Open Access
Open access
volume 60 issue 1 pages 25-37

Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK

Jozaa Z. ALTamimi 1
Ghedeir M. Alshammari 2
Nora Abdullah AlFaris 1
Reham I Alagal 1
Dalal H Aljabryn 1
Norah A Albekairi 3
Mahmoud Ahmad Alkhateeb 4
Mohammed Abdo Yahya 2
Publication typeJournal Article
Publication date2021-12-06
scimago Q1
wos Q1
SJR0.964
CiteScore9.2
Impact factor4.8
ISSN13880209, 17445116
Drug Discovery
General Medicine
Pharmacology
Pharmaceutical Science
Molecular Medicine
Complementary and alternative medicine
Abstract
Ellagic acid (EA) is used in traditional medicine to treated hyperlipidaemia.This study examined if AMPK mediates the anti-steatotic effect of ellagic acid (EA) in streptozotocin (STZ)-induced type 1 diabetes mellitus in rats.Adult male Wistar rats (130 ± 10 g) were divided into 6 groups (n = 8 rats/group) as control, control + EA, control + EA + CC an AMPK inhibitor), T1DM, T1DM + EA, and T1DM + EA + CC. The treatments with EA (50 mg/kg/orally) and CC (200 ng/rat/i.p.) were given the desired groups for 12 weeks, daily.In T1DM-rats, EA reduced fasting glucose levels (44.8%), increased fasting insulin levels (92.8%), prevented hepatic lipid accumulation, and decreased hepatic and serum levels of total triglycerides (54% & 61%), cholesterol (57% & 48%), and free fatty acids (40% & 37%). It also reduced hepatic levels of ROS (62%), MDA (52%), TNF-α (62%), and IL-6 (57.2%) and the nuclear activity of NF-κB p65 (54%) but increased the nuclear activity of Nrf-2 (4-fold) and levels of GSH (107%) and SOD (87%). Besides, EA reduced downregulated SREBP1 (35%), SREBP2 (34%), ACC-1 (36%), FAS (38%), and HMG-CoAR (49%) but stimulated mRNA levels of PPARα (1.7-fold) and CPT1a (1.8-fold), CPT1b (2.9-fold), and p-AMPK (4-fold). All these events were prevented by the co-administration of CC.These findings encourage the use of EA to treat hepatic disorders, and non-alcoholic fatty liver disease (NAFLD). Further in vivo and in vitro studies are needed to validate its potential in clinical medicine.
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ALTamimi J. Z. et al. Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK // Pharmaceutical Biology. 2021. Vol. 60. No. 1. pp. 25-37.
GOST all authors (up to 50) Copy
ALTamimi J. Z., Alshammari G. M., AlFaris N. A., Alagal R. I., Aljabryn D. H., Albekairi N. A., Alkhateeb M. A., Yahya M. A. Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK // Pharmaceutical Biology. 2021. Vol. 60. No. 1. pp. 25-37.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1080/13880209.2021.1990969
UR - https://doi.org/10.1080/13880209.2021.1990969
TI - Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK
T2 - Pharmaceutical Biology
AU - ALTamimi, Jozaa Z.
AU - Alshammari, Ghedeir M.
AU - AlFaris, Nora Abdullah
AU - Alagal, Reham I
AU - Aljabryn, Dalal H
AU - Albekairi, Norah A
AU - Alkhateeb, Mahmoud Ahmad
AU - Yahya, Mohammed Abdo
PY - 2021
DA - 2021/12/06
PB - Taylor & Francis
SP - 25-37
IS - 1
VL - 60
PMID - 34870551
SN - 1388-0209
SN - 1744-5116
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2021_ALTamimi,
author = {Jozaa Z. ALTamimi and Ghedeir M. Alshammari and Nora Abdullah AlFaris and Reham I Alagal and Dalal H Aljabryn and Norah A Albekairi and Mahmoud Ahmad Alkhateeb and Mohammed Abdo Yahya},
title = {Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK},
journal = {Pharmaceutical Biology},
year = {2021},
volume = {60},
publisher = {Taylor & Francis},
month = {dec},
url = {https://doi.org/10.1080/13880209.2021.1990969},
number = {1},
pages = {25--37},
doi = {10.1080/13880209.2021.1990969}
}
MLA
Cite this
MLA Copy
ALTamimi, Jozaa Z., et al. “Ellagic acid protects against non-alcoholic fatty liver disease in streptozotocin-diabetic rats by activating AMPK.” Pharmaceutical Biology, vol. 60, no. 1, Dec. 2021, pp. 25-37. https://doi.org/10.1080/13880209.2021.1990969.