The role of Neu1 in the protective effect of dipsacoside B on acetaminophen-induced liver injury

Shuang Chen; Mengzhen Li; Wei Jiang; Hao Zheng; Lian-Wen Qi; Shujun Jiang

doi:10.21037/atm-19-3850

. 2020 Jul;8(13):823. doi: 10.21037/atm-19-3850

The role of Neu1 in the protective effect of dipsacoside B on acetaminophen-induced liver injury

Shuang Chen ^1,², Mengzhen Li ^1,², Wei Jiang ^1,², Hao Zheng ^1,², Lian-Wen Qi ^1,^2,^3,^✉, Shujun Jiang ^1,^2,^3,^✉

PMCID: PMC7396229 PMID: 32793668

Abstract

Background

Pharmacological induction of autophagy can protect against acetaminophen (APAP) induced acute liver failure (ALF) by removing APAP adducts (APAP-AD), but its mechanism is not well understood. Hepatoprotective effect of saponins from traditional Chinese medicine has attracted widespread attention from all over the world. The content of saponins in Lonicerae Flos (Shanyinhua in Chinese) is up to 15–25%. Dipsacoside B (DB) is a common bioactive ingredient of different Shanyinhua, but its hepatoprotective effect and mechanism are still unknown. The present investigation aimed to study the benefit of DB in APAP-induced hepatotoxicity mouse model and different cell model.

Methods

Mice were treated with DB by intraperitoneal injection 1 h before treated with 500 mg/kg APAP, which caused ALF after 4 h. HepG2 cells were treated with DB for 1 h before treated with 10 mM APAP for 12 h. Hepatotoxicity was assessed via ALT and AST. Neuraminidase 1 (Neu1), lysosomal autophagy marker LC3 and P62 were examined by western blot. Neu1 activity was assayed using its substrate 2-(4-methylumbelliferyl)-D-N-acetylneuraminic acid. Apoptosis level was examined by TUNEL and caspase 3 activity. Molecular docking was used to predict the interaction between DB and protein Neu1.

Results

Our results demonstrated that pretreatment with 0.5 μM DB (in vitro) and 50 mg/kg DB (in vivo) respectively reversed increased level of AST and ALT induced by APAP. Histopathological examinations showed reduced necrosis and apoptosis in the liver of DB-treated APAP mice. DB promoted the removal of APAP-AD by lysosomal autophagy. These effects were associated with significant decrease in the level of Neuraminidase 1 (Neu1), a negative regulator of lysosomal exocytosis. Molecular docking results showed that DB could bind to Neu1 protein (binding energy =−7.86 kcal/mol). Akt/mTOR-mediated autophagy and inhibition of apoptosis may be the main mechanisms for the hepatoprotective effects of DB in acetaminophen-induced liver injury.

Conclusions

These data indicate that DB alleviated hepatotoxicity caused by APAP at least in part via Neu1 inhibition, Akt/mTOR pathway is involved in the detoxification effect of DB on acetaminophen-induced hepatotoxicity.

Keywords: Acetaminophen (APAP), acute liver failure (ALF), dipsacoside B, neuraminidase 1

Introduction

Acetaminophen (APAP) is currently widely used as an antipyretic and analgesic drug, but an overdose can cause severe liver injury and even acute liver failure (ALF) in animals and humans (1). At therapeutic doses, 90% of APAP binds to glucuronide and sulfuric acid to form non-toxic APAP complex, and excreted by the kidneys (2). The remaining part forms a reactive metabolite, N-acetyl-p-benzoquinone imine (NAPQI) via the activity of cytochrome P450 enzymes. NAPQI then conjugates with hepatic glutathione (GSH), and is consequently secreted into the bile without damage (3). Overdose of APAP can generate excess NAPQI, which deplete cellular GSH and cause APAP protein adduct (APAP-AD) formation, resulting in liver injury as result. NAPQI, as APAP metabolite, can react with protein in mitochondria to form APAP-AD, which results in mitochondrial damage causing hepatic cell necrosis and liver damage (4,5).

