Glycyrrhizic acid attenuates CCl4-induced hepatocyte apoptosis in rats via a p53-mediated pathway

Abstract

AIM: To investigate the effect of glycyrrhizic acid (GA) on carbon tetrachloride (CCl₄)-induced hepatocyte apoptosis in rats via a p53-dependent mitochondrial pathway.

METHODS: Forty-five male Sprague-Dawley rats were randomly and equally divided into three groups, the control group, the CCl₄ group, and the GA treatment group. To induce liver fibrosis in this model, rats were given a subcutaneous injection of a 40% solution of CCl₄ in olive oil at a dose of 0.3 mL/100 g body weight biweekly for 8 wk, while controls received the same isovolumetric dose of olive oil by hypodermic injection, with an initial double-dose injection. In the GA group, rats were also treated with a 40% solution of CCl₄ plus 0.2% GA solution in double distilled water by the intraperitoneal injection of 3 mL per rat three times a week from the first week following previously published methods, with modifications. Controls were given the same isovolumetric dose of double distilled water. Liver function parameters, such as alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were determined. Pathologic changes in the liver were detected by hematoxylin and eosin staining. Collagen fibers were evaluated by Sirius red staining. Hepatocyte apoptosis was investigated using the terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-triphosphate nick end labeling (TUNEL) assay and the cleaved caspase-3 immunohistochemistry assay. The expression levels of p53 and apoptosis-related proteins were evaluated by immunohistochemistry or Western blotting analysis.

RESULTS: After 8 wk of treatment, GA significantly reduced serum activity of ALT (from 526.7 ± 57.2 to 342 ± 44.8, P < 0.05) and AST (from 640 ± 33.7 to 462.8 ± 30.6, P < 0.05), attenuated the changes in liver histopathology and reduced the staging score (from 3.53 ± 0.74 to 3.00 ± 0.76, P < 0.05) in CCl₄-treated rats. GA markedly reduced the positive area of Sirius red and the ratio of the hepatic fibrotic region (from 7.87% ± 0.66% to 3.68% ± 0.32%, P < 0.05) compared with the CCl₄ group. GA also decreased the expression level of cleaved caspase-3 compared to the CCl₄ group. TUNEL assay indicated that GA significantly diminished the number of TUNEL-positive cells compared with the CCl₄ group (P < 0.05). GA treatment clearly decreased the level of p53 (P < 0.05) detected by immunohistochemistry and Western blotting analysis. Compared with the CCl₄ group, we also found that GA reduced the Bax/Bcl-2 ratio (P < 0.05), the expression of cleaved caspase-3 (P < 0.05), cleaved caspase-9 (P < 0.05), and inhibited cytochrome C and second mitochondria-derived activator of caspases (Smac) release from mitochondria to cytoplasm, i.e., GA reduced the expression level of Smac, which inhibited c-IAP1 activity (P < 0.05), ultimately inhibiting the activity of caspase-3, according to Western blotting analysis. As a result, GA suppressed activation of the caspase cascades and prevented hepatocyte apoptosis.

CONCLUSION: GA can inhibit CCl₄-induced hepatocyte apoptosis via a p53-dependent mitochondrial pathway to retard the progress of liver fibrosis in rats.

Core tip: This study is the first to investigate the effects of glycyrrhizic acid (GA) on p53-dependent apoptosis in carbon tetrachloride (CCl₄)-induced hepatic injury. The results indicated that GA can attenuate hepatocyte apoptosis via a p53-mediated mitochondrial pathway and retard the progression of liver fibrosis induced by CCl₄ in rats.

INTRODUCTION

Liver fibrosis, induced by various pathological factors, is a common outcome in many chronic liver diseases, and is a serious threat to human health. It is known that the foundation of liver fibrosis is the imbalance between synthesis and degradation of extracellular matrix (including collagen, glycoproteins, polysaccharides, amines, etc.).

