1. Introduction
Liver inflammation is one common initiator of liver illness and is considered as the main contributor of hepatic tissue damage [1]. Consequently, inflammation leads to tissue modifications with the developing of fibrosis, cirrhosis, and finally, in many cases ending in primary liver cancer, and death [2,3]. Worldwide, more than 1 million deaths each year are due to the chronic liver inflammation associated with fibrosis and cirrhosis [4]. Inflammation of injured hepatocytes activates immune processes in liver. Inflammatory signaling of the liver is regulated by the action of immune cells, including Kupffer cells and inflammatory cells, such as infiltrating macrophages, T lymphocytes, neutrophils, and dendritic cells [5]. Consequently, such processes initiate and maintain the hepatic inflammation through the release of cytokines, such as zinc finger e-box binding protein 2 (ZEB-2), phosphatase and tensin homolog (PTEN), tumor necrosis factor (TNF-α), interleukins (IL-1 and IL-6), as well as interferon gamma (IFN-γ) [6,7,8,9,10]. These inflammatory mediators activate hepatic stellate cells (HSCs), which are the major source of the development of fibrosis in liver after interaction with HSCs via transforming growth factor (TGF-β) [1].
Flavonoids are a group of natural products which are important for human health [11]. Flavonoids exhibit broad therapeutic potential in cardiovascular, gastric, and liver diseases. Furthermore, flavonoids exhibited anti-inflammatory properties through regulation of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and other inflammatory-related factors [12,13,14,15,16,17,18]. Among these flavonoids, the C-glycosylated type including orientin, isoorientin, vitexin, and isovitexin are reported to possess anxiolytic, antioxidative activities [19,20]. Orientin is one in this bioactive category isolable from many medicinal plants such as basil, bamboo, passion flower, golden queen, flax, dayflower, and lavender. Orientin exhibits a diversity of medicinal properties, which comprise anti-inflammation, antioxidant, antimicrobial, neuroprotective, vasodilation, and cardio-protective effects [19,21]. Carbon tetrachloride (CCl4) is commonly used in industries as a solvent and in medicine as an anthelmintic. CCl4 is a well-known hepatotoxic in both humans and experimental animals. Previous studies reported its wide application in scientific research including flavonoids, as a model of hepatotoxicity associated with the release of TNF-α from activated hepatic macrophages [22,23,24]. Lipopolysaccharide (LPS) is an endotoxin made up of a polysaccharide and induces inflammation in various organs, including the liver, kidney, and brain, as well as murine macrophages and HSCs. Most of the toxicities observed in LPS-induced injury have been attributed to toxic mediators produced by activated cells, including TNF-α, iNOS, IL-1β, IL-6, ZEB-2, PTEN, and other pro-inflammatory molecules [25,26,27,28,29]. However, to the best of our knowledge, there was no previous detailed information about the effects of orientin on LPS-mediated pro-inflammatory responses on HSCs, as well as its anti-inflammatory activity towards CCl4-induced liver inflammation on experimental mice. Hence, the current study was designed to assess the effect of orientin on anti-inflammatory activity and its molecular mechanisms towards a CCl4-induced in vivo model and inflamed in vitro model including an in silico docking approach.
2. Materials and Methods
2.1. Animals and Experimental Design
Male C57Bl6j mice (at age of 6–8 weeks and weight range 20–25 g) were maintained in the College of Science, King Faisal University and accommodated in animal ethical conditions with a 12/12 h light/dark cycle and unrestricted access to nutrition conditions. Animal protocols were approved by the Deanship of Scientific Research (KFU-REC-2022-JAN-EA000401), King Faisal University, Saudi Arabia, and all animal experiments conformed to the appropriate standards. CCl4 was used to induce liver injury models. Mice were divided into four groups as follows: control group (corn oil was administered via oral gavage); inflammatory group (15% CCl4 (Merck-Sigma, Darmstadt, Germany) was used at a concentration of 5 mL/kg twice a week); inflammatory and orientin group (1 mg/Kg body weight of orientin (Carbosynth, Rietlistrasse, Staad, St. Gallen, Switzerland) was injected via intra peritoneal); and orientin alone group (1 mg/Kg was injected via intra peritoneal). HCSs were extracted in naïve mice and extracted cells used for ex vivo inflammatory studies. To assess the effect of orientin on liver protection and anti-inflammatory properties, the mice were sacrificed 3 weeks after injection.