Autophagy can selectively remove cytosolic macromolecules and damaged organelles, thereby preventing mitochondrial damage-induced cell death (6,7). Recent reports indicated PI3K/Akt/mTOR signaling pathway regulated autophagy and apoptosis in different tissue injury (8,9). Accumulating evidence indicate that pharmacological induction of autophagy can protect against APAP-induced liver injury by removing APAP-AD (10,11), but the underlying mechanism remains unclear. Neuraminidase 1 (Neu1), a sialidase (SA), is widely found on the cell membrane and in lysosomes. It desialylates sialo-glycoconjugates by removing their terminal sialic acid residues (12). Most of the studies on Neu1 mainly focused on hepatic glucose and lipid metabolism (13,14), but very little is known about its role in drug-induced ALF. Autophagy starts with the formation of the phagophore, followed by autophagosome, and then fuses with lysosomes to form autolysosomes, wherefrom the contents are degraded by lysosomal enzymes (6,15). Lysosomal function and acidification are fundamental mechanisms for autophagosome–lysosome fusion. Lysosomal membrane protein 1 (LAMP-1) is predominantly localized in lysosomal membrane (LM), which protects LM from self-digestion, plays important physiological roles in maintaining lysosomes structures and functions (16). It has been reported that Neu1 negatively mediated lysosomal exocytosis in hematopoietic cells by LAMP-1 desialyation (17). Whether Neu1 can mediate drug-induced liver damage by affecting lysosomal exocytosis has not been reported yet.

N-acetyl-L-cysteine (NAC) is the first line detoxification drug for treating APAP-induced ALF in the initial rise in toxicity, but lots of patients present to the hospital after this stage (18). Furthermore, Lack of suitable biomarkers which can indicate progression of liver failure and provide liver transplantation operative basis (19).Therefore it is urgent to explore novel candidates and find new target for APAP-induced hepatotoxicity treatment.

Saponin extracts from traditional Chinese medicine have been widely reported to be resistant to drug-induced acute liver damage. From the chemical structural point of view, most saponins with hepatoprotective effects are triterpenoids, such as Ginseng saponins, saikosaponins, aescin etc. (20-22). The aforementioned studies suggest that hepatoprotection may be a common effect among saponins. The content of saponins in Lonicerae Flos (Shanyinhua in Chinese) is up to 15%, with regard to reported protective effects against CC1₄- and D-galactosamine-induced liver injury (23). Dipsacoside B (DB) is a common triterpenoid bioactive ingredient of different Lonicerae Flos without rhamnose in its branch chain compared to akebia saponin D (ASD). ASD is reported to alleviate hepatic steatosis via increased autophagic flux in both ob/ob mice and Buffalo rat liver cells (24). However, the hepatoprotective potential of DB remains unclear.

In the present study, we found that DB ameliorated APAP-induced hepatotoxicity via promoted autophagy and alleviated apoptosis, which contributed to the alteration of Akt/mTOR signal pathway. Upregulation of Neu1 caused by APAP was inhibited by DB, which can be a potential target for ALF therapy. Our data indicate that DB has the capacity to prevent APAP-induced hepatotoxicity due to autophagy activation and anti-apoptosis effects.

We present the following article in accordance with the ARRIVE reporting checklist (available at http://dx.doi.org/10.21037/atm-19-3850).

Methods

Reagents and chemicals

Assay kits for alanine aminotransferase (ALT), aspartate aminotransferase (AST), and glutathione disulfide (GSSG) were purchased from Nanjing Jiancheng Bioengineering Institute (Nanjing, China). Neu1 antibody was purchased from signal way antibody (Baltimore, USA). Antibodies LC3, P62, LAMP1, Akt, phosphorylate-Akt, mTOR, phosphorylate-mTOR were ordered from Cell Signaling Technology (Danvers, America). Acetaminophen (APAP) was obtained from Aladdin (Shanghai, China). Dipsacoside B (PubChem CID: 21627940) was bought from Chengdu Alfa Biothechnology Co., Ltd (Chengdu, China). 2-(4-methylumbelliferyl) -D-N-acetylneuraminic acid (4MU-NeuAc) was obtained from Sigma (St. Louis, MO, USA), Caspase 3 Activity Assay Kit (Beyotime Biotechnology, China) were purchased from Beyotime Biotechnology.

