Prenatal Environmental Hypoxia Enhances Adult Hypoxia Tolerance in Brandt's Voles (Lasiopodomys brandtii): Behavioral and Transcriptomic Insights.

IF 3.7 1区 生物学 Q1 ZOOLOGY
Mengyang Li, Congcong Qiao, Xiujuan Li, Maolin Huang, Zhenlong Wang, Luye Shi
{"title":"Prenatal Environmental Hypoxia Enhances Adult Hypoxia Tolerance in Brandt's Voles (Lasiopodomys brandtii): Behavioral and Transcriptomic Insights.","authors":"Mengyang Li, Congcong Qiao, Xiujuan Li, Maolin Huang, Zhenlong Wang, Luye Shi","doi":"10.1111/1749-4877.70010","DOIUrl":null,"url":null,"abstract":"<p><p>Prenatal hypoxia poses significant risks to mammalian brain development, often leading to long-term cognitive and memory deficits. However, certain hypoxia-tolerant species, such as Brandt's vole (Lasiopodomys brandtii), have evolved unique adaptations to thrive in low-oxygen environments. This study explores the effects of prenatal environmental hypoxia on the cognitive abilities and molecular responses of Brandt's voles in adulthood. Using behavioral tests (novel object recognition and Y maze) and transcriptomic analysis, we found that Brandt's voles exposed to prenatal environmental hypoxia exhibited intact cognitive and memory functions, contrasting with the deficits observed in model organisms. Transcriptomic profiling, validated by RT-qPCR experiments, revealed adaptive changes in energy metabolism, oxygen transport, and neuroprotective mechanisms, particularly in voles exposed to hypoxia both prenatally and in adulthood. These findings suggest that moderate prenatal environmental hypoxia exposure induces developmental plasticity in Brandt's voles, enhancing their hypoxia tolerance in adulthood, which contrasts with the detrimental effects observed in model organisms under similar conditions. Our study highlights the importance of investigating non-model organisms with natural hypoxia exposure histories, providing novel insights into the mechanisms of hypoxia adaptation and potential strategies for mitigating hypoxia-related neurological damage.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative zoology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/1749-4877.70010","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Prenatal hypoxia poses significant risks to mammalian brain development, often leading to long-term cognitive and memory deficits. However, certain hypoxia-tolerant species, such as Brandt's vole (Lasiopodomys brandtii), have evolved unique adaptations to thrive in low-oxygen environments. This study explores the effects of prenatal environmental hypoxia on the cognitive abilities and molecular responses of Brandt's voles in adulthood. Using behavioral tests (novel object recognition and Y maze) and transcriptomic analysis, we found that Brandt's voles exposed to prenatal environmental hypoxia exhibited intact cognitive and memory functions, contrasting with the deficits observed in model organisms. Transcriptomic profiling, validated by RT-qPCR experiments, revealed adaptive changes in energy metabolism, oxygen transport, and neuroprotective mechanisms, particularly in voles exposed to hypoxia both prenatally and in adulthood. These findings suggest that moderate prenatal environmental hypoxia exposure induces developmental plasticity in Brandt's voles, enhancing their hypoxia tolerance in adulthood, which contrasts with the detrimental effects observed in model organisms under similar conditions. Our study highlights the importance of investigating non-model organisms with natural hypoxia exposure histories, providing novel insights into the mechanisms of hypoxia adaptation and potential strategies for mitigating hypoxia-related neurological damage.

产前环境缺氧增强勃兰特田鼠(Lasiopodomys brandtii)成年缺氧耐受性:行为和转录组学的见解。
产前缺氧对哺乳动物的大脑发育有重大风险,经常导致长期的认知和记忆缺陷。然而,某些耐缺氧物种,如勃兰特田鼠(Lasiopodomys brandtii),已经进化出独特的适应能力,可以在低氧环境中茁壮成长。本研究探讨了产前环境缺氧对成年期布氏田鼠认知能力和分子反应的影响。通过行为测试(新物体识别和Y迷宫)和转录组学分析,我们发现暴露于产前环境缺氧的勃兰特田鼠表现出完整的认知和记忆功能,与模式生物观察到的缺陷形成对比。转录组学分析通过RT-qPCR实验验证,揭示了能量代谢、氧转运和神经保护机制的适应性变化,特别是在产前和成年期暴露于缺氧的田鼠中。这些发现表明,适度的产前环境缺氧暴露诱导了勃兰特田鼠的发育可塑性,增强了它们成年后的缺氧耐受性,这与模式生物在类似条件下观察到的有害影响形成了对比。我们的研究强调了研究具有自然缺氧暴露史的非模式生物的重要性,为缺氧适应机制和减轻缺氧相关神经损伤的潜在策略提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.40
自引率
12.10%
发文量
81
审稿时长
>12 weeks
期刊介绍: The official journal of the International Society of Zoological Sciences focuses on zoology as an integrative discipline encompassing all aspects of animal life. It presents a broader perspective of many levels of zoological inquiry, both spatial and temporal, and encourages cooperation between zoology and other disciplines including, but not limited to, physics, computer science, social science, ethics, teaching, paleontology, molecular biology, physiology, behavior, ecology and the built environment. It also looks at the animal-human interaction through exploring animal-plant interactions, microbe/pathogen effects and global changes on the environment and human society. Integrative topics of greatest interest to INZ include: (1) Animals & climate change (2) Animals & pollution (3) Animals & infectious diseases (4) Animals & biological invasions (5) Animal-plant interactions (6) Zoogeography & paleontology (7) Neurons, genes & behavior (8) Molecular ecology & evolution (9) Physiological adaptations
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信