Steady-state thermal homeostasis model of heat generated and dissipated in the human retina.

IF 1.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Physical biology Pub Date : 2026-08-19 DOI:10.1088/1478-3975/ae9665
Christina Kiel, Alexander J E Foss
{"title":"Steady-state thermal homeostasis model of heat generated and dissipated in the human retina.","authors":"Christina Kiel, Alexander J E Foss","doi":"10.1088/1478-3975/ae9665","DOIUrl":null,"url":null,"abstract":"<p><p>The retina is both metabolically active and exposed to light, resulting in persistent heat generation. However, the quantitative contributions of metabolic and irradiative heat sources, and the mechanisms responsible for dissipating this thermal load, remain incompletely characterized. Here we develop a steady-state quantitative thermal balance model of the retina that integrates heat production from metabolic activity and light absorption with multiple heat dissipation pathways into a unified energy balance framework. Metabolic heat was estimated from reported ATP consumption rates under dark-and light-adapted conditions, while irradiative heat input was quantified based on environmental luminance, pupil size, and ocular optics. These inputs were incorporated into a lumped energy balance in the form of, allowing calculation of the retinal temperature elevation relative to blood,. Heat dissipation pathways, including conduction to surrounding tissue, choroidal blood perfusion, convection, and radiation, were expressed as thermal conductances,and analyzed within the same framework,. Under sunlight, total retinal heat input reached approximately 10 mW, approximately threefold higher than at night. Despite this, the predicted steady-state retinal temperature elevation remained very small (∼10<sup>-3</sup>K), suggesting that heat is dissipated highly efficiently. The analysis shows that conduction and choroidal blood perfusion dominate retinal heat removal under physiological conditions, whereas radiation and convection contribute negligibly. The results suggest that retinal heat redistribution via conduction plays a major role in retinal thermal homeostasis, whereas choroidal blood perfusion primarily contributes to subsequent systemic heat removal rather than acting as a dominant limiting mechanism itself. This analysis provides quantitative support for the long-standing hypothesis that the choroid functions as a heat sink for the retina.</p>","PeriodicalId":20207,"journal":{"name":"Physical biology","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2026-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1088/1478-3975/ae9665","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The retina is both metabolically active and exposed to light, resulting in persistent heat generation. However, the quantitative contributions of metabolic and irradiative heat sources, and the mechanisms responsible for dissipating this thermal load, remain incompletely characterized. Here we develop a steady-state quantitative thermal balance model of the retina that integrates heat production from metabolic activity and light absorption with multiple heat dissipation pathways into a unified energy balance framework. Metabolic heat was estimated from reported ATP consumption rates under dark-and light-adapted conditions, while irradiative heat input was quantified based on environmental luminance, pupil size, and ocular optics. These inputs were incorporated into a lumped energy balance in the form of, allowing calculation of the retinal temperature elevation relative to blood,. Heat dissipation pathways, including conduction to surrounding tissue, choroidal blood perfusion, convection, and radiation, were expressed as thermal conductances,and analyzed within the same framework,. Under sunlight, total retinal heat input reached approximately 10 mW, approximately threefold higher than at night. Despite this, the predicted steady-state retinal temperature elevation remained very small (∼10-3K), suggesting that heat is dissipated highly efficiently. The analysis shows that conduction and choroidal blood perfusion dominate retinal heat removal under physiological conditions, whereas radiation and convection contribute negligibly. The results suggest that retinal heat redistribution via conduction plays a major role in retinal thermal homeostasis, whereas choroidal blood perfusion primarily contributes to subsequent systemic heat removal rather than acting as a dominant limiting mechanism itself. This analysis provides quantitative support for the long-standing hypothesis that the choroid functions as a heat sink for the retina.

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
人体视网膜产生和散发热量的稳态热稳态模型。
视网膜既代谢活跃又暴露于光下,导致持续发热。然而,代谢和辐射热源的定量贡献,以及负责消散这种热负荷的机制,仍然没有完全表征。本研究建立了视网膜稳态定量热平衡模型,该模型将代谢活动产热和光吸收与多种散热途径整合到一个统一的能量平衡框架中。代谢热是根据报道的在黑暗和光适应条件下的ATP消耗率来估计的,而辐射热输入是根据环境亮度、瞳孔大小和眼睛光学来量化的。这些输入以Q_“in”=Q_“out”的形式被合并到一个集中能量平衡中,从而可以计算视网膜相对于血液的温度升高∆T。散热途径,包括传导到周围组织、脉络膜血液灌注、对流和辐射,用热导率G表示,并在同一框架下进行分析,∆T=Q_out/G。在阳光下,视网膜总热输入约为10 mW,约为夜间的三倍。尽管如此,预测的稳态视网膜温度升高仍然非常小(~ 10-3 K),表明热量被高效地消散。分析表明,在生理条件下,传导和脉络膜血流灌注是视网膜热去除的主要方式,而辐射和对流的作用可以忽略不计。结果表明,通过传导的视网膜热再分配在视网膜热稳态中起主要作用,而脉络膜血液灌注主要有助于随后的全身热清除,而不是作为主要的限制机制本身。这一分析为长期存在的脉络膜作为视网膜热沉的假设提供了定量支持。
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
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
期刊最新文献
An alphabet of allostery: A transferable transfer entropy contact pattern predicts allosteric-site character and conformational rewiring. Decoupling Bulk Stiffness and Pore Size in 3D Rat Tail Collagen I Matrices. Learning the mechanism of collective microbial function via random community-media pairing. Testing the Avrami-Dobrzyński model of cancer transformation using mutation-count clinical data across multiple tumour types. Spanning-tree thermostatistics of protein allostery: an exact Kirchhoff framework with application to oncogenic KRAS.
wanfang
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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