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Soybean soluble polysaccharide prevents obesity in high-fat diet-induced rats via lipid metabolism regulation.

Abstract
Soybean soluble polysaccharide (SSPS) was reported to possess the anti-obesity activity and improve metabolic syndrome. Unfortunately, the underlying mechanisms are not well understood. Here, we treated high-fat diet (HFD) Sprague Dawley rats with 250 mg per kg of SSPS, the SSPS treatment significantly decreased their body weight (P < 0.001), liver index value (P < 0.01), as well as the concentration levels of Triglyceride (TG), total cholesterol (TC), low-density cholesterol (LDL-C)), and inflammatory cytokines in the serum. Furthermore, we uncovered 276 differently expressed proteins (P < 0.05) highly involved in lipid metabolism processes. Additionally, after SSPS treatment, both fatty acid binding protein 5 and 7 were downregulated, consistent with the in vivo results. However, peroxisome proliferator-activated receptor γ expression in liver tissue was up-regulated, contradictory to in vitro results. We deduced that two different lipid metabolism mechanisms exist between in vivo and in vitro. Furthermore, in the in vitro experiments, SSPS exerted a lipid-lowering effect. Altogether, the study's results provide an overview of SSPS-induced changes in the liver proteome, which could help us understand the molecular mechanism by which SSPS alleviates obesity.
AuthorsHaiyan He, Chong Chen, Wei Zhao
JournalInternational journal of biological macromolecules (Int J Biol Macromol) Vol. 222 Issue Pt B Pg. 3057-3065 (Dec 01 2022) ISSN: 1879-0003 [Electronic] Netherlands
PMID36252627 (Publication Type: Journal Article)
CopyrightCopyright © 2022 Elsevier B.V. All rights reserved.
Chemical References
  • Dietary Carbohydrates
  • Polysaccharides
  • Cholesterol
Topics
  • Rats
  • Animals
  • Diet, High-Fat (adverse effects)
  • Lipid Metabolism
  • Soybeans
  • Rats, Sprague-Dawley
  • Obesity (drug therapy, etiology, prevention & control)
  • Liver
  • Dietary Carbohydrates (pharmacology)
  • Polysaccharides (pharmacology, metabolism)
  • Cholesterol (metabolism)

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