2.2. Isolation and Culture of Primary Hepatic Stellate Cells
HSCs were isolated from male C57Bl6j mice as described previously [30]. Briefly, after in situ perfusion of the liver with 2-step proteinase–collagenase digestion, and HSCs were maintained in RPMI (Sigma-Aldrich, Taufkirchen, Germany) supplemented with 10% fetal bovine serum (Applied Biosystems, Waltham, MA, USA) and 1% anti-mycotic/antibacterial solution (Gibco, Waltham, MA, USA) at 37 °C in humidified conditions with 5% CO2. The purity of cells was quantified by a Bio-Rad cell counter. The media were changed after the 5th day of culture. The cultured cells were regarded to be HSCs and used to carry out experiments after 3 passages. Orientin- and CCl4-supplemented cell treatments were initiated 12 h after isolation.
2.3. Estimation of Cytokines for Liver Inflammation
HSCs were plated into 6-well plates, and when the cells were 80% confluent, 10 ng/mL LPS was added for 12 h. The cytokines from HSCs derived from liver tissue of naïve mice were quantified. Cayman scientific kits (Cayman Chemical Co., Ann Arbor, MI, USA) were used to quantify the TNF-α, IL-6, IL-8, and IFN-γ according to manufacturer instructions.
2.4. Nitrate Detection Assay
HSCs were cultured into 6-well plates, and at 80% of cells confluent, 10 ng/mL of LPS was inserted for 12 h. After that, 1 mL of fresh serum-free media was inserted into the culturing plate. Adjusted experimental media were cropped after 24 h. Nitric oxide in experimentally adjusted medium was evaluated by Griess assay (Beyotime Biotechnology, Shanghai, China) according to the manufacturer’s protocol [31].
2.5. RNA Extraction and RT-PCR Analysis
In brief, the cell culture dish was embedded on ice, TRIzol (Thermo Fisher, San Jose, California, USA) was added to lyse the cells for 5–10 min, and then followed by the method described in Khalil et al. [30]. Then, total cellular RNA was extracted according to the manufacturer’s protocol. One microgram of total RNA was reverse transcribed using the Prime Script TM RT-reagent kit (Takara, RR047A, Kusatsu, Shiga, Japan) [32].
The primer sequences used for amplification were as follows: GAPDH forward, 5′-GCAAGGATACTGAGAGCAAGAG-3′ and reverse, 5′-GGATGGAATTGTGAGGGAGATG-3′; ZEB-2 forward, 5′-AGCGACACGGCCATTATTTAC-3′ reverse, 5′-GTTGGGCAAAAGCATCTGGAG-3′; PTEN forward, 5′-TGTGGTCTGCCAGCTAAAGG-3′ and reverse, 5′-ACACACAGGTAACGGCTGAG-3′.
2.6. Western Blot
An overnight incubation of cells was performed prior to exposure to the specified treatments. The lysates of cultured cells were prepared using RIPA lysis buffer, then separated on an SDS-PAGE gel and transferred to a PVDF membrane. Western blot assays were performed with the aid of specified primary antibodies: ZEB-2 (mouse monoclonal antibody 1:1500) (Invitrogen, Waltham, MA, USA), PTEN (rabbit polyclonal antibody 1:1000) (Invitrogen, Waltham, MA, USA), iNOS (rabbit polyclonal antibody 1:1000) (Biorbyt, Cambridge, UK), β-actin (rabbit polyclonal antibody 1:2000) (Cell Signaling Technology, Beverly, MA, USA) and its HRP-labeled secondary antibodies [33], followed by detection with an enhanced chemiluminescence reagent. Chemiluminescence of expressed bands were examined to confirm the linear range of the chemiluminescence signals, and the quantifications were performed using the densitometry tool in ImageJ software v1.8.