It has been shown that hepatocyte apoptosis can induce liver fibrosis[1-3]. Hepatocyte apoptosis is a major form of cell death which is primarily triggered by activation of the caspase family of cysteine proteases during the progression of chronic liver disease[4]. Many reports have shown that p53 is accumulated in hepatocytes in several fibrotic liver diseases[5-7]. The protein p53 can lead to apoptosis predominantly through p53-regulated genes such as P21, PUMA, NOXA and Bax[8]. The intensity of inflammation induces pro-apoptotic protein p53 with inhibition of anti-apoptotic Bcl-2 in non-alcoholic fatty liver disease[5]. Thioacetamide activates p53, increases caspase-3, Bax and Bad protein contents, and possibly causes the release of cytochrome C from mitochondria and the disintegration of membranes, eventually leading to apoptosis of cells in thioacetamide (TAA)-induced liver fibrosis and cirrhosis[9]. The pro-apoptotic protein, Bax, is a positive regulator and the anti-apoptotic protein, Bcl-xL, is a negative regulator that regulates the release of cytochrome C from mitochondria to the cytoplasm[10,11]. The presence of Bax protein is a direct result of the release of cytochrome C from mitochondria and activation of caspase-9[12]. Inhibitors of apoptosis proteins (IAPs), which regulate apoptosis through various factors, play a vital role in inhibition of the apoptotic process[13]. c-IAP1, c-IAP2 and Survivin, as key members of IAPs, can inhibit the activity of caspase-3 and -7, thus blocking cell apoptosis[14,15]. During the apoptotic process, second mitochondria-derived activator of caspases (Smac), released from mitochondria into the cytoplasm, bind and antagonize IAPs, subsequently reducing the inhibition of caspases by IAPs resulting in apoptosis[16-18]. p53 activation enhances X-IAP inhibition-induced cell death by promoting mitochondrial release of Smac[19]. Therefore, inhibiting p53-dependent hepatocyte apoptosis may be an effective therapeutic strategy for the treatment and prevention of hepatic fibrosis.

Chinese herbal medicine has been widely used to cure diseases for thousands of years in China, especially chronic liver diseases. In recent years, the efficacy of Chinese herbal medicine has been appraised by modern biological technology[20,21]. Glycyrrhizic acid (GA), also known as Glycyrrhizin[22], is the major bioactive component of licorice root extract. GA, a glycosylated saponin, which has one molecule of glycyrrhetinic acid and two molecules of glucuronic acid, has adrenal cortex hormone-like effects[23,24]. GA has numerous pharmacologic effects, such as anti-inflammatory, anti-viral, anti-tumor and hepatoprotective activities[25]. GA also exerts an anti-apoptotic effect through the inhibition of hepatocyte apoptosis[26,27]. Recent findings indicate that GA significantly inhibits hepatocyte apoptosis by down-regulating the expression of caspase-3 and inhibiting the release of cytochrome C from mitochondria into the cytoplasm[28].

It has been reported that carbon tetrachloride (CCl₄) can induce hepatocyte apoptosis and liver fibrosis in animal models[29-33]. The damage responses, induced by CCl₄ injection in rat and mouse models, are similar to liver cirrhosis in humans[34]. Thus, we presumed here that GA treatment started from the early stage of chronic liver disease could effectively attenuate hepatocyte apoptosis, consequently inhibit liver fibrosis and retard disease progression in rats. This study sought to investigate the effects of GA on p53-dependent apoptosis in CCl₄-induced hepatic injury.