Experimental animals

Eight weeks old male C57BL/6J (18–22 g, RRID: IMSR_JAX:000664) mice were housed in a temperature-controlled (23–25 °C) and humidity 40–60% specific pathogen-free facility with free access to standard food and water under 12 h light-12 h dark cycle. All mice were provided by the Laboratory Animal Center of Nanjing Qinglongshan (Nanjing, China). Mice were randomly assigned to five groups (n=10 each group): (I) Normal control group: treated with saline by intraperitoneal injection, (II) APAP induced group: treated with 500 mg/kg APAP by intraperitoneal injection, (III) APAP + DB group: 25 mg/kg DB was given by intraperitoneal injection 1h before treated with 500 mg/kg APAP, (IV) APAP + DB group: 50 mg/kg DB was given by intraperitoneal injection 1h before treated with 500 mg/kg APAP, (V) APAP + OS group: 25 mg/kg OS was given by intraperitoneal injection 1 h before treated with 500 mg/kg APAP. The number of dead mice was recorded in every 2 h after APAP with or without DB injection, the survival rate of the mice was evaluated within 24 h. After APAP administration at 4 h, 6–8 animals were anesthetized and sacrificed for experimental analysis. All experiments were approved by the Animal Ethics Committees of China Pharmaceutical University and performed in adherence with the Guide for the Care and Use of Laboratory Animals of China Pharmaceutical University.

Biochemical parameters

Serum ALT and AST activity after 4 h of APAP induction were measured by ALT and AST reagent kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Oxidized glutathione (GSSG) content in HepG2 cells after 12 h of APAP treatment was measured by GSSG reagent kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Serum Caspase 3 activity was examined by Caspase 3 Activity Assay Kit (Beyotime Biotechnology, China).

Sialidase activity assay

We used the protocol described by Alexey V. Pshezhetsky and Michel Potier with minor modifications (25). Freshly isolated liver (100 mg) or cells (10⁶) were homogenized 5 times by sonication (50 hz, 5 s/time) in 200 µL H₂O, and incubated with 0.25 mM 4MU-NeuAc (Sigma, M8639) at 37 °C for 1 h in Na-acetate buffer (pH =4.6); 0.4 M glycine buffer (pH =10.4) was used to terminate the reaction. Fluorescence of liberated 4-methylumbelliferone (ex. 365 nm, em. 450 nm) was measured using a Thermofisher Multiskan™ FC spectrofluorometer.

Quantitative real-time polymerase chain reaction (qRT-PCR)

High-quality total RNA from liver and HepG2 cells were isolated via extraction with TRIeasyTM Total RNA Extraction Reagent (10606ES60, Yeasen, China). cDNA was synthesized using Hifair^® II 1st Strand cDNA Synthesis SuperMix for qPCR (gDNA digester plus) (11123ES60, Yeasen, China). The primers used for mice Neu1, mice 36B4, human Neu1, and human HPRT were as follows: mNeu1-F 5'-CCAACACCTTTGCTTCCTTGG-3' (Forward) and 5'-AGGGTAATGGGGAGCC TGAGT-3' (Reverse); m36b4-F 5'- AGCCTAAGATGAGCGCAAGT-3' (Forward) and 5'- TTACTAGGCAGATGGCCACA-3' (Reverse); hNeu1-F 5'- TGTGACCTTC ACCCTGAGC-3' (Forward) and 5'- TCGCAGGGTCAGGTTCACTC-3' (Reverse); hHPRT-F 5'- ACCAGTCAACAGGGGACATAAAAG-3' (Forward) and 5'- GTCTGCATTGTTTGCCAGTGTC -3' (Reverse). Quantitative RT-PCR for each gene was performed using Hieff™ qPCR SYBR^® Green Master Mix (No Rox) (11201ES03, Yeasen, China) in a Biorad CFX96 Touch real time PCR system (Biorad, USA.). The relative abundance of target gene transcripts was normalized via 36b4 (mice) or HPRT (human) expression.

Histological analysis and immunohistochemistry (IHC) and TUNEL assay

Livers were collected post 4 h intervention in different groups. Liver was fixed in 4% paraformaldehyde (PFA), sections (5 µm) were created and stained with hematoxylin and eosin according to standard procedures. Immunohistochemistry (IHC) was performed on paraffin sections as previously described (26). The TUNEL assay was performed by apoptosis detection kits (Beyotime Biotechnology, China) to detect apoptosis in liver tissues according to the manufacturer’s instructions. Images were captured by a Leica Upright Microscope DM2500, and calculated semi-quantitatively at magnification ×400 with Image Pro Plus software.

Cell culture

The human hepatoma cell line HepG2 (ATCC number:HB-8065™) was kindly supplied by Stem Cell Bank, Chinese Academy of Sciences. HepG2 cells were supported in Minimum Essential Medium (MEM, KGM31600-500, KeyGEN BioTECH) supplemented with 10% fetal bovine serum (FBS). Cells were maintained at 37 ºC in a humidified atmosphere with 5% CO₂.

Western blotting

The livers and cells were homogenized in protein lysis buffer to harvest total protein (P0013, Beyotime Biotechnology). The lysates were centrifuged at 12,000 g for 15 min at 4 °C. Protein concentrations in supernatants were determined with the enhanced BCA Protein Assay Kit (P0009, Beyotime Biotechnology). Proteins in same amount were separated by 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The membrane was further stained with Ponceau red (Nanjing Jiancheng Bioengineering Institute, Nanjing, China) to analyze APAP-AD.

Molecular docking

Search for the amino acid sequence of human NEU1 (Gene ID: 4758) was conducted. A homology model of human Neu1 was built at SWISS-MODEL website. Molecular docking of dipsacoside B (PubChem CID: 21627940) and Neu1 was performed by AutoDock (version 4.2.6). A genetic algorithm was performed 100 times to obtain 100 docking conformations, from which the best conformation was selected.

Statistical analysis

Statistically significant differences between control group and experimental group are presented as the means ± SD. All data were analyzed by one-way ANOVA (when three groups are compared) or repeated measurement ANOVA (for time course data) and unpaired Student's t-test. P<0.05 was considered statistically significant.

Results

Protective effect of DB treatment against APAP-induced hepatotoxicity

To investigate the hepatoprotective effect of DB (Figure 1A) in mice treated with an overdose of APAP (500 mg/kg) for 4 h, we checked the circulating level of ALT and AST which were widely used as biochemical markers for the evaluation of hepatic injury. As shown in Figure 1B, serum ALT and AST levels were dramatically raised in the APAP group compared with the control group (P<0.001). However, DB pretreatment significantly reduced the serum ALT (P<0.01) and AST (P<0.05) levels than in the APAP group (Figure 1B). To investigate the effects of DB on APAP-induced mortality, the survival rate was observed every 2 h within 24 h after DB treatment. We found 50 mg/kg DB pretreatment could significantly improve the survival rate of APAP-induced mice. Mice in APAP group began to die at 14 h, and the final survival rate was 20%, while 50 mg/kg DB increased the survival rate to 50% (Figure 1C). Histopathology of liver tissues was performed using H&E staining. Centrilobular necrosis in the necrotic area was markedly increased in APAP-treated mice compared to control mice (Figure 1D). In addition, we also found that DB pretreatment can partly suppress the hepatotoxicity caused by LPS/D-GalN in mice. The elevations of ALT and AST were both reduced but without significance by DB pretreatment for LPS/D-GalN mice (Figure S1A,S1B), and inflammatory cell infiltration was decreased (Figure S1C). Those results indicated that DB has hepatoprotective effect on APAP-induced liver injury.

Protective effect of DB on liver histopathological alterations in APAP induced mice. (A) The chemical structure of Dipsacoside B (DB). (B) Serum ALT and AST levels in APAP-treated mice with or without DB were detected after APAP treatment for 4 h. (C) Survival rate of mice were pretreated with DB by intraperitoneal injection for 1 h before APAP induction. (D) Representative liver histopathology with hematoxylin/eosin staining of APAP-induced liver injury in mice, assessed by images capture (Scale bar=100 μm). n=6–8, *, P<0.05; **P<0.01; ***, P<0.005.

Effects of pretreatment with DB on autophagy

Emerging evidence indicate that autophagy is an important protective mechanism against APAP-induced Liver injury (4,7,27). To study whether DB pretreatment protects against APAP-induced ALF via autophagy activation, the levels of autophagy marker LC3 and P62 were examined in liver of APAP-induced mice. Our data showed that pretreatment with DB increased the ratio of LC3 II/LC3-I in liver of APAP-treated mice, while P62 level slightly reduced (Figure 2A), which indicated that DB promoted autophagy in APAP mice. Immunohistochemistry confirmed that autophagy was raised in APAP-treated mice (Figure 2B). The predominant forms of APAP-AD were 34 kDa −60 kDa, increased after 1 h treatment with APAP, reached a maximum around 2 h, declined at 6–24 h with overdose of APAP, which is the critical initiation event for mitochondrial damage involved in hepatic necrosis with overdose of APAP (11). Ponceau red staining qualitatively revealed that DB protected against the APAP-induced hepatic necrosis by increasing APAP-AD removal (Figure 2C).

Activation of autophagy by DB alleviated APAP-induced hepatotoxicity. (A) Total liver lysates were subjected to Western blot analysis for LC3 and P62 (n=4). (B) lysosome autophagy was examined by immunohistochemistry. LC3 was increased in DB-treated APAP-mice (n=3), scale bar =50 μm. (C) Mice liver was subjected to Western blot analysis for APAP-AD. The membrane for the liver samples was further stained with Poncea red (n=3). *, P<0.05; **, P<0.01.

Protective effect of DB treatment against APAP induced HepG2 cell

NAPQI, the toxic metabolite of acetaminophen, binds to GSH covalently and forms glutathione disulfide (GSSG), causing GSH depletion (3). In order to determine whether DB affected the metabolism of acetaminophen, we examined the GSSG level in APAP-treated HepG2 cell. As expected, 0.5 µM DB potently inhibited the increase of GSSG caused by 10 mM APAP (Figure 3A). Meanwhile, enhancement of ALT level was markedly prevented in 0.5 µM DB-treated HepG2 cell pretreated with 10 mM APAP (Figure 3B). To investigate whether DB can alleviate APAP-induced hepatotoxicity in HepG2 cells by autophagy, we examined LC3-II and P62 levels. We found that LC3-II was significantly increased in APAP-treated HepG2 cells with 0.5 µM DB treatment, while P62 was reduced (Figure 3C). To confirm the hepatoprotective effect of DB, we examined the autophagy in two other liver cell lines—Huh7 and SMMC-7721 HCC cells treated by APAP. Our results show that DB can promote autophagy no significant change of LC3 II and P62 in these cells (Figure S2A,S2B). These results also showed that DB could ameliorate APAP-induced ALF by autophagy in HepG2 cells.

The inhibitory effects of DB treatment in APAP-induced hepatotoxicity. (A) Total content of GSSG in APAP-treated HepG2 cells with or without DB was measured after 12 h (n=7). (B) The effect of DB treatment on ALT levels in APAP-induced HepG2 cells (n=6). (C) Total cell lysate was subjected to Western blot analysis for LC3 and P62 (n=4). (D) Relative intensity of LC3 and P62. *, P<0.05; **, P<0.01.

DB suppressed APAP-induced hepatocyte apoptosis in vitro and in vivo

It has been reported that hepatocyte apoptosis is involved in the development of acute liver injury (28). To confirm the effects of DB on apoptosis induced by APAP both in vivo and in vitro, we performed TUNEL staining to evaluate apoptosis level in liver tissue sections, and examined the Caspase 3 activity both in liver tissue and HepG2 cells induced by APAP. We found that the number of TUNEL-positive hepatocytes in APAP group was significantly higher than the control group, while DB pretreatment effectively decreased the number of TUNEL-positive hepatocytes, indicating that DB significantly inhibited APAP induced apoptosis (Figure 4A). Consistent with the TUNEL assay results, DB treatment suppressed Caspase 3 activity in mice and HepG2 cells caused by APAP (Figure 4B,C).

DB pretreatment suppressed apoptosis caused by APAP. (A) TUNEL staining of apoptotic hepatocytes counterstained with DAPI in liver tissue sections from mice treated with Vehicle (Control group), APAP (Model group), APAP + DB (50 mg/kg) for 4 h (n=3, original magnifications, ×200). (B) Capase 3 activity in liver tissues from mice treated with Vehicle (Control group), APAP (Model group), APAP + DB (50 mg/kg) for 4 h (n=6). (C) Capase3 activity in HepG2 cells treated with Vehicle (Control group), APAP (Model group), APAP + DB (0.5 μM) for 12 h (n=5). *, P<0.05; **, P<0.01.