2.7. Molecular Docking
2.7.1. Protein Preparation
Three-dimensional structures of proposed anti-apoptotic proteins, such as PTEN (PDB-ID-1D5R) and ZEB-2 (PDB-ID-2D8V), were retrieved from the RCSB PDB Protein Data Bank (
2.7.2. Ligand Preparation
The structure of orientin was retrieved from the PubChem compound database of the National Center for Biotechnology Information (PubChem ID: 5281675). The downloaded structure was converted into PDB format using a freely available open-source tool, using pymol and AutoDock docking tools. In the edit tool, the orientin structure in PDB format was converted to pdbqt and selected the root of the ligand using AutoDock followed by Autogrid tools [34].
2.8. Statistical Analysis
Data are expressed as mean ± SD. The significant difference was analyzed by the Student’s t-test. The multiple analyses were performed by one-way ANOVA using MS Office Excel. Comparisons between the means of various treatment groups were analyzed using the post hoc analysis of the Excel worksheet. A value of p < 0.05 was considered to be statistically significant. Data are represented from at least three independent experiments.
3. Results
3.1. Effect of Orientin on CCl4-Induced Liver Inflammation and Immune Dysfunction
In this study, the protective effect of orientin on CCl4-induced liver inflammation in a mice model was investigated. As shown in Figure 1, induced liver inflammation was observed in disease groups, including the cirrhosis and inflammatory cellular infiltrations in the right lobe, and widespread hepatic fibrosis was observed as well. Moreover, the score of the liver injury was significantly higher in the CCl4 group compared to orientin alone and orientin with CCl4-treated groups. These orientin-treated disease mice distinctly alleviated the CCl4-induced liver damage and reduced infiltration of inflamed cells (Figure 2A). The serum liver functional markers ALT and AST of orientin-treated mice were quantified using the BioVision ELISA method [35]. Fibrosis and cirrhosis increased the aspartate aminotransferase (AST) and alanine aminotransferase (ALT) marker in mice (Figure 2B). Orientin attenuated the liver damage in CCl4-treated mice and evidently the ALT and AST markers were increased 1.91-fold in CCl4-treated mice, whereas the orientin-treated mice showed ALT/AST at a 1.23-fold ratio level compared to the control group (Figure 2B).
3.2. Effect of Orientin on Expression of Inflammatory Markers in CCl4-Induced Liver Tissues
Natural molecules play a major role in anti-inflammatory mechanisms in mice. As shown in Figure 3, orientin reduced pro-inflammatory markers such as TNF-α, IL-6, IL-8, and IFN-γ, which were quantified in CCl4-induced mice. The CCl4-treated mice showed an elevated level of these markers compared to the control group and orientin-treated group. Accordingly, the tissue lysate of orientin-treated mice showed significant reduction of TNF-α (from 421 to 241 pg/mL), IL-6 (from 214 to 133 pg/mL), IL-8 (from 800 to 580 pg/mL), and IFN-γ (from 228 to 175 pg/mL) compared to the CCl4 inflammatory group (Figure 3A–D). However, the orientin alone and orientin with CCl4-treated mice groups had strongly reduced inflammatory markers (p < 0.05). The fibrotic markers were potentially regulated by orientin, as it was regulated significantly in CCl4-induced liver tissues. The ZEB-2 mRNA was downregulated from 4.1-fold of the CCl4-induced condition to 2.2-fold of the orientin-treated condition. Similar findings were observed for PTEN mRNA and reduced from 9-fold to 4-fold (Figure 3E). The protein expression of ZEB-2 and PTEN were quantified in orientin-treated CCl4-induced mice and were downregulated from 2.7- and 2.5-fold of CCl4-induced inflammatory group to 1.6- and 1.9-fold in orientin-treated groups. respectively (Figure 3F,G). The orientin alone group showed insignificant expression of ZEB-2 and PTEN compared to the untreated control group. These results indicated that orientin significantly controlled the inflammatory and fibrotic markers in CCl4-induced mouse liver tissues.
