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Madecassoside modulates lipid metabolism in visceral adipocytes: exploring the browning, lipolysis, and lipogenesis mechanisms for potential obesity treatment.
Cho, Wonjun; Hong, Mineui; Mobarak, Enas H; Birdal, Oguzhan; Lim, Min Chan; Jung, Min Seok; Hong, Soon Auck; Jeong, Ji Hoon; Jung, Tae Woo.
Afiliación
  • Cho W; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Hong M; Department of Pathology, College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Mobarak EH; Department of Restorative Dentistry, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
  • Birdal O; Department of Cardiology, Medical Faculty, Atatürk University, Erzurum 25240, Turkey.
  • Lim MC; College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Jung MS; College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Hong SA; Department of Pathology, College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Jeong JH; Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
  • Jung TW; Department of Global Innovative Drugs, Graduate School of Chung-Ang University, Seoul 06974, Republic of Korea.
J Pharm Pharmacol ; 76(7): 834-841, 2024 Jul 05.
Article en En | MEDLINE | ID: mdl-38588466
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 PPARα and FGF21 in 3T3-L1 adipocytes as well as the secretion of FGF21 into the culture medium. Knockdown of PPARα 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triterpenos / Células 3T3-L1 / PPAR alfa / Lipogénesis / Factores de Crecimiento de Fibroblastos / Lipólisis / Obesidad Límite: Animals Idioma: En Revista: J Pharm Pharmacol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triterpenos / Células 3T3-L1 / PPAR alfa / Lipogénesis / Factores de Crecimiento de Fibroblastos / Lipólisis / Obesidad Límite: Animals Idioma: En Revista: J Pharm Pharmacol Año: 2024 Tipo del documento: Article