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. 2020 Nov 30;58(1):1186–1192. doi: 10.1080/13880209.2020.1845747

Effects of wogonoside on the inflammatory response and oxidative stress in mice with nonalcoholic fatty liver disease

Guangyu Jiang a,b,*, Dayin Chen a,*, Wenpeng Li a, Chengcheng Liu c,✉, Jiguang Liu a,✉, Yingxue Guo a,✉
PMCID: PMC7875554  PMID: 33253604

Abstract

Context

Wogonoside has many pharmacological activities, but whether it has a protective effect against non-alcoholic fatty liver disease (NAFLD) has not been reported.

Objective

This study investigates the protective effect of wogonoside against NAFLD in mice and its potential mechanism.

Materials and methods

C57BL/6 mice were randomly divided into control group, NAFLD group and low-, medium- and high-dose wogonoside groups (5, 10 and 20 mg/kg, respectively) (n= 12). Mice in the control group were fed with the standard diet, and those in NAFLD group and low-, medium- and high-dose wogonoside groups were fed with a high-fat diet. The different doses of wogonoside were administered by gavage once a day for 12 weeks.

Results

Compared with those in NAFLD group, the liver mass, liver index and the LDL, TG, TC, IL-2, IL-6, TNF-α, MDA and NF-κB p65 levels were decreased, and the SOD and GSH-Px activities, and HDL, IκBα, Nrf2 and HO-1 contents were increased in wogonoside groups. Compared with those in the NAFLD group, wogonoside (5, 10 and 20 mg/kg) reduced AST (132.21 ± 14.62, 115.70 ± 11.32 and 77.94 ± 8.86 vs. 202.35 ± 19.58 U/L) and ALT (104.37 ± 11.92, 97.53 ± 10.12 and 56.74 ± 6.33 vs. 154.66 ± 14.23 U/L) activities in the serum.

Discussion and conclusions

Wogonoside has a protective effect against NAFLD in mice, which may be related to its anti-inflammation and inhibition of oxidative stress, suggesting that wogonoside may be a potential therapeutic agent for the treatment of NAFLD.

Keywords: Inflammation, NF-κB pathway, Nrf2/HO-1 pathway

Introduction

Non-alcoholic fatty liver disease (NAFLD) is characterized by the excessive fat deposition in the liver and the steatosis of liver cells (Boutari and Mantzoros 2020). With the change of people's eating habits and the improvement of their living standards, the population of obesity, hypertension, hyperlipidaemia and non-insulin-dependent diabetes is increasing, so the risk of people suffering from NAFLD is also increasing year by year and then NAFLD will further induce the occurrence of cardiovascular and cerebrovascular events (Danford and Lai 2019). NAFLD has posed a serious threat to social development and human health, and is a new major health problem.

Wogonoside, a flavonoid monomer (Figure 1), is one of the active components of traditional Chinese medicine Scutellaria baicalensis Georgi (Scutellaria) (Yan et al. 2020). Wogonoside has many pharmacological activities, such as neuroprotection, cardiovascular protection, antidiabetic, antioxidative, antibacterial, anti-inflammatory and antitumor (Ku and Bae 2014; Zhang et al. 2014; Chen et al. 2019). It has been found that wogonoside can protect against the acute liver injury induced by lipopolysaccharide (LPS) and d-galactosamine (d-GalN) by activating Nrf2 and inhibiting the activation of NLRP3 inflammasome (Gao et al. 2016). In addition, wogonoside also has a significant protective effect against CCl4-induced liver fibrosis (Wang et al. 2015). So far, the therapeutic effect of wogonoside on NAFLD has not been reported. Given the importance of inflammation and oxidative stress in NAFLD (Pan and An 2018; Farzanegi et al. 2019), the current study explored the effects of wogonoside on the inflammation and oxidative stress in mice induced by a high-fat diet.

Figure 1.

Figure 1.

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Chemical structure of wogonoside.

Materials and methods

Drugs and reagents

Wogonoside (purity > 90.0%) was purchased from DESITE Pharmaceutical Co., Ltd., Chengdu, China; serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), high density lipoprotein (HDL), low density lipoprotein (LDL), triglyceride (TG) and total cholesterol (TC) detection kits were purchased from Yuanye Biological Co. Ltd., Shanghai, China; interleukin-2 (IL-2), IL-6, tumour necrosis factor-α (TNF-α), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and malonyldialdehyde (MDA) detection kits were purchased from Jiancheng Bioengineering Institute of Nanjing, Nanjing, China; anti-NF-κB p65, anti-IκBα, anti-Nrf2, anti-HO-1 and anti-β-actin primary antibodies were purchased from Cell Signalling Technology, Beverly, MA. All other reagents were of analytical grade.

