HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice

Authors
Lee, Heon-MyungRim, Hong-KunSeo, Jong-HwanKook, Yoon-BumKim, Sung-KewOh, Chang-HyunYoo, Kyung HoJin, Jong-SikAn, Hyo-Jin
Issue Date
2014-12
Publisher
BIOMED CENTRAL LTD
Citation
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, v.14
Abstract
Background: HOX-7 is a newly developed dietary formula composed of traditional oriental herbal medicines. The formula was developed with the aim of improving weight control. We investigated the anti-obesity effect of HOX-7 on high-fat-diet (HFD)-induced obesity in C57BL/6 mice. Methods: The mice were divided into four groups and were fed a normal diet (ND), HFD, or HFD with oral administration of HOX-7 at 100 or 200 mg/kg/day for 12 weeks. Body and fat weight, histological changes of fat tissue, and the expression of key adipogenic transcription factors were investigated. Results: The body weight of mice fed the HFD with HOX-7 was significantly decreased compared to the HFD group. There were no obvious differences in weekly food intake among the 4 groups. The weight of the epididymal and total fat pads was reduced in mice fed the HFD with HOX-7. Treatment with HOX-7 also substantially attenuated the expression of key adipogenic transcription factors, including peroxisome proliferatoractivated receptor., CCAAT/enhancer binding protein a, sterol regulatory element binding protein 1c, adipocyte P2, liver X receptor, and lipoprotein lipase in the epididymal adipose tissue. Conclusion: Overall, this study highlighted the anti-obesity effects of HOX-7, a finding that could contribute to the development of natural anti-obesity herbal medicines.
Keywords
RECEPTOR-GAMMA EXPRESSION; ADIPOCYTE DIFFERENTIATION; SALICORNIA-HERBACEA; ANTIOBESITY; METABOLISM; REGULATOR; EXTRACT; RATS; C/EBPa; Mice; Obesity; PPAR gamma; SREBP1c; Traditional herbal medicine
ISSN
1472-6882
URI
https://pubs.kist.re.kr/handle/201004/126018
DOI
10.1186/1472-6882-14-505
Appears in Collections:
KIST Article > 2014
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