MATERIALS AND METHODS

Materials

GA was purchased from Sigma (St Louis, MO, United States). Anti-caspase-3, anti-caspase-9, anti-c-IAP1, anti-cytochrome C, anti-Smac, anti-Bcl-2, anti-Bax and anti-COXIV antibodies were purchased from Cell Signaling Technology (Beverly, MA, United States). Anti-GADPH and anti-p53 antibodies were bought from Abcam (Cambridge, United Kingdom), horseradish peroxidase-conjugated anti-mouse and anti-rabbit immunoglobin G antibodies were purchased from Cell Signaling Technology. The chemiluminescence reaction kit (ECL Plus) was purchased from Millipore (Billerica, MA, United States). Anti-cleaved-caspase-3 antibody and the mitochondria/cytoplasm fractionation kit were purchased from Beyotime Biotechnology (Haimen, Jiangsu Province, China).

Animal model of liver fibrosis and treatment

Male SD rats weighing 150-200 g were purchased from the Experimental Animal Center of Zhongshan Hospital, Fudan University. Rats were kept in a temperature-controlled room with an alternating 12-h dark and light cycle. Forty-five rats were randomly and equally divided into three groups, the control group, the CCl₄ group, and the GA treatment group. To induce liver fibrosis in this model, rats were given a subcutaneous injection of a 40% solution of CCl₄ (Wako Pure Chemical, Osaka, Japan) in olive oil at a dose of 0.3 mL/100 g body weight biweekly for 8 wk, while controls received the same isovolumetric dose of olive oil by hypodermic injection, with an initial double-dose injection. In the GA group, rats were also treated with a 40% solution of CCl₄ plus 0.2% GA solution in double distilled water by the intraperitoneal injection of 3 mL per rat three times a week from the first week following previously published methods[35,36], with modifications. Controls were given the same isovolumetric dose of double distilled water. Animals were sacrificed 24 h after the last injection. Blood was obtained from the left ventricular apex for measurements of aminotransferases and the samples were stored at -20 °C. The liver was removed and rinsed with 0.9% saline, some liver sections were fixed in 10% buffered formaldehyde and embedded in paraffin for, and the remaining liver was stored at -70 °C for protein experiments.

Liver function

Blood was centrifuged at 3500 g at 4 °C for 10 min to separate the plasma. The activity of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were detected using a Siemens Advia 1650 automatic analyzer.

Sirius-red and hematoxylin and eosin staining

The thick sections (5 μm) were stained with hematoxylin and eosin (HE) and Sirius-red. HE staining was performed to assess pathologic changes in the liver. The standard of pathological grade was according to consensus on evaluation of the diagnosis and severity of hepatic fibrosis[37]. Sirius-red staining was performed to detect hepatic fibrosis. The Sirius red-positive areas were assessed in four different fields for each section by Image J Software (National Institutes of Health, Bethesda, MD, United States) and were in accordance with the following expression (collagen area/total area-vascular lumen area) × 100[38].

Immunohistochemical staining

Liver tissue sections were subjected to dewaxing, hydration and thermal induction antigen retrieval. Slices were blocked and incubated with anti-p53 antibody (1:50) and anti-cleaved-caspase-3 antibody (1:100) which were diluted in TBS-5% bovine serum albumin (BSA) at 4 °C overnight. Negative-control antibody was species-matched. The following day, the slices were washed and incubated with secondary antibodies. The slices were then incubated with 3, 3’-diaminobenzidine tetrachloride for 5-10 min to develop the color, and staining was observed under light microscopy (Olympus, Japan).

Terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-triphosphate nick end labeling assay

The terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-triphosphate nick end labeling (TUNEL) assay (Roche, Germany) was performed in accordance with the manufacturer’s protocol. Nuclei were redyed with 4,6-diamidino-2-phenylindole (DAPI) staining. Cells marked by TUNEL were evaluated using fluorescence microscopy (Olympus, Japan).

Protein preparation

Mitochondria were isolated with a tissue mitochondria isolation kit according to the manufacturer’s instructions. During mitochondria preparation, all samples were placed on ice. Eighty mg liver tissue was cut into pieces, tissue mitochondria isolation reagent A with phenylmethylsulfonyl fluoride (PMSF) was added, and then homogenized in an ice bath approximately 10 times. The homogenate was centrifuged at 600 rpm at 4 °C for 5 min. The supernatant was then collected and centrifuged at 11000 g at 4 °C for 10 min. The supernatant contained the cytoplasmic protein, and the precipitate contained the mitochondria. The cytoplasmic and mitochondrial fractions of the lysate were estimated by Western blotting. Liver tissues were homogenized in RIPA Lysis Buffer with PMSF and then centrifuged at 12000 g for 15 min at 4 °C, and the supernatant was the total protein.

Western blotting analysis

Proteins were separated by 10% or 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis and then transferred to polyvinylidene difluoride membranes (Millipore). The membranes were blocked with 5% BSA for 2 h, and then incubated overnight at 4 °C with rabbit anti-caspase-9, anti-caspase-3, anti-Smac, anti-cytochrome C, anti-c-IAP1, anti-Bcl-2, anti-Bax antibodies and mouse anti-p53, anti-GAPDH and anti-COXIV antibodies. The membranes were then incubated with HRP-conjugated goat anti-rabbit IgG and goat anti-mouse IgG (1:5000, diluted) at room temperature for 2 h, and then washed again and detected by the enhanced chemiluminescence (ECL) reaction. The intensities of the bands were analyzed by Image J software.

Statistical analysis

Each experiment was repeated at least 3 times. Data were estimated using analysis of variance and all values are expressed as mean ± SD. A P value < 0.05 was considered significant. All analyses in the study were implemented by SPSS 11.5 software for Windows (Chicago, IL, United States).

RESULTS

Function of GA on serum parameters of hepatic fibrosis induced by CCl₄

The activities of ALT and AST were significantly increased in the CCl₄ treated group compared with those in the control group (P < 0.05). In the GA group, the activities of ALT and AST were markedly decreased compared with those in rats with liver fibrosis not treated with GA (P < 0.05) (Table 1).

Table 1.

Effect of glycyrrhizic acid on plasma alanine aminotransferase and aspartate aminotransferase activity in CCl₄-induced rats

Group	ALT (U/L)	AST (U/L)
Control	42.4 ± 6.0	70.2 ± 2.3
CCl4	526.7 ± 57.2	640 ± 33.7
GA	342 ± 44.8a	462.8 ± 30.6a

^aP < 0.05 vs the carbon tetrachloride (CCl₄) group. GA: Glycyrrhizic acid; ALT: Alanine aminotransferase; AST: Aspartate aminotransferase.

Role of GA in the improvement of liver fibrosis induced by CCl₄

After 8 wk of CCl₄ administration, liver histopathology was significantly changed in the CCl₄ group. The livers, in the control group, showed an integrated lobular structure with central venous and hepatic cord radiation (Figure 1). The staging score was 0 (Table 2). The positive area of Sirius red staining in the control group was around the central vein rather than in the hepatic parenchyma. There were numerous Steatosis and ballooning of hepatocytes in the GA and CCl₄ groups. In the CCl₄ group, the liver showed fibrous connective tissue proliferation, fiber interval formation which was associated with disorder of lobular structure in the portal area, and most rat livers appeared to have pseudo lobules (Figure 1). The score of hepatic fibrosis in the CCl₄ group increased to 3.53 ± 0.74 (Table 2). The positive areas of Sirius red staining in the CCl₄ group were in the boundaries of the hepatic lobules and the ratio of the hepatic fibrotic region was 7.87% ± 0.66%. In the GA group, livers appeared to have fibrous connective tissue proliferation, the formation of a few fiber intervals in the portal area, and the occasional pseudo lobule (Figure 1). The score was 3.00 ± 0.76 (P < 0.05) in the GA group (Table 2). The positive area of Sirius red staining in the GA group was decreased, and the ratio of the hepatic fibrotic region (3.68% ± 0.32%, P < 0.05) was reduced compared with the CCl₄ group (Figure 1).

