Xingyao Yu , Pai Pang , Tao Liu , Xiufang Jiang , Jiayi Zhang , Xiangpei Yue , Jianjun Guo , Xiang Cheng , Tong Zhao , Yongqi Zhao , Zhonghua Dai , Lingling Zhu
{"title":"小鼠急性缺氧诱导神经元激活的全脑定位:c-Fos免疫荧光研究","authors":"Xingyao Yu , Pai Pang , Tao Liu , Xiufang Jiang , Jiayi Zhang , Xiangpei Yue , Jianjun Guo , Xiang Cheng , Tong Zhao , Yongqi Zhao , Zhonghua Dai , Lingling Zhu","doi":"10.1016/j.ibneur.2025.08.013","DOIUrl":null,"url":null,"abstract":"<div><div>Acute hypobaric hypoxic exposure, defined as rapid ascent to high altitude with brief sojourn, triggers profound physiological adaptations while increasing risks of acute mountain sickness (e.g., gastrointestinal distress, pulmonary/cerebral edema). Beyond these somatic manifestations, cognitive deficits frequently emerge under hypoxic stress, yet the neural substrates mediating these impairments remain poorly mapped. To systematically characterize hypoxia-induced brain activation patterns, we conducted whole-brain mapping of neuronal activity changes in mice exposed to acute hypobaric hypoxia versus normoxic controls using c-Fos immunofluorescence, a robust marker of neuronal activation. Our functional analysis focused on key brain regions governing: cardiorespiratory homeostasis, attention, memory, emotional processing, motivation and reward. Quantitative c-Fos mapping revealed increased neural activity in several brainstem nuclei and repressed neural activity in higher-order forebrain after exposure to 24 h-6000 m hypobaric hypoxia. These datas establish the first brain-wide map of hypoxia-responsive neural networks, providing mechanistic insights into physiological adaptation and cognitive vulnerability after acute hypobaric hypoxic exposure.</div></div>","PeriodicalId":13195,"journal":{"name":"IBRO Neuroscience Reports","volume":"19 ","pages":"Pages 519-531"},"PeriodicalIF":2.9000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Brain-wide mapping of acute hypoxia-induced neuronal activation in mice: A c-Fos immunofluorescence study\",\"authors\":\"Xingyao Yu , Pai Pang , Tao Liu , Xiufang Jiang , Jiayi Zhang , Xiangpei Yue , Jianjun Guo , Xiang Cheng , Tong Zhao , Yongqi Zhao , Zhonghua Dai , Lingling Zhu\",\"doi\":\"10.1016/j.ibneur.2025.08.013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Acute hypobaric hypoxic exposure, defined as rapid ascent to high altitude with brief sojourn, triggers profound physiological adaptations while increasing risks of acute mountain sickness (e.g., gastrointestinal distress, pulmonary/cerebral edema). Beyond these somatic manifestations, cognitive deficits frequently emerge under hypoxic stress, yet the neural substrates mediating these impairments remain poorly mapped. To systematically characterize hypoxia-induced brain activation patterns, we conducted whole-brain mapping of neuronal activity changes in mice exposed to acute hypobaric hypoxia versus normoxic controls using c-Fos immunofluorescence, a robust marker of neuronal activation. Our functional analysis focused on key brain regions governing: cardiorespiratory homeostasis, attention, memory, emotional processing, motivation and reward. Quantitative c-Fos mapping revealed increased neural activity in several brainstem nuclei and repressed neural activity in higher-order forebrain after exposure to 24 h-6000 m hypobaric hypoxia. These datas establish the first brain-wide map of hypoxia-responsive neural networks, providing mechanistic insights into physiological adaptation and cognitive vulnerability after acute hypobaric hypoxic exposure.</div></div>\",\"PeriodicalId\":13195,\"journal\":{\"name\":\"IBRO Neuroscience Reports\",\"volume\":\"19 \",\"pages\":\"Pages 519-531\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IBRO Neuroscience Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667242125001290\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IBRO Neuroscience Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667242125001290","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Brain-wide mapping of acute hypoxia-induced neuronal activation in mice: A c-Fos immunofluorescence study
Acute hypobaric hypoxic exposure, defined as rapid ascent to high altitude with brief sojourn, triggers profound physiological adaptations while increasing risks of acute mountain sickness (e.g., gastrointestinal distress, pulmonary/cerebral edema). Beyond these somatic manifestations, cognitive deficits frequently emerge under hypoxic stress, yet the neural substrates mediating these impairments remain poorly mapped. To systematically characterize hypoxia-induced brain activation patterns, we conducted whole-brain mapping of neuronal activity changes in mice exposed to acute hypobaric hypoxia versus normoxic controls using c-Fos immunofluorescence, a robust marker of neuronal activation. Our functional analysis focused on key brain regions governing: cardiorespiratory homeostasis, attention, memory, emotional processing, motivation and reward. Quantitative c-Fos mapping revealed increased neural activity in several brainstem nuclei and repressed neural activity in higher-order forebrain after exposure to 24 h-6000 m hypobaric hypoxia. These datas establish the first brain-wide map of hypoxia-responsive neural networks, providing mechanistic insights into physiological adaptation and cognitive vulnerability after acute hypobaric hypoxic exposure.