
In this study, we investigated the physiological regulation of energy metabolism in wild-type (WT) and WFS1-deficient (Wfs1KO) mice by measuring the effects of menthol treatment on the O2 consumption, CO2 production, rectal body temperature, and heat production. The basal metabolism and behavior was different between these genotypes as well as TRP family gene expressions. Wfs1KO mice had a shorter life span and weighed less than WT mice. The food and water intake of Wfs1KO mice was lower as well as the body temperature when compared to their WT littermates. Furthermore, Wfs1KO mice had higher basal O2 consumption, and CO2 and heat production than WT mice. In addition, Wfs1KO mice showed a higher response to menthol administration in comparison to WT mice. The strongest menthol effect was seen on different physiological measures 12 h after oral administration. The highest metabolic response of Wfs1KO mice was seen at the menthol dose of 10 mg/kg. Menthol increased O2 consumption, and CO2 and heat production in Wfs1KO mice when compared to their WT littermates. In addition, the expression of Trpm8 gene was increased. In conclusion, our results show that the Wfs1KO mice develop a metabolic phenotype characterized with several physiological dysfunctions.
Male, Mice, Knockout, 570, Mice, 129 Strain, Dose-Response Relationship, Drug, Body Weight, Membrane Proteins, Thermogenesis, Menthol, Mice, Oxygen Consumption, Genetics, developmental biology, physiology, Menthol, metabolism, Trpm8, Wfs1, Animals, Energy Metabolism, Original Research
Male, Mice, Knockout, 570, Mice, 129 Strain, Dose-Response Relationship, Drug, Body Weight, Membrane Proteins, Thermogenesis, Menthol, Mice, Oxygen Consumption, Genetics, developmental biology, physiology, Menthol, metabolism, Trpm8, Wfs1, Animals, Energy Metabolism, Original Research
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