DB prevented the increase in hepatic Neu1 level due to APAP treatment

Maintenance of the structural and functional integrity of lysosomes is vital for autophagosome-lysosome fusion. Neu1 is mainly located in lysosome, and acts as a negative regulator of lysosome exocytosis in hematopoietic cells by removal of sialic acids on LAMP-1 (17). We found that mRNA and protein levels of Neu1 were increased in both HepG2 cells and liver of mice by APAP induction. Treatment with 0.5 µM (in vitro) and 50 mg/kg (in vivo) DB inhibited the elevation of Neu1 level (Figure 5A,B,C,D). But DB showed no significant effect on Neu1 level in Huh7 and SMMC-7721 HCC cells induced by APAP (Figure S2A,S2B). This phenotype may be caused by the lower Neu1 level in these cells compared to HepG2 cells (Figure S2C). We further tested whether enzyme activity of Neu1was also changed by APAP in vitro and in vivo. Our results demonstrated that DB (0.5 μM in vitro and 50 mg/kg in vivo) prevented the increase of Neu1 activity caused by APAP (Figure 5E,F). In line with this, DB (0.5 µM in vitro and 50 mg/kg in vivo) restored the level of lysosome marker (LAMP1) (Figure 5G,H). These data suggested that DB could restore the structural integrity of lysosome in ALF through inhibition of Neu1.

DB restored the increase of Neu1 in APAP-induced hepatotoxicity. (A) Protein levels of Neu1 were decreased in APAP-treated HepG2 cells (n=3) and mice (n=8) treated with DB by Western Blot. (B) Relative density of Neu1 in liver of APAP-treated mice by Western Blot. (C and D) Transcript levels of Neu1 were decreased in APAP-treated HepG2 cells (n=4) and mice (n=6–8) treated with DB by qRT-PCR. (E and F) Enzyme activity of Neu1 were inhibited in APAP-treated HepG2 cells and mice treated with DB (n=6–8). (G) Total cell lysate and liver lysates were subjected to Western blot analysis for LAMP1 (n=4). (H) lysosome marker was examined by immunohistochemistry. LAMP1 was increased in DB treated mice (n=3), scale bar =50 µm. *, P<0.05; **, P<0.005; ***, P<0.001.

Neu1 is a negative regulator of autophagy

The above results indicated that the inhibition of Neu1 plays a role in protecting against APAP-induced hepatotoxicity through autophagy. In order to confirm the role of Neu1 in autophagy, we treated mice with Neu1 inhibitor-Oseltamivir (OS, 25 mg/kg) 1 h before APAP induction. Histological analyses revealed that centrilobular necrosis in the necrotic area was markedly decreased in OS-treated mice compared to APAP-treated mice (Figure 6A). The predominant forms of APAP-AD (34-60kD) were also reduced in the liver of OS-treated mice (Figure 6B). To investigate whether Neu1 was involved in autophagy, we treated HepG2 cells with Torin 1 (an mTOR inhibitor and autophagy inducer, 10 µM) or OS (0.25 µM) 1 h before APAP induction. As shown in Figure 6C and 6D, enzyme activity and protein level of Neu1 were both downregulated in Torin 1-treated and OS-pretreatment HepG2 cells, which was consistent with DB (0.5 µM)-treated HepG2 cells. In line with these observations, ALT levels were reduced in DB-, OS- and Torin1-treated HepG2 cells by APAP induction (Figure 6E), which indicated that DB ameliorated the hepatotoxic effects of APAP via inhibition of Neu1 activity. To investigate whether Neu1 alteration is correlated with autophagy, we checked LC3 and P62 level in OS or Torin1 pretreated HepG2 induced by APAP. OS and Torin1 significantly promoted the LC3-II caused by APAP, but without markedly effect for P62 (Figure 6F). Taken together, these above results lend credence to the hepatoprotective potential of DB particularly against APAP-induced acute liver injury.

