4.7 Article

Bioactivity-based molecular networking-guided identification of guttiferone J from Garcinia cambogia as an anti-obesity candidate

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 180, 期 5, 页码 589-608

出版社

WILEY
DOI: 10.1111/bph.15979

关键词

anti-obesity; bioactivity-based molecular networking; Garcinia cambogia; guttiferone J; sirtuin 3; white adipose tissue browning

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This study discovered that polycyclic polyprenylated acylphloroglucinols from the fruits of Garcinia cambogia have lipid-lowering effects and can induce browning of adipocytes. Among them, guttiferone J (GOJ) is the most potent inducer of browning, which activates the deacetylase SIRT3 to enhance mitochondrial biogenesis and thermogenesis. In high-fat diet-induced obese mice, GOJ protected against obesity and related disorders by promoting browning of adipose tissue.
Background and PurposePharmacological intervention to induce browning of white adipose tissue provides a promising anti-obesity therapy. The fruits of Garcinia cambogia (Clusiaceae) have been widely applied to manage body weight; however, the chemical principles remain unclear. The current study aims to discover browning inducers from the fruits of G. cambogia and investigate the underlying mechanisms. Experimental ApproachThe bioactivity-based molecular networking and Oil Red O staining on 3T3-L1 and C3H10T1/2 adipocytes were applied for guided isolation. High-fat diet-induced obese mice were recruited to evaluate the anti-obesity activity. Key ResultsThe bioactivity-based molecular networking-guided isolation yielded several polycyclic polyprenylated acylphloroglucinols from the fruits of G. cambogia with lipid-lowering effect in adipocytes, including guttiferone J (GOJ), garcinol and 14-deoxygarcinol. As the most potent one, GOJ (10 mu M) reduced lipid accumulation by 70% and 76% in 3T3-L1 and C3H10T1/2 adipocytes, respectively. Furthermore, GOJ (2.5-10 mu M) increased the expression of the deacetylase sirtuin 3 (SIRT3) and activated it, which, in turn, reduced the acetylation level of PPAR gamma coactivator-1 alpha to boost mitochondrial biogenesis and promoted uncoupling protein 1 expression to enhance thermogenesis, resulting in browning of adipocytes. In high-fat diet-induced-obese mice, GOJ (10 and 20 mg center dot kg(-1)center dot day(-1) for 12 weeks) protected against adiposity, hyperlipidaemia, insulin resistance and liver lipotoxicity, through boosting SIRT3-mediated browning of inguinal adipose tissue. Conclusion and ImplicationsGOJ represents a new scaffold of thermogenic inducer, which is responsible for the anti-obesity property of G. cambogia and can be further developed as a candidate for treating obesity and its related disorders.

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