@article {Fink699, author = {Brian D. Fink and Judith A. Herlein and Deng Fu Guo and Chaitanya Kulkarni and Benjamin J. Weidemann and Liping Yu and Justin L. Grobe and Kamal Rahmouni and Robert J. Kerns and William I. Sivitz}, title = {A Mitochondrial-Targeted Coenzyme Q Analog Prevents Weight Gain and Ameliorates Hepatic Dysfunction in High-Fat{\textendash}Fed Mice}, volume = {351}, number = {3}, pages = {699--708}, year = {2014}, doi = {10.1124/jpet.114.219329}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {We hypothesized that the mitochondrial-targeted antioxidant, mitoquinone (mitoQ), known to have mitochondrial uncoupling properties, might prevent the development of obesity and mitigate liver dysfunction by increasing energy expenditure, as opposed to reducing energy intake. We administered mitoQ or vehicle (ethanol) to obesity-prone C57BL/6 mice fed high-fat (HF) or normal-fat (NF) diets. MitoQ (500 {\textmu}M) or vehicle (ethanol) was added to the drinking water for 28 weeks. MitoQ significantly reduced total body mass and fat mass in the HF-fed mice but had no effect on these parameters in NF mice. Food intake was reduced by mitoQ in the HF-fed but not in the NF-fed mice. Average daily water intake was reduced by mitoQ in both the NF- and HF-fed mice. Hypothalamic expression of neuropeptide Y, agouti-related peptide, and the long form of the leptin receptor were reduced in the HF but not in the NF mice. Hepatic total fat and triglyceride content did not differ between the mitoQ-treated and control HF-fed mice. However, mitoQ markedly reduced hepatic lipid hydroperoxides and reduced circulating alanine aminotransferase, a marker of liver function. MitoQ did not alter whole-body oxygen consumption or liver mitochondrial oxygen utilization, membrane potential, ATP production, or production of reactive oxygen species. In summary, mitoQ added to drinking water mitigated the development of obesity. Contrary to our hypothesis, the mechanism involved decreased energy intake likely mediated at the hypothalamic level. MitoQ also ameliorated HF-induced liver dysfunction by virtue of its antioxidant properties without altering liver fat or mitochondrial bioenergetics.}, issn = {0022-3565}, URL = {https://jpet.aspetjournals.org/content/351/3/699}, eprint = {https://jpet.aspetjournals.org/content/351/3/699.full.pdf}, journal = {Journal of Pharmacology and Experimental Therapeutics} }