Neu1 negatively regulated autophagy in ALF. (A) Representative photomicrographs of liver samples of mice subjected to hematoxylin and eosin staining (magnification, ×10; n=5, Scale Bars: 50 μm). (B) Liver samples of mice were subjected to Western blot analysis for APAP-AD. The membrane for the liver samples was further stained with Poncea red (n=3). (C) Protein levels of Neu1 were decreased in APAP-treated HepG2 cell (n=3) upon treatment with OS and Torin1 as captured through Western blot analysis. (D) Enzyme activity of Neu1 was decreased in APAP-treated HepG2 cells (n=6) treated with OS and Torin1. (E) The effect of OS and Torin1 treatment on ALT levels in APAP-treated HepG2 cells (n=6). (F) Protein levels of LC3 and P62 in APAP-treated HepG2 cells subsequently treated with OS and Torin1 as evidenced by Western blot analysis (n=4). *, P<0.05; **, P<0.005.

DB alleviated acute liver injury induced by APAP via inhibition of Akt/mTOR signal

PI3k/Akt/mTOR signal is a classical signal pathway for autophagy regulation (29). As shown in Figure 6E, Torin1(mTOR inhibitor) significantly reduced the ALT in APAP-induced HepG2 cells, we confirmed whether DB protected against APAP hepatotoxicity via Akt/mTOR signal. We assessed the hepatic protein expression levels of Akt, p-Akt, mTOR, p-mTOR. The level of p-Akt and p-mTOR were both elevated in APAP group but reduced after DB administration (Figure 7A). Our results indicated that APAP-induced ALF might be due to the alterations in Akt/mTOR pathway in the liver.

DB ameliorated hepatotoxicity via interaction with Neu1. (A) Protein levels of P-AKT and p-mTOR were decreased in APAP-treated HepG2 cell with DB as captured through Western blot analysis. (n=4) (*, P<0.05). (B) Protein is shown as cartoon and DB as sticks. TYR370, ARG280, GLU264, ASP226, SER102, and ALA162 with important interactive hydrogen-bonds with DB are labeled, and the dashed lines represent hydrogen bonds. The binding energy =−7.86 kcal/mol.

Neu1 is a negative regulator of lysosomal exocytosis. We also tested whether DB alleviated liver injury by directly targeting Neu1. Molecular docking experiment showed that DB docked into the cavity of protein Neu1, with the possibility of forming hydrogen-bond with six amino acid residues (TYR370, ARG280, GLU264, ASP226, SER102, and ALA162). The binding energy predicted by Autodock was –7.86 kcal/mol (Figure 7B). Consistent with this, DB has no significant impact on autophagy in Huh7 and SMMC-7721 HCC cells with lower neu1 level (Figure S2A,S2B). The aforementioned observation indicated that DB could directly inhibit Neu1 activity.

Discussion

APAP-induced liver injury is one of the major causes of acute liver failure in clinical practice (30). The present work evaluated the protective effects of DB against ALF induced by APAP. The major findings of this study are as follows: (I) DB reduced APAP-induced hepatotoxicity both in vivo (50 mg/kg) and in vitro (0.5 µM); (II) the hepatoprotective effect of DB was mediated through the activation of autophagy and inhibition of apoptosis by Akt/mTOR signal pathway; (III) DB restored the equilibrium of lysosome structure by inhibiting Neu1 activity in APAP-induced liver damage.

Mitochondrial damage and APAP-AD formation are critical factors for APAP-induced hepatocyte necrosis. Various lines of evidence have shown that pharmacological induction of autophagy by Torin1 offers protection against APAP-induced ALF by the removal of damaged mitochondria and APAP-AD (10,11). However, the mechanisms that underlie this activity of the hepatocytes remain largely unclear. Phosphatase and tensin homolog (PTEN)-induced kinase 1 (PINK1), a mitochondrial serine/threonine kinase, mediates Ser65 phosphorylation of ubiquitin and enhances Parkin E3 ligase activity to facilitate mitophagy in ALF induced by APAP (31-33). Emerging evidence indicates that autophagy receptor protein-SQSTM1/p62 binds directly with LC3 via its LC3-interaction region (LIR), and thus promotes recruitment of autophagosomes to mitochondria (34,35). P62 has been reported to bind with APAP-AD and facilitate APAP-AD transition to the detergent insoluble form, which can only be removed by autophagy (11). In the present study, histological analysis and Ponceau red staining showed that DB enhanced the removal of APAP-AD (34–60 kD) leading to protection against APAP-induced necrosis. Pretreatment with DB improved the level of LC3-II in APAP-induced hepatotoxicity model, suggesting that activation of autophagy played a key role in the hepatoprotective effect of DB. Excessive autophagy may cause apoptosis in pathological conditions, but our study revealed that DB moderately promoted autophagy in APAP injury model without increase of apoptosis, supplementation of DB partially inhibited activity of Caspase 3 and prevented DNA damage caused by APAP. Our results were supported by Gong’s study, who reported that ASD (with one more rhamnose compared to DB could protect against apoptosis and activated autophagy in liver of NAFLD mice (23).

