HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Antimetabolic Syndrome Effect of Phytosome Containing the Combined Extracts of Mulberry and Ginger in an Animal Model of Metabolic Syndrome.

Abstract
Due to the antimetabolic syndrome effect of mulberry and ginger together with the advantages of the synergistic effect and phytosome encapsulation technique, we hypothesized that phytosome containing the combined extracts of mulberry and ginger (PMG) should be able to manage MetS. PMG was developed and assessed the phenolic content and biological activities associated with the pathophysiology of MetS. The antimetabolic syndrome effect and the possible underlying mechanisms in the animal model of MetS were also assessed. Male Wistar rats induced MetS by subjecting to a 16-week high-carbohydrate high-fat diet. MetS rats were orally given PMG at doses of 50, 100, and 200 mg/kg for 21 days. They were determined metabolic parameter changes in serum, histomorphology changes of adipose tissue, the inflammatory cytokines such as IL-6 and TNF-α, oxidative stress status, PPAR-γ, and HDAC3 in adipose tissue. Our in vitro data showed that PMG increased phenolic contents and biological activities. PMG significantly improved MetS parameters including body weight gain, lipid profiles, plasma glucose, HOMA-IR, and ACE. In addition, the density and size of adipocyte, adiposity index, and weights of adipose tissues were also improved. Moreover, the decrease in TNF-α and IL-6, oxidative stress status, and HDAC3 expression together with the increase in PPAR-γ expression in adipose tissue was also observed. These data suggest that PMG exhibit antimetabolic syndrome and the possible underlying mechanism may be associated partly with the modulation effect on HDAC3, PPAR-γ, and adipose tissue. In addition, PMG also improves oxidative stress and inflammation in MetS. Therefore, PMG can be served as the potential supplement to manage MetS. However, a clinical trial study is essential to confirm this health benefit.
AuthorsNut Palachai, Jintanaporn Wattanathorn, Supaporn Muchimapura, Wipawee Thukham-Mee
JournalOxidative medicine and cellular longevity (Oxid Med Cell Longev) Vol. 2019 Pg. 5972575 ( 2019) ISSN: 1942-0994 [Electronic] United States
PMID31827683 (Publication Type: Journal Article)
CopyrightCopyright © 2019 Nut Palachai et al.
Chemical References
  • Antioxidants
  • Blood Glucose
  • Cholesterol, LDL
  • PPAR gamma
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Histone Deacetylases
  • histone deacetylase 3
Topics
  • Adipose Tissue (metabolism, pathology)
  • Animals
  • Antioxidants (chemistry)
  • Blood Glucose (analysis)
  • Cholesterol, LDL (blood)
  • Diet, High-Fat
  • Disease Models, Animal
  • Zingiber officinale (chemistry, metabolism)
  • Histone Deacetylases (genetics, metabolism)
  • Male
  • Metabolic Syndrome (drug therapy, metabolism, pathology)
  • Morus (chemistry, metabolism)
  • Oxidative Stress (drug effects)
  • PPAR gamma (metabolism)
  • Plant Extracts (chemistry, pharmacology, therapeutic use)
  • Rats
  • Rats, Wistar
  • Tumor Necrosis Factor-alpha (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: