Crotonis Fructus and Its Constituent, Croton Oil, Stimulate Lipolysis in OP9 Adipocytes.

Evid Based Complement Alternat Med

Center for Metabolic Function Regulation, Wonkwang University School of Medicine, No. 460 Iksan-Daero, Iksan, Jeonbuk 570-749, Republic of Korea ; BK21 Plus Program and Department of Smart Life-Care Convergence, Graduate School, Wonkwang University, No. 460 Iksan-Daero, Iksan, Jeonbuk 570-749, Republic of Korea ; Department of Korean Physiology, Wonkwang University School of Korean Medicine, No. 460 Iksan-Daero, Iksan, Jeonbuk 570-749, Republic of Korea.

Published: December 2014

AI Article Synopsis

  • Crotonis fructus (CF), derived from Croton tiglium L., has traditionally been used for gastrointestinal issues in Asia, with croton oil (CO) as its main active component.
  • The study investigates the effects of CF extracts (CFE) and CO on lipolysis in adipocytes, using glycerol release as a marker for fat breakdown.
  • Results show that CFE and CO enhance glycerol release in a dose-dependent manner, outperforming isoproterenol, and their lipolytic effect involves increased activity of phosphorylated hormone sensitive lipase (pHSL), suggesting potential for CFE and CO in developing lipolysis-stimulating treatments.

Article Abstract

Introduction. Crotonis fructus (CF) is the mature fruit of Croton tiglium L. and has been used for the treatment of gastrointestinal disturbance in Asia. It is well known that the main component of CF is croton oil (CO). The present study is to investigate the effects of CF extracts (CFE) and CO on lipolysis in OP9 adipocytes. Methods. Glycerol release to the culture supernatants was used as a marker of adipocyte lipolysis. Results. Treatment with various concentrations of CFE and CO stimulates glycerol release in a dose-dependent manner. The increase in glycerol release by CFE is more potent than isoproterenol, which is a β-adrenergic agonist as a positive control in our system. The increased lipolysis by CFE and CO was accompanied by an increase of phosphorylated hormone sensitive lipase (pHSL) but not nonphosphorylated HSL protein and mRNA. Pretreatment with H89, which is a protein kinase A inhibitor, significantly abolished the CFE- and CO-induced glycerol release in OP9 adipocytes. These results suggest that CFE and CO may be a candidate for the development of a lipolysis-stimulating agent in adipocytes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244682PMC
http://dx.doi.org/10.1155/2014/780385DOI Listing

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