Differential regulation of metabolic parameters by energy deficit and hunger

• Published in: Metabolism, clinical and experimental Vol. 64; no. 10; pp. 1235 - 1239
• Main Authors: Kitka, Tamás, Tuza, Sebestyén, Varga, Balázs, Horváth, Csilla, Kovács, Péter
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.2015
• Subjects: Animals; Appetite Depressants - pharmacology; Appetite Regulation - drug effects; Caloric Restriction; Cyclobutanes - pharmacology; Diet; Endocrinology & Metabolism; Energy expenditure; Energy Metabolism - drug effects; Food Deprivation - physiology; Hunger - drug effects; Hunger - physiology; Indirect calorimetry; Male; Mice; Mice, Inbred C57BL; Obesity; Obesity - etiology; Obesity - metabolism; Respiratory exchange rate; Respiratory quotient; Tramadol - pharmacology; Energy expenditure; Obesity; Respiratory quotient; Respiratory exchange rate; Indirect calorimetry
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/j.metabol.2015.06.017

Abstract Aims Hypocaloric diet decreases both energy expenditure (EE) and respiratory exchange rate (RER), affecting the efficacy of dieting inversely. Energy deficit and hunger may be modulated separately both in human and animal studies by drug treatment or food restriction. Thus it is important to separate the effects of energy deficit and hunger on EE and RER. Methods Three parallel and analogous experiments were performed using three pharmacologically distinct anorectic drugs: rimonabant, sibutramine and tramadol. Metabolic parameters of vehicle- and drug-treated and pair-fed diet-induced obese mice from the three experiments underwent common statistical analysis to identify effects independent of the mechanisms of action. Diet-induced obesity (DIO) test of tramadol was also performed to examine its anti-obesity efficacy. Results RER was decreased similarly by drug treatments and paired feeding throughout the experiment irrespective of the cause of reduced food intake. Contrarily, during the passive phase, EE was decreased more by paired feeding than by both vehicle and drug treatment irrespective of the drug used. In the active phase, EE was influenced by the pharmacological mechanisms of action. Tramadol decreased body weight in the DIO test. Conclusions Our results suggest that RER is mainly affected by the actual state of energy balance; conversely, EE is rather influenced by hunger. Therefore, pharmacological medications that decrease hunger may enhance the efficacy of a hypocaloric diet by maintaining metabolic rate. Furthermore, our results yield the proposal that effects of anorectic drugs on EE and RER should be determined compared to vehicle and pair-fed groups, respectively, in animal models.