Animals

Male C57BL/6 mice, aged 4 weeks, were purchased from Beijing Weitonglihua Company (clean grade; licence no.: SYXK (Beijing, China) 2017-0025). They were housed in 50% relative humidity and at 23 °C according to the national standards for experimental animals. The animal experiments were carried out in a manner that was consistent with the provisions of China Animal Welfare Act and the Guide of NIH Experimental Animal Management and Use after being approved by the Ethical Committee of Experimental Animals of Jiamusi University.

Animal grouping, modelling and administration

The male C57BL/6 mice were randomly divided into control group, NAFLD group and low-, medium- and high-dose wogonoside groups (5, 10 and 20 mg/kg, respectively) (n= 12). The mice in the control group were fed with the standard diet, and those in the NAFLD group and low-, medium and high-dose wogonoside groups with a high-fat diet (0.5% cholic acid, 2% cholesterol and 15% lard in the standard diet). The mice were administered the corresponding doses of drugs by gavage once a day for 12 weeks.

Pathological observation of liver tissue

At the end of the last administration, two mice in each group were randomly selected and sacrificed by cervical dislocation. The liver samples were perfused with sterile saline to remove the blood cells and fixed in 10% formaldehyde solution for 24 h, then dehydrated, hyalinized, immersed in wax and paraffin-embed and continuously sliced into 5 μm thick slices by a microtome. The slices were dried for use. The dried slices were stained by haematoxylin–eosin (HE) and mounted for the preparation of sections. The sections were examined under a light microscope for the observation of the pathological changes of liver tissue.

Measurement of body mass, liver mass and liver index

At the end of the last administration, the body mass of the remaining mice in each group was weighed. The blood samples were collected by removing their eyeballs, and then the mice were sacrificed by cervical dislocation. The liver was separated and weighed accurately, and the liver index was calculated according to the following formula.

Liver index = liver mass/body mass × 100%

Determination of serum biochemical indicators

The blood was collected in the same way as described above and 1.5 mL of the blood sample was placed into a centrifuge tube and centrifuged at 3000 rpm for 10 min to obtain the serum. AST and ALT activities and HDL, LDL, TG and TC contents in the serum of mice were detected by an automatic biochemical analyser.

Measurement of inflammatory factors and oxidative stress-related indicators in the liver tissue

The liver tissue (100 μg) of mice taken from the same part was placed into a cup containing 0.9 mL cold sterile saline and homogenized on ice, and then the liver tissue-saline solution was centrifuged (3000 rpm for 5 min at 4 °C) to prepare a homogenate containing 10% of the liver tissue. The contents of IL-2, IL-6 and TNF-α in the liver tissue were determined by enzyme-linked immunosorbent assay (ELISA), and the SOD and GSH-Px activities and the MDA contents in the liver tissue were determined by spectrophotometry.

Western blot analysis

The total protein and nucleoprotein of liver tissue were extracted, respectively. The proteins were quantified by BCA method and denatured in a boiling water bath, and then the SDS gel electrophoresis on the proteins was performed. The proteins were transferred onto PVDF membranes by semi-dry method, then the first antibodies (1:1000) were added onto the membranes after the blocking with the skimmed milk powder for 2 h and the membranes were incubated at 4 °C overnight. The membranes were washed three times with TBST and then incubated with the corresponding second antibody (1:2000) labelled by HRP for 2 h. ECL was used for the colour development and the films were exposed in a darkroom. The images were scanned and the absorbance value of each band was analysed with Image J software (Bethesda, MD), in which β-actin was used as the internal reference for the standard control of the relative expression calculation of the target proteins.

Statistical methods

SPSS 20.0 software (SPSS Inc., Chicago, IL) was used to analyse the data. The measurement data were expressed as ‘mean ± SD’ and the differences between the mean values were analysed for significance using a one-way analysis of variance (ANOVA). p < 0.05 or p < 0.01 indicated that the difference was a highly significant, respectively.

