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Madecassoside modulates lipid metabolism in visceral adipocytes: exploring the browning, lipolysis, and lipogenesis mechanisms for potential obesity treatment

Authors
Cho, WonjunHong, MineuiMobarak, Enas H.Birdal, OguzhanLim, Min ChanJung, Min SeokHong, Soon AuckJeong, Ji HoonJung, Tae Woo
Issue Date
Apr-2024
Publisher
OXFORD UNIV PRESS
Keywords
Madecassoside; Obesity; PPAR alpha; FGF21; Adipocyte
Citation
JOURNAL OF PHARMACY AND PHARMACOLOGY
Journal Title
JOURNAL OF PHARMACY AND PHARMACOLOGY
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/73494
DOI
10.1093/jpp/rgae042
ISSN
0022-3573
2042-7158
Abstract
Objectives: Madecassoside (MA) is a triterpene derived from Centella asiatica that has been recognized for its antioxidant and anti-inflammatory properties in various disease models. However, its direct impact on cultured white adipocytes and the underlying mechanisms, mainly through gene knockdown, have not been thoroughly explored. Methods: Western blot analysis was utilized to assess the expression levels of various proteins, while oil red O staining was used to measure lipid deposition. The adipocyte shapes were confirmed using H&E staining. Key findings: MA treatment enhanced browning and lipolysis in 3T3-L1 adipocytes and adipose tissue from experimental mice while suppressing lipogenesis. Furthermore, MA treatment increased the expression of PPAR alpha and FGF21 in 3T3-L1 adipocytes as well as the secretion of FGF21 into the culture medium. Knockdown of PPAR alpha or FGF21 using siRNA diminished the effects of MA on lipid metabolism in cultured adipocytes. Conclusions: These findings demonstrate that MA promotes thermogenic browning and lipolysis while inhibiting adipocyte lipogenesis, thus showing the potential for attenuating obesity. The study suggested that MA could be a viable therapeutic approach for treating obesity. [GRAPHICS]
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