Cell Reports (Aug 2024)

Housing mice near vs. below thermoneutrality affects drug-induced weight loss but does not improve prediction of efficacy in humans

  • Julie M. Jacobsen,
  • Natalia Petersen,
  • Lola Torz,
  • Marina K. Gerstenberg,
  • Kent Pedersen,
  • Søren Østergaard,
  • Birgitte S. Wulff,
  • Birgitte Andersen,
  • Kirsten Raun,
  • Berit Ø. Christoffersen,
  • Linu M. John,
  • Marc L. Reitman,
  • Rune E. Kuhre

Journal volume & issue
Vol. 43, no. 8
p. 114501

Abstract

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Summary: Evaluation of weight loss drugs is usually performed in diet-induced obese mice housed at ∼22°C. This is a cold stress that increases energy expenditure by ∼35% compared to thermoneutrality (∼30°C), which may overestimate drug-induced weight loss. We investigated five anti-obesity mechanisms that have been in clinical development, comparing weight loss in mice housed at 22°C vs. 30°C. Glucagon-like peptide-1 (GLP-1), human fibroblast growth factor 21 (hFGF21), and melanocortin-4 receptor (MC4R) agonist induced similar weight losses. Peptide YY elicited greater vehicle-subtracted weight loss at 30°C (7.2% vs. 1.4%), whereas growth differentiation factor 15 (GDF15) was more effective at 22°C (13% vs. 6%). Independent of ambient temperature, GLP-1 and hFGF21 prevented the reduction in metabolic rate caused by weight loss. There was no simple rule for a better prediction of human drug efficacy based on ambient temperature, but since humans live at thermoneutrality, drug testing using mice should include experiments near thermoneutrality.

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