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Role of Beetroot (Beta vulgaris) Juice on Chronic Nanotoxicity of Silver Nanoparticle-Induced Hepatotoxicity in Male Rats

Authors Albrahim T, Alonazi MA

Received 2 February 2020

Accepted for publication 1 May 2020

Published 15 May 2020 Volume 2020:15 Pages 3471—3482


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Prof. Dr. Anderson Oliveira Lobo

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Tarfa Albrahim,1 Mona A Alonazi2

1College of Health and Rehabilitation Sciences, Department of Health Sciences, Clinical Nutrition, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia; 2Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia

Correspondence: Tarfa Albrahim Email [email protected]

Introduction: Nanoparticles are at the forefront of rapidly developing nanotechnology and have gained much attention for their application as an effective drug delivery system and as a mediated therapeutic agent for cancer. However, the cytotoxicity of nanoparticles is still relatively unknown and, therefore, additional study is required in order to elucidate the potential toxicity of these nanoparticles on cells.
Materials and Methods: Thus, the following work aimed to investigate the capability of Beta vulgaris (beetroot) water extract (BWE; 200 mg/kg) to protect hepatic tissue following silver nanoparticles (AgNPs; 80 mg/kg; > 100 nm) intoxication in male rats.
Results: AgNPs-intoxication elevated the liver function markers – including serum transaminases and alkaline phosphatase activities – and decreased serum levels of albumin and total proteins, in addition to disturbing the oxidation homeostasis. This is evidenced by the increased lipid peroxidation, the depleted glutathione, and the suppressed activity of superoxide dismutase and catalase. In addition, an apoptotic reaction was observed following AgNPs treatment, as indicated by the up-regulation of p53 and down-regulating Bcl-2 expressions, examined by the immunohistochemistry method. Furthermore, AgNPs exhibited a marked elevation in liver DNA damage that was indicated by an increase in tail length, tail DNA% and tail movement. However, BWE eliminated the biochemical and histological alterations, reflecting its hepatoprotection effect in response to AgNPs.
Discussion: Collectively, the present data suggest that BWE could be used following AgNPs as a potential therapeutic intervention to minimize AgNPs-induced liver toxicity.

Keywords: silver nanoparticles, Beta vulgaris, oxidative stress, p53 and Bcl-2 expression, hepatotoxicity


Nanotechnology, a facilitative technology that deals with nanometre-sized objects, is currently in the process of being developed at several levels. Due to their distinctive physicochemical and electrical properties, nano-sized materials have gained considerable traction in the fields of electronics, biotechnology, and aerospace engineering. In the field of medicine, NPs are being employed as a novel delivery system for drugs, proteins, DNA, and monoclonal antibodies.1,2 The small size of NPs means that they are able to easily enter the body and cross a variety of biological obstructions to reach the most vulnerable organs.3

Silver has long been known as an anti-bacterial substance thus the use of silver NPs (AgNPs) in a commercial and medical products – such as in wound dressings, the coating of surgical instruments, and prostheses4,5 - is extensive. Animal and human studies have demonstrated that, after inhalation and through oral exposure, AgNPs are distributed to the liver, heart, spleen, and brain, in addition to the lungs and gastrointestinal tract.6 Based on the special biokinetic characteristics of AgNPs discussed earlier, it is necessary to address the toxicity-related issues of AgNPs in appropriate experimental models, particularly in light of standard protocols with respect to the livers of experimental animals.

A wide range of plants are cultivated globally for food and for medicinal purposes, with several traditional medicinal plants displaying significant potential in the management and treatment of various modern health problems. These include beetroot (Beta vulgaris L), known in the Middle East as Shamandar, a plant of the family Amaranthaceae.7 The roots of beet have long been used in traditional medicine to treat a wide variety of diseases, and beetroot itself contains large quantities of pigments such as betaxanthins and betacyanin from the betalain family, a group of water-soluble nitrogen-containing pigments derived from betalamicacid. Studies indicate that the betalains in beetroot can act as protective molecules and, in addition, it is claimed that beetroot has a multitude of therapeutic uses due to its anti-depressant, hepatoprotective, anti-hypertensive, antioxidant, anti-hyperlipidaemic, radioprotective, and immunostimulatory effects. Moreover, they possess anti-cancer, immunomodulatory, anti-inflammatory, anti-mutagenic, anti-microbial and anti-fungal properties, and can be used as expectorants and carminatives.79

This study aims to investigate the relief of chronic nanotoxicity effects on the structure and function of the liver in male rats from the application of silver nanoparticles (AgNPs), by examining the role played by the administration of beetroot.

