Open Access
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 type: Journal Article
Publication date: 2021-12-06
scimago Q1
wos Q1
SJR: 0.964
CiteScore: 9.2
Impact factor: 4.8
ISSN: 13880209, 17445116
PubMed ID:
34870551
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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Total citations:
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Citations from 2024:
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GOST
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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.
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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.
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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 -
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@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}
}
Cite this
MLA
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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.