Department of Evolutionary Anthropology, Duke University, Durham, NC, United States.
Kalahari Research Trust, Kuruman River Reserve, Northern Cape, South Africa.
Front Endocrinol (Lausanne). 2024 Sep 30;15:1418056. doi: 10.3389/fendo.2024.1418056. eCollection 2024.
Mammalian reproductive and somatic development is regulated by steroid hormones, growth hormone (GH), and insulin-like growth factor-1 (IGF-1). Based largely on information from humans, model organisms, and domesticated animals, testosterone (T) and the GH/IGF-1 system activate sexually differentiated development, promoting male-biased growth, often at a cost to health and survivorship. To test if augmented prenatal androgen exposure in females produces similar developmental patterns and trade-offs, we examine maternal effects in wild meerkats (), a non-model species in which adult females naturally, albeit differentially by status, express exceptionally high androgen concentrations, particularly during pregnancy. In this cooperative breeder, the early growth of daughters predicts future breeding status and reproductive success.
We examine effects of normative and experimentally induced variation in maternal androgens on the ontogenetic patterns in offspring reproductive hormones (androstenedione, A; T; estradiol, E), IGF-1, growth from pup emergence at 1 month to puberty at 1 year, and survivorship. Specifically, we compare the male and female offspring of dominant control (DC or high-T), subordinate control (SC or lower-T), and dominant treated (DT or blocked-T) dams, the latter having experienced antiandrogen treatment in late gestation.
Meerkat offspring showed sex differences in absolute T and IGF-1 concentrations, developmental rates of A and E expression, and survivorship - effects that were sometimes socially or environmentally modulated. Atypical for mammals were the early male bias in T that disappeared by puberty, the absence of sex differences in A and E, and the female bias in IGF-1. Food availability was linked to steroid concentrations in females and to IGF-1, potentially growth, and survival in both sexes. Maternal treatment significantly affected rates of T, E, and IGF-1 expression, and weight, with marginal effects on survivorship; offspring of DT dams showed peak IGF-1 concentrations and the best survivorship.
Maternal effects thus impact offspring development in meerkats, with associated trade-offs: Whereas prenatal androgens modify postnatal reproductive and somatic physiology, benefits associated with enhanced competitiveness in DC lineages may have initial costs of reduced IGF-1, delay in weight gain, and decreased survivorship. These novel data further confirm the different evolutionary and mechanistic pathways to cooperative breeding and call for greater consideration of natural endocrine variation in both sexes.
哺乳动物的生殖和躯体发育受类固醇激素、生长激素(GH)和胰岛素样生长因子-1(IGF-1)的调节。基于来自人类、模式生物和家养动物的大量信息,睾酮(T)和 GH/IGF-1 系统激活了性分化发育,促进了雄性偏向的生长,这通常是以健康和生存为代价的。为了测试雌性中增强的产前雄激素暴露是否产生类似的发育模式和权衡,我们研究了野生猫鼬()中的母体效应,这是一种非模式物种,其中成年雌性自然地、尽管因地位而异地表达极高的雄激素浓度,特别是在怀孕期间。在这种合作繁殖者中,女儿的早期生长预测未来的繁殖状态和繁殖成功。
我们研究了母体雄激素的正常和实验诱导变化对后代生殖激素(雄烯二酮、T;雌二醇、E)、IGF-1、从 1 个月大的幼崽到 1 岁的青春期的生长以及生存的个体发育模式的影响。具体来说,我们比较了优势控制(DC 或高-T)、从属控制(SC 或低-T)和优势处理(DT 或阻断-T)的母鼠的雄性和雌性后代,后者在妊娠后期接受了抗雄激素治疗。
猫鼬后代在 T 的绝对浓度、A 和 E 表达的发育速度以及生存方面表现出性别差异——这些效应有时受到社会或环境的调节。与哺乳动物不同的是,T 的早期雄性偏向在青春期消失,A 和 E 没有性别差异,而 IGF-1 则偏向雌性。食物供应与雌性的类固醇浓度以及 IGF-1 相关,这可能与两性的生长和生存有关。母体处理显著影响 T、E 和 IGF-1 的表达速度和体重,对生存有边缘影响;DT 母鼠的后代表现出最高的 IGF-1 浓度和最佳的生存能力。
因此,母体效应对猫鼬的后代发育产生了影响,伴随着权衡:产前雄激素改变了产后的生殖和躯体生理学,在 DC 谱系中增强竞争力的好处可能最初会导致 IGF-1 减少、体重增加延迟和生存能力下降。这些新数据进一步证实了合作繁殖的不同进化和机制途径,并呼吁在两性中更多地考虑自然内分泌变化。