Materials and Methods


Silver Nanoparticles

Silver nanopowder, with a particle size less than 100 nm and a 99.9% trace metals basis, was purchased from Sigma-Aldrich (St. Louis, MO, USA). According to the supplier, the prepared AgNPs is characterized using transmission electron microscopy (TEM), dynamic light scattering (DLS), Zeta potential measurements, and UV/Visible spectral analysis to guarantee consistent materials (monodisperse AgNPs free from agglomeration; refractive index n20/D 1.333; fluorescence—λem 388 nm) ( For an additional characterization of the size distribution of the particles, scanning electron microscope (SEM) was performed. Briefly, the AgNPs was dissolved in 0.5% aqueous carboxymethylcellulose (Sigma-Aldrich) and the prepared solution was then coated with carbon, mounted on an electron microscope grid (200 mesh), and visualized using a scanning electron microscope (SEM; type S-4700, JEOL Ltd., Tokyo, Japan) operating at 80kV. However, AgNPs in the injected doses should be distributed more uniformly by sonication for 10 minutes just before injection, to be taken by systemic circulation.10

Beetroot Preparation and Extraction

Red beetroot (B. vulgaris L.) was purchased from a local market in Riyadh, KSA. They were washed with tap water, chopped into small pieces, crushed with deionized water (1:2 w/v), and were then filtered and lyophilized to powder, according to the methods of Sana and Rahila.11

Experimental Design

Adult male Sprague-Dawley (SD) rats (n=40, 3 months old, 150–170 g weight). Animals were kept on basal diet and tap water, both of which were provided ad libitum. After two weeks of acclimation, animals were randomly divided into four equal groups (n=10): Group 1 (Control) received saline and served as control; group 2 (BWE) had beetroot water extract orally administered (200 mg/kg BWE/day); group 3 (AgNPs) received intraperitoneal injections of AgNPs (80 mg/kg; >100 nm) for 4 weeks; and group 4 (AgNPs+BWE) was treated intraperitoneally with AgNPs (80 mg/kg; >100 nm) for 4 weeks and then treated with beetroot water extract (200 mg/kg/day) for further 4 weeks. The dose of AgNPs was selected based on the study conducted by Singh et al12 unlike the dose of beetroot water extract, which was selected according to the work of El Gamal et al.13 The study protocols were approved by the Ethics Committee for Laboratory Animal Care of Princess Nourah bint Abdulrahman University in Riyadh (KSA; H-01-R-059; IRB long number: 19-0201) in accordance with the National Institutes of Health (NIH) Guidelines for the Care and Use of Laboratory Animals, 8th edition (NIH Publication No. 85-23, revised 1985).

At the end of the experimental period, the rats were euthanized with intraperitoneal injection of sodium pentobarbital (200 mg/kg i.p.) and subjected to a complete necropsy. Blood samples were individually collected from the inferior vena cava of each rat and stored in anti-coagulant and non-heparinized glass tubes for hematological analysis and estimation of liver function biomarkers. Blood samples were incubated at room temperature for 10 minutes and left to clot then centrifuged at 3000 × g for 15 min. Following this, the sera was separated and kept in a clean stopper plastic vial at –80°C for analysis of serum parameters.

Hematological Analysis

The hematological parameters were determined on whole blood utilizing an automated analyzer (Abacus junior, Radim, Italy).

Liver Function Biomarkers

Serum liver parameters of alanine transaminase (ALT) and aspartate transaminase (AST), alkaline phosphatase (ALP), albumin (Alb) and total proteins were estimated in order to assess liver function, using commercial diagnostic kits (Randox/Laboratory, Crumlin, United Kingdom) and following the manufacture’s protocols.

Preparation of Liver Homogenates

The livers from all experimental groups were removed, weighed and stored at −20°C. Thereafter, a 10% w/v homogenate was prepared by grinding 0.3 g of tissue in 3 mL of 50 mM phosphate buffer saline, pH 7.4.

Oxidative Stress Status Assays

The liver homogenates were assayed for the purpose of analyzing their oxidant/antioxidant status, using a variety of biomarkers. The measurement of lipid peroxidation (LPO) was performed according to the parameters outlined in the protocol of Ohkawa et al and was based on determining the amount of formed malondialdehyde (MDA), a lipid peroxidation end-product marker.14 The content of glutathione (GSH) was determined according to the method described by Ellman15 and the hepatic activity of superoxide dismutase (SOD) was assayed based on the method described by Nishikimi et al.16 Finally, catalase (CAT) activity was estimated according to the method devised by Aebi, measuring the decomposition rate of hydrogen peroxide (H2O2) at 240 nm.17

Comet Assay (Determination of DNA Damage)

A comet assay (single cell gel electrophoresis) was employed to assess and quantify the levels of liver tissue DNA damage, based on the described method of Olive and Banáth.18

Histological Preparation

After necropsy, the liver was immediately removed and repaired by immersion in 10% neutral buffered formalin solution for 24–48 hours. The specimens were subsequently dehydrated, cleared and embedded in paraffin. Serial sections of 5 µm thick were cut by means of rotary microtome (Litz, Wetzlar; Germany) and were then stained with hematoxylin and eosin.19 For silver particle detection in the liver, semithin sections were prepared on glass slides through cutting at 1-um using an ultramicrotome (EM UC7 from Leica Microsystems). Following this preparation, the sections were stained with Toluidine blue for 25 s and examined by a light microscope.

Apoptotic (p53) and Anti-Apoptotic (Bcl-2) Markers Expression

The expression of apoptotic p53 proteins and anti-apoptotic Bcl-2 proteins in liver sections was detected using avidin Biotin Complex (ABC) (Elite–ABC, Vector Laboratories, CA, USA). Sections were incubated with anti-rabbit p53 or anti-rabbit Bcl-2 monoclonal antibody (dilution 1:80 and 1:2000; DAKO Japan Co, Ltd, Tokyo, Japan) according to the methodology of Harrison-Bernard et al.20

Statistical Analysis

Data were expressed as mean values ± SE (standard error). Significant differences among treatment groups were statistically analyzed by one way ANOVA. The criterion for statistical significance was set at p<0.05 for the biochemical data. All statistical analyses were performed using SPSS statistical version 21 software package (SPSS® Inc., USA).


AgNPs Characterization

AgNPs used in the study were formed in spheroids of 80–90 nm in diameter, as seen by the SEM (Figure 1).

Figure 1 Scanning electron micrograph of AgNPs. Bar=100 nm.

Effect of Silver Nanoparticles and/or Beta vulgaris on Hematological Parameters

Compared with the data obtained from the control group of rats, the administration of AgNPs in the other groups led to a significant decrease in both the Hb content and RBC count, whilst there was a significant increase in WBCs and platelet counts (Table 1). However, the post-administration of BWE to AgNPs induced a significant amelioration in the AgNPs-mediated modulation in hematological parameters and restored those values towards the results observed in the control. Interestingly, BWE treatment alone substantially increased the Hb content compared with the control value.

Table 1 Changes in Complete Blood Pictures in Different Groups Under Study

Effect of Silver Nanoparticles and/or Beta vulgaris on Liver Functions

The rats treated with AgNPs exhibited a significant increase in the activity of serums ALT, AST and ALP, and a significant decrease in serum albumin (Alb) and total protein levels in comparison with the control and BWE groups (Figure 2). Nevertheless, treatment of rats chronically exposed to AgNPs with BWE (AgNPs+BWE) exhibited a considerable decrease in the activity of serums ALT, AST and ALP and a notable increase in albumin serum and total proteins level, compared to the AgNPs group.

Figure 2 Serum levels of AST, ALT, ALP, albumin and total protein following sliver nanoparticles (AgNPs, 80 mg/kg; >100 nm) and/or beetroot water extract (BWE, 200 mg/kg, orally) exposure in male rats. The values are the means ± SE (n = 10). Columns with different symbols are statistically significant at p<0.05.

Effect of Silver Nanoparticles and/or Beta vulgaris on Liver Oxidative Stress

There was a substantial increase in liver LPO and a substantial decrease in GSH content in the rats treated with silver nanoparticles, as well as a decrease in the activity of SOD and CAT, in comparison with the control and BWE groups (Figure 3). On the other hand, the rats chronically treated with silver nanoparticles along with Beta vulgaris (AgNPs+BWE) exhibited a significant decrease in LPO level, whilst there was a significant increase in the liver content of GSH and activities of SOD and CAT, compared to the AgNPs-treated group.

