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.2018 Dec;56(1):183-191.
doi: 10.1080/13880209.2018.1436073.

Desalted Salicornia europaea powder and its active constituent, trans-ferulic acid, exert anti-obesity effects by suppressing adipogenic-related factors

Affiliations

Desalted Salicornia europaea powder and its active constituent, trans-ferulic acid, exert anti-obesity effects by suppressing adipogenic-related factors

Md Mahbubur Rahman et al. Pharm Biol.2018 Dec.

Abstract

Context: Salicornia europaea (Amaranthaceae) (SE) has been shown to reduce obesity, but it remains a problem as a food supplement because of its high salt content (25-35% NaCl).

Objectives: This study investigated the anti-obesity effects and mechanism of action of desalted SE powder (DSP).

Materials and methods: Sprague-Dawley rats (n = 50) were divided into a normal control group (NC), a high-fat diet (HFD)-induced obesity control group (HFD), and HFD groups co-administered DSP (250 and 500 mg/kg) or Garcinia cambogia (Clusiaceae) extract (GE, 200 mg/kg, standard control) orally each day for 12 weeks.

Results: The body weight was significantly reduced by co-administration of DSP (596.51 ± 19.84 kg, 4.60% and 562.08 ± 9.74 kg, 10.10%, respectively) and GE (576.00 ± 11.29 kg, 7.88%) relative to the HFD group (625.25 ± 14.02 kg) and was accompanied by reduced abdominal fat mass, and serum lipid levels, with no effects on feed intake. To find the underlying mechanism of the anti-obesity effects, trans-ferulic acid (TFA) was identified as the main ingredient and investigated with regard to whether it attenuated adipogenesity in 3T3L-1 cells. DSP-derived TFA suppressed adipocyte differentiation and accumulation of intracellular lipids. TFA also down-regulated the adipogenesis-related gene expression of sterol regulatory element-binding protein 1, peroxisome proliferator-activated receptor γ, CCAAT/enhancer binding protein-α and fatty acid synthase.

Conclusions: These findings suggest that DSP may be considered for use as a food supplement intent of controlling obesity through its antiobesity and antiadipogenic properties.

Keywords: 3T3L-1 cells; Desaltation; abdominal fat mass; adipogenesis.

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Figures

Figure 1.
Figure 1.
Analytical and preparative HPLC profiles of desaltedSalicornia europaea L. powder (DSP). (A) Analytical HPLC profile of DSP-EW; (B) analytical HPLC profile of authentictrans-ferulic acid; (C) Multiple preparative HPLC profile of DSP-EW; (1) caffeic acid; (2)p-coumaric acid; (3)trans-ferulic acid; (4) isorhamnetin-3-β-D-glucoside.
Figure 2.
Figure 2.
ESI-MS spectra of DSP-EW-3 (compound 1) (top, positive;bottom, negative).
Figure 3.
Figure 3.
Effect of co-administration of DSP on body weight in high fat induced obese rat. NC: normal control; HFD: high-fat diet induced obese group; HFD + DSP-250, rat supplemented HFD and desaltedS. europea powder at dose 250 mg/kg; HFD + DSP-500, rat supplemented 500 mg/kg DSP; HFD + GE-200, rat supplemented 200 mg/kgGarcinia cambogea extract. The data are reported as the mean ± SD (n = 10). *p < 0.05, **p < 0.01, ***p < 0.001, Bonferronipost hoc test following two-way ANOVA versus the NC group.
Figure 4.
Figure 4.
Effect of co-administration of DSP on body weight in high fat induced obese rat. NC: normal control; HFD: high-fat diet induced obese group; HFD + DSP-250, rat supplemented HFD and desaltedS. europea powder at dose 250 mg/kg; HFD + DSP-500, rat supplemented 500 mg/kg DSP; HFD + GE-200, rat supplemented 200 mg/kg Garcinia cambogea extract. (A) 3-D micro-CT images of abdominal adiposity. (B–D) numerical presentation of abdominal adiposity. TAF: total abdominal fat; VAF: visceral abdominal fat, and SAF: subcutaneous abdominal fat volume. The data are reported as the mean ± SD (n = 10). *p < 0.05, **p < 0.01, ***p < 0.001, analyzed by parametric multiple comparison procedures, One-way ANOVA test. When the result of ANOVA was significant, and Dunnett’s multiple comparison test was applied versus the NC group; #p < 0.05; ##p < 0.01; and ###p < 0.001, versus high-fat diet supplemented group (HFD).
Figure 5.
Figure 5.
DSP-derived trans-ferulic acid on cell viability in 3T3-L1 cells. The data are reported as the mean ± SD (n = 10). Analyzed by Bonferronipost hoc test following one-way ANOVA versus the NC group. But there was no significant change was observed either versus normal control (NC) or versus DMI group.
Figure 6.
Figure 6.
Effect of co-administration of DSP-derivedtrans-ferulic acid on lipid accumulation in 3T3-L1 cells. The data are reported as the mean ± SD (n = 10). *p < 0.05, **p < 0.01, ***p < 0.001, analyzed by parametric multiple comparison procedures, One-way ANOVA test. When the result of ANOVA was significant, and Dunnett’s multiple comparison test was applied versus the NC group; #p < 0.05; ##p < 0.01; and ###p < 0.001, versus DMI.
Figure 7.
Figure 7.
Effect of co-administration of DSP-derivedtrans-ferulic acid on gene/protein expression in 3T3-L1 cells. The data are reported as the mean ± SD (n = 10). *p < 0.05, **p < 0.01, ***p < 0.001, analyzed by parametric multiple comparison procedures, One-way ANOVA test. When the result of ANOVA was significant, and Dunnett’s multiple comparison test was applied versus the NC group; #p < 0.05; ##p < 0.01; and ###p < 0.001, versus DMI group.
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