从恒定光照下恢复后,生理反应随分子损伤结果而变化。

IF 2.2 3区 生物学 Q1 ZOOLOGY
Kevin Pham, Madeline Lazenby, Natalie R Gassman, Christine R Lattin, Haruka Wada
{"title":"从恒定光照下恢复后,生理反应随分子损伤结果而变化。","authors":"Kevin Pham, Madeline Lazenby, Natalie R Gassman, Christine R Lattin, Haruka Wada","doi":"10.1093/icb/icaf075","DOIUrl":null,"url":null,"abstract":"<p><p>The Damage-Fitness model describes how stress is linked to damage and repair pathways that drive health and fitness outcomes across taxa. However, we lack an understanding of how variation in hypothalamic-pituitary-adrenal (HPA) responses (i.e., endocrine flexibility) affects damage, especially after recovery from stressors. In this study, adult female zebra finches were exposed to a normal photoperiod or constant light for 23 days followed by a recovery period. Using path analysis, we combined a suite of morphological and physiological traits to examine the mechanisms related to cellular damage outcomes. In control individuals, HPA axis reactivity was condition-dependent, such that birds with higher body mass had stronger HPA axis reactivity. HPA axis reactivity was associated with two specific relationships: a strong, positive, relationship with glucose reactivity and a slightly negative relationship with liver 4-hydroxynonaneal that covaried. Interestingly, this condition-dependency disappeared in birds recovering from constant light. While HPA axis reactivity was positively associated with glucose reactivity, this path relationship was not associated with any damage marker. Liver glucocorticoid receptor abundance was negatively associated with liver protein carbonyl damage in control birds, but this relationship was lost in birds recovering from light. These patterns indicate that long-term exposure to a stressor such as constant light can alter biologically linked relationships, even after cessation and recovery from that stressor. Yet, whether rewiring of physiological network connectivity is related to adaptive physiological outcomes, fitness-related traits, or performance remains unclear.</p>","PeriodicalId":54971,"journal":{"name":"Integrative and Comparative Biology","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Physiological responses vary with molecular damage outcomes after recovery from constant light.\",\"authors\":\"Kevin Pham, Madeline Lazenby, Natalie R Gassman, Christine R Lattin, Haruka Wada\",\"doi\":\"10.1093/icb/icaf075\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The Damage-Fitness model describes how stress is linked to damage and repair pathways that drive health and fitness outcomes across taxa. However, we lack an understanding of how variation in hypothalamic-pituitary-adrenal (HPA) responses (i.e., endocrine flexibility) affects damage, especially after recovery from stressors. In this study, adult female zebra finches were exposed to a normal photoperiod or constant light for 23 days followed by a recovery period. Using path analysis, we combined a suite of morphological and physiological traits to examine the mechanisms related to cellular damage outcomes. In control individuals, HPA axis reactivity was condition-dependent, such that birds with higher body mass had stronger HPA axis reactivity. HPA axis reactivity was associated with two specific relationships: a strong, positive, relationship with glucose reactivity and a slightly negative relationship with liver 4-hydroxynonaneal that covaried. Interestingly, this condition-dependency disappeared in birds recovering from constant light. While HPA axis reactivity was positively associated with glucose reactivity, this path relationship was not associated with any damage marker. Liver glucocorticoid receptor abundance was negatively associated with liver protein carbonyl damage in control birds, but this relationship was lost in birds recovering from light. These patterns indicate that long-term exposure to a stressor such as constant light can alter biologically linked relationships, even after cessation and recovery from that stressor. Yet, whether rewiring of physiological network connectivity is related to adaptive physiological outcomes, fitness-related traits, or performance remains unclear.</p>\",\"PeriodicalId\":54971,\"journal\":{\"name\":\"Integrative and Comparative Biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative and Comparative Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/icb/icaf075\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ZOOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative and Comparative Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/icb/icaf075","RegionNum":3,"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

摘要

损害-健康模型描述了压力是如何与损害和修复途径联系在一起的,这些途径推动了整个分类群的健康和健康结果。然而,我们缺乏对下丘脑-垂体-肾上腺(HPA)反应(即内分泌灵活性)的变化如何影响损伤的理解,特别是在从压力源恢复后。在这项研究中,成年雌性斑胸草雀暴露在正常光周期或恒定光下23天,然后进行恢复期。利用通径分析,我们结合了一套形态和生理特征来检查与细胞损伤结果相关的机制。在对照个体中,HPA轴的反应性是条件依赖的,如体重越大的鸟类HPA轴的反应性越强。HPA轴反应性与两种特定关系相关:与葡萄糖反应性有强烈的正相关关系,与肝脏4-羟基苯胺有轻微的负相关关系。有趣的是,这种条件依赖性在持续光照下恢复的鸟类中消失了。虽然HPA轴反应性与葡萄糖反应性呈正相关,但这种路径关系与任何损伤标志物无关。在对照组中,肝糖皮质激素受体丰度与肝蛋白羰基损伤呈负相关,但在光照恢复的鸟类中,这种关系不存在。这些模式表明,长期暴露在压力源(如恒定的光线)下,即使在停止并从压力源中恢复后,也会改变生物学上的相关关系。然而,生理网络连接的重新布线是否与适应性生理结果、健康相关特征或表现有关尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physiological responses vary with molecular damage outcomes after recovery from constant light.

The Damage-Fitness model describes how stress is linked to damage and repair pathways that drive health and fitness outcomes across taxa. However, we lack an understanding of how variation in hypothalamic-pituitary-adrenal (HPA) responses (i.e., endocrine flexibility) affects damage, especially after recovery from stressors. In this study, adult female zebra finches were exposed to a normal photoperiod or constant light for 23 days followed by a recovery period. Using path analysis, we combined a suite of morphological and physiological traits to examine the mechanisms related to cellular damage outcomes. In control individuals, HPA axis reactivity was condition-dependent, such that birds with higher body mass had stronger HPA axis reactivity. HPA axis reactivity was associated with two specific relationships: a strong, positive, relationship with glucose reactivity and a slightly negative relationship with liver 4-hydroxynonaneal that covaried. Interestingly, this condition-dependency disappeared in birds recovering from constant light. While HPA axis reactivity was positively associated with glucose reactivity, this path relationship was not associated with any damage marker. Liver glucocorticoid receptor abundance was negatively associated with liver protein carbonyl damage in control birds, but this relationship was lost in birds recovering from light. These patterns indicate that long-term exposure to a stressor such as constant light can alter biologically linked relationships, even after cessation and recovery from that stressor. Yet, whether rewiring of physiological network connectivity is related to adaptive physiological outcomes, fitness-related traits, or performance remains unclear.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.70
自引率
7.70%
发文量
150
审稿时长
6-12 weeks
期刊介绍: Integrative and Comparative Biology ( ICB ), formerly American Zoologist , is one of the most highly respected and cited journals in the field of biology. The journal''s primary focus is to integrate the varying disciplines in this broad field, while maintaining the highest scientific quality. ICB''s peer-reviewed symposia provide first class syntheses of the top research in a field. ICB also publishes book reviews, reports, and special bulletins.
×
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