Author:
Kagawa Syota,Tanabe Katsuya,Hiromura Makoto,Ogawa Kakuyou,Koga Takayuki,Maeda Takahiro,Amo-Shiinoki Kikuko,Ochi Hiroyuki,Ichiki Yui,Fukuyama Shogo,Suzuki Saori,Suizu Natsuki,Ohmine Takaaki,Hamachi Sakurako,Tsuneki Hiroshi,Okuya Shigeru,Sasaoka Toshiyasu,Tanizawa Yukio,Nagashima Fumihiro
Abstract
Hachimijiogan (HJG) has originally been used to ameliorate a variety of symptoms associated with low ambient temperatures. However, its pharmacological action in metabolic organs remains unclear. We hypothesized that HJG may modulate metabolic function and have a potential therapeutic application to metabolic diseases. To test this hypothesis, we investigated metabolic action of HJG in mice. Male C57BL/6J mice chronically administered with HJG showed a reduction in adipocyte size with increased transcription of beige adipocyte-related genes in subcutaneous white adipose tissue. HJG-mixed high-fat diet (HFD)-fed mice showed alleviation of HFD-induced weight gain, adipocyte hypertrophy, liver steatosis with a significant reduction in circulating leptin and Fibroblast growth factor 21 despite no changes in food intake or oxygen consumption. Feeding an HJG-mixed HFD following 4-weeks of HFD feeding, while a limited effect on body weight, improved insulin sensitivity with a reversal of decreased circulating adiponectin. In addition, HJG improved insulin sensitivity in the leptin-deficient mice without significant effects on body weight. Treatment with n-butanol soluble extracts of HJG potentiated transcription of Uncoupling protein 1 mediated by β3-adrenergic agonism in 3T3L1 adipocytes. These findings provide evidence that HJG modulates adipocyte function and may exert preventive or therapeutic effects against obesity and insulin resistance.
Funder
Japan Society for the Promotion of Science
Subject
Pharmacology (medical),Pharmacology
Cited by
1 articles.
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