Literature DB >> 21177944

Nonshivering thermogenesis and its adequate measurement in metabolic studies.

Barbara Cannon1, Jan Nedergaard.   

Abstract

Alterations in nonshivering thermogenesis are presently discussed as being both potentially causative of and able to counteract obesity. However, the necessity for mammals to defend their body temperature means that the ambient temperature profoundly affects the outcome and interpretation of metabolic experiments. An adequate understanding and assessment of nonshivering thermogenesis is therefore paramount for metabolic studies. Classical nonshivering thermogenesis is facultative, i.e. it is only activated when an animal acutely requires extra heat (switched on in minutes), and adaptive, i.e. it takes weeks for an increase in capacity to develop. Nonshivering thermogenesis is fully due to brown adipose tissue activity; adaptation corresponds to the recruitment of this tissue. Diet-induced thermogenesis is probably also facultative and adaptive and due to brown adipose tissue activity. Although all mammals respond to injected/infused norepinephrine (noradrenaline) with an increase in metabolism, in non-adapted mammals this increase mainly represents the response of organs not involved in nonshivering thermogenesis; only the increase after adaptation represents nonshivering thermogenesis. Thermogenesis (metabolism) should be expressed per animal, and not per body mass [not even to any power (0.75 or 0.66)]. A 'cold tolerance test' does not examine nonshivering thermogenesis capacity; rather it tests shivering capacity and endurance. For mice, normal animal house temperatures are markedly below thermoneutrality, and the mice therefore have a metabolic rate and food consumption about 1.5 times higher than their intrinsic requirements. Housing and examining mice at normal house temperatures carries a high risk of identifying false positives for intrinsic metabolic changes; in particular, mutations/treatments that affect the animal's insulation (fur, skin) may lead to such problems. Correspondingly, true alterations in intrinsic metabolic rate remain undetected when metabolism is examined at temperatures below thermoneutrality. Thus, experiments with animals kept and examined at thermoneutrality are likely to yield an improved possibility of identifying agents and genes important for human energy balance.

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Year:  2011        PMID: 21177944     DOI: 10.1242/jeb.050989

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


  295 in total

1.  Cold but not sympathomimetics activates human brown adipose tissue in vivo.

Authors:  Aaron M Cypess; Yih-Chieh Chen; Cathy Sze; Ke Wang; Jeffrey English; Onyee Chan; Ashley R Holman; Ilan Tal; Matthew R Palmer; Gerald M Kolodny; C Ronald Kahn
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-04       Impact factor: 11.205

2.  FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis.

Authors:  Ffolliott M Fisher; Sandra Kleiner; Nicholas Douris; Elliott C Fox; Rina J Mepani; Francisco Verdeguer; Jun Wu; Alexei Kharitonenkov; Jeffrey S Flier; Eleftheria Maratos-Flier; Bruce M Spiegelman
Journal:  Genes Dev       Date:  2012-02-01       Impact factor: 11.361

3.  Red blood cell β-adrenergic receptors contribute to diet-induced energy expenditure by increasing O2 supply.

Authors:  Eun Ran Kim; Shengjie Fan; Dmitry Akhmedov; Kaiqi Sun; Hoyong Lim; William O'Brien; Yuanzhong Xu; Leandra R Mangieri; Yaming Zhu; Cheng-Chi Lee; Yeonseok Chung; Yang Xia; Yong Xu; Feng Li; Kai Sun; Rebecca Berdeaux; Qingchun Tong
Journal:  JCI Insight       Date:  2017-07-20

4.  Defective daily temperature regulation in a mouse model of amyotrophic lateral sclerosis.

Authors:  Maurine C Braun; Alexandra Castillo-Ruiz; Premananda Indic; Dae Young Jung; Jason K Kim; Robert H Brown; Steven J Swoap; William J Schwartz
Journal:  Exp Neurol       Date:  2018-07-18       Impact factor: 5.330

5.  Mice Housed at Elevated Vivarium Temperatures Display Enhanced T-cell Response and Survival to Francisella tularensis.

Authors:  Robert L Rubin
Journal:  Comp Med       Date:  2017-12-01       Impact factor: 0.982

6.  Mouse Thermoregulation: Introducing the Concept of the Thermoneutral Point.

Authors:  Vojtěch Škop; Juen Guo; Naili Liu; Cuiying Xiao; Kevin D Hall; Oksana Gavrilova; Marc L Reitman
Journal:  Cell Rep       Date:  2020-04-14       Impact factor: 9.423

7.  Cardiac-specific VLCAD deficiency induces dilated cardiomyopathy and cold intolerance.

Authors:  Dingding Xiong; Huamei He; Jeanne James; Chonan Tokunaga; Corey Powers; Yan Huang; Hanna Osinska; Jeffrey A Towbin; Enkhsaikhan Purevjav; James A Balschi; Sabzali Javadov; Francis X McGowan; Arnold W Strauss; Zaza Khuchua
Journal:  Am J Physiol Heart Circ Physiol       Date:  2013-11-27       Impact factor: 4.733

8.  The hidden cost of housing practices: using noninvasive imaging to quantify the metabolic demands of chronic cold stress of laboratory mice.

Authors:  John M David; Arion F Chatziioannou; Richard Taschereau; Hongkai Wang; David B Stout
Journal:  Comp Med       Date:  2013-10       Impact factor: 0.982

9.  Interleukin-6 is important for regulation of core body temperature during long-term cold exposure in mice.

Authors:  Emil Egecioglu; Fredrik Anesten; Erik Schéle; Vilborg Palsdottir
Journal:  Biomed Rep       Date:  2018-07-02

10.  Inappropriate heat dissipation ignites brown fat thermogenesis in mice with a mutant thyroid hormone receptor α1.

Authors:  Amy Warner; Awahan Rahman; Peter Solsjö; Kristina Gottschling; Benjamin Davis; Björn Vennström; Anders Arner; Jens Mittag
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-17       Impact factor: 11.205

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