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. 2009 Jun 16;297(2):E545–E551. doi: 10.1152/ajpendo.00255.2009

Fig. 1.

Fig. 1.

Metabolic and circadian phenotype of neuromedin U receptor 2 knockout (KO; NMUr2−/−) mice. NMUr2−/− mice exhibited normal body weight (A; body weight at 10 wk of age) and daily food intake (B) compared with congenic wild-type (WT) mice (n = 12 mice/genotype), although the KO mice did consume a greater amount of food during the light phase of the day (B; *P < 0.05, 2-way ANOVA with Bonferroni's post hoc test). Daily profiles of metabolic rate were determined for both genotypes, and no pronounced differences were observed in V̇o2 (C), V̇co2 (D), or respiratory quotient (RQ; E). Running wheel activity of WT (F) and NMUr2−/− (G) mice was monitored under both light-dark and constant dark conditions (n = 10 mice/genotype). The period of wheel running activity based on activity onset was significantly shorter in KO mice (F; **P < 0.01, Student's t-test.). No differences were observed in animals' phase-shift response to a 1-h light pulse delivered at circadian time 14 (CT14; F, G). F and G: shading in indicates dark period; red lines illustrate activity onsets from which circadian periods were calculated, with the break showing the day the light pulse was administered.