Effect of silymarin on the relative gene expressions of some inflammatory cytokines in the liver of CCl4-intoxicated male rats

The intensive exposure of the liver cells to any type of noxae, such as viruses, drugs, alcohols, and xenobiotics could induce hepatic inflammation through the upregulation of gene expression of several fibrotic and inflammatory mediators. So, our study assessed the role of silymarin on the inflammatory response induced by carbon tetrachloride (CCl4) as an example of xenobiotics on liver tissues in male rats. Forty-eight Wister male rats (weight: 130 ± 10) were housed for 14 days and then divided randomly into six groups: control, SLY: rats received only silymarin orally for 12 weeks (daily), CO: rats were injected with corn oil for 8 weeks (3 times weekly), CCl4: rats were injected with CCl4 solubilized in corn oil for 8 weeks (day by day), Treated: rats received silymarin for 4 weeks after CCl4 injection, Protected: rats received silymarin for 4 weeks before and 8 weeks during CCl4 injection. When the treatment period for the rats was over, they underwent scarification after anesthesia. Then, the sera were extracted from the collected blood for the determination of irisin levels, liver functions, and lipid profiles. Liver tissues were separated for the histopathological examinations, the determination of oxidative stress (OS) parameters content, and the relative gene expression of inflammatory cytokines; nuclear factor kappa (NF)-κB, tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, cyclooxygenase (COX)-2, and transforming growth factor beta (TGF-β). The findings showed that silymarin reduced liver inflammation by overcoming the OS process and inflammatory cytokines production which was stimulated by CCl4. These results were confirmed by histopathology of liver tissues.


Methods.
All experiments were performed in accordance with relevant guidelines and regulations.
Animals.Forty-eight male Wister rats, whose ages ranged from 60 to 65 days (130 ± 5 g), were purchased from the animal room of the Faculty of Agriculture, Alexandria University.They were kept in suitable cages with environmentally relevant circumstances (temp.25 ± 0.5 °C, 12:12 sleep/wake phase).Rats were fed on a common pellet diet and tap water ad libitum 23,24 .They were left for 2-week adaptation before starting the treatments.Figure 1 resembles the experimental design.
In brief, rats were distributed randomly into 6 groups, (8 rats/each) as bellow: 1. Control group (Ctrl) healthy rats with no treatment.2. SLY rats were administered with silymarin (100 mg/Kg body weight) orally every day for 3 months 25 .
When the experiment period was completed, feeding was stopped for 12 hs, and the rats were anesthetized by inhalation with 5% isoflurane.After dissection, blood samples were gathered from the portal vein and underwent centrifugation at 1000×g over 10 min; the separated sera were reserved in a deep freezer until analysis.Additionally, livers were detached rapidly and divided into three pieces after washing with cold saline.The first piece of the liver was bored by a needle and fixed (in 10% formalin/saline) for histological examinations.The next piece was transmitted to vials containing RNA later solution and saved at − 80 °C until the process for the detecting the relative gene expression of fibrotic and inflammatory mediators.The last portion was homogenized with the homogenizer in cold sodium phosphate buffer/saline solution and centrifuged at 10,000×g over 20 min.The supernatants were distributed over some vials to avoid sample freezing and thawing and stored at − 80 °C till use for the oxidative and nitrosative stress (OS/NSS) markers detection 23,24 .
Ethics statement.The ethical standards of the animal protocol have been certified by the Institutional Animal Care and Use Committee of Alexandria University (ALEXU-IACUC; Code No. AU14-220,529-3-2).This work was carried out following ARRIVE guidelines (https:// arriv eguid elines.org).