Figure 3 Hepatic levels of LPO and GSH and activities of SOD and CAT following sliver nanoparticles (AgNPs, 80 mg/kg; >100 nm) and/or beetroot water extract (BWE, 200 mg/kg, orally) exposure in male rats. The values are the means ± SE (n = 10). Columns with different symbols are statistically significant at p<0.05.

Liver DNA Fragmentation in Rats Treated with Silver Nanoparticles and/or Beta vulgaris

Rats treated with silver nanoparticles exhibited a significant increase in liver DNA damage (P < 0.05) that was indicated by an increase in tail length, tail DNA% and tail movement, compared to the control and Beta vulgaris groups. A significant decrease in liver DNA damage was observed in the rats that were chronically treated with silver nanoparticles and Beta vulgaris (AgNPs+BWE), in comparison with the DNA damage observed in the livers of the group that were treated solely with AgNPs (Figure 4 and Table 2).

Table 2 Liver DNA Damage (Comet Assay Parameters Obtained by Image Analysis in Cells) in Different Groups

Figure 4 Photomicrographs representation of liver DNA damage in different groups using comet assay. ((A), control; (B), Beta vulgaris; (C), silver nanoparticles; (D), silver nanoparticles with Beta vulgaris groups).

Effect of Silver Nanoparticles and/or Beta vulgaris on Liver Histopathology

The liver sections from both the control group and the group of rats treated with BWE revealed a normal hepatocyte structure, where the hepatocytes are polygonal in shape with eosinophilic granular cytoplasm and vesicular basophilic nuclei (Figure 5A and B). A variety of major histopathological lesions were observed in the liver sections of rats chronically treated with AgNPs, as well as the diffused infiltration of inflammatory cells, mainly eosinophils, atrophied and vacuolated hepatocytes, and degeneration with focal area necrosis (Figure 5C). Liver sections in rats treated with AgNPs and BWE (AgNPs+BWE) revealed a moderate degree of improvement in hepatocytes, where there were only a few atrophied and/or vacuolated hepatocytes and a mild infiltration of inflammatory cells (Figure 5D).

Figure 5 Photomicrographs of rat Liver sections of different experimental groups stained with hematoxylin & eosin. (A and B) Liver sections of control and BWE groups showed normal structure of hepatocytes (hp) and central veins (CV). (C) Liver sections in treated rats with sliver nanoparticles (AgNPs) showed severe infiltration of inflammatory cells (Black arrows), atrophied and vacuolated hepatocytes (White arrows), and degeneration with focal area, focal necrosis. (D) Liver sections in AgNPs+BWE revealed a few atrophied and/or vacuolated hepatocytes and mild infiltration of inflammatory cells (Black arrows).

Furthermore, Toluidine blue staining revealed that the presence of AgNPs had formed within the cytoplasm of hepatocytes (Figure 6C). Nonetheless, the number of AgNPs within the hepatocytes decreased in the liver sections of rats post-treated with the BWE (AgNPs+BWE) (Figure 6D), suggesting the ability of beetroot to facilitate the removal of AgNPs from the liver. Both Figure 6A and B of the control and BWE-treated alone liver revealed no silver has appeared within the cells.

Figure 6 Photomicrographs representation of AgNPs precipitated in liver tissue in different groups using Toluidine blue. ((A), control; (B), Beta vulgaris; (C), silver nanoparticles; (D), silver nanoparticles with Beta vulgaris groups). Arrow reveals the precipitation of AgNPs within the hepatocytes. Scale bar =50.

Effect of Silver Nanoparticles and/or Beta vulgaris on Liver p53 Expressions

Expression of cytoplasmic p53 and the incidence of apoptotic cells were faintly positive reactions in liver sections in both the control and BWE groups (Figure 7A and B). In contrast, (Figure 7C) demonstrated strong p53 expression in the liver sections in rats treated with AgNPs, while liver sections in AgNPs+BWE revealed mildly positive reactions for p53 expression (Figure 7D).

Figure 7 Photomicrographs of rat liver sections stained by apoptotic p53 antibody in different groups under study. (A and B) Faint positive reactions (arrows) for p53 in liver sections in control and BWE groups. (C) Strong positive reactions (arrows) for p53 in liver sections in rats treated with AgNPs. (D) Mild positive reactions (arrows) for p53 in liver sections in rats treated with AgNPs and BWE.

