肽水平和端粒长度。在此,我们测试了圈养鸟类(斑胸草雀)中总谷胱甘肽浓度与端粒长度之间的联系。在鸟类生长期间,使用谷胱甘肽合成的特异性抑制剂(丁硫氨酸亚砜胺;BSO)实验性地降低了总谷胱甘肽水平。我们在鸟类出生后的第一个月在室外鸟舍中监测它们的繁殖性能,并监测它们近9年的寿命。在对照个体中,发育期间红细胞谷胱甘肽水平可正向预测成年期红细胞端粒长度。然而,经BSO处理的雌性而非雄性在成年期显示出比对照雌性更长的端粒。这一违反直觉的发现表明雌性产生了一种补偿反应。这种补偿与同一群体中先前的发现一致,即在该群体中,BSO处理增加了雌性而非雄性的生长和成年体重。BSO对任何性别的寿命或繁殖产出均无影响。然而,早期谷胱甘肽水平和成年端粒长度仅在对照雌性中交互预测寿命。那些在雏鸟期“自然”谷胱甘肽水平低(未操控)但成年期能够产生更长端粒的雌性似乎寿命更长。结果表明,由早期低谷胱甘肽水平引发的应激效应反应能力可通过端粒长度提高适应性。总体而言,结果可能表明谷胱甘肽与端粒值之间存在性别特异性联系。端粒酶活性和性类固醇(雌激素)是解释氧化应激对成年端粒长度的早期影响背后性别偏向机制的良好候选因素。