Developmental programming: Preconceptional and gestational exposure of sheep to biosolids on offspring ovarian dynamics.

IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY Biology of Reproduction Pub Date : 2024-11-19 DOI:10.1093/biolre/ioae166
Katherine M Halloran, Yiran Zhou, Michelle Bellingham, Richard G Lea, Neil P Evans, Kevin Sinclair, Peter Smith, Vasantha Padmanabhan
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Abstract

Developmental exposure to environmental chemicals (ECs) perturbs establishment and maintenance of the ovarian reserve across the reproductive lifetime, leading to premature follicle depletion and ovarian aging. Considering humans are exposed to a complex mixture of ECs, real-life models assessing their cumulative impact on the ovarian reserve are needed. Biosolids is a source of real-life mixture of ECs. While earlier studies demonstrated that grazing pregnant sheep on biosolids-treated pastures (BTP) did not influence establishment of the ovarian reserve in fetal life, its impact on subsequent depletion of ovarian reserve during reproductive life of offspring is unknown. We hypothesized that developmental exposure to biosolids accelerates depletion of ovarian reserve. Ovaries were collected from F1 juveniles (9.5 weeks) and adults (2.5 years) born to F0 ewes grazed on control inorganic fertilizer pastures or BTP from before conception and throughout gestation. The impact on follicular density, activation rate, and Anti-Müllerian hormone (AMH; mediator of activation) expression by immunohistochemistry was determined. Activation rate was increased in F1 BTP juveniles with a corresponding reduction in primordial follicle density. In contrast, activation rate and ovarian reserve were similar between control and F1 BTP adults. The density of AMH-positive antral follicles was lower in BTP juveniles, whereas AMH expression tended to be higher in antral follicles of BTP adults, consistent with the changes in the ovarian reserve. These findings of detrimental effects of developmental exposure to biosolids during juvenile life that normalizes in adults is supportive of a shift in activation rate likely related to peripubertal hormonal changes.

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发育编程:绵羊受孕前和妊娠期接触生物固体对后代卵巢动态的影响。
发育过程中暴露于环境化学物质(ECs)会扰乱整个生育期卵巢储备的建立和维持,导致卵泡过早耗竭和卵巢衰老。考虑到人类暴露于复杂的环境化学物质混合物中,需要建立真实的模型来评估它们对卵巢储备的累积影响。生物固体是现实生活中ECs混合物的来源。早期研究表明,在生物固体处理过的牧场(BTP)上放牧怀孕绵羊不会影响胎儿期卵巢储备的建立,但其对后代生殖期卵巢储备耗竭的影响尚不清楚。我们假设,在发育过程中接触生物固体会加速卵巢储备的消耗。我们从受孕前和整个妊娠期采集了在无机肥料对照牧场或生物固体废弃物中放牧的 F0 母羊所生的 F1 幼羊(9.5 周)和成年羊(2.5 岁)的卵巢。通过免疫组化测定了对卵泡密度、活化率和抗苗勒氏管激素(AMH,活化介质)表达的影响。F1 BTP幼鼠的活化率增加,原始卵泡密度相应降低。相比之下,对照组和 F1 BTP 成体的活化率和卵巢储备量相似。BTP幼鼠的AMH阳性前卵泡密度较低,而BTP成鼠的前卵泡中AMH表达往往较高,这与卵巢储备的变化一致。这些研究结果表明,在幼年时期接触生物固体会对发育产生不利影响,而在成年后则会恢复正常,这支持了可能与围青春期激素变化有关的激活率变化。
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来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
期刊最新文献
Pyrroloquinoline-quinone supplementation restores ovarian function and oocyte quality in a mouse model of advanced maternal age. Attenuation of Ampullary Anoctamin 1 by the Peritoneal Fluid in Rhesus Macaques with Spontaneous Endometriosis. CSPG4 involvement in endometrial decidualization contributes to the pathogenesis of preeclampsia. CTNND1 affects trophoblast proliferation and specification during human embryo implantation. Developmental programming: Preconceptional and gestational exposure of sheep to biosolids on offspring ovarian dynamics.
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