Effect of Silver Nanoparticles and/or Beta vulgaris on Liver Bcl-2 Expressions

The expression of cytoplasmic anti-apoptotic Bcl-2 and the incidence of apoptotic cells in the liver sections of rats in the control and BWE groups showed strong positive reactions (Figure 8A and B). In contrast, (Figure 8C) showed faint Bcl-2 expression in the liver sections of rats treated with AgNPs while liver sections in AgNPs+BWE revealed moderately positive reactions for Bcl-2 expression (Figure 8D).

Figure 8 Photomicrographs of rat liver sections stained by anti-apoptotic Bcl-2 antibody in different groups under study. (A and B) Strong positive reactions (arrows) for Bcl-2 in liver sections in control BWE groups. (C) Faint positive reactions (arrows) for Bcl-2 in liver sections in rats treated with silver nanoparticles. (D) Moderate positive reactions (arrows) for Bcl-2 in liver sections in rats treated with silver nanoparticles and Beta vulgaris.


Despite the growing beneficial biomedical purposes of AgNPs, there is a limit to their uses due to the scarcity of knowledge about the interaction between AgNPs and different cellular processes. Nonetheless, recent studies suggest that AgNPs have a range of cellular targets, among which is the stimulation of the apoptosis pathway, as well as oxidative stress due to the overproduction of reactive oxygen species (ROS) leading to liver injury.21,22 Hence, in this study, the potential role of beetroot was examined in relation to the stimulation of the apoptotic pathway and oxidative stress caused by AgNPs in rats. After exposure, AgNPs can be absorbed, reach the blood and then deposited predominantly in the liver, leading to liver damage.23 In the present study, AgNPs administrated at 80 mg/kg caused liver damage, evidenced by the distribution in serum liver markers, apoptosis and DNA damage. These findings are in accordance with previous studies performed by Patlolla et al24 and Heydrnejad et al.23 The results obtained in previous studies demonstrated that the oral administration of AgNPs in rats (50–100 mg/kg) could significantly increase liver markers and oxidative stress, causing DNA damage.

In toxicological studies, the size of AgNPs is important. Gliga et al25 found that AgNPs measuring 10 nm in diameter were toxic, whereas 40–75 nm AgNPs were not. In the same manner, Park et al26 found that 4 nm AgNPs considerably elevated the production of ROS and pro-inflammatory cytokines released from macrophage immune cells, unlike those AgNPs measuring 20–70 nm. Additionally, Cho et al27 discovered that the single intraperitoneal injection of AgNPs measuring 10 nm in diameter at a dose of 0.2 mg per mouse, induced hepatotoxicity characterized by congestion, vacuolation, single cell necrosis, and focal necrosis. This is a direct contrast with the results obtained with 60 and 100 nm of AgNPs. Indeed, the previous studies demonstrated that the sizes of the nanoparticles may be the foremost factor influencing the toxicity of AgNPs.

In the current study, the RBC count and hemoglobin content decreased in the AgNPs-treatment group. Similar findings were also reported in Carassius auratus gibelio larval exposed to 1, 2, and 3 ppm AgNPs (5 nm), which may be indicators of acute anemia, erythropoiesis disorder leading to deformation of RBCs and inhibition of heme synthesis.28 Adragna et al29 suggested that silver particles cause stress, leading to loss of RBCs. Increases in WBCs and platelet counts after exposure to AgNPs are considered a normal reaction in rats, due to the stimulatory effect on their immune system.30,31 However, Forouhar Vajargah et al28 found that long‐term exposure to AgNPs in Carassius auratus gibelio larval caused stressful conditions, leading to a decrease in WBC count due to cortisol secreted during stress reaction. This could encourage lymphocytes apoptosis and thus shorten their life span, and also reduce their proliferation.32

