Department of Biology, Indiana University at Bloomington, Bloomington, IN, USA; Department of Biology, Indiana University at Bloomington, 915 East 3(rd) Street, Myers Hall, Bloomington, IN 47405, USA.
Department of Biology, Indiana University at Bloomington, Bloomington, IN, USA.
Gen Comp Endocrinol. 2024 Jun 1;352:114490. doi: 10.1016/j.ygcen.2024.114490. Epub 2024 Mar 8.
Stressful experiences in early life can alter phenotypic expression later in life. For instance, in vertebrates, early life nutrient restriction can modify later life activity of the hypothalamic-pituitary-adrenal/interrenal axis (the HPI in amphibians), including the up- and downstream regulatory components of glucocorticoid signaling. Early life nutrient restriction can also influence later life behavior and metabolism (e.g., fat accumulation). Yet, less is known about whether nutrient stress-induced carryover effects on HPA/HPI axis regulation can vary across environmental contexts, such as the type of diet on which nutrient restriction occurs. Here, we experimentally address this question using the plains spadefoot toad (Spea bombifrons), whose larvae develop in ephemeral habitats that impose intense competition over access to two qualitatively distinct diet types: detritus and live shrimp prey. Consistent with diet type-specific carryover effects of early life nutrient restriction on later life HPI axis regulation, we found that temporary nutrient restriction at the larval stage reduced juvenile (i.e., post-metamorphic) brain gene expression of an upstream glucocorticoid regulator (corticotropin-releasing hormone) and two downstream regulators (glucocorticoid and mineralocorticoid receptors) only on the shrimp diet. These patterns are consistent with known diet type-specific effects of larval nutrient restriction on juvenile corticosterone and behavior. Additionally, larval nutrient restriction increased juvenile body fat levels. Our study indicates that HPA/HPI axis regulatory responses to nutrient restriction can vary remarkably across diet types. Such diet type-specific regulation of the HPA/HPI axis might provide a basis for developmental or evolutionary decoupling of stress-induced carryover effects.
早期生活中的压力经历会改变后期的表型表达。例如,在脊椎动物中,早期的营养限制可以改变下丘脑-垂体-肾上腺/间肾轴(两栖动物中的 HPI)后期的活性,包括糖皮质激素信号的上下游调节成分。早期的营养限制也会影响后期的行为和代谢(例如,脂肪积累)。然而,人们对营养应激引起的 HPA/HPI 轴调节的跨环境影响知之甚少,例如发生营养限制的饮食类型。在这里,我们使用平原铲足蟾蜍(Spea bombifrons)实验性地解决了这个问题,其幼虫在短暂的栖息地中发育,这些栖息地对两种不同质量的饮食类型(碎屑和活虾猎物)的获取存在强烈竞争。与早期营养限制对后期 HPI 轴调节的特定饮食类型的延续效应一致,我们发现幼虫期的短暂营养限制降低了幼体(即变态后)大脑中一种上游糖皮质激素调节剂(促肾上腺皮质激素释放激素)和两种下游调节剂(糖皮质激素和盐皮质激素受体)的基因表达仅在虾类饮食中。这些模式与已知的幼虫营养限制对幼体皮质酮和行为的特定饮食类型效应一致。此外,幼虫营养限制增加了幼体的体脂水平。我们的研究表明,HPA/HPI 轴对营养限制的反应可以在不同的饮食类型之间发生显著变化。HPA/HPI 轴的这种特定于饮食类型的调节可能为应激诱导的延续效应的发育或进化解耦提供基础。