Results

Effects of wogonoside on the body mass, liver mass, liver index and serum AST and ALT activities in NAFLD mice

In order to verify the protective effect of wogonoside against the liver injury in NAFLD mice, the effects of wogonoside on the body mass, liver mass, liver index and AST and ALT activities in the serum of NAFLD mice were detected. The results showed that compared with those in the control group, the body mass, liver mass and liver index of mice in NAFLD group were significantly higher (p < 0.01), suggesting that the NAFLD model was successfully established; compared with that in NAFLD group, the body mass of mice in wogonoside groups was not significantly different (p> 0.05), but the liver mass and liver index were significantly lower, respectively (p < 0.01) (Figure 2(a–c)). Compared with those in the control group, the serum AST (202.35 ± 19.58 vs. 53.48 ± 7.91 U/L) and ALT (154.66 ± 14.23 vs. 17.84 ± 1.79 U/L) activities of mice in NAFLD group were significantly increased (p < 0.01), and compared with those in NAFLD group, the serum AST (132.21 ± 14.62, 115.70 ± 11.32 and 77.94 ± 8.86 vs. 202.35 ± 19.58 U/L) and ALT (104.37 ± 11.92, 97.53 ± 10.12 and 56.74 ± 6.33 vs. 154.66 ± 14.23 U/L) activities of mice in wogonoside groups were significantly decreased (p < 0.01) (Figure 2(d,e)), suggesting that wogonoside could have a protective effect against the liver injury of NAFLD mice.

Figure 2.

Figure 2.

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Effects of wogonoside on the body mass (a), liver mass (b), liver index (c) and the serum AST (d) and ALT (e) activities in NAFLD mice. Values are expressed as mean ± SD, n= 10. Compared with the control group: **p< 0.01; Compared with NAFLD group: ##p< 0.01.

Effects of wogonoside on the pathological morphology of liver in NAFLD mice

HE staining was used to detect the effect of wogonoside on the pathological morphology of liver tissue in NAFLD mice. It was found that in the control group, the structure of liver lobules was clear, the structure of liver tissue was normal, the surrounding cell cords were radially arranged and there was no cell with fatty degeneration; in NAFLD group, the boundary of liver lobules was not clear, the structure of liver tissue showed some pathological changes, such as a large number of globular lipid droplets and inflammatory cells infiltrated; compared with NAFLD group, the pathological morphology of liver tissue was improved to some extent in the low-, medium- and high-dose wogonoside groups, such as the reduced globular lipid droplets and infiltration of inflammatory cells, especially in the high-dose wogonoside group, as shown in Figure 3.

Figure 3.

Figure 3.

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Effects of wogonoside on the pathological morphology of liver tissue in NAFLD mice (HE, ×200).

Effects of wogonoside on the serum HDL, LDL, TG and TC contents of in NAFLD mice

As shown in Figure 4, compared with those in the control group, the serum HDL contents were significantly decreased, while the serum LDL, TG and TC contents were significantly increased in NAFLD group (p < 0.01); compared with those in NAFLD group, the serum HDL contents were significantly increased, while the serum LDL, TG and TC contents were significantly decreased (p < 0.05 or p < 0.01), suggesting that wogonoside could play a protective role against the liver injury by regulating the lipid metabolism disorder in NAFLD mice.

Figure 4.

Figure 4.

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Effects of wogonoside on the serum HDL (a), LDL (b), TG (c) and TC (d) contents in NAFLD mice. Values are expressed as mean ± SD, n= 10. Compared with the control group: **p< 0.01; Compared with NAFLD group: #p< 0.05, ##p< 0.01.

Effects of wogonoside on the inflammatory response of liver tissue in NAFLD mice

Compared with those in the control group, the contents of IL-2 (1345.28 ± 123.30 vs. 510.73 ± 56.43 pg/mL), IL-6 (101.81 ± 10.54 vs. 40.76 ± 5.73 pg/mL) and TNF-α (270.30 ± 31.48 vs. 54.50 ± 5.14 pg/mL) in the liver tissue of mice in NAFLD group increased significantly (p < 0.01), and compared with those in NAFLD group, the contents of IL-2 (940.86 ± 107.47, 886.71 ± 90.69 and 649.92 ± 68.11 vs. 1345.28 ± 123.30 pg/mL), IL-6 (81.37 ± 8.26, 63.34 ± 7.71 and 60.83 ± 5.08 vs. 101.81 ± 10.54 pg/mL) and TNF-α (184.04 ± 19.20, 125.79 ± 10.65 and 106.74 ± 11.48 vs. 270.30 ± 31.48 pg/mL) in the liver tissue of mice in the wogonoside-treated groups decreased significantly (p < 0.01), as shown in Figure 5(a–c). Western blot analysis showed that compared with that in the control group, the expression of NF-κB p65 in the liver tissue of mice in NAFLD group increased significantly, while that of IκBα decreased significantly (p < 0.01), and compared with that in NAFLD group, the expression of NF-κB p65 in the liver tissue of mice decreased significantly, while that of IκBα increased significantly in the wogonoside-treated groups (p < 0.01), as shown in Figure 5(d–f). The results suggest that wogonoside can protect NAFLD mice from the liver injury by regulating the NF-κB pathway to inhibit the inflammation.

