Abstract

Background Currently, obesity and its comorbidities have become a serious threat to human health necessitating urgent development of safe and effective therapy for their management. Materials and Methods In this research, a novel polyherbal formulation (F2) was prepared by mixing specific proportions of royal jelly and lemon juice with ethanol extracts of Orostachys japonicus, Rhus verniciflua, and Geranium thunbergii. The antioxidant activity was assessed using DPPH and ABTS assay methods. The antiobesity potential of the F2 was assessed in vitro using 3T3-L1 fibroblast and in vivo using a high-fat diet (HFD) fed C57BL/6J mice model. F2 was administered in mice at the dose of 23 mg/kg and 46 mg/kg, twice daily by oral gavage. A well-accepted antiobesity agent, Garcinia cambogia (GC), at 200 mg/kg was used as a positive control. Results F2 was observed to exhibit synergistic antiadipogenic activity in 3T3-L1 cells. This inhibition was reinforced by the downregulation of specific adipogenic transcription factors. Furthermore, F2 was also found to reduce mice body weight gain, food efficiency ratio, fasting blood glucose level, fat deposition into the liver, and mass of white adipose tissue. F2 also played a role in the excretion of fat consumed by the mice. For most of the assays performed, the F2 (46 mg/kg) was comparable to the positive control GC (200 mg/kg). In addition, potential and synergistic antioxidant activity was observed on F2. Conclusion The results revealed that the formulation F2 exhibited potential antiobesity activity through the inhibition of adipocyte differentiation, dietary fat absorption, and reduction of free fatty acids deposition in tissues.

Highlights

  • According to World Health Organization (WHO), obesity is the accumulation of abnormal or excessive fat into the body to the extent that may impair health condition

  • We found evidence that Geranium thunbergii (GT), Rhus verniciflua (RV), Orostachys japonicus (OJ), and Royal jelly (RJ) showed potential antiadipogenic and/or antiobesity activity in 3T3-L1 adipocytes or Sprague-Dawley Rats [13, 16, 28,29,30,31]. erefore, our objective was to develop an effective antiobesity herbal formulation using these natural medicines

  • Astragalin, fustin, fisetin, and sulfuretin were detected at 210 nm, whereas ellagic acid was detected at 250 nm. e retention times of astragalin, fustin, fisetin, sulfuretin, and ellagic acid were 29.445, 14.792, 33.657, 42.800, and 25.718 min, and the concentrations of these compounds in F2 were 3.64, 35.83, 5.90, 3.22, and 1.82 mg/g, respectively

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Summary

Introduction

According to World Health Organization (WHO), obesity is the accumulation of abnormal or excessive fat into the body to the extent that may impair health condition. E antioxidant activity was assessed using DPPH and ABTS assay methods. E antiobesity potential of the F2 was assessed in vitro using 3T3-L1 fibroblast and in vivo using a high-fat diet (HFD) fed C57BL/6J mice model. F2 was found to reduce mice body weight gain, food efficiency ratio, fasting blood glucose level, fat deposition into the liver, and mass of white adipose tissue. Potential and synergistic antioxidant activity was observed on F2. E results revealed that the formulation F2 exhibited potential antiobesity activity through the inhibition of adipocyte differentiation, dietary fat absorption, and reduction of free fatty acids deposition in tissues Conclusion. e results revealed that the formulation F2 exhibited potential antiobesity activity through the inhibition of adipocyte differentiation, dietary fat absorption, and reduction of free fatty acids deposition in tissues

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