Optimal housing temperatures for mice to mimic the thermal environment of humans: An experimental study

被引:203
作者
Fischer, Alexander W. [1 ,2 ]
Cannon, Barbara [1 ]
Nedergaard, Jan [1 ]
机构
[1] Stockholm Univ, Wenner Gren Inst, Arrhenius Labs F3, Dept Mol Biosci, SE-10691 Stockholm, Sweden
[2] Univ Med Ctr Hamburg Eppendorf, Dept Biochem & Mol Cell Biol, DE-20246 Hamburg, Germany
基金
瑞典研究理事会;
关键词
Ambient temperature; Basal metabolic rate; Human; Lower critical temperature; Mouse; Thermoneutral; Thermoregulation; ENERGY-EXPENDITURE; THERMOREGULATORY RESPONSES; BODY-TEMPERATURE; MOUSE; MODEL; THERMONEUTRALITY; ATHEROSCLEROSIS; THERMOGENESIS; INFLAMMATION;
D O I
10.1016/j.molmet.2017.10.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The laboratory mouse is presently the most common model for examining mechanisms of human physiology and disease. Housing temperatures can have a large impact on the outcome of such experiments and on their translatability to the human situation. Humans usually create for themselves a thermoneutral environment without cold stress, while laboratory mice under standard conditions (approximate to 20 degrees C) are under constant cold stress. In a well-cited, theoretical paper by Speakman and Keijer in Molecular Metabolism, it was argued that housing mice under close to standard conditions is the optimal way of modeling the human metabolic situation. This tenet was mainly based on the observation that humans usually display average metabolic rates of about 1.6 times basal metabolic rate. The extra heat thereby produced would also be expected to lead to a shift in the 'lower critical temperature' towards lower temperatures. Methods: To examine these tenets experimentally, we performed high time-resolution indirect calorimetry at different environmental temperatures on mice acclimated to different housing temperatures. Results: Based on the high time-resolution calorimetry analysis, we found that mice already under thermoneutral conditions display mean diurnal energy expenditure rates 1.8 times higher than basal metabolism, remarkably closely resembling the human situation. At any temperature below thermoneutrality, mice metabolism therefore exceeds the human equivalent: Mice under standard conditions display energy expenditure 3.1 times basal metabolism. The discrepancy to previous conclusions is probably attributable to earlier limitations in establishing true mouse basal metabolic rate, due to low time resolution. We also found that the fact that mean energy expenditure exceeds resting metabolic rate does not move the apparent thermoneutral zone (the lower critical temperature) downwards. Conclusions: We show that housing mice at thermoneutrality is an advantageous step towards aligning mouse energy metabolism to human energy metabolism. (C) 2017 The Authors. Published by Elsevier GmbH.
引用
收藏
页码:161 / 170
页数:10
相关论文
共 36 条
[11]   Warming the mouse to model human diseases [J].
Ganeshan, Kirthana ;
Chawla, Ajay .
NATURE REVIEWS ENDOCRINOLOGY, 2017, 13 (08) :458-465
[12]   Thermoneutral housing exacerbates nonalcoholic fatty liver disease in mice and allows for sex-independent disease modeling (vol 23, pg 829, 2017) [J].
Giles, Daniel A. ;
Moreno-Fernandez, Maria E. ;
Stankiewicz, Traci E. ;
Graspeuntner, Simon ;
Cappelletti, Monica ;
Wu, David ;
Mukherjee, Rajib ;
Chan, Calvin C. ;
Lawson, Matthew J. ;
Klarquist, Jared ;
Suenderhauf, Annika ;
Softic, Samir ;
Kahn, C. Ronald ;
Stemmer, Kerstin ;
Iwakura, Yoichiro ;
Aronow, Bruce J. ;
Karns, Rebekah ;
Steinbrecher, Kris A. ;
Karp, Christopher L. ;
Sheridan, Rachel ;
Shanmukhappa, Shiva K. ;
Reynaud, Damien ;
Haslam, David B. ;
Sina, Christian ;
Rupp, Jan ;
Hogan, Simon P. ;
Divanovic, Senad .
NATURE MEDICINE, 2017, 23 (07) :829-+
[13]   Modulation of ambient temperature promotes inflammation and initiates atherosclerosis in wild type C57BL/6 mice [J].
Giles, Daniel A. ;
Ramkhelawon, Bhama ;
Donelan, Elizabeth M. ;
Stankiewicz, Traci E. ;
Hutchison, Susan B. ;
Mukherjee, Rajib ;
Cappelletti, Monica ;
Karns, Rebekah ;
Karp, Christopher L. ;
Moore, Kathryn J. ;
Divanovic, Senad .
MOLECULAR METABOLISM, 2016, 5 (11) :1121-1130
[14]   The mouse thermoregulatory system: Its impact on translating biomedical data to humans [J].
Gordon, Christopher J. .
PHYSIOLOGY & BEHAVIOR, 2017, 179 :55-66
[15]   The mouse: An "average" homeotherm [J].
Gordon, Christopher J. .
JOURNAL OF THERMAL BIOLOGY, 2012, 37 (04) :286-290
[16]   RELATIONSHIP BETWEEN AUTONOMIC AND BEHAVIORAL THERMOREGULATION IN THE MOUSE [J].
GORDON, CJ .
PHYSIOLOGY & BEHAVIOR, 1985, 34 (05) :687-690
[17]   Behavioral thermoregulatory responses of single- and group-housed mice [J].
Gordon, CJ ;
Becker, P ;
Ali, JS .
PHYSIOLOGY & BEHAVIOR, 1998, 65 (02) :255-262
[18]  
IUPS Thermal Commission, 2003, J THERM BIOL, V28, P75
[19]   MITOTIC-ACTIVITY IN MICE IS SUPPRESSED BY ENERGY RESTRICTION-INDUCED TORPOR [J].
KOIZUMI, A ;
TSUKADA, M ;
WADA, Y ;
MASUDA, H ;
WEINDRUCH, R .
JOURNAL OF NUTRITION, 1992, 122 (07) :1446-1453
[20]   Baseline tumor growth and immune control in laboratory mice are significantly influenced by subthermoneutral housing temperature [J].
Kokolus, Kathleen M. ;
Capitano, Maegan L. ;
Lee, Chen-Ting ;
Eng, Jason W. -L. ;
Waight, Jeremy D. ;
Hylander, Bonnie L. ;
Sexton, Sandra ;
Hong, Chi-Chen ;
Gordon, Christopher J. ;
Abrams, Scott I. ;
Repasky, Elizabeth A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (50) :20176-20181