Sea cucumbers-derived sterol sulfate alleviates insulin resistance and inflammation in high-fat-high-fructose diet-induced obese mice.
Adiponectin
/ metabolism
Adipose Tissue
/ drug effects
Animals
Anti-Inflammatory Agents
/ therapeutic use
Blood Glucose
/ metabolism
Cytokines
/ metabolism
Diet, High-Fat
/ adverse effects
Fructose
/ adverse effects
Glucose Tolerance Test
Glycogen
/ metabolism
Inflammation
/ drug therapy
Insulin Resistance
Male
Mice
Mice, Inbred C57BL
Obesity
/ complications
Sea Cucumbers
/ chemistry
Signal Transduction
/ drug effects
Sterols
/ therapeutic use
Inflammation
Insulin resistance
Marine
Metabolic syndrome
Sterol sulfate
Journal
Pharmacological research
ISSN: 1096-1186
Titre abrégé: Pharmacol Res
Pays: Netherlands
ID NLM: 8907422
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
05
06
2020
revised:
08
08
2020
accepted:
31
08
2020
pubmed:
11
9
2020
medline:
14
8
2021
entrez:
10
9
2020
Statut:
ppublish
Résumé
Sea cucumbers are widely consumed in traditional medicine and food. Sea cucumbers-derived sulfated sterol exhibits a sulfate group at C-3 position, which is different from phytosterol with a hydroxyl group. However, the effect of sterol sulfate on metabolic syndrome remains unknown. The purpose of the present study is to investigate the alleviation of sterol sulfate on high-fat-high-fructose diet (HFFD)-induced insulin resistance and inflammation. After 2 weeks feeding with HFFD, male C57BL/6J mice were continuously fed with HFFD plus 0.4 % (w/w) sterol sulfate or phytosterol for 6 weeks. The OGTT was carried out at 7 weeks. At the end of the experimental period, the changes of glycogen, circulating glucose, insulin, pro-inflammatory cytokine and adiponectin were measured. H&E staining was used to observe the morphological changes in adipose tissue. Furthermore, the underlying molecular mechanisms were investigated. Dietary sterol sulfate was superior to phytosterol in reducing body weight gain, adipocyte hypertrophy, and levels of circulating glucose and insulin, as well as increasing the glycogen content of tissues. Furthermore, sterol sulfate ameliorated insulin resistance mainly due to the inhibition of gluconeogenesis, the promotion of glycogen synthesis and GLUT4 translocation by activating PI3K/Akt signaling pathway. Additionally, sterol sulfate effectively attenuated inflammation by increasing serum adiponectin and reducing pro-inflammatory cytokine release. Sterol sulfate exhibited a more significant effect than phytosterol in alleviating HFFD -induced insulin resistance and inflammation, which might be closely related to the sulfate group. The results might provide insights into the prevention and alleviation of metabolic syndrome.
Identifiants
pubmed: 32911073
pii: S1043-6618(20)31499-7
doi: 10.1016/j.phrs.2020.105191
pii:
doi:
Substances chimiques
Adiponectin
0
Anti-Inflammatory Agents
0
Blood Glucose
0
Cytokines
0
Sterols
0
Fructose
30237-26-4
Glycogen
9005-79-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105191Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.