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Reducing Effect of Farnesylquinone on Lipid Mass in C. elegans by Modulating Lipid Metabolism.


ABSTRACT: Bioassay-guided fractionation of marine-derived fungi revealed that the EtOAc fraction from the fermentation broth of a mutated fungal strain Streptomyces nitrosporeus YBH10-5 had lipid-lowering effects in HepG2 cells. Chromatographic separation of the EtOAc fraction resulted in the isolation of 11 PKS-based derivatives, including a structurally unique meroterpenoid namely nitrosporeunol H (1). The structure of compound 1 was determined by the analysis of spectroscopic data. Further bioassay resulted in farnesylquinone (2) and its analogues to exert in vivo fat-reducing effects in C. elegans worm model. The underlying mode of action of compound 2 in the context of live worms was investigated, uncovering that compound 2 enhanced the mitochondrial ?-oxidation rate and changed the transcriptional level of energy metabolism genes. Additional experiments revealed that compound 2 exerted its effects in C. elegans partially through repressing FAT-5, an isoform of stearoyl-CoA desaturase (SCD) which catalyzes the conversion of saturated fatty acids to monounsaturated fatty acids, thereafter leading to the modification of the fatty acid profile. Thus, compound 2 was suggested to be a promising lead for further optimization to treat obesity.

SUBMITTER: Jia X 

PROVIDER: S-EPMC6627328 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Reducing Effect of Farnesylquinone on Lipid Mass in <i>C. elegans</i> by Modulating Lipid Metabolism.

Jia Xihua X   Xu Manglin M   Yang Aigang A   Zhao Yan Y   Liu Dong D   Huang Jian J   Proksch Peter P   Lin Wenhan W  

Marine drugs 20190605 6


Bioassay-guided fractionation of marine-derived fungi revealed that the EtOAc fraction from the fermentation broth of a mutated fungal strain <i>Streptomyces nitrosporeus</i> YBH10-5 had lipid-lowering effects in HepG2 cells. Chromatographic separation of the EtOAc fraction resulted in the isolation of 11 PKS-based derivatives, including a structurally unique meroterpenoid namely nitrosporeunol H (<b>1</b>). The structure of compound <b>1</b> was determined by the analysis of spectroscopic data.  ...[more]

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