Histological, biochemical, and molecular examinations. Histopathological examinations of liver tis-
sues.Liver pieces were transferred to 10% formalin/Saline solution, fixed, embedded in paraffin, and then sliced into 5 μm thickness Sections 27 .The grade of histological changes in liver tissue was performed by hematoxylin and eosin (H&E) dye and Gomori's Trichrome (fibrosis detector) staining.All slides underwent examination and imaging using a light microscope.
Determination of the hepatic oxidative and nitrosative stress (OS/NSS) parameters.Markers of OS/NSS were assessed in the liver tissue homogenate supernatant using commercial kits.Lipid peroxidation, the peroxidation and decomposition of polyenic fatty acids of the lipids, was assessed following the method of Ellman 28 .TBARS, including lipid aldehydes, and hydroperoxides, are predicted in terms of malondialdehyde (MDA) equivalents.Under high temperatures and low PH, MDA reacts with thiobarbituric acid, giving a pinky solution, which is detected at 532 nm.The concentration of NO, an indicator of NSS, was valued after adding of Griess reagent to the homogenate 29 .The level of GSH was performed according to the method of Ellman 30 .Ellman's reagent reacts with GSH, producing a yellow product, which is observed at 412 nm.The SOD activity was assessed by the indirect method using pyrogallol, as cited by Marklund and Marklund 31 .At high PH, pyrogallol autooxidation takes place spontaneously, forming superoxide anion radicals (O 2 − •), which are removed by SOD.The GPx activity was evaluated spectrophotometrically using hydrogen hydroperoxide as a substrate 32 .The GR catalyzes the production of GSH from the oxidized form GSSG in the presence of NADPH 33 .Glutathione-S-transferase (GST) activity was valued based on the modified methodology of Habig et al., since the p-nitrobenzyl chloride (GST substrate) reacts with the GSH forming a conjugate product detected at 310 nm 34 .The hepatic total protein in the homogenate was estimated to calculate of enzyme activity based on the Lowry et al. method 35 .
Biochemical Analysis of irisin, Liver Enzymes, and Lipid Profile in serum.Irisin was measured in the rat's serum by commercial ELISA kits 12 .Liver enzymes (TP, ALT, AST, and ALP) and lipid profiles (HDL, LDL, and TG) were measured using commercial kits.
Assessment of the hepatic inflammatory and fibrotic mediators' relative gene expression.The relative gene expressions of NF-κB, COX-2, TNF-α, IL-6, and TGF-β were assessed by the reverse transcription-polymerase chain reaction (qRT-PCR).The isolation of the total RNA from the frozen liver tissues (nearly 50 mg) was performed using Biozol reagent according to Shaban et al 23 .The mixture was treated with chloroform and centrifuged at 4 °C over 20 min.The aqueous layer was collected, and the ethanol was added to precipitate the mRNA.The purity was assessed at the absorption ratio of 260/280 nm, which was regularly higher than 1.8.Using a onestep RT-PCR reaction, the cDNA was synthesized from 5 µg of the purified mRNA by the High-Capacity cDNA Reverse Transcription Kit and used for amplification of transcripts primer sequences.qRT-PCR was done using 3 µL of isolated RNA in a 30 µL reaction mixture, which was contain 0.25 µM of the requested gene primer  .The expression of all the genes were standardized to that of β-actin mRNA in the same liver sample, and the fold difference was calculated using the Eq. 2 −ΔΔ Ct, as described before 23,36,37 .
Statistical analysis.Data were provided as mean ± standard deviation (SD).Results were analyzed for statistical variances using one-way analysis of variance (ANOVA).A p value ≤ 0.05 was marked statistically significant.Comparisons between groups were performed using the post hoc analysis by SPSS 25.0 software.Pearson correlation coefficient was applied to parametrical data.Still, Spearman rank correlation coefficient was performed on the non-parametrical data to determine the association between irisin hormones and all parameters in all groups.