Figure 1.

Histological examination of liver by hematoxylin and eosin and Sirius red staining. A: Histological examination. Rats were treated with carbon tetrachloride (CCl₄) and/or glycyrrhizic acid (GA). Liver tissue sections were stained with hematoxylin and eosin or Sirius red (original magnification, × 100); B: Quantitative analysis of liver fibrosis by Sirius red staining. Results are represented as fibrotic area (%), which signifies the proportion of area stained red/area of total area-vascular lumen. Values are mean ± SD. ^aP < 0.05 vs CCl₄.

Table 2.

Histopathological semiquantitative scores in the liver

Group	n	0	+ 1	+ 2	+ 3	+ 4	Staging scores
Control	15	15	0	0	0	0	0
CCl4	15	0	0	2	3	10	3.53 ± 0.74
GA	15	0	10	1	10	3	3.00 ± 0.76a

^aP < 0.05 vs the carbon tetrachloride (CCl₄) group. GA: Glycyrrhizic acid.

Impact of GA on hepatic apoptosis induced by CCl₄

The expression level of cleaved caspase-3 was high in the livers of rats in the CCl₄ group. Interestingly, this level was reduced in the GA-treated group as detected by immunohistochemistry (Figure 2A). Under fluorescence microscopy, the TUNEL assays showed no stain and non-apoptotic nuclei in the normal liver tissue. High quantities of TUNEL cells were observed in the livers of the CCl₄ group and numerous condensed and fragmented nuclei. In the GA-treated group, there were few TUNEL cells, and less DAPI staining was observed in the same slice. The merged images indicated that TUNEL-positive cells were different, as numerous fused cells were observed in the CCl₄ group, while a significant reduction in these cells was detected in the GA-treated group (Figure 2B). Overall, these findings indicated that GA reduced apoptosis in liver lesion progression.

Figure 2.

Impact of glycyrrhizic acid treatment on hepatic apoptosis induced by carbon tetrachloride in rats. A: Liver tissue sections from the different groups were subjected to immunohistochemistry to determine the expression level of cleaved caspase-3 (original magnification, × 400); B: Fluorescence microscopy image showing terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-triphosphate nick end labeling (TUNEL) stain (dashed arrows), and the same tissue slices were respectively counterstained with 4’6-diamidino-2-phenylindole (DAPI) to localize the nuclei (arrows). Images of combined with DAPI, indicated TUNEL-positive cells (arrow heads) (original magnification, × 200). GA: Glycyrrhizic acid; CCl₄: Carbon tetrachloride.

Effect of GA on the level of proteins induced by CCl₄

The level of p53 was significantly higher in the livers of rats in the CCl₄ group than in the other two groups as detected by immunohistochemical staining, while in the GA group, the expression level of p53 was reduced (Figure 3A). This is consistent with the Western blotting analysis (Figure 3B) which showed that p53 was activated in the CCl₄ group and clearly reduced in the GA group.

Figure 3.

Effect of glycyrrhizic acid treatment on the expression level of p53 in the livers of rats injured by carbon tetrachloride. A: Liver tissue slices from the different groups were subjected to immunohistochemistry (original magnification, × 400). B: Total protein fractions prepared from livers were analyzed by Western blotting to assess the expression level of p53 and GAPDH to confirm the same sample loading. The results of Western blotting analysis were similar in at least three replicate independent experiments. All values are presented as mean ± SD. Statistical significance was defined as follows: ^aP < 0.05 vs the carbon tetrachloride (CCl₄) group. GA: Glycyrrhizic acid.