3.3. Docking of Orientin with Mouse PTEN and ZEB-2
The docking study demonstrated the virtual interactions of orientin with phosphate membrane domains of mouse PTEN and stem cell membrane protein of mouse ZEB-2 using molecular docking software tools. The binding energy, ligand bonds, bond distance, and amino acid residue interaction were recorded in Table 1 and Table 2 and Figure 4A,B. Orientin interacted with PTEN (−6.44) amino acid residue of the chain A domain (Figure 4A), such as asparagine, threonine, glycine, and arginine forming a hydrogen bond. Interestingly, the strong binding interactions were observed as a carbon hydrogen bond in asparagine and arginine residue of the PTEN protein. The cation and hydrophobic bonds were observed at tyrosine, proline, and arginine positions of 163 to 170 amino acid residues. Totally, ten different bonds were formed between orientin with mouse PTEN protein. The ZEB-2 protein interacted with orientin with a binding energy of (−6.17) and, in total, six different amino acid residues in a position from 19 to 51 interacted with orientin chain B and C. Orientin formed a sigma bond between ZEB-2 at a position of arginine 166 and confirmed the formation of an overlapped covalent bond (Figure 4B). These interactions demonstrated the involvement of orientin in signaling of hepatic cellular fibrosis and inflammatory markers.
3.4. Effect of Orientin on LPS-Induced Inflammation in Hepatic Stellate Cells
Orientin controlled cell proliferation, nitric oxide, iNOS, and inflammatory structural stress in LPS-induced inflammatory mouse-derived HSCs (Figure 5A–D). As shown in Figure 5A, orientin significantly inhibited the LPS 10 ng/mL-induced proliferation in mice-derived HSCs. The LPS-challenged cells were exposed to orientin in concentration (10 to 80 μM) for 24 h and cell proliferation was quantified. The cell proliferation was inhibited gradually based on the dose of orientin concentration and it was found that 20 and 40 μM significantly controlled the proliferation and was non-toxic to murine hepatic cells. Thus, we selected an orientin concentration of 30 μM for our further ex vivo studies to evaluate the effect of orientin on LPS-induced HSC inflammation. LPS statistically stimulated HSC proliferation (Figure 5A), indicating that LPS could increase the functional metabolic and inflammatory markers of HSCs. The treatment of orientin reduces LPS-related cell functioning markers. The effect of orientin on anti-inflammatory markers in LPS-activated HSCs was evaluated; we treated murine HSCs with either LPS alone, or LPS with orientin concentrations of 30 μM. Nitric oxide (nitrate μM) was used to determine pro-inflammatory activity of the host cells. Orientin significantly decreased LPS-induced nitric oxide from 35 to 27 μM, whereas orientin alone showed a similar nitric oxide concentration compared to untreated control HSCs (Figure 5B). LPS-stimulated expression of iNOS was determined by immunoblot. Orientin alleviated iNOS expression in the LPS-induced group (2.2-fold) comparatively to the LPS alone group (4.3-fold) (p < 0.05) (Figure 5C,D). These results were co-related with HSC differentiation and maturation in LPS-induced conditions (Figure 6).