Results
Silymarin overcomes the changes induced by CCl 4 in liver architecture.Examination of H&E and Gomori's Trichrome stained sections of all studied groups existed in Figs. 2 and 3.The control and SLY groups showed that they displayed nearly identical histological pictures.Livers of the control and SLY groups showed no morphometric or histological alterations between them.The livers seemed to be composed of the normal architecture of the central compartment of the hepatic lobule.Each one was occupied centrally by a central vein.Cords of mono-nucleated hepatocytes with normal granular and eosinophilic cytoplasm radiated from the central vein (CV) departed by narrow sinusoids.Oil-treated liver (CO group) showed some binucleated hepatocytes with cytoplasm vacuolation and dilatation of blood sinusoids among hepatocytes.Additionally, the Gomori's Trichrome stain demonstrated the supporting stroma in the liver tissue with minimal collagen fiber content, which appeared in the portal tracts (PT).Rat liver treated with CCl 4 revealed focal areas with eosinophilic hepatocytes and zones of vacuolated pale hepatocytes in the liver tissue.Some PT shows compact cellular infiltration surrounded by fibers.There are clusters of degenerated hepatocytes without nuclei.The Gomori's Trichrome stain demonstrated dense green assemblies of fibers between the liver lobules with vacuolated hepatocytes.It also illustrated abnormal inspissation of erythrocytes within the hepatic sinusoids as in the PT tributaries.While, Treatment with silymarin (Treat-CCl 4 ) displayed regaining the eosinophilic granular existence in the hepatocytes cytoplasm, general restoration of hepatic cords arrangement, and intervening blood sinusoids with some blood congestion in the branch of the portal artery and nuclei of the cellular infiltrate in the stroma of the PT.In the protected group (Prot-CCl 4 ) administration with silymarin pre and during CCl 4 injection showed recovery of hepatocytes and general architecture of the hepatic lobule.It also reduced the deposition of collagen fibers, which was induced by CCl 4 around the CV and in the PT stroma.

Silymarin terminated lipid peroxidation induced by CCl 4 .
The effects of silymarin on the lipid peroxidation parameters, NO and MDA, in rat liver are shown in Table 2.The NO and MDA content had non-remarkable (p > 0.05) changes in the hepatic homogenates of rats treated with silymarin alone (SLY group) compared to the control.The levels of those parameters in rats injected with corn oil alone (CO group) were increased significantly (p ≤ 0.05) compared with the Ctrl group.In addition, rats injected with CCl 4 dissolved in corn oil (CCl 4 group) demonstrated a significant (p ≤ 0.05) elevation in NO and MDA concentrations compared with the Ctrl and CO group, while the administration of silymarin in the treated and protected groups (Treat-CCl 4 and Prot-CCl 4 ) alleviated NO and MDA levels significantly (p ≤ 0.05) compared to the CCl 4 group but did not achieve the control.
Silymarin endorsed the antioxidant system.The effects of silymarin on the antioxidant markers (GSH, GR, GPx, GST, and SOD) in rat liver are shown in Table 2.The GSH level, as well as GR, GPx, GST, and SOD activities had non-remarkable (p > 0.05) changes in the SLY group compared to the Ctrl group.The activity of GR was noticeably (p ≤ 0.05) higher while the concentration of GSH and the activities of GPx, GST, and SOD were significantly (p ≤ 0.05) lower in the CO group in comparison to the Ctrl group.Additionally, the CCl 4 group demonstrated a significant (p ≤ 0.05) elevation in the activity of GR and a significant (p ≤ 0.05) decline in the level of GSH and the activities of GPx, GST, and SOD in comparison to the Ctrl and CO groups.Conversely, Treat-CCl 4 and Prot-CCl 4 groups demonstrated a significant (p ≤ 0.05) decline in the activity of GR and a significant (p ≤ 0.05) elevation in the level of GSH and the activities of GPx, GST, and SOD in comparison to the CCl 4 groups but did not achieve the control (p ≤ 0.05).
Table 1.qRT-PCR primers sequences.The anti-inflammatory effects of silymarin.The impacts of silymarin on the relative gene expression of the inflammatory parameters in all studied groups are presented in Fig. 4. The NF-κB and TNF-α relative gene expressions were noticeably (p ≤ 0.05) lower, while the IL-6 and COX-2 relative gene expressions were noticeably (p ≤ 0.05) higher in the SLY group compared to the healthy group.However, the relative gene expression of those genes was significantly (p ≤ 0.05) higher in the CO group in comparison to the Ctrl.Also, CCl 4 group showed significant (p ≤ 0.05) elevation in the NF-κB, TNF-α, IL-6, and COX-2 gene expressions as compared to CO and Ctrl groups.However, the administration of silymarin in the treated and protected groups presented a www.nature.com/scientificreports/significant (p ≤ 0.05) decline in the gene expressions of those parameters compared to the CCl 4 group but did not achieve the control.

