Altered Oxidative Status as a Cost of Reproduction in a Seabird with High Reproductive Costs.

IF 1.8 3区 生物学 Q3 PHYSIOLOGY Physiological and Biochemical Zoology Pub Date : 2022-01-01 DOI:10.1086/717916
Yimei Lin, Allison Patterson, Ana Gabriela Jimenez, Kyle Elliott
{"title":"Altered Oxidative Status as a Cost of Reproduction in a Seabird with High Reproductive Costs.","authors":"Yimei Lin,&nbsp;Allison Patterson,&nbsp;Ana Gabriela Jimenez,&nbsp;Kyle Elliott","doi":"10.1086/717916","DOIUrl":null,"url":null,"abstract":"<p><p>AbstractLife history theory posits that reproduction is constrained by a cost of reproduction such that any increase in breeding effort should reduce subsequent survival. Oxidative stress refers to an imbalance between the prooxidant reactive oxygen species (ROS) and antioxidant defense. If not thwarted, ROS can cause damage to DNA, lipids, and proteins, potentially increasing the rate of senescence and decreasing cellular function. Reproduction is often associated with higher metabolic rates, which could increase production of ROS and lead to oxidative damage if the animal does not increase antioxidant protection. Thus, oxidative stress could be one mechanism creating a cost of reproduction. In this study we explored how reproduction may affect oxidative status differently between male and female thick-billed murres during early and late breeding seasons over three consecutive years. We manipulated breeding efforts by removing an egg from the nest of some individuals, which forced females to relay, and by handicapping other individuals by clipping wings. We measured total antioxidant capacity (TAC), uric acid (UA) concentration, and malondialdehyde (MDA; an index of lipid oxidative damage) concentration in blood plasma as well as activities of superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) in red blood cells. Oxidative status was highly variable across years, and year was consistently the most important factor determining oxidative status; inconsistent results in previous field studies may be because reproductive oxidative stress occurs only in some years. Females had lower SOD and GPx and higher MDA and TAC than males immediately after egg laying, suggesting that the cost of egg laying required investment in cheaper nonenzymatic antioxidant defenses that had lower capacity for defending against lipid peroxidation. Delayed birds had lower UA and lower SOD, GPx, and CAT activity compared with control birds. In conclusion, when reproductive costs increase via higher energy costs or longer breeding seasons, the oxidative status of both male and female murres deteriorated as a result of reduced antioxidant defenses.</p>","PeriodicalId":54609,"journal":{"name":"Physiological and Biochemical Zoology","volume":"95 1","pages":"35-53"},"PeriodicalIF":1.8000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological and Biochemical Zoology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1086/717916","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 6

Abstract

AbstractLife history theory posits that reproduction is constrained by a cost of reproduction such that any increase in breeding effort should reduce subsequent survival. Oxidative stress refers to an imbalance between the prooxidant reactive oxygen species (ROS) and antioxidant defense. If not thwarted, ROS can cause damage to DNA, lipids, and proteins, potentially increasing the rate of senescence and decreasing cellular function. Reproduction is often associated with higher metabolic rates, which could increase production of ROS and lead to oxidative damage if the animal does not increase antioxidant protection. Thus, oxidative stress could be one mechanism creating a cost of reproduction. In this study we explored how reproduction may affect oxidative status differently between male and female thick-billed murres during early and late breeding seasons over three consecutive years. We manipulated breeding efforts by removing an egg from the nest of some individuals, which forced females to relay, and by handicapping other individuals by clipping wings. We measured total antioxidant capacity (TAC), uric acid (UA) concentration, and malondialdehyde (MDA; an index of lipid oxidative damage) concentration in blood plasma as well as activities of superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) in red blood cells. Oxidative status was highly variable across years, and year was consistently the most important factor determining oxidative status; inconsistent results in previous field studies may be because reproductive oxidative stress occurs only in some years. Females had lower SOD and GPx and higher MDA and TAC than males immediately after egg laying, suggesting that the cost of egg laying required investment in cheaper nonenzymatic antioxidant defenses that had lower capacity for defending against lipid peroxidation. Delayed birds had lower UA and lower SOD, GPx, and CAT activity compared with control birds. In conclusion, when reproductive costs increase via higher energy costs or longer breeding seasons, the oxidative status of both male and female murres deteriorated as a result of reduced antioxidant defenses.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
高繁殖成本海鸟的氧化状态改变作为繁殖成本。
【摘要】生活史理论认为,繁殖受到繁殖成本的限制,因此任何繁殖努力的增加都会减少随后的存活率。氧化应激是指促氧化活性氧(ROS)与抗氧化防御之间的失衡。如果不加以抑制,活性氧会对DNA、脂质和蛋白质造成损害,可能会增加衰老速度,降低细胞功能。繁殖通常与较高的代谢率有关,如果动物不增加抗氧化保护,这可能会增加ROS的产生并导致氧化损伤。因此,氧化应激可能是造成繁殖成本的一种机制。在本研究中,我们在连续三年的研究中探讨了繁殖在繁殖季节的早期和晚期对雄性和雌性厚嘴莺氧化状态的不同影响。我们通过从一些个体的巢中取出一个卵来操纵繁殖努力,这迫使雌性进行接力,并通过剪断其他个体的翅膀来妨碍繁殖。我们测量了总抗氧化能力(TAC)、尿酸(UA)浓度和丙二醛(MDA);血浆脂质氧化损伤指数)浓度及红细胞超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)、过氧化氢酶(CAT)活性。氧化状态在不同年份变化很大,年份一直是决定氧化状态的最重要因素;以往的实地研究结果不一致可能是因为生殖氧化应激只发生在某些年份。产卵后,雌性的SOD和GPx低于雄性,而MDA和TAC高于雄性,这表明产卵成本需要投资更便宜的非酶抗氧化防御,而非酶抗氧化防御能力较低。与对照鸟相比,延迟鸟的UA和SOD、GPx、CAT活性较低。综上所述,当生殖成本通过更高的能量成本或更长的繁殖季节而增加时,雄性和雌性小鼠的氧化状态都因抗氧化防御能力降低而恶化。
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 去求助
来源期刊
CiteScore
3.20
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Physiological and Biochemical Zoology: Ecological and Evolutionary Approaches primarily publishes original research in animal physiology and biochemistry as considered from behavioral, ecological, and/or evolutionary perspectives. Studies at all levels of biological organization from the molecular to the whole organism are welcome, and work that integrates across levels of organization is particularly encouraged. Studies that focus on behavior or morphology are welcome, so long as they include ties to physiology or biochemistry, in addition to having an ecological or evolutionary context. Subdisciplines of interest include nutrition and digestion, salt and water balance, epithelial and membrane transport, gas exchange and transport, acid-base balance, temperature adaptation, energetics, structure and function of macromolecules, chemical coordination and signal transduction, nitrogen metabolism and excretion, locomotion and muscle function, biomechanics, circulation, behavioral, comparative and mechanistic endocrinology, sensory physiology, neural coordination, and ecotoxicology ecoimmunology.
期刊最新文献
IGF-1 Levels Increase during an Immune but Not an Oxidative Challenge in an Avian Model, the Japanese Quail Infection Causes Trade-Offs between Development and Growth in Larval Amphibians. Announcement: Physiological and Biochemical Zoology Is Changing Its Name to Ecological and Evolutionary Physiology. Environmental stress and the morphology of Daphnia pulex The rate of cooling during torpor entry drives torpor patterns in a small marsupial
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1