3.5. Effect of Orientin on Hepatic Fibrotic Signaling Markers ZEB-2, PTEN, and TNF-α
Orientin regulated the fibrotic markers in HSCs. The mRNA and protein expression of ZEB-2, PTEN, and TNF-α were quantified in orientin-treated LPS-challenged HSCs (Figure 7). The ZEB-2 mRNA was downregulated from 4.4-fold of the LPS-induced condition to 3.1-fold of the orientin-treated condition (Figure 7A). Similar findings were observed in protein expression of ZEB-2 and reduced from 6.2-fold to 2.4-fold (Figure 7B,C). This indicates orientin controlled the mesenchymal modification of HSCs and inhibited the hepatic inflammation. HSC activator PTEN was inhibited by orientin treatment. The mRNA and protein expression of PTEN was significantly downregulated in orientin-treated HSCs. Orientin inhibited the LPS-induced PTEN 3.4-fold of mRNA and 2.5-fold of protein expression into 2.6-fold and 1.9-fold of mRNA and protein, respectively (Figure 7A–C). The inflammatory marker TNF-α was significantly inhibited by orientin treatment and it was downregulated from 4.9-fold of LPS-induced mRNA to 3.1-fold of mRNA. Orientin treatment of LPS-treated HSC led to a decrease of TNFα protein levels (2.8-fold), when compared to HSCs treated only with LPS (4.5-fold) (Figure 7A–C). The ZEB-2 expression was increased in the orientin alone treated group compared to the untreated control group (Figure 7B,C).
4. Discussion
The need of for herbal supplements has been increased because of their merits to control oxidative hepatic damage [36]. Hepatotoxicity induced by CCl4 leads to liver injury, hepatic cell death, and activation of cell necrotic pathways [37]. The long-term exposure of CCl4 leads to chronic liver damage and hepatic carcinoma. Recent strategies focused on usage of plant-derived flavonoids, such as luteolin, as hepato-protective, anti-oxidative, and anti-inflammatory agents [38]. In this study, the effect of orientin on liver protection and anti-inflammatory mechanisms in liver tissues in mice were examined. The pathological score and disease index were significantly reduced by orientin treatment in a concentration of 1 mg/kg bw of mouse. The pathophysiology of liver tissue showed that orientin significantly reduced cirrhosis, necrotic cellular morphology, and inflamed infiltration in hepatic tissue (Figure 1). Some studies showed that the flavonoids improve the hepatic cellular architecture from CCl4-induced hepatic damage [39,40]. Liver metabolic enzymes play a major role in detoxification, fibrotic steatosis, and inflammatory modifications of the host. Several studies showed plant flavonoids potentially augmented the AST/ALT level in a CCl4-induced mouse model [41,42,43]. In this present study, AST/ALT was potentially reduced by orientin 1 mg/kg bw compared to the CCl4-induced mice group. The orientin alone treated mice showed similar levels compared to untreated groups (Figure 2A,B). These data are concurrent with the reported modulatory action of extracts of orientin using acetaminophen-induced liver damage in a mice model showing boosted ALT/AST levels, maintaining a normal liver structure, and moderate activity against the iNOS. The current study demonstrated detailed mechanisms of orientin towards reduction of TNF-α, IL-6, IL-8, and IFN-γ in a CCl4-induced mice model and downregulation of ZEB-2 and PTEN fibrotic markers in LPS-induced murine HSCs [44,45,46].
The inflammatory cytokines are key players of fibrotic mediators and are associated with worse prognosis of the inflammatory liver disease [26]. The CCl4 administration led to a rise in the level of pro-inflammatory mediators such as TNF-α, IL-6, IL-8, and IFN-γ (Figure 3A–D). However, the orientin treatment showed marked reduction in the inflammatory cytokines compared to the CCl4 control group. Some previous reports showed the similar ameliorative effect of naringenin and orientin on TNF-α, IL-6, and iNOS in mice models [15,44,45,46,47]. The liver fibrotic markers, ZEB-2 and PTEN, were upregulated in the CCl4-treated group, whereas orientin potentially reduced the expression of ZEB-2 and reached 1.7-fold from a 2.8-fold expression (Figure 3E–G). The PTEN expression was downregulated in the orientin treatment compared to the CCl4 treatment. Protein expression was reduced to 13% compared to the CCl4 group (Figure 3G). The virtual binding of orientin with ZEB-2 and PTEN was achieved and potent binding was observed (Figure 4A,B). The formation of pi-Alkyl hydrophobic bonds between orientin and PTEN changed the structural confirmation and led to less potent receptor molecules. The amino acid residues interacting with orientin from residue 160 to 167 played a major role in coupled complex regulations (Table 1). Regarding the ZEB-2 interaction with orientin, it formed a sigma bond between ZEB-2 at the position of residue 166 and confirmed the formation of an overlapped covalent bond. The coupled complex formations demonstrated the involvement of orientin, with ZEB-2 downregulating the signaling process of protein and controlling the fibrotic formation in intracellular regulatory elements (Table 2).