Silymarin reduced fibrosis.
The relative gene expression of the fibrotic marker; TGF-β in different studied groups is shown in Fig. 4F.The TGF-β relative gene expression in the SLY group was significantly (p ≤ 0.05) lower than the control.In contrast, the TGF-β relative gene expression in the CO group was significantly (p ≤ 0.05) higher compared to the control.Moreover, the relative gene expression of that parameter in the CCl 4 group was significantly (p ≤ 0.05) higher compared to the CO and Ctrl groups.In Treat-CCl 4 and Prot-CCl 4 groups, silymarin administration upset the fibrotic effect of CCl 4 significantly (p ≤ 0.05) but didn't achieve the control.MDA (nmol/mg protein) 1.71 ± 0.1 a 1.68 ± 0.1 a 3.14 ± 0.2 b 6.00 ± 0.2 c 3.39 ± 0.2 d 1.95 ± 0.3 e GSH (mg/mg protein) 2.01 ± 0.0 a 2.01 ± 0.0 a 1.65 ± 0.1 b 0.25 ± 0.0 c 1.57 ± 0.0 d 1.90 ± 0.0 e GR (µmol/min/mg protein) 0.02 ± 0.0 a 0.02 ± 0.0 a 0.03 ± 0.0 b 0.06 ± 0.0 c 0.04 ± 0.0 d 0.02 ± 0.0 a GST (µmol/min/mg protein) 6.41 ± 0.2 a 6.45 ± 0.  Experimental summary.All results of the present experiment were concise in Fig. 5.

