Acute Homeostatic Responses to Increased Fat Consumption in MCH1R Knockout Mice
- First Online:
- Cite this article as:
- Chung, S., Wong, T., Nagasaki, H. et al. J Mol Neurosci (2010) 42: 459. doi:10.1007/s12031-010-9358-5
Melanin-concentrating hormone (MCH) is a hypothalamic neuropeptide which has been shown to regulate energy homeostasis. Using genetic knockout mice lacking the MCH1 receptor (MCH1R), we investigated how these mice adapt to metabolic changes caused by excessive caloric consumption. We show that the MCH system is one of the players mediating behavioral and metabolic responses upon increased caloric consumption. MCH1R knockout mice showed decreased tendency of food intake upon exposure to a high-fat diet. They also are resistant to gain weight upon high-fat diet by increasing fat metabolism. Therefore, the MCH system is important in regulating metabolic responses upon various environmental stimuli such as high-fat diet.
KeywordsMelanin-concentrating hormone Energy homeostasis G protein-coupled receptor Neuropeptide
Melanin-concentrating hormone (MCH) is a cyclic neuropeptide originally isolated from salmon pituitary where it induces paling of the skin (Kawauchi et al. 1983). In rodents and human, MCH exists as a 19-amino-acid-long peptide which is mainly synthesized in the lateral hypothalamus and the zona incerta (Mouri et al. 1993; Qu et al. 1996; Vaughan et al. 1989). In rodents, MCH interacts with one receptor, MCH1R (Bachner et al. 1999; Chambers et al. 1999; Lembo et al. 1999; Saito et al. 1999; Shimomura et al. 1999). MCH1R is widely expressed in the brain suggesting that the MCH system might have diverse physiological functions (Bittencourt et al. 1992; Saito et al. 2001). In rodents, MCH has been shown to regulate energy homeostasis (Pissios et al. 2006). Acute central MCH administration increases food intake, and chronic administrations increase body weight, white adipose tissue mass, and liver mass in mice (Ito et al. 2003). MCH levels are increased upon fasting and MCH is overexpressed in the hypothalamus of ob/ob mice (Qu et al. 1996). Mice lacking prepro-MCH are lean due to hypophagia and an increase in metabolic rate (Shimada et al. 1998). MCH1R knockout mice are lean; however, they are hyperphagic and hyperactive (Marsh et al. 2002). Furthermore, MCH1R knockout mice are resistant to diet-induced obesity (Chen et al. 2002). These evidences suggest that MCH is important in regulating energy homeostasis.
To identify specific roles of the MCH system in coordinating energy homeostasis, we examined the metabolic and behavioral responses of MCH1R knockout (KO) mice subjected to increased dietary fat. This environmental stimulus affects energy homeostasis through the hypothalamic pathways which maintain the integrity of the body’s basal metabolism. Since MCH is a hypothalamic peptide which has been shown to modulate feeding response and metabolism, we studied its roles in metabolic adaptations to high-fat diet by using mice lacking the MCH1R.
Previous studies have shown that MCH1R KO mice have lower body weight and fat mass than wild-type (WT) mice upon chronic high-fat diet (Chen et al. 2002; Marsh et al. 2002). These studies, however, focused only on the long-term consequences of exposure to high-fat diet (Chen et al. 2002). MCH1R KO mice have been subjected to moderate high-fat (MHF) diet and have exhibited similar level of enhanced running wheel activity to WT mice (Zhou et al. 2005). This suggests that MCH1R is not required for acute activity-based energy expenditure upon a change in diet composition. Our study therefore focused on how acute exposure to high-fat diet affects metabolic adaptations in MCH1R KO mice.
Materials and Methods
MCH1R knockout mice obtained from Merck (Marsh et al. 2002), backcrossed to a C57BL/6 backgrounds, were used for all the experiments. Animals were group-housed and maintained on a 12-h light/dark cycle (lights on at 07:00) with food and water available ad libitum. For studies measuring feeding and metabolism, mice were single housed for the accurate measurement of individual animal. All experimental procedures were performed in compliance with NIH Guide for Care and Use of Laboratory Animals and approved by the UCI Institutional Animal Care and Use Committee.
VO2 and VCO2 were simultaneously measured by indirect calorimetry (Oxymax, Columbus Instruments, Columbus, OH, USA). Mice were acclimatized to the chamber at least for 2 days. Mice were individually housed in specially built plexiglass cages (20 cm × 10.5 cm × 12 cm) through which room air is passed at a flow rate of 0.52 l/min. Exhaust air from each chamber will be sampled at 5-min intervals. Sample air was sequentially passed through O2 and CO2 analyzers (Columbus Instruments) for determination of O2 and CO2 content. Metabolic rate (calorie per hour) was calculated from the following equation: (3.815 + 1.232 × RER) × vO2, where RER is the respiratory exchange ratio [volume of CO2 produced (ml/kg body weight/h) per volume of O2 consumed (ml/kg body weight/h)] and vO2 is the volume of O2 consumed per hour. After they were adapted to the chamber, food was switched to a high-fat diet (HF) diet (D12451, 45% kcal fat; Research Diets, New Brunswick, NJ, USA). Mice were left in the chamber three more days to examine any changes in their metabolism.
Prism software (GraphPad, San Diego, CA, USA) was used for statistical analysis. Results were analyzed by t test or ANOVA followed by the appropriate post hoc comparisons, and p < 0.05 was considered statistically significant.
Metabolic Responses of MCH1R Knockout Mice to High Fat Diet Consumption
Diet-induced thermogenesis is proportionate to caloric consumption and represents an important component of energy homeostasis. To study whether the MCH system regulates diet-induced thermogenesis upon exposure to a high-fat diet, energy expenditure was monitored in WT and MCH1R KO mice when they were exposed to a high-fat diet.
These data indicate that reduced feed efficiency of the MCH1R KO mice upon high-fat diet is not caused by a decrease in appetite alone. It correlates with an increased fatty acid oxidation which is evidenced by their lower RER value (Fig. 2b). This suggests that blockade of the endogenous MCH system might boost fat burning process upon increased dietary fat consumption and that this might have caused the resistance to body weight gain in MCH1R KO mice.
The MCH system has been extensively studied for its roles in regulating energy homeostasis (Pissios et al. 2006). These data have suggested that the MCH system may be involved in many situations where energy homeostasis is perturbed. We chose to study the MCH system’s potential role in diet-induced thermogenesis induced by increased dietary fat consumption. This stimulus has been shown to affect the hypothalamic pathway which maintains homeostasis. In this report, we use MCH1R KO mice to show that the MCH system is involved in maintaining homeostasis when animals are exposed to increased fat consumption.
We show that the MCH system is involved in the adaptation to high-fat diet provided acutely. When they were fed with normal chow, MCH1R KO mice showed hyperphagia as previously described, possibly secondary to their increased metabolism and activity (Marsh et al. 2002). In young and lean animals, transition from low- to high-fat diet leads to a marked hyperphagia due to the novelty and palatability of the high-fat diet. This transition is then followed by a reduced food intake to account for the higher energy content of the diet. MCH1R KO mice, however, did not exhibit hyperphagia but instead an immediate reduction in food intake. This suggests that MCH1R KO mice do not show a tendency to prefer high-fat diet. Most notably, the feed efficiency of MCH1R KO mice during the 72 h of HF diet was significantly lower than that of WT mice which suggests that the MCH system might regulate metabolic responses upon exposure to high-fat diet. This led us to monitor the acute metabolic changes of these mice upon high-fat diet consumption by monitoring their RER and VO2.
When exposed to high calorific food in mice, VO2 increases due to increase in locomotor activity. Both WT and MCH1R KO mice have been shown to exhibit an increase in locomotor activity upon transition to a MHF diet (Zhou et al. 2005), but the effect on VO2 was not reported. Our results show no significant difference in the VO2 of MCH1R KO mice upon exposure to high-fat diet. This is surprising especially since mice lacking ppMCH exhibit a higher VO2 and a higher locomotor activity after 24 h of high-fat diet than WT mice (Kokkotou et al. 2005). It may, however, be explained at least in part by our RER results. RER values represent the energy fuel that animals use. High RER indicates increased utilization of carbohydrates for energy consumption whereas low RER indicates increased utilization of fatty acids. Therefore, high RER values in animals lead to increased risk of weight gain. Transition to HF diet usually decreases RER values to increase fat oxidation so that animals do not gain weight. Our study shows that RER values of WT mice increased significantly during the first 24-h HF diet before decreasing during the 24–72 h of HF diet, as expected. On the other hand, the RER values of MCH1R KO mice subjected to the same paradigm are high on LF diet and gradually decrease when put on HF diet. They do not show the burst in increase in the first 24 h of HF diet as do the WT mice. This suggests that the MCH1R KO mice can increase fat oxidation more efficiently. This might also have contributed to the resistance to weight gain in MCH1R KO mice upon HF diet. This finding suggests that the MCH system can modulate fat/carbohydrate oxidation, especially when animals are acutely exposed to HF diet. This is in agreement with the studies that have reported that MCH1R antagonists induce significant weight loss than a pair-fed group (Huang et al. 2005; Ito et al. 2010). Ito et al. reported that chronic MCH1R antagonist treatments into DIO mice slightly increased fatty acid oxidation and reduced serum-free fatty acid level, but not triglyceride level (Ito et al. 2010). These findings suggest that MCH1R signaling modulates fatty acid oxidation when animals are exposed to HF diet. Also, it has been reported that MCH1R KO mice have slightly lower triglyceride level than WT mice (77 ± 10 mg/dl for WT vs. 69 ± 6 mg/dl for MCH1R KO; Marsh et al. 2002). We therefore predict that the reduced body weight gains of MCH1R KO mice upon HF diet might be accompanied by lower triglyceride/free fatty acid levels. Together, these data point at the MCH system as being involved in the adaptation of the organism to excess caloric consumption.
In summary, our experiments show that the endogenous MCH system has an important role in regulating energy homeostasis upon high-fat diet consumption. It, however, remains to be described how the MCH system regulates these processes.
We would like to thank Dr. Su Qian in Merck for providing us with MCH1R KO mice. We would also like to thank Dr. Qun-Yong Zhou and Dr. Jia-Da Li for helpful discussion and helping us with metabolism assay. This work was supported by grants MH60231 and DA024746 to O.C. S.C. is supported by Davis Foundation Postdoctoral Fellowship Program in Eating Disorders Research supported by Hilda and Preston Davis Foundation.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.