HSCs play major role in liver cirrhosis and lipid metabolism [48]. Previous studies evidenced that inhibition of HSC proliferation led to prevention of liver injury and fibrosis [49,50,51]. Therefore, natural molecules are focused on liver protection and host health. In this study, we first examined the effect of orientin on LPS-induced murine HSCs and estimated the ZEB-2 and PTEN fibrotic markers. The results indicated that orientin treatment caused cell protection from LPS-induced hepatotoxicity (Figure 5 and Figure 6A). The inflammatory nitric oxide marker was potentially reduced (from 36 to 27 μM) by orientin in LPS-induced HSCs (Figure 6B), indicating the negative progression of fibrosis in LPS-induced inflamed HSCs. The induced nitric oxide synthase is a key regulator of nitric oxide production and its signaling pathways [52]. The orientin treatment reduced the LPS-induced iNOS expression in HSCs and consequently confirmed the reduction of nitric oxide release (Figure 6C,D).
Fibrotic markers such as ZEB-2, PTEN, and TNF-α played a key role in hepatic fibrosis and mesenchymal transition of liver tissues [53,54,55]. In this study, transcripts and protein expressions of these markers were significantly reduced by orientin, which consequently control the transition of HSCs from mesenchymal to fibroblastic architecture. Significant downregulation of ZEB-2, PTEN, and TNF-α in the orientin treatment group confirmed that this phytochemical is able to inhibit the LPS-induced fibrotic process (Figure 7A–C).
5. Conclusions
The present study demonstrated that orientin significantly diminished liver cirrhosis, inflamed infiltration, and boosted AST/ALT levels in CCl4-induced mice. In addition, the levels of inflammatory markers (TNF-α, IL-6, IL-8, and IFN-γ) and fibrotic markers (ZEB-2 and PTEN) were decreased by orientin treatment in CCl4-induced liver toxicity. On the other hand, significant downregulation of ZEB-2, PTEN, and TNF-α was demonstrated in orientin treatment against LPS-induced HSC fibrotic processes. Orientin also showed reduction of iNOS expression and nitric oxide release in HSCs of the LPS-induced fibrotic cells. The results were supported with virtual binding studies. In conclusion, transcripts and protein expression of inflammatory, as well as fibrotic, markers were significantly attenuated by orientin in HSCs and subsequently control the transition of HSCs from mesenchymal to fibroblastic fashion.
H.E.K.: conceptualization, funding acquisition, methodology, writing—review and editing, writing—original draft preparation and supervision; H.-I.M.I.: formal analysis, methodology, validation, software, writing—review and editing, writing—original draft preparation; K.A.E.-F.: writing—review and editing; S.H.A.: writing—review and editing; M.A.M.: validation, writing—review and editing. All authors have read and agreed to the published version of the manuscript.
This project was funded by the Deanship of Scientific Research (DSR), King Faisal University, Al-Ahsa, Saudi Arabia (Nasher Track, project No. 216092).
The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of King Faisal University (KFU-REC-2022-JAN-EA000401).
Not applicable.
Not applicable.
The authors acknowledge with thanks the Deanship of Scientific Research (DSR), King Faisal University, Al-Ahsa, Saudi Arabia (Nasher Track, project No. 216092).
The authors declare no conflict of interest is associated with this work.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Enlarge this image.Figure 1. Morphological and histological evaluation of liver in mice. (A) Control group, (B) CCl4-treated group, (C) orientin (1 mg/kg)-treated group, and (D) CCl4 orientin (1 mg/kg)-treated group. Magnification ×200.