Discussion
The current study purveys evidence for the OS/NSS, which is progressed by CCl 4 .The levels of MDA and NO were increased significantly in liver homogenates of rats in both CO and CCl 4 groups (Table 2).In addition, the antioxidant system was also interrupted by rigorous depletions of the GSH backup and the GPx, GST, and SOD activities with an obvious increase in GR activity (Table 2).Previous studies showed that the corn oil administration causes significant elevation in liver MDA level with a significant decline in GSH level, SOD and GPx activities [38][39][40] .They recommended that animals administrated with corn oil (containing a high amount of polyunsaturated fatty acids) have low scavenging activity to diminish free radicals and more predisposed to lipid peroxidation than animals fed with monounsaturated fats or saturated fatty acids diets 40 .As mentioned before, CCl 4 promotes the production of various free radical metabolites, which induce the overproduction and accumulation of ROS (reactive oxygen species) and enhance the β-oxidation of polyunsaturated fatty acids of the liver cell phospholipid bilayer consequently increasing the level of MDA 9,23 .Reactive nitrogen species (RNS) are also elevated because the metabolites of CCl 4 activate the inducible nitric oxide synthase (iNOS) activity, the key enzyme for the excessive production of NO.The depletion of GSH concentration is the main step in the initiation of hepatic necrosis.The GSH was consumed by the two enzymes; GPx and GST to detoxify CCl 4 and its metabolites, which explains the reason for GSH deficiency.The increment of GR activity may be considered a natural response to compensate for the continuous depletion of GSH backup.The accumulation of ROS may cause damage to the catalytic activity of SOD.The enzyme activity of t-GPx and GST may possibly inhibit due www.nature.com/scientificreports/ to the depletion in the GSH level and the direct attack of the free radicals to the enzyme active sites 23,41 .Previous studies indicated that the administration of CO with CCl 4 amplified the hepatotoxic effects of CCl 4 40 .In our experiment, CO and/or CCl 4 administration triggered an obvious increment of ALT, AST, and ALP with considerable depletion in TP concentration, which indicates liver cell damage in both CO and CCl 4 groups (Table 3).The elevated levels of those hepatic enzymes in serum are due to the cellular leakage of those enzymes into the blood circulation which reflects the image of cell membrane integrity damage of the hepatocytes.The decline of serum TP may be due to decreasing protein biosynthesis 23,41 .In this study also, the hepatic injury altered the lipid profiles, where the LDL-c and TG concentrations were increased, whereas the HDL-c concentration decreased (Table 3).The results were approved and agreed with the last literatures which indicated that CO and/or CCl 4 induced toxic hepatotoxicity 23,[40][41][42][43][44] .
The CO and CCl 4 groups showed a significant upregulation of the NF-κB, COX-2, TGF-β, TNF-α, and IL-6 gene expression in rats' livers compared to the control (Fig. 4).OS is the primary mechanism in the induction of chronic hepatic inflammation which mainly evolved from fibrosis and progressed to liver cirrhosis.It encourages cytokine biosynthesis such as NF-κB via the provoking of Kupffer cells.NF-κB is a primary transcription factor regulating the induction of a series of pro-inflammatory cytokines gene expression and involves in the progression of inflammation and apoptosis.COX-2 is an inducible isozyme of cyclooxygenases and a key player in initiating the inflammatory response 45 .Biernacki et al. reported that the proteasomal degradation of NF-κB can terminate the pro-inflammatory cascade reaction mediated by NF-κB then stop the gene expression of several pro-inflammatory genes, COX-2, and TNF-α 46 .Rusyn et al., indicated that single dose of corn oil upregulated the expression of NF-κB and TNF-α 47 .CCl 4 enhances the activation of cytoplasmic NF-κB, which then Trans-locates to the nucleus and induces TGF-β gene expression.TGF-β activates human hepatic stellate cells and transforms them into myofibroblasts by increasing the deposition of collagen in between cells 24 .The activated NF-κB also induces the transcription of TNF-α and iNOS gene, which give us another explanation for the overproduction of NO 23,[48][49][50] .TNF-α, is a multifunctional cytokine, initiates the up-regulation of some interleukins (IL-6, IL-8, IL-12), and other inflammatory intermediates gene expression through inflammatory cascade reactions 51,52 .
In addition, the histological examinations confirmed the biochemical results (Figs. 2C,D and 3D) where CCl 4 influenced extensive modifications in the liver tissue architecture as severe hepatocellular degenerations, inflammatory cells, and the existence of fatty changes.
The results demonstrated that the MDA and NO levels were decreased significantly in the hepatic homogenates of rats administrated with silymarin in the protected and treated groups while the GSH concentration and the GPx, GR, GST, and SOD activities were increased (Table 2).Silymarin maintains the integrity of liver cells through several mechanisms 53 .First, it increases the plasma membrane stability by reacting with the hydrophobic compounds in the inner layer of the cell membrane.This reaction avoids the access of pro-oxidants such as CCl 4 through the cell membrane, decreasing the rate of lipids peroxidation and decreasing MDA levels, thereby preserving the SOD catalytic enzyme activities which are affected by the free radicals.Second, the depletion in the contents of the GSH is probably antagonized by silibinin (silymarin isomer).Silibinin may increase the generation of the hepatic GSH via an increment in the substrate (i.e., cysteine) bioavailability, thereby preserving the antioxidants enzymes relay on the GSH (i.e., GSH-Px, GST) and GR enzyme activity due to the stable consumption of GSH 25 .
In the current study, silymarin decreased the elevation of ALT, AST, and ALP enzyme activities, TG and cholesterol levels with a decline of TP level in the sera which are detected after CCl 4 injection in both treat-CCl 4 and prot-CCl 4 groups (Table 3).In hepatocytes, the impacts of silymarin on the plasma membranes permeability is linked to the modifications of phospholipids and cholesterol (membrane lipids) which interprets that silymarin may implicate with the secretion of lipoproteins and hepatic enzymes in the blood 54 .Additionally, silibinin can reduce the glycerol integration into lipids of the hepatocytes 55 .While the elevation of the TP levels was attuned by inducing the gene expression of the protein during the silymarin administration 56 .Mereish et al. showed that silymarin had an antagonistic effect against the production of the total lipids and triglycerides in the liver of rats injected with CCl 4 55,57,58 .Moreover, Treat-CCl 4 and Prot-CCl 4 groups showed significant decreases in the relative gene expressions of NF-кB, TGF-β, TNF-α, IL-6, and COX-2 in the hepatic tissues compared to the intoxicated group (Fig. 4).Silymarin hinders the translocation of NF-кB by preventing its activation, thereby switching off the expression and productions of TGF-β, TNF-α, interferon-gamma, IL-2, IL-4, and COX-2 genes.The reduction in the TNF-α gene expression ceases the IL-6 transcription, as shown in Fig. 4. The drop in NF-κB, TGF-β, TNF-α, COX-2, and IL-6, repairs the defects which happened to the liver due to the administration of CCl 4 .
In the current experiment, we found that CCl 4 decreased serum irisin levels, and this might have contributed to the increased level of inflammation and OS 59,60 .Our study showed that there are a negative correlation between irisin and MDA, NF-κB, and TNF-α in CCl 4 -intoxicated group.This is evidenced by exogenous irisin treatment decreased inflammatory intermediates including IL-6 and TNF-α that are controlled by NF-κB, indicating that there is a negative correlation between irisin level and the level of this cytokines 14,61 .Meanwhile, the level of irisin was improved in the treated and protected groups, which may be due to the antioxidant powers of silymarin 62 .The positive effect of silymarin in achieving normal hepatic function is through irisin production since irisin is intricate with lipid metabolism, and the inflammatory reaction encouraged through AMPK-NF-κB pathway [63][64][65] .In addition, it was found that the extracts of Silymarin have positive effects on hepatic PGC-1α mRNA expression of diabetic rats, PGC-1α is a main promoter of mitochondrial biogenesis, including ROSdetoxification and irisin production 61,62 .Li et al. 66 suggested that low circulating irisin levels lead to non-alcoholic fatty liver and that Nicotinamide adenine dinucleotide + boosting therapy improves non-alcoholic fatty liver disease via stimulating a novel Fndc5/irisin.Furthermore, a significant reduction in levels of FNDC5/irisin has been indicated in both liver tissue and serum of diabetic rats 67 .In addition, since irisin is expressed and secreted by many tissues, the elevated serum irisin level in this research may be due to the positive impacts of silymarin on the hepatic cells.

