Doctoral School of University of Białystok, Białystok, Poland.
Mammal Research Institute, Polish Academy of Sciences, Białowieża, Poland.
Biol Lett. 2024 Oct;20(10):20240257. doi: 10.1098/rsbl.2024.0257. Epub 2024 Oct 30.
Oxidative stress (OS) and impaired immune function (IF) have been proposed as key physiological costs of reproduction. The relationship between OS and IF remains unresolved, particularly in long-living iteroparous species. We studied physiological markers of maintenance (OS, IF markers) in lactating, post-lactating and non-lactating females of edible dormice-a long-living rodent. We predicted the OS balance and IF to be compromised by lactation, especially in older females expected to face stronger trade-offs between life functions. We found that the age predictor (body size) correlated negatively with white blood cell level (WBC), positively with neutrophils to lymphocytes ratio and had no effect on OS markers. Oxidative damage markers (reactive oxygen metabolites (ROMs); but not antioxidant capacity) and body size-adjusted WBC were the lowest in lactating, higher in post-lactating and the highest in non-lactating females. Body size/age did not affect this correlation suggesting a similar age-independent allocation strategy during reproduction in this species. The path analysis testing the causal relationship between ROMs and WBC revealed that IF is more likely to affect OS than . Our study indicates the trade-off between crucial life functions during reproduction and suggests that immunosuppression reduces the risk of OS; therefore, mitigating oxidative costs of reproduction.
氧化应激(OS)和免疫功能受损(IF)被认为是生殖的关键生理代价。OS 和 IF 之间的关系仍未解决,特别是在长寿的多次产卵物种中。我们研究了哺乳期、哺乳期后和非哺乳期食虫松鼠(一种长寿的啮齿动物)的维持生理标志物(OS、IF 标志物)。我们预测,哺乳期会使 OS 平衡和 IF 受到损害,特别是在预期面临生命功能之间更强权衡的老年雌性中。我们发现,年龄预测因子(体型)与白细胞计数(WBC)呈负相关,与中性粒细胞与淋巴细胞比值呈正相关,与 OS 标志物无关。氧化损伤标志物(活性氧代谢物(ROMs);但抗氧化能力不受影响)和体型调整后的 WBC 在哺乳期最低,哺乳期后最高,非哺乳期最高。体型/年龄不影响这种相关性,表明在该物种的繁殖过程中存在一种类似的与年龄无关的分配策略。测试 ROMs 和 WBC 之间因果关系的路径分析表明,IF 更有可能影响 OS 而不是 OS 影响 IF。我们的研究表明,在繁殖期间,关键生命功能之间存在权衡,并表明免疫抑制降低了 OS 的风险;因此,减轻了生殖的氧化代价。