Enlarge this image.Figure 2. Effect of orientin on liver. (A) The disease pathology scores for liver injury. (B) Effect of orientin on CCl4-induced changes in hepatic functional markers of ALT activity and AST activity. Orientin-treated liver tissues were excised after the 7th day of ip injection and homogenate using ice cold PBS. All values are expressed as mean ± SD. * Represents the significant comparison with the control. # Represents the significant comparison with control and CCl4-induced groups.
Enlarge this image.Figure 3. Effect of orientin on liver inflammatory markers. The CCl4-induced mice were administered for orientin 1 mg/kg body weight of mice for 7 days and liver tissues were excised. Liver homogenate was prepared using ice cold cell lysis buffer with 0.1% DTT. (A) The TNF-α was estimated using a Cayman ELISA kit. (B) IL-6 was estimated in liver lysate using a mouse Cayman ELISA kit. (C) IFN-γ was estimated in liver lysate using a mouse Cayman ELISA kit. (D) IL-8 was estimated in liver lysate using a mouse Cayman ELISA kit. (E) mRNA expression of ZEB-2 and PTEN using real time PCR. (F,G) Protein quantification of ZEB-2 and PTEN in CCl4-induced and CCl4 with orientin treatment using immunoblot-based techniques. (The data are represented as the mean ± SD.) p < 0.05. * Represents the significant comparison with control and CCl4-induced groups.
Enlarge this image.Figure 4. In silico docking of orientin (CID: 5281675) and (A) mouse PTEN (PDB-ID-1D5R) and (B) ZEB-2 (PDB-ID-2D8V) proteins binding analysis. Computational binding was performed using AutoDock software to demonstrate the illustration of interactions in the hydrophobic bond and other polar bonds of PTEN and ZEB-2. It shows the amino acid residue analysis of the interacted bond and its length, together with the binding pocket of ligand–receptor interactions.
Enlarge this image.Figure 5. Effect of orientin on LPS-induced inflammatory HSCs. Naïve mouse-derived HSCs were isolated and cultured in an adherent-coated 12-well plate. Cultured cells were stimulated with LPS 10 ng for 2 h and orientin was treated for 12 h. Treated cells were evaluated for cell proliferation, nitrate quantification, and iNOS protein. (A) Cell proliferation of LPS-stimulated HSCs and LPS with orientin-treated cells were quantified using SRB assay. (B) Nitric oxide level as nitrate (μM) in LPS-stimulated and orientin-treated HSCs. (C,D) iNOS protein quantification using immunoblot. Values are expressed as three independent experiments and all values are expressed as mean ± SD. * Represents the significant comparison with control and LPS-induced groups.
Enlarge this image.Figure 6. Effect of orientin on LPS-induced inflammatory HSCs. Naïve mouse-derived HSCs were isolated and cultured in an adherent-coated 12-well plate. Cultured cells were stimulated with LPS 10 ng for 2 h and treated with orientin (30 µM) for 12 h. (A) Control group, (B) LPS-treated group, (C) orientin (30 µM)-treated group, and (D) LPS and orientin (30 µM)-treated group.
Enlarge this image.Figure 7. Effect of orientin on hepatic fibrotic signaling markers ZEB-2 and PTEN. Naïve mouse-derived HSCs were stimulated with LPS 10 ng for 2 h and treated for 12 h with orientin (30 µM). Treated cells were evaluated for ZEB-2, PTEN, and TNF-α mRNA and protein were quantified. (A) mRNA quantification of ZEB-2, PTEN, and TNF-α in LPS-stimulated HSCs and LPS with orientin-treated cells was undertaken using SYBR green-based real time PCR assay. (B,C) Protein quantification of ZEB-2, PTEN, and TNF-α in LPS-stimulated HSCs and LPS with orientin (30 µM)-treated cells using immunoblot-based techniques. Values are expressed as three independent experiments and all values are expressed as mean ± SD. * Represents the significant comparison with the control and LPS-induced groups.