Consistent with the previous studies, AgNPs measuring less than 100 nm in diameter in the present study caused liver damage. Elevated levels of hepatic enzymes (ALT, AST and ALP) as well as decreased serum levels of albumin and total proteins are crucial indicators of liver injury. Moreover, Hassanen et al31 reported that 25 and 50 mg/kg of chitosan-coated AgNPs produced histopathological alterations and disturbances in liver markers in rats. The possible mechanism for liver damage could be due to the accumulation of Ag+ hepatocytes, which generate excessive amounts of ROS, leading to the loss of the functional integrity of hepatocyte membranes. This then leads to cellular enzyme leakage into the blood and, subsequently, liver dysfunction. Nonetheless, post-administration of beetroot to AgNPs-treated rats decreased serum levels of ALT, AST, and ALP, and increased albumin and total protein levels to those of the control group. The obtained results indicate the ability of BWE to protect against AgNPs-induced hepatotoxicity, which is in accordance with the earlier work of Krajka-Kuzniak et al,33 who demonstrated that beetroot protected liver from N-nitrosodiethylamine and carbon tetrachloride-induced liver damage. Similarly, Iahtisham-Ul-Haq et al34 reported the beneficial effect of beetroot‐based beverages on serum levels of these enzymes. The hepatoprotective effect of beetroot, however, could be attributed to the antiradical scavenging activity of the extract.

In the current study, after 28 days exposure to AgNPs in rats, a significant increase in the LPO level and a significant depletion in reduced GSH content – as well as inhibition in SOD and CAT activities – were observed in liver tissue. This data demonstrates that AgNPs may cause oxidative injury through a ROS-mediated process. AgNPs toxicity appears to boost ROS generation, through the liberation of Ag+ ions inside the cells, as documented by Hassanen et al.31 Dabrowska-Bouta et al35 found that AgNPs altered the expression of oxidative stress-related genes, as well as biochemical markers in myelin membranes extracted from AgNPs-exposed rats. They also suggested that Ag may interact with metal–proteins, such as thiol-proteins, and causing conformational changes and dysfunction. GSH depletion has a marked effect on lipid and protein oxidation. Notably, these entire disturbances can be improved by BWE post-treatment. The free radical scavenging activity of beetroot has been documented previously.36,37 The antiradical activity of BWE may be due to its high source of polyphenols and flavonoids, such as betalains. Further evidence supports the ability of polyphenols to enhance detoxifying/antioxidant enzymes of Phase II, exerting hepatoprotective effect.38 Indeed, BWE post-administration in the present study maintained the endogenous antioxidant defense system at normal cellular concentrations following AgNPs.

Oxidative stress and ROS overproduction in hepatocytes following exposure to AgNPs mediated p53 overexpression. Our results are in accordance with Barcińska et al39 who found that induced apoptosis and cell cycle arrest in pancreatic ductal adenocarcinoma cells (PANC-1) through inducing up-regulation in p53. The ability of AgNPs to induce apoptosis was extensively studied and supported in its use in cancer therapy. AgNPs with a diameter of less than 10 nm can interact extracellularly with cellular membrane proteins and deactivate signaling pathways, causing inhibition of cell proliferation.40 AgNPs can enter cells through diffusion or endocytosis to cause production of ROS, resulting in apoptosis. Although p53 enhances the antioxidant defense system against ROS, after extensive and prolonged exposure to ROS, p53 instead promotes cellular senescence or apoptosis. p53 plays a vital role in distributing cellular homeostasis, ultimately activating apoptosis in severe or protracted protein damage.41 Furthermore, in oxidative damage, p53 mediates apoptosis by enhancing the expression of pro-apoptotic proteins and inhibiting anti-apoptotic proteins. In the present study, AgNPs also down-regulated Bcl-2 expression in liver tissue. The findings of the present study align with those recorded by Zielinska et al,42 who reported that AgNPs significantly down-regulated Bcl-2 expression in PANC-1 cells. Conversely, BWE post-administration augmented the increase in p53, and enhanced Bcl-2 in the liver tissue. In the same manner, El Gamal et al13 found that BWE administration up-regulated the anti-apoptotic proteins and down-regulated the pro-apoptotic proteins in response to toxicants. Thus, our findings suggest that BWE protects against AgNPs-induced hepatotoxicity in rats via the modulation of the apoptotic pathway.

In conclusion, AgNPs (>100 nm in diameter) were found to elicit toxicity in the liver tissue of rats through different mechanisms, including disturbing liver function, inducing oxidative stress and enhancing apoptotic signaling. Nevertheless, BWE augmented the changes provoked by AgNPs, reflecting its hepatoprotective activity.


This research was funded by the Deanship of Scientific Research at Princess Nourah bint Abdulrahman University through the Fast-track Research Funding Program.


The authors report no conflicts of interest in this work.


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