Neu1, the most abundant sialidase in mammals, is involved in the regulation of energy homeostasis, inflammation, proliferation, cell adhesion, phagocytosis, and exocytosis (36,37). Neu1 regulates LAMP-1, a structural component of the lysosomal membrane, via its sialic acid cleavage. Hypersialylated LAMP-1 has a longer half-life and accumulates at plasma membrane, which is correlated with excessive lysosomal exocytosis of serine proteases in o mice bone (16). Our results revealed the function of Neu1 in APAP-induced ALF mice models those were pretreated with DB. Compared to HepG2 cells, SMMC-7721 and Huh7 HCC cells showed lower Neu1, which exhibited no significant change of Neu1 and autophagy marker by APAP and DB treatment, and cells with lower Neu1 level are more resistant to APAP injury. Taken together, our data demonstrate that DB ameliorated the hepatotoxic effects of APAP by regulating lysosome mediated autophagy through Neu1 inhibition. The AutoDock result showed that DB could bind with protein Neu1, which may be the cause of Neu1 enzyme activity variation by DB. Moreover, how DB influences the protein level of Neu1 both in vitro and in vivo still needs further study.

It is generally accepted that defective autophagy results in excessive inflammation that contributes to disease pathology (37,38). And Neu1 was positive enhancers of inflammation in monocytes/macrophages for atherosclerosis (39). LPS/D-Gal-induced acute liver injury mainly results from the release of massive inflammatory cytokines, such as interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α. We found that 50 mg/kg DB can partly inhibited the elevation of AST, ALT and inflammatory infiltration by LPS/D-Gal. Whether higher dose of DB can significantly reverse the LPS/D-Gal-induced acute liver injury is needs deeply study. It has been confirmed that activation of autophagy by pharmacotherapy can protect against acute liver injury induced by various stimulus has been confirmed (11,28,40). It is beneficial for the treatment of acute liver injury through restore the dysfunction of autophagy. We identified DB as a factor that exerted hepatoprotective activity through possible mechanisms involved in the inhibition of Neu1 and induction of autophagy.

Conclusions

In summary, our results identified a critical role of autophagy and Neu1 in the hepatoprotective effects of DB in APAP-induced hepatotoxicity models. DB inhibited liver toxicity through regulation of autophagy, basically via increasing the removal of APAP-AD, and thus preventing hepatic necrosis. Furthermore, the inhibition of Neu1 by DB could restore the excessive lysosome exocytosis. Therefore, Neu1 inhibition may be a new target for treating APAP-induced liver injury as exemplified with DB treatment.

Supplementary

The article’s supplementary files as

atm-08-13-823-rc.pdf^{(154.3KB, pdf)}

DOI: 10.21037/atm-19-3850

atm-08-13-823-dss.pdf^{(65.6KB, pdf)}

DOI: 10.21037/atm-19-3850

atm-08-13-823-coif.pdf^{(195.1KB, pdf)}

DOI: 10.21037/atm-19-3850

Acknowledgments

The authors thank Dr. Raphael N. Alolga, a native English teacher for editing our manuscript. We thank YingJian Hou and Minhui Sun from the Cellular and Molecular Biology Center of China Pharmaceutical University for their technical help in histological microscopy and qRT-PCR.

Funding: This project funded by China Postdoctoral science foundation (Grant No. 2018M630640) and the National Natural Science Foundation of China (Grant No. 81900780).