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Unripe Rubus coreanus Miquel Extract Containing Ellagic Acid Regulates AMPK, SREBP-2, HMGCR, and INSIG-1 Signaling and Cholesterol Metabolism In Vitro and In Vivo.

Authors :
Lee KH
Jeong ES
Jang G
Na JR
Park S
Kang WS
Kim E
Choi H
Kim JS
Kim S
Source :
Nutrients [Nutrients] 2020 Feb 26; Vol. 12 (3). Date of Electronic Publication: 2020 Feb 26.
Publication Year :
2020

Abstract

Our previous study demonstrated that a 5% ethanol extract of unripe Rubus coreanus (5- u RCK) has hypo-cholesterolemic and anti-obesity activity. However, the molecular mechanisms of its effects are poorly characterized. We hypothesized that 5- u RCK and one of its major bioactive compounds, ellagic acid, decrease cellular and plasma cholesterol levels. Thus, we investigated the hypocholesterolemic activity and mechanism of 5- u RCK in both hepatocytes and a high-cholesterol diet (HCD)-induced rat model. Cholesterol in the liver and serum was significantly reduced by 5- u RCK and ellagic acid. The hepatic activities of HMG-CoA and CETP were reduced, and the hepatic activity of LCAT was increased by both 5- u RCK extract and ellagic acid, which also caused histological improvements. The MDA content in the aorta and serum was significantly decreased after oral administration of 5- u RCK or ellagic acid. Further immunoblotting analysis showed that AMPK phosphorylation in the liver was induced by 5- u RCK and ellagic acid, which activated AMPK, inhibiting the activity of HMGCR by inhibitory phosphorylation. In contrast, 5- u RCK and ellagic acid suppressed the nuclear translocation and activation of SREBP-2, which is a key transcription factor in cholesterol biosynthesis. In conclusion, our results suggest that 5- u RCK and its bioactive compound, ellagic acid, are useful alternative therapeutic agents to regulate blood cholesterol.<br />Competing Interests: The authors declare no conflict of interest.

Details

Language :
English
ISSN :
2072-6643
Volume :
12
Issue :
3
Database :
MEDLINE
Journal :
Nutrients
Publication Type :
Academic Journal
Accession number :
32110925
Full Text :
https://doi.org/10.3390/nu12030610