Mitochondrial function in skeletal muscle contributes to reproductive endothermy in tegu lizards (Salvator merianae)

IF 5.6 2区 医学 Q1 PHYSIOLOGY Acta Physiologica Pub Date : 2024-05-13 DOI:10.1111/apha.14162
Livia Saccani Hervas, Lara do Amaral-Silva, Marina Rincon Sartori, Ane Guadalupe-Silva, Luciane H. Gargaglioni, Johannes Lerchner, Marcos Túlio Oliveira, Kênia Cardoso Bícego
{"title":"Mitochondrial function in skeletal muscle contributes to reproductive endothermy in tegu lizards (Salvator merianae)","authors":"Livia Saccani Hervas,&nbsp;Lara do Amaral-Silva,&nbsp;Marina Rincon Sartori,&nbsp;Ane Guadalupe-Silva,&nbsp;Luciane H. Gargaglioni,&nbsp;Johannes Lerchner,&nbsp;Marcos Túlio Oliveira,&nbsp;Kênia Cardoso Bícego","doi":"10.1111/apha.14162","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aim</h3>\n \n <p>In cyclic climate variations, including seasonal changes, many animals regulate their energy demands to overcome critical transitory moments, restricting their high-demand activities to phases of resource abundance, enabling rapid growth and reproduction. Tegu lizards (<i>Salvator merianae</i>) are ectotherms with a robust annual cycle, being active during summer, hibernating during winter, and presenting a remarkable endothermy during reproduction in spring. Here, we evaluated whether changes in mitochondrial respiratory physiology in skeletal muscle could serve as a mechanism for the increased thermogenesis observed during the tegu's reproductive endothermy.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We performed high-resolution respirometry and calorimetry in permeabilized red and white muscle fibers, sampled during summer (activity) and spring (high activity and reproduction), in association with citrate synthase measurements.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>During spring, the muscle fibers exhibited increased oxidative phosphorylation. They also enhanced uncoupled respiration and heat production via adenine nucleotide translocase (ANT), but not via uncoupling proteins (UCP). Citrate synthase activity was higher during the spring, suggesting greater mitochondrial density compared to the summer. These findings were consistent across both sexes and muscle types (red and white).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>The current results highlight potential cellular thermogenic mechanisms in an ectothermic reptile that contribute to transient endothermy. Our study indicates that the unique feature of transitioning to endothermy through nonshivering thermogenesis during the reproductive phase may be facilitated by higher mitochondrial density, function, and uncoupling within the skeletal muscle. This knowledge contributes significant elements to the broader picture of models for the evolution of endothermy, particularly in relation to the enhancement of aerobic capacity.</p>\n </section>\n </div>","PeriodicalId":107,"journal":{"name":"Acta Physiologica","volume":"240 7","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Physiologica","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/apha.14162","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Aim

In cyclic climate variations, including seasonal changes, many animals regulate their energy demands to overcome critical transitory moments, restricting their high-demand activities to phases of resource abundance, enabling rapid growth and reproduction. Tegu lizards (Salvator merianae) are ectotherms with a robust annual cycle, being active during summer, hibernating during winter, and presenting a remarkable endothermy during reproduction in spring. Here, we evaluated whether changes in mitochondrial respiratory physiology in skeletal muscle could serve as a mechanism for the increased thermogenesis observed during the tegu's reproductive endothermy.

Methods

We performed high-resolution respirometry and calorimetry in permeabilized red and white muscle fibers, sampled during summer (activity) and spring (high activity and reproduction), in association with citrate synthase measurements.

Results

During spring, the muscle fibers exhibited increased oxidative phosphorylation. They also enhanced uncoupled respiration and heat production via adenine nucleotide translocase (ANT), but not via uncoupling proteins (UCP). Citrate synthase activity was higher during the spring, suggesting greater mitochondrial density compared to the summer. These findings were consistent across both sexes and muscle types (red and white).

Conclusion

The current results highlight potential cellular thermogenic mechanisms in an ectothermic reptile that contribute to transient endothermy. Our study indicates that the unique feature of transitioning to endothermy through nonshivering thermogenesis during the reproductive phase may be facilitated by higher mitochondrial density, function, and uncoupling within the skeletal muscle. This knowledge contributes significant elements to the broader picture of models for the evolution of endothermy, particularly in relation to the enhancement of aerobic capacity.

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
骨骼肌中的线粒体功能有助于巨蜥(Salvator merianae)的生殖内温。
目的:在包括季节变化在内的周期性气候变化中,许多动物会调节能量需求以克服关键的过渡时刻,将高需求活动限制在资源丰富的阶段,从而实现快速生长和繁殖。泰谷蜥(Salvator merianae)是一种外温动物,具有强健的年周期,夏季活跃,冬季冬眠,春季繁殖时表现出显著的内温性。在此,我们评估了骨骼肌线粒体呼吸生理的变化是否可以作为凫蛙繁殖内热期间产热增加的机制:我们在夏季(活动)和春季(高活动和繁殖)对渗透红肌和白肌纤维进行了高分辨率呼吸测定和热量测定,并对柠檬酸合成酶进行了测量:结果:春季,肌肉纤维的氧化磷酸化增加。结果:春季,肌肉纤维的氧化磷酸化增加,它们还通过腺嘌呤核苷酸转位酶(ANT)增强了非偶联呼吸和产热,但没有通过非偶联蛋白(UCP)。与夏季相比,春季柠檬酸合成酶的活性更高,这表明线粒体密度更大。这些发现在性别和肌肉类型(红肌和白肌)上都是一致的:目前的研究结果突显了外温爬行动物潜在的细胞生热机制,这种机制有助于瞬时内热。我们的研究表明,在繁殖期通过非颤抖性产热过渡到内热的独特特征可能是由于骨骼肌内线粒体密度较高、功能较强和解偶联。这方面的知识为更广泛的内热进化模型,特别是与提高有氧能力有关的模型,提供了重要元素。
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
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
期刊最新文献
Correction to "Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease". Issue Information Impaired suppression of fatty acid release by insulin is a strong predictor of reduced whole-body insulin-mediated glucose uptake and skeletal muscle insulin receptor activation. Differential production of mitochondrial reactive oxygen species between mouse (Mus musculus) and crucian carp (Carassius carassius) A quantitative analysis of bestrophin 1 cellular localization in mouse cerebral cortex.
×
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