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. 2018 Dec 12;23(12):3296.
doi: 10.3390/molecules23123296.

Oleiferasaponin A₂, a Novel Saponin from Camellia oleifera Abel. Seeds, Inhibits Lipid Accumulation of HepG2 Cells Through Regulating Fatty Acid Metabolism

Affiliations

Oleiferasaponin A₂, a Novel Saponin from Camellia oleifera Abel. Seeds, Inhibits Lipid Accumulation of HepG2 Cells Through Regulating Fatty Acid Metabolism

Tai-Mei Di et al. Molecules. .

Abstract

A new triterpenoid saponin, named oleiferasaponin A₂, was isolated and identified from Camellia oleifera defatted seeds. Oleiferasaponin A₂ exhibited anti-hyperlipidemic activity on HepG2 cell lines. Further study of the hypolipidemic mechanism showed that oleiferasaponin A₂ inhibited fatty acid synthesis by significantly down-regulating the expression of SREBP-1c, FAS and FAS protein, while dramatically promoting fatty acid β-oxidation by up-regulating the expression of ACOX-1, CPT-1 and ACOX-1 protein. Our results demonstrate that the oleiferasaponin A₂ possesses potential medicinal value for hyperlipidemia treatment.

Keywords: Camellia oleifera; fatty acid metabolism; hypolipidemic activity; oleiferasaponin A2; triterpenoid saponin.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(A) Structure of oleiferasaponin A2; and (B) Key HMBC correlations of oleiferasaponin A2.
Figure 2
Figure 2
(A) The effect of oleiferasaponin A2 on HepG2 cells proliferation; (B) the lipid lowering activity of oleiferasaponin A2 under oleic acid treatment; and (C) the content of triglyceride under OA inducement. NC, blank control without oleic acid; 0, model group with 80 μM oleic acid; SVST, group with 80 μM oleic acid and 10 μM simvastain; A2, group with 80 μM oleic acid and 10 μM oleiferasaponin A2. ** p < 0.01, * p < 0.05.
Figure 3
Figure 3
The relative expression of genes related to fatty acid metabolism on fatty acid synthesis genes (SREBP-1c, FAS and ACC) and fatty acid β-oxidation genes (PPARα, ACOX-1 and CPT-1). NC, blank control; OA, 80 μM oleic Acid; OA + SVST, 80 μM Oleic Acid + 10 μM simvastatin; OA + A2, 80 μM Oleic Acid + 10 μM Oleiferasapoin A2. Compared to the control, ** p < 0.01.
Figure 4
Figure 4
The relative expression of proteins related to fatty acid metabolism. NC, blank control without oleic acid; 0, model group with 80 μM oleic acid; SVST, group with 80 μM oleic acid and 10 μM simvastain; A2, group with 80 μM oleic acid and 10 μM oleiferasapoin A2; ACOX-1, fatty acid oxidation protein; FAS, fatty acid synthesis protein; β-actin, reference protein.

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