Figure 5.

Figure 5.

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Effects of wogonoside on the inflammatory response of liver tissue in NAFLD mice. (a) IL-2 levels; (b) IL-6 levels; (c) TNF-α levels; (d) Western blot analysis; (e) protein relative expression of NF-κB p65; (f) protein relative expression of IκBα. Values are expressed as mean ± SD, n= 10. Compared with the control group: **p< 0.01; Compared with NAFLD group: ##p< 0.01.

Effect of wogonoside on the oxidative stress level of liver tissue in NAFLD mice

Compared with that in the control group, the activities of SOD (37.34 ± 4.76 vs. 59.63 ± 6.21 U/mg protein) and GSH-Px (12.68 ± 1.08 vs. 16.21 ± 2.17 U/mg protein) decreased significantly, while the content of MDA (3.61 ± 0.40 vs. 1.24 ± 0.13 nmol/mg protein) increased significantly in the liver tissue of mice in NAFLD group (p < 0.01); compared with that in NAFLD group, the activities of SOD (45.57 ± 5.09, 48.21 ± 4.30 and 53.35 ± 5.97 vs. 37.34 ± 4.76 U/mg protein) and GSH-Px (14.46 ± 1.53, 15.09 ± 1.76 and 16.31 ± 2.04 vs. 12.68 ± 1.08 U/mg protein) increased significantly, while the content of MDA (2.95 ± 0.33, 2.70 ± 0.25 and 1.86 ± 0.21 vs. 3.61 ± 0.40 nmol/mg protein) decreased significantly in the low-, medium- and high-dose wogonoside groups (p < 0.05 or p < 0.01), as shown in Figure 6(a–c). Western blot analysis showed that the expression of Nrf2 and HO-1 proteins in the liver tissue of mice in NAFLD group was significantly lower than that in the control group (p < 0.01), and the expression of Nrf2 and HO-1 proteins in the liver tissue of mice in the low-, medium- and high-dose wogonoside groups was significantly higher than that in NAFLD group (p < 0.01), as shown in Figure 6(d–f). These results suggest that wogonoside can protect NAFLD mice from the liver injury by regulating the Nrf2/HO-1 pathway to inhibit the oxidative stress.

Figure 6.

Figure 6.

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Effect of wogonoside on the oxidative stress level of liver tissue in NAFLD mice. (a) SOD activities; (b) GSH-Px activities; (c) MDA levels; (d) Western blot analysis; (e) protein relative expression of Nrf2; (f) protein relative expression of HO-1. Values are expressed as mean ± SD, n= 10. Compared with the control group: **p< 0.01; compared with NAFLD group: #p < 0.05, ##p < 0.01.

Discussion

Fat metabolism mainly occurs in the liver and a large amount of high-fat diet for a long time will increase the fat intake of the liver, and when the rate of fat intake in the liver is greater than that of its excretion, the fatty degeneration in the liver will be induced (Kashyap et al. 2019). The animal model induced by high-fat diet can better simulate the occurrence and development of human non-alcoholic fatty liver, with the characteristics of insulin resistance and obesity, and is widely used in the related studies (Braud et al. 2017). In this study, mice were fed on a high-fat diet for 12 weeks for preparing a model of NAFLD mice. The results showed that the body mass, liver mass, liver index and serum AST and ALT activities of mice in the NAFLD model group were significantly increased, and there were a large number of lipid droplets and inflammatory infiltrating cells in the liver tissue of NAFLD mice, suggesting that the NAFLD mouse model was successfully established, while the liver mass, liver index and the activities of AST and ALT in the serum of mice in the wogonoside-treated groups were significantly lower than those in NAFLD group, and the pathological changes of the liver were also improved in wogonoside-treated groups, indicating that wogonoside could protect the liver of NAFLD mice. The serum HDL, LDL, TG and TC contents are the most commonly used indexes for NAFLD (Liang et al. 2018). The results of this study show that wogonoside could reduce the content of serum HDL, LDL and TG in NAFLD mice, and increase the content of HDL, further confirming the protective effect of wogonoside against the liver injury in NAFLD mice.

