Articles citing this Article
PubMed
PubMed Citation
Articles by Masuda, Y.
Articles by Fushiki, T.
Upregulation of uncoupling proteins by oral administration of capsiate, a nonpungent capsaicin analog
Yoriko Masuda,1 Satoshi Haramizu,1 Kasumi Oki,1 Koichiro Ohnuki,1 Tatsuo Watanabe,2 Susumu Yazawa,3 Teruo Kawada,1 Shu-ichi Hashizume,4 and Tohru Fushiki1
1Laboratory of Nutrition Chemistry, Division of Food Science and Biotechnology, and 3Laboratory of Vegetable and Ornamental Horticulture, Division of Agriculture, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502; 2School of Food and Nutritional Sciences, University of Shizuoka, Shizuoka 422-8526; and 4Research Institute, Morinaga and Company, Limited, Yokohama 230-8504, Japan
Submitted 11 September 2002 ; accepted in final form 14 August 2003
ABSTRACT
TOP
ABSTRACT
MATERIALS AND METHODS
RESULTS
DISCUSSION
DISCLOSURES
REFERENCES
Capsiate is a nonpungent capsaicin analog, a recently identified principle of the nonpungent red pepper cultivar CH-19 Sweet. In the present study, we report that 2-wk treatment of capsiate increased metabolic rate and promoted fat oxidation at rest, suggesting that capsiate may prevent obesity. To explain these effects, at least in part, we examined uncoupling proteins (UCPs) and thyroid hormones. UCPs and thyroid hormones play important roles in energy expenditure, the maintenance of body weight, and thermoregulation. Two-week treatment of capsiate increased the levels of UCP1 protein and mRNA in brown adipose tissue and UCP2 mRNA in white adipose tissue. This dose of capsiate did not change serum triiodothyronine or thyroxine levels. A single dose of capsiate temporarily raised both UCP1 mRNA in brown adipose tissue and UCP3 mRNA in skeletal muscle. These results suggest that UCP1 and UCP2 may contribute to the promotion of energy metabolism by capsiate, but that thyroid hormones do not.
oxygen consumption; body fat; energy expenditure; CH-19 Sweet; thermogenesis---itabenice if one of our board sponcers could sell sweet bell pepper extract
PubMed
PubMed Citation
Articles by Masuda, Y.
Articles by Fushiki, T.
Upregulation of uncoupling proteins by oral administration of capsiate, a nonpungent capsaicin analog
Yoriko Masuda,1 Satoshi Haramizu,1 Kasumi Oki,1 Koichiro Ohnuki,1 Tatsuo Watanabe,2 Susumu Yazawa,3 Teruo Kawada,1 Shu-ichi Hashizume,4 and Tohru Fushiki1
1Laboratory of Nutrition Chemistry, Division of Food Science and Biotechnology, and 3Laboratory of Vegetable and Ornamental Horticulture, Division of Agriculture, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502; 2School of Food and Nutritional Sciences, University of Shizuoka, Shizuoka 422-8526; and 4Research Institute, Morinaga and Company, Limited, Yokohama 230-8504, Japan
Submitted 11 September 2002 ; accepted in final form 14 August 2003
ABSTRACT
TOP
ABSTRACT
MATERIALS AND METHODS
RESULTS
DISCUSSION
DISCLOSURES
REFERENCES
Capsiate is a nonpungent capsaicin analog, a recently identified principle of the nonpungent red pepper cultivar CH-19 Sweet. In the present study, we report that 2-wk treatment of capsiate increased metabolic rate and promoted fat oxidation at rest, suggesting that capsiate may prevent obesity. To explain these effects, at least in part, we examined uncoupling proteins (UCPs) and thyroid hormones. UCPs and thyroid hormones play important roles in energy expenditure, the maintenance of body weight, and thermoregulation. Two-week treatment of capsiate increased the levels of UCP1 protein and mRNA in brown adipose tissue and UCP2 mRNA in white adipose tissue. This dose of capsiate did not change serum triiodothyronine or thyroxine levels. A single dose of capsiate temporarily raised both UCP1 mRNA in brown adipose tissue and UCP3 mRNA in skeletal muscle. These results suggest that UCP1 and UCP2 may contribute to the promotion of energy metabolism by capsiate, but that thyroid hormones do not.
oxygen consumption; body fat; energy expenditure; CH-19 Sweet; thermogenesis---itabenice if one of our board sponcers could sell sweet bell pepper extract