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Phytochemical Combination (p-Synephrine, p-Octopamine Hydrochloride, and Hispidulin) for Improving Obesity in Obese Mice Induced by High-Fat Dietopen access

Authors
Lee, DahaeLee, Ji HwanKim, Byoung HaLee, SanghyunKim, Dong-WookKang, Ki Sung
Issue Date
May-2022
Publisher
MDPI
Keywords
adipocytes; adipogenesis; hispidulin; p-octopamine hydrochloride; p-synephrine
Citation
Nutrients, v.14, no.10
Journal Title
Nutrients
Volume
14
Number
10
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/58196
DOI
10.3390/nu14102164
ISSN
2072-6643
2072-6643
Abstract
Obesity treatment efficiency can be increased by targeting both central and peripheral pathways. In a previous study, we identified two natural compounds (hispidulin and p-synephrine) that affect adipocyte differentiation. We tested whether obesity treatment efficiency may be improved by adding an appetite-controlling agent to the treatment in the present study. Alkaloids, such as p-octopamine, are adrenergic agonists and are thus used as dietary supplements to achieve weight loss. Here, we assessed anti-obesity effects of a mixture of p-synephrine, p-octopamine HCl, and hispidulin (SOH) on murine preadipocyte cells and on mice receiving a high-fat diet (HFD). SOH showed stronger inhibition of the formation of red-stained lipid droplets than co-treatment with hispidulin and p-synephrine. Moreover, SOH reduced the expression of adipogenic marker proteins, including CCAAT/enhancer-binding protein alpha, CCAAT/enhancer-binding protein beta, and peroxisome proliferator-activated receptor gamma. In the HFD-induced obesity model, body weight and dietary intake were lower in mice treated with SOH than in the controls. Additionally, liver weight and the levels of alanine aminotransferase and total cholesterol were lower in SOH-treated mice than in the controls. In conclusion, our results suggest that consumption of SOH may be a potential alternative strategy to counteract obesity. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
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