Inflammation plays an important role in the occurrence and development of NAFLD, and IL-2, IL-6 and TNF-α are closely related to the occurrence of inflammation (Oliveira et al. 2019). Inflammatory factors, such as IL-2, IL-6 and TNF-α, can promote the steatosis of hepatocytes, and eventually lead to NAFLD (Ezquerro et al. 2019). In vitro and in vivo studies show that wogonoside could reduce the expression of TNF-α, IL-6 and IL-1 and improve the symptoms of osteoarthritis in mice (Tang et al. 2017). It was also found in this study that the content of IL-2, IL-6 and TNF-α in the liver tissue of NAFLD mice increased significantly, while that of IL-2, IL-6 and TNF-α in the wogonoside groups decreased significantly, suggesting that wogonoside could effectively inhibit the inflammatory response of liver tissue of NAFLD mice. NF-κB pathway plays a key role in inflammatory response, mediating the transcription and expression of many inflammatory factors (Deng et al. 2018). Normally, NF-κB exists in the cytoplasm and is activated by some signals, such as oxidative stress, then the inhibitory subunit IкB will be dissociated and the functional subunits such as p65 subunit will be translocated into the nucleus to play the role of transcriptional regulation (Zeng et al. 2015; Sindhu et al. 2019). Previous studies found that wogonoside could promote the glucose uptake of HepG2 cells and increase the glycogen synthesis to improve the liver ischaemia and reperfusion (IR) injury, which may be related to NF-κB inflammatory pathway (Zhu et al. 2019). The results of this study also showed that compared with that in NAFLD group, the expression of NF-κB p65 decreased and that of IκBα increased in the wogonoside-treated groups, further indicating that wogonoside can protect NAFLD mice from the liver injury by regulating the NF-κB pathway and inhibiting the inflammation.

Oxidative stress, one factor leading to the pathogenesis of NAFLD, refers to the accelerated production of ROS in the body, which is beyond the body’s ability to scavenge it, leading to the injury of tissues (Yang and Jo 2018). Liver is not only the main site of ROS production, but also the main target organ of ROS attack (Zhang et al. 2020). SOD, an important ROS scavenger, can keep ROS in balance in the body and in NAFLD model, the activity of SOD is reduced and the accumulation of ROS is increased, and finally the injury hepatocytes will be aggravated (Kobyliak et al. 2016). GSH-Px exists in all tissues of human body, among which the activity of GSH-Px is the highest in the liver, and GSH-Px is an important part of endogenous antioxidant system, with the function of clearing ROS and preventing the oxidative stress injury of liver (Niu et al. 2018). MDA, a highly toxic lipid peroxidation product, can spread to the inside and outside of cells, and then aggravate the damage range of an oxidative stress (El-Din et al. 2014). It has been reported that the content of MDA in NAFLD patients increases significantly and is positively correlated with the fatty degeneration, fibrosis, inflammation and necrosis of liver tissue (Świderska et al. 2019). Our results showed that the activities of SOD and GSH-Px decreased significantly, while the content of MDA increased significantly in the liver tissue of mice in NAFLD group, indicating an oxidative damage in the liver tissue; the activities of SOD and GSH-Px increased, while the content of MDA decreased in each wogonoside-treated group significantly, suggesting that wogonoside can effectively inhibit the oxidative stress level of liver tissue in NAFLD mice.

Nrf2 is an important transcription factor regulating antioxidant status, and under normal conditions, Nrf2 and Keap1 form a complex in the cytoplasm to inhibit the activity of Nrf2 (Wu et al. 2019). In the case of oxidative stress, Nrf2 dissociates from Keap1, and Nrf2 translocates into the nucleus to bind to antioxidant response element (ARE) to activate the expression of HO-1, an antioxidant gene, thus enhancing the antioxidant capacity of cells (Fan et al. 2017). The increase of Nrf2 and HO-1 protein expression can enhance the antioxidant capacity of the body and protect the body from the damage of reactive oxygen species (Xu et al. 2018). A number of studies have confirmed that in NAFLD model, the regulation of Nrf2 pathway activation is an important mechanism to play the role of liver protection (Feng et al. 2017; Yan et al. 2018).

The results of this study showed that the expression of Nrf2 and HO-1 in the liver tissue of mice treated with the different doses of wogonoside was significantly increased compared with that in NAFLD group, further confirming that wogonoside can protect NAFLD mice from the liver injury by regulating the Nrf2/HO-1 pathway and inhibiting the oxidative stress.

Conclusions

Wogonoside has a protective effect against liver injury in NAFLD mice induced by high-fat diet. Regulation of the NF-κB pathway and the inhibition of inflammatory response are mechanisms through which wogonoside can protect NAFLD mice from liver injury. In addition, regulation of the Nrf2/HO-1 pathway and the inhibition of oxidative stress may be another mechanism through which wogonoside can play the protective effect against liver injury in NAFLD mice.

Funding Statement

This work was supported by the Scientific Research Projects of Education Department of Heilongjiang Province [No. 2017-KYYWF-0603].

Disclosure statement

The authors declare that there is no conflict of interest regarding the publication of this paper.

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