We examined the impact of GA on Bcl-2 and Bax protein expression in CCl₄-induced liver injury by Western blot analysis. As shown in Figure 4A, the expression level of the anti-apoptotic protein, Bcl-2, was decreased, while the expression of the pro-apoptotic protein, Bax, was increased in mitochondrial fraction of CCl₄-induced hepatic injury, and the Bax/Bcl-2 ratio was elevated in the CCl₄ group. In contrast, GA reversed the expression levels of Bcl-2 and Bax, and improved the Bax/Bcl-2 ratio. Both pro- and anti-apoptotic Bcl-2 proteins regulate cytochrome C from mitochondria to cytoplasm. The cytoplasmic fraction in the control group contained a negligible amount of cytochrome C. However, cytochrome C accumulated in the cytoplasm of liver tissue in the CCl₄ group, and GA inhibited the release of cytochrome C (Figure 4B). Caspase activation plays an important role in apoptosis, and caspase-3 cleavage is a typical feature of apoptosis[39]. In the current study, we found that there was increased cleavage of caspase-9 (37 kDa) and caspase-3 (17 kDa) in the CCl₄ group, suggesting severe apoptosis. Intriguingly, the levels of caspase-9 and caspase-3 cleavage diminished in the GA group (Figure 4C and D).

Figure 4.

Impact of glycyrrhizic acid on CCl₄-treated hepatocyte apoptosis signal cascades. Protein extracts from livers in the different groups were subjected to Western blotting. A: Expression levels of Bax and Bcl-2 in the mitochondria; B: Expression levels of cytochrome C (Cyt.c) in the cytoplasm and mitochondria; C: Expression level of caspase-9 in the total protein; D: Expression level of caspase-3 in the total protein; E: Expression level of Smac in the cytoplasm; F: Expression level of c-IAP1 the total protein. In all these experiments glyceraldehyde-3-phosphate dehydrogenase (GAPDH), COXIV were used to ensure equal sample loading. The Western blotting results represent three independent tests. The bar graph represents the value of in the different proteins via the density of bands from at least three independent tests. All values are presented as mean ± SD. Statistical significant was defined as follows: ^aP < 0.05 vs the CCl₄ group. GA: Glycyrrhizic acid; CCl_4: Carbon tetrachloride.

We also found that the cytoplasmic fraction in the control group contained a negligible amount of Smac. However, Smac accumulated in the cytoplasm of livers in rats exposed to CCl₄. GA treatment significantly inhibited the release of Smac induced by CCl₄ (Figure 4E). The expression level of c-IAP1 corresponded to the decreased expression of Smac in the GA-treated group compared with the CCl₄ group (Figure 4F), and the consequence was in accordance with the view that Smac has an antergic effect on c-IAP1 activity which can inhibit the activity of caspases[16-18]. These results indicated that GA could prevent CCl₄-induced apoptosis by suppressing the activation of upstream caspase-3. GA treatment ameliorated CCl₄-induced hepatic injury, and indicated the involvement of the p53 pathway in CCl₄-induced hepatocyte apoptosis.

DISCUSSION

Liver fibrosis is a common outcome in many chronic liver diseases. Liver fibrosis and cirrhosis, as shown in recent studies, are reversible processes[40,41]. However, there have been few effective therapies for the treatment of hepatic fibrosis in recent years[42]. There is an urgent need to investigate the effect of innocuous anti-fibrotic agents[43]. CCl₄-induced liver injury is one of the best-characterized models of hepatotoxicity, and can be used in the clinic to examine anti-hepatotoxic and/or hepatoprotective drugs[44].

GA, used in the treatment and control of chronic viral hepatitis, is now routinely used in Japan, due to its well-recognized transaminase-lowering effect in clinical applications[25,45,46]. Neominophagen C is a Japanese preparation containing 0.2% glycyrrhizin, 0.1% cysteine, and 2% glyceine, and mainly acts as an anti-inflammatory or cytoprotective drug rather than an antiviral. It can improve mortality in patients with subacute liver failure and ameliorate liver function in patients with subacute hepatic failure, chronic hepatitis, and cirrhosis[47].

