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
Department of Natural Products Chemistry, Daiichi University of Pharmacy, Fukuoka, Japan.
Division of Endocrinology, Metabolism, Hematological Sciences and Therapeutics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
Front Pharmacol. 2023 May 12;14:1167934. doi: 10.3389/fphar.2023.1167934. eCollection 2023.
(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 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 -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.
(HJG)最初被用于改善与环境低温相关的各种症状。然而,其在代谢器官中的药理作用仍不清楚。我们推测HJG可能调节代谢功能,并对代谢性疾病具有潜在的治疗应用价值。为了验证这一假设,我们研究了HJG在小鼠体内的代谢作用。长期给予HJG的雄性小鼠皮下白色脂肪组织中脂肪细胞大小减小,米色脂肪细胞相关基因的转录增加。喂食HJG混合高脂饮食(HFD)的小鼠显示HFD诱导的体重增加、脂肪细胞肥大、肝脏脂肪变性得到缓解,循环瘦素和成纤维细胞生长因子21显著降低,尽管食物摄入量或耗氧量没有变化。在喂食4周HFD后再喂食HJG混合HFD,虽然对体重的影响有限,但改善了胰岛素敏感性,使循环脂联素的降低得到逆转。此外,HJG改善了瘦素缺乏小鼠的胰岛素敏感性,对体重没有显著影响。用HJG的正丁醇可溶性提取物处理可增强3T3L1脂肪细胞中由β3-肾上腺素能激动介导的解偶联蛋白1的转录。这些发现提供了证据表明HJG调节脂肪细胞功能,并可能对肥胖和胰岛素抵抗发挥预防或治疗作用。