Zhe Shi, Xue-Min Wang, Wen-Wen Duan, Yong-Lan Du, Shu-Kuan Ling, Zhe Zhang, Guo-Dong Wang, Di Zhao, Jin-Jun Ding, Ke Zhang, Ang Li, Lan Yan, Yi Zhang, Dan Cheng, Tai-Cheng Huang, Wei-Jie Xie, Li-Mei Lin, Qin-Hui Tuo, Bo-Hou Xia, Ti-Fei Yuan, Ren-Rong Wu, Xiang-Fang Chen
{"title":"Neuroplasticity and brain health: insights from natural torpor.","authors":"Zhe Shi, Xue-Min Wang, Wen-Wen Duan, Yong-Lan Du, Shu-Kuan Ling, Zhe Zhang, Guo-Dong Wang, Di Zhao, Jin-Jun Ding, Ke Zhang, Ang Li, Lan Yan, Yi Zhang, Dan Cheng, Tai-Cheng Huang, Wei-Jie Xie, Li-Mei Lin, Qin-Hui Tuo, Bo-Hou Xia, Ti-Fei Yuan, Ren-Rong Wu, Xiang-Fang Chen","doi":"10.1111/brv.70069","DOIUrl":null,"url":null,"abstract":"<p><p>Natural torpor is a seasonal adaptation that ensures very low energy expenditure to survive periods of harsh conditions. The brains of hibernating mammals can survive prolonged periods with a low body temperature and low energy supply. Moreover, they exhibit marked changes in neuronal morphology, function, and network connectivity during the torpor-arousal transition. Intriguingly, these changes are fully restored soon after arousal under suitable conditions, with no apparent signs of injury. Their distinct phenotypic plasticity reflects a remarkable capacity for neural regrowth and reorganization. To some extent, the brains of hibernating mammals possess the ability to \"reset\" upon arousal. Their natural advantages and unique neural plasticity traits hold great translational promise and value for various brain health application scenarios. In addition, the brains of hibernating mammals represent ideal model systems for exploring the foundations of memory engrams. However, the exact operating principles involved in the brains of hibernating mammals, and their profound impacts on brain function, remain enigmatic. Thus, dissecting the neurobiological underpinnings of these features of the brains of hibernating mammals and their neural plasticity traits during the torpor-arousal cycle could not only shed light on the mysteries of memory but also facilitate the translation of natural torpor into practical implications for human health. Herein, we focus specifically on this topic, as well as on identifying the possible difficulties and challenges that lie ahead, with the hope of 1 day achieving therapeutic synthetic torpor in humans.</p>","PeriodicalId":133,"journal":{"name":"Biological Reviews","volume":" ","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Reviews","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/brv.70069","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Natural torpor is a seasonal adaptation that ensures very low energy expenditure to survive periods of harsh conditions. The brains of hibernating mammals can survive prolonged periods with a low body temperature and low energy supply. Moreover, they exhibit marked changes in neuronal morphology, function, and network connectivity during the torpor-arousal transition. Intriguingly, these changes are fully restored soon after arousal under suitable conditions, with no apparent signs of injury. Their distinct phenotypic plasticity reflects a remarkable capacity for neural regrowth and reorganization. To some extent, the brains of hibernating mammals possess the ability to "reset" upon arousal. Their natural advantages and unique neural plasticity traits hold great translational promise and value for various brain health application scenarios. In addition, the brains of hibernating mammals represent ideal model systems for exploring the foundations of memory engrams. However, the exact operating principles involved in the brains of hibernating mammals, and their profound impacts on brain function, remain enigmatic. Thus, dissecting the neurobiological underpinnings of these features of the brains of hibernating mammals and their neural plasticity traits during the torpor-arousal cycle could not only shed light on the mysteries of memory but also facilitate the translation of natural torpor into practical implications for human health. Herein, we focus specifically on this topic, as well as on identifying the possible difficulties and challenges that lie ahead, with the hope of 1 day achieving therapeutic synthetic torpor in humans.
期刊介绍:
Biological Reviews is a scientific journal that covers a wide range of topics in the biological sciences. It publishes several review articles per issue, which are aimed at both non-specialist biologists and researchers in the field. The articles are scholarly and include extensive bibliographies. Authors are instructed to be aware of the diverse readership and write their articles accordingly.
The reviews in Biological Reviews serve as comprehensive introductions to specific fields, presenting the current state of the art and highlighting gaps in knowledge. Each article can be up to 20,000 words long and includes an abstract, a thorough introduction, and a statement of conclusions.
The journal focuses on publishing synthetic reviews, which are based on existing literature and address important biological questions. These reviews are interesting to a broad readership and are timely, often related to fast-moving fields or new discoveries. A key aspect of a synthetic review is that it goes beyond simply compiling information and instead analyzes the collected data to create a new theoretical or conceptual framework that can significantly impact the field.
Biological Reviews is abstracted and indexed in various databases, including Abstracts on Hygiene & Communicable Diseases, Academic Search, AgBiotech News & Information, AgBiotechNet, AGRICOLA Database, GeoRef, Global Health, SCOPUS, Weed Abstracts, and Reaction Citation Index, among others.