Conclusion
The present experiment indicates the laboratory results of the protective role of silymarin against OS/NSS and liver inflammation induced through the OS induced by xenobiotics.Irisin could be a mediator by which silymarin could induce its hepatoprotective effects by suppressing OS and inflammatory factors.Silymarin pharmaceutical products are struggling seriously to challenge the synthetic drug's expensive costs, risk factors, and ineffective.Further studies may be performed to test the efficacy of exogenous irisin treatment in hepatic damage induced by xenobiotics and to illustrate the involved mechanisms.

Figure 2 .
Figure 2. Microscopic examination of liver tissues stained by H&E; (A) Ctrl group: control rat liver demonstrating the normal architecture of the central compartment of the hepatic lobule.The central vein (CV) occupies the core of the lobule.Strings of hepatocytes arrayed from the CV.They are departed by narrow sinusoids (s).The hepatocytes demonstrate a normal granular and eosinophilic cytoplasm.Hepatocytes have a single nucleus (h); (B) SLY group: Liver section from a rat receiving silymarin for 12 weeks revealing the unaltered organization of cords of hepatocytes radiating around the CV and focal aggregates of cellular infiltrates (arrow) are depicted around the portal tract (PT); (C) CO group: The PT of the Oil-treated rat liver demonstrating vacuolation of the hepatocyte cytoplasm (H). the portal vein (PV) tributary, the branch of the portal artery (PA), (b) = bile ductules, scanty stromal cells (arrow); (D) CCl 4 group: The PT of the liver of rat injected with CCl 4 induced lesion revealing consistent increased connective tissue stroma (black star) with dilation of biliary cholangioles (ch).Some hepatocytes have a single nucleus (h1); others are binucleated (h2).Pivotal clumps of cellular infiltrate (arrow) are depicted.(E) Treat-CCl 4 group: Treatment with silymarin after CCl 4 -induced lesion depicting focal areas (arrows) with vacuolated hepatocytes (H1) among the majority of normal hepatocytes (H2).(F) Prot-CCl 4 group: Liver section of rat treated with silymarin before and during CCl 4 injection; showing recovery of hepatocytes (H3) and general architecture of the hepatic lobule.All images are original with microscopic magnification × 400.