Apoptosis is one of the events involved in the process of liver fibrosis. Thus, factors that affect apoptosis may be used to modulate liver fibrosis[33]. A line of evidence has shown that loss of p53 function is a common and considerable occurrence in the development of many human malignancies. In unstressed cells, expression of p53 is regulated and maintained at a low level through the ubiquitin/proteasome pathway[48]. Endogenous p53 activation in hepatocytes causes spontaneous liver fibrosis in double minute 2-knockout mice[3]. It also appears to modulate ethanol-induced hepatocyte apoptosis, since it was completely abrogated in mice with a p53 null background[49]. Mitochondria react to different cytotoxic stimuli, are central death regulators and play a vital role in p53-dependent death, in other words, the p53-dependent signal induces cell death through the mitochondrial pathway[50,51]. When the death signal is conducted to the mitochondria, the cell membrane permeability is increased and apoptosis-related proteins are released[52].

Many reports have demonstrated that drugs can ameliorate CCl₄-mediated hepatic apoptosis in rats, such as branched-chain amino acids[32] and the water-soluble extract of Salvia miltiorrhiza[33]. GA has an anti-apoptotic effect through the inhibition of hepatic apoptosis[26,27]. It significantly inhibited hepatocyte apoptosis by down-regulating the expression of caspase-3 and inhibiting the release of cytochrome C from mitochondria into the cytoplasm[28]. GA can alter Kaposi sarcoma-associated herpesvirus latency by triggering p53-mediated apoptosis[53]. Here we demonstrated that intervention with GA from the early stage of chronic liver disease effectively attenuated p53-dependent hepatocyte apoptosis and liver fibrosis, thus retarding disease progression in rats.

Apoptosis and necrosis contribute to the process of liver fibrosis[29,33]. Whether necrotic liver injury or apoptosis is dominant in CCl₄-induced liver injury models remains controversial. A previous study showed that CCl₄ can induce acute hepatocellular damage which is characterized by necrotic cell death[54], while another study indicated that a substantial number of hepatocytes undergo apoptosis in the acute stage after CCl₄ administration[29]. In the present study, we found both apoptosis and necrosis occurred in the CCl₄-induced chronic liver injury model. These results were consistent with other reports[32,33]. Discrepancies may be attributed to the time points of observation.

Steatosis and ballooning of hepatocytes are the earliest, most frequent, and most striking pathological changes observed in CCl₄-induced liver injury[29,55,56], and we found this pathological change using H and E staining. According to immunohistochemical staining, p53 expression level was significantly increased in the CCl₄ group compared with the GA group. Western blot analysis showed that p53 was sharply up-regulated in the CCl₄ group compared to the GA group. This indicated that p53 was activated after CCl₄ administration, however, GA reduced the expression level of p53.

To date, TUNEL assay[27], cleaved caspase-3 immunohistochemical staining[57] and serum CK18 fragment[58] have been identified as the markers of apoptosis. In the study we first detected DNA fragmentation of hepatocytes using the TUNEL assay. TUNEL-positive cells in the CCl₄ group were significantly increased compared with the GA group. GA reduced the number of TUNEL-labeled cells[27]. However, the TUNEL assay is not a specific marker of apoptosis, thus we performed cleaved caspase-3 immunohistochemical staining. The results coincided with those from the TUNEL assay. Apoptosis, a form of cell death, is principally caused by activation of the caspase family of cysteine proteases[4]. In accordance with Western blotting analysis, accompanied by the reduction in p53, the expression level of Bcl-2 was sharply decreased and the expression level of Bax was obviously increased in the mitochondrial fraction of the CCl₄ group, and the Bax/Bcl-2 ratio was elevated, while this tendency was reversed in the GA-treated group. Our results demonstrated that GA suppressed p53 activity, resulting in an increase in Bcl-2 and a decrease in Bax. In addition, GA inhibited the release of cytochrome C into the cytoplasm from mitochondria, and then inactivated caspase-9 and caspase-3. GA also reduced the expression of Smac, which was released from mitochondria, and bound to and antagonized c-IAP1, subsequently increased the inhibitory effect of c-IAP1 on caspase-3 and finally suppressed hepatocyte apoptosis. The degree of hepatic injury was associated with a substantial number of hepatocytes undergoing apoptosis[27]. The results also demonstrated that hepatic injury in the CCl₄ group was more serious than that in the GA group on the basis of histological observation, Sirius red staining assay, serum transaminase and TUNEL analyses. To our knowledge, these findings were to report that the effects of GA on p53-mediated activity in hepatocyte apoptosis in the liver of CCl₄-treated rats. Whether other mechanisms or pathways are involved in liver fibrosis requires further exploration.