Interactions of orientin and ZEB2 receptor residues of target protein.
| Binding |
Ligand |
Intermole |
Ligand Atoms (Ring) | Docked Amino Acid Residue (Bond Length) |
|---|---|---|---|---|
| −6.17 | −0.19 | −6.38 | Conventional Hydrogen Bond: | |
| Chain B—C3′-O | Chain A: ARG′36 ′HN′ (2.80 Å) | |||
| Chain B—C3′-OH | Chain A: ALA′32 ′O′ (1.80 Å) | |||
| Chain B—C4′-OH | Chain A: ALA′32 ′O′ (1.80 Å) | |||
| Chain C—C4-O | Chain A: THR′49 ′HG1′ (1.88 Å) | |||
| Chain A—C5-OH | Chain A: THR′49 ′OG1′ (1.93 Å) | |||
| C2-OH | Chain A: THR′19 ′O′ (2.20 Å) | |||
| C3-OH | Chain A: THR′19 ′OG1′ (2.18 Å) | |||
| C3-OH | Chain A: THR′19 ′O′ (2.61 Å) | |||
| Pi-Alkyl Hydrophobic bond: | ||||
| O | Chain A: ALA′32′ (4.36 Å) | |||
| O | Chain A: LEU′20′ (5.00 Å) | |||
| O | Chain A: LEU′20′ (5.41 Å) | |||
| O | Chain A: PRO′51′ (5.18 Å) | |||
| Pi-sigma bond: | ||||
| O | Chain A: LEU′20′ CD2′ (3.44 Å) | |||
| O | Chain A: ARG′166′ (4.77 Å) | |||
ALA, alanine; ARG, arginine; LEU, leucine; ASN, asparagine; PRO, proline; THR, threonine.
Interactions of orientin and PTEN receptor residues of target protein.
| Binding |
Ligand |
Intermole |
Ligand Atoms |
Docked Amino Acid Residue |
|---|---|---|---|---|
| −6.44 | −0.2 | −6.44 | -Conventional Hydrogen Bond: | |
| Chain B—C4′-O | Chain A: ASN′323 ′HD22′ (1.92 Å) | |||
| Chain B—C4′-OH | Chain A: THR′161 ′O′ (1.83 Å) | |||
| Chain B—C3′-OH | Chain A: THR′161 ′O′ (2.24 Å) | |||
| Chain C—C4′-O | Chain A: GLN′143 ′HE22′ (1.90 Å) | |||
| Chain C—C4′-O | Chain A: GLN′143 ′HE21′ (2.44 Å) | |||
| C4-OH | Chain A: ARG′167 ′HH12′ (2.35 Å) | |||
| -Carbon Hydrogen Bond | ||||
| C | Chain A: ASP′318′OD2′ (3.19 Å) | |||
| C | Chain A: ARG′167′CD′ (2.90 Å) | |||
| -Pi-Alkyl Hydrophobic bond: | ||||
| O | Chain A: TRY′170′ (5.65 Å) | |||
| O | Chain A: TRY′170′ (4.81 Å) | |||
| -Pi-Pi T-shaped bond: | ||||
| O | Chain A: PRO′163′ (4.56 Å) | |||
| O | Chain A: ARG′166′ (4.77 Å) | |||
| -Pi-cation bond: | ||||
| O | Chain A: ARG′166′ NH2′ (4.35 Å) | |||
ARG, arginine; ASN, asparagine; ASP, aspartic acid; GLN, glutamine; PRO, proline; TRY, tyrosine.
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Details
; Hairul-Islam, Mohamed Ibrahim 2
; Kareem Ahmed El-Fass 3 ; Akrawi, Sabah H 4 ; Morsy, Mohamed A 5
1 Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia;
2 Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia;
3 Department of Pharmacy Practice, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia;
4 Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia;
5 Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, Saudi Arabia;