Figure 3 .
Figure 3. Microscopic examination of liver tissue stained by Gomori's trichrome stain; (A) Ctrl group: Negative control rat liver demonstrates the supporting stroma and minimal collagen fiber content (arrow) depicted in the PT.(B) SLY group: Liver section from a rat receiving silymarin for 12 weeks showing average connective tissue content (arrow pointing to greenish collagen fibers) (C) CO group: liver of rat treated with oil vehicle showing average connective tissue deposit (arrow) in the PT (D) CCl 4 group: Liver section from rat treated with CCl 4 induction of lesion illustrating non-resolving of the fibrous tissue (arrow pointing to green collagen fibers) deposited in the PT and the CV.Note the extensive diffusion of degenerated cells (yellow arrow) appeared between the hepatocytes.Abnormal inspissation of erthrocytes (*) noticed in the hepatic sinusoids as in the PT tributaries.(E) Treat-CCl 4 group: liver of rat treated with silymarin 4 weeks after CCl 4 induced lesion demonstrating persisting collagen bands arrow pointing to a greenish band of fibers) around the dilated central vein.(F) Prot-CCl 4 group: Liver section from rats treated with silymarin before and during CCl 4 induced lesion demonstrating an evident reduction in the greenish deposits of collagen fibers around the CV and the PT stroma.All images are original with microscopic magnification × 100.

Figure 4 .
Figure 4. Effect of silymarin administration on (A) the concentrations of Serum Irisin and the gene expression of the hepatic; (B) NF-κB, (C) TNF-α, (D) IL-6, (E) COX-2, and (F) TGF-β against CCl 4 -injection.The findings are expressed as mean ± SD (n = 8).Different characters for the same parameter are significantly different at p ˂ 0.05.

Table 3
.05) lower in the CO group as compared with the ctrl group.Moreover, the CCl 4 group showed significant (p ≤ 0.05) elevations in the ALT, AST, ALP, LDL-c, and TG levels, whereas the TP and HDL-c levels were considerably (p ≤ 0.05) declined as compared to the Ctrl and CO groups.However, the ALT, AST, ALP, LDL-c, and TG levels of Treat-CCl 4 and Prot-CCl 4 groups were reduced significantly (p ≤ 0.05).Still, the concentrations of TP and HDL-c were improved significantly (p ≤ 0.05) as compared to the CCl 4 group but didn't achieve the control.
. The TP, ALT, and TG levels in the SLY group had non-significant (p > 0.05) changes, whereas the AST, ALP, and LDL-c levels were increased significantly (p ≤ 0.05), and the HDL-c level was elevated significantly (p ≤ 0.05) when compared with the Ctrl group.The concentrations of ALT, AST, ALP, LDL-c, and TG were noticeably (p ≤ 0.05) higher, while the concentrations of TP and HDL-c were significantly (p ≤ 0

Table 2 .
Effects of Silymarin on OS/NSS parameters.All values are presented as mean ± SD (n = 8), Different characters with the same parameters are significantly different at p < 0.05.

Table 4 .
Correlation analysis between Irisin hormone and all studied parameters in all studied groups (n = 8).Where; a Correlation is significant at the 0.05 level (2-tailed), b Correlation is significant at the 0.01 level (2-tailed).