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Ameliorating Effect of Green Tea Aqueous Extract against Histo
pathophysiological Changes Induced by Ciprofibrate in the liver
of Male Albino Rats
Fikry Ali Abushofa
1
, Azab Elsayed Azab
2*
, Tahani S. AL-Jelany Sakah
3
, and Nadia M. Kermani
4
1, 4
Department of Zoology, Faculty of Science, Zawia University, Libya
2
Department of Physiology, Faculty of Medicine, Sabratha University, Libya
3
Department of Biological Sciences, School of Basic Sciences, Libyan Academy of Graduate Studies, Tripoli, Libya.
Corresponding Author: Azab Elsayed Azab, Department of Physiology, Faculty of Medicine, Sabratha University, Libya.
Received date: November 26, 2020; Accepted date: November 30, 2020; Published date: December 12, 2020
Citation: Fikry A. Abushofa, Azab E. Azab, Tahani S. AL-Jelany Sakah and Nadia M. Kermani (2020) Ameliorating Effect of Green Tea Aqueous
Extract against Histopathophysiological Changes Induced by Ciprofibrate in the liver of Male Albino Rats J, Biotech. and Bioprocessing 1(3); DOI:
10.31579/2766-2314/013
Copyright: © 2020, Azab Elsayed Azab, This is an open access article distributed under the Creative Commons Attribution License, which
permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background: The liver is a specific target for drug toxicity because of its role in removal and metabolism of
chemicals by converting drugs into another forms that can be readily removed from the body. It is known that the
main function of the liver is the elimination of toxins that may enter the body, thus becoming vulnerable damaged
during this mechanism, which can be revealed as bleeding, congestion, necrosis or other conditions of liver injury.
Ciprofibrate belongs to widely used class of lipid-regulating agents, which stimulate hepatic cells and the hepatic
cell becomes uncontrollably divided, causing liver growth. It causes liver cell proliferation in addition to other
pleiotropic effects such as peroxisome proliferation and induction of certain peroxisomal and cytosolic enzymes in
liver.
Objective: The present study aimed to evaluate the potential beneficial effects of green tea aqueous extract
administration against the biochemical and histological alterations induced in the liver by ciprofibrate in male rats.
Materials and Methods: In the current study 3 groups of 6 male rats were used (Control group, 100mg\Kg body
weight, and Cipro 100mg\Kg body weight with green tea). The rats have been treated daily orally by gavages for 21
days. On the last day of the experiment the animals were killed then blood samples and parts from the liver were
collected. Liver function was examined for the serum Alanine Aminotransferase (ALT), Aspartate Aminotransferase
(AST), alkaline phosphates (ALP), enzyme activities, and serum total & direct bilirubin concentrations. The
histopathological investigation was conducted for the liver tissues of all groups.
Results: Treatment of male rats with 100 mg\Kg body weight of ciprofibrate caused a significant increase in serum
ALT, AST, and ALP activities, total, and direct bilirubin concentration. Histologically, there were histological
changes in central vein area and portal zones, revealed congestion in blood sinusoids, necrosis in hepatic cells, and
damage in central vein lining epithelium. Co-administration of green tea aqueous extract with Ciprofibrate
significantly improved the structural changes in the liver and the serum ALT, AST, and ALP activities, total, and
direct bilirubin concentrations were significantly declined.
Conclusion: It can be concluded that Ciprofibrate treatment induced elevation in liver function tests and severe
histopathological changes and green tea aqueous extract was able to protect the liver against these effects in male
rats. So, the patients should be advised to take green tea aqueous extract while they are treated by ciprofibrate.
Key words: hypolipidemic agent; ciprofibrate; green tea aqueous extract; hepatotoxicity; hepatophysiological
change
1. Introduction
The liver is responsible for the metabolism of xenobiotics and
endogenous hormones, and the detoxification of exogenous compounds
[1]. It is known that the main function of the liver is the elimination of
toxins that may enter the body, thus becoming vulnerable damaged during
this mechanism, which can be revealed as bleeding, congestion, necrosis
or other conditions of liver injury [2].
The liver plays an essential role in transforming and clearing chemicals
and is susceptible to the toxicity from these agents. The drugs can be
administered to the body by many ways, including orally, intramuscular
injection, intravenous, dermal absorption, and nasally [3]. Some
medicinal agents, when taken in overdoses and sometimes even when
introduced within therapeutic ranges, may lead to serious adverse effects.
The liver is a specific target for drug toxicity because of its role in removal
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