Paulo De Melo, Nayara Pereira, Rafaela Braun Araujo, William T Festuccia, Thiago Mattar Cunha, Luiz Osório Leiria
{"title":"Behavior-driven monitoring of thermogenesis in mice using a thermal gradient ring.","authors":"Paulo De Melo, Nayara Pereira, Rafaela Braun Araujo, William T Festuccia, Thiago Mattar Cunha, Luiz Osório Leiria","doi":"10.1152/ajpendo.00133.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Accurately assessing whole body heat production requires reliable thermometry methods. In mice, common approaches include rectal temperature (RT) measurement, infrared (IR) thermography, and implanted probes. However, factors such as stress, handling, surgery, and variability limit their applicability for evaluating thermogenesis. The Thermal Gradient Ring (TGR), widely used in neuropathic pain and ion channel studies, consists of a circular structure with 12 temperature zones and an integrated camera for real-time behavior monitoring. This system allows for precise analysis of independent behavioral measures, including preferred temperature (PT), distance accumulation in the zones, locomotion pattern, and zone occupancy over time, thereby offering an indirect readout of thermoregulatory state. In this study, we evaluated TGR as a noninvasive tool to detect thermoregulatory behavior adaptations, quantifying zone occupancy time, mobility patterns across temperature gradients, and preferred temperature. Using models with both elevated (β-adrenergic stimulation and high-fat diet feeding) and reduced core body temperature [brown adipose tissue (BAT) lipectomy, uncoupling protein 1 (UCP1) deficiency, and cold exposure], we found that the TGR system reliably detects context-specific thermoregulatory behaviors that contribute to energy homeostasis, while simultaneously serving as a quantitative tool for evaluating thermogenic status. These findings suggest that TGR is a valuable tool for metabolic research, offering a reliable additional assessment for thermogenesis in mice.<b>NEW & NOTEWORTHY</b> The integration between adaptive thermogenesis and behavioral strategies governing metabolic state regulation in mice remains poorly characterized. Using a TGR system, we developed and validated a novel methodology for noninvasive, unbiased, and continuous monitoring of behavior-driven thermogenic capacity. Using loss- and gain-of-function models of BAT thermogenesis, we identified distinct behavioral strategies, mice dynamically adjusted locomotor activity and thermal zone occupancy to modulate heat production, directly reflecting their real-time monitoring of metabolic status.</p>","PeriodicalId":7594,"journal":{"name":"American journal of physiology. Endocrinology and metabolism","volume":" ","pages":"E241-E253"},"PeriodicalIF":3.1000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Endocrinology and metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpendo.00133.2025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/30 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Accurately assessing whole body heat production requires reliable thermometry methods. In mice, common approaches include rectal temperature (RT) measurement, infrared (IR) thermography, and implanted probes. However, factors such as stress, handling, surgery, and variability limit their applicability for evaluating thermogenesis. The Thermal Gradient Ring (TGR), widely used in neuropathic pain and ion channel studies, consists of a circular structure with 12 temperature zones and an integrated camera for real-time behavior monitoring. This system allows for precise analysis of independent behavioral measures, including preferred temperature (PT), distance accumulation in the zones, locomotion pattern, and zone occupancy over time, thereby offering an indirect readout of thermoregulatory state. In this study, we evaluated TGR as a noninvasive tool to detect thermoregulatory behavior adaptations, quantifying zone occupancy time, mobility patterns across temperature gradients, and preferred temperature. Using models with both elevated (β-adrenergic stimulation and high-fat diet feeding) and reduced core body temperature [brown adipose tissue (BAT) lipectomy, uncoupling protein 1 (UCP1) deficiency, and cold exposure], we found that the TGR system reliably detects context-specific thermoregulatory behaviors that contribute to energy homeostasis, while simultaneously serving as a quantitative tool for evaluating thermogenic status. These findings suggest that TGR is a valuable tool for metabolic research, offering a reliable additional assessment for thermogenesis in mice.NEW & NOTEWORTHY The integration between adaptive thermogenesis and behavioral strategies governing metabolic state regulation in mice remains poorly characterized. Using a TGR system, we developed and validated a novel methodology for noninvasive, unbiased, and continuous monitoring of behavior-driven thermogenic capacity. Using loss- and gain-of-function models of BAT thermogenesis, we identified distinct behavioral strategies, mice dynamically adjusted locomotor activity and thermal zone occupancy to modulate heat production, directly reflecting their real-time monitoring of metabolic status.
期刊介绍:
The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.