In summary, our findings showed that GA exerted anti-apoptotic effects via a p53-dependent mitochondrial pathway (Figure 5). GA protected against CCl₄-induced hepatocyte apoptosis by regulating the Bcl-2 family of proteins, expression of Smac and caspase cleavage. These anti-apoptotic effects were related to decreases in the expression of pro-apoptotic proteins in the cytoplasm and the inhibition of proteins associated with apoptosis in the mitochondria. These findings suggest that GA can attenuate CCl₄-induced hepatocyte apoptosis via a p53-mediated mitochondrial pathway and can retard the progression of liver fibrosis induced by CCl₄ in rats.

Figure 5.

Schematic diagram of the effect of glycyrrhizic acid on the interruption of p53 signaling in carbon tetrachloride-induced hepatocyte apoptosis (blue arrows). Glycyrrhizic acid (GA) suppressed the activation of p53, decreased the expression level of Bax and increased the expression level of Bcl-2, which resulted in reduced cytochrome C release from the mitochondria into the cytoplasm, and inactivated caspase-9 and -3; GA also significantly inhibited Smac release from mitochondria into the cytoplasm and elevated the expression level of c-IAP1, resulting in inhibition of caspase-3 activity. Ultimately, GA suppressed the apoptosis of hepatocytes.

COMMENTS

Background

Liver fibrosis, induced by various pathological factors, is a common outcome in many chronic liver diseases, and is a serious threat to human health. However, there have been few effective therapies for the treatment of hepatic fibrosis in recent years. The authors investigated whether glycyrrhizic acid (GA) could attenuate hepatocyte apoptosis via a p53-mediated mitochondrial pathway and retard the progression of liver fibrosis induced by CCl₄ in rats.

Research frontiers

In this study, the authors found that GA attenuated hepatocyte apoptosis via a p53-mediated mitochondrial pathway and retarded the progression of liver fibrosis induced by carbon tetrachloride (CCl₄) in rats, which may be a potential alternative treatment approach in patients with liver injury.

Innovations and breakthroughs

This study sought to investigate the effects of GA on p53-dependent apoptosis in CCl₄-induced hepatic injury. The study data showed that GA protected against CCl₄-induced hepatocyte apoptosis by regulating the Bcl-2 family of proteins, expression of Smac and caspase cleavage.

Applications

This study provides valuable experimental evidence for future anti-liver fibrosis drug studies, and may provide an effective therapy for retarding the process of liver fibrosis.

Terminology

Liver fibrosis, induced by various pathological factors, is a common outcome in many chronic liver diseases, and eventually leads to liver cirrhosis. Apoptosis is gene-controlled and auto-programmed cell death in order to maintain homeostasis. Apoptosis is different from necrosis, as it is an initiative process rather than a passive process and involves gene activation, expression and regulation.

Peer review

This is a good study in which the authors presented experimental evidence that GA exerts anti-apoptotic effects via a p53-dependent mitochondrial pathway in CCl₄-induced hepatocyte apoptosis in rats. The results are interesting and suggest that GA could protect against CCl₄-induced hepatocyte apoptosis by regulating Bcl-2 family of proteins, expression of Smac and caspases cleavage.