Panax notoginseng saponins promote liver regeneration through activation of the PI3K/AKT/mTOR cell proliferation pathway and upregulation of the AKT/Bad cell survival pathway in mice
The regenerative capacity of the liver is crucial for the host to survive after serious hepatic injuries, tumor resection, or living donor liver transplantation. Panax notoginseng saponins (PNS) have been reported to exert protective effects during organ injuries. The present study aimed to evaluate the effect of PNS on liver regeneration(LR) and on injuries induced by partial hepatectomy (PH).
We performed 70% partial PH on C57BL/6 J mice treated with or without PNS. LR was estimated by liver weight/body weight, serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels and cell proliferation, and the related cellular signals were analyzed by Western blot.
Different concentrations of PNS promoted hepatocyte proliferation in vitro. Mice in the PNS group showed higher liver/body weight ratios at 2 d and 7 d (P < 0.05) after PH and lower levels of serum ALT and AST (P < 0.05) compared to those of mice in the normal control (NC) group. Histological analysis showed that the expression of proliferating cell nuclear antigen(PCNA) at 2 d and 7 d after PH was significantly higher in the PNS group than in the NC group (P < 0.05). Mechanistically, the AKT/mTOR cell proliferation pathway and AKT/Bad cell survival pathway were activated by PNS, which accelerated hepatocyte proliferation and inhibited apoptosis (P < 0.05).
PNS promoted liver regeneration through activation of PI3K/AKT/mTOR and upregulated the AKT/Bad cell pathways in mice.
KeywordsPanax notoginseng saponins Liver regeneration Protein kinase B Mammalian target of rapamycin
Protein kinase B
Bovine serum albumin
Hanks balanced salt solution
Inferior vena cava
Mammalian target of rapamycin
Proliferating cell nuclear antigen
Panax notoginseng saponins
Specific pathogen free
The liver, which has a remarkable regenerative capability, is able to fully regenerate to its original mass, even with less than 30% of its tissue left . This regenerative capacity is crucial for the host to survive after serious hepatic injuries, tumor resection, or living donor liver transplantation. Liver function recovery depends on increased energy production, which is indispensable for restoring liver mass . However, the mechanisms underlying the response of the liver to acute and chronic injury and signaling pathways that are critical for regenerative capacity still require further study.
The traditional Chinese medicinal herb Panax notoginseng(Sanqi), which is known as a hemostatic medicine, has been used to accelerate blood clotting, alleviate swelling and relieve pain for more than a thousand years . Panax notoginseng saponins (PNSs)contains more than 20 dammarane type saponins including ginsenoside Rg1, Rg2, Rb1, Rb2, Rb3, Rc, Rd., Re, Rh, F2 and notoginsenoside R1, R2, R3, R4, R6, Fa, Fc, Fe, etc., among which panax notoginsenoside R1, ginsenoside Rg1, Rd., Re and Rb1 are the major active components [4, 5, 6]. More than 200 compounds have been isolated from PNS, including saponins, flavonoids, cyclopeptides, sterols, polyacetylenes, volatile oil, amino acids, and polysaccharides . Various PNS preparations are commercially available and widely applied in pharmaceutical forms, including capsules, injections, and powders . Increasing evidences has indicated that PNS can not only prevent the aggregation of platelets to invigorate the circulation of blood but can also stimulate angiogenesis to repair injured vessels and recover the blood supply for different organs . In addition, PNS prevents cardiomyocyte apoptosis and alleviates oxidative stress-induced damage . PNS protects human umbilical vascular endothelium cell against oxidative damage in vitro . Moreover, PNS has been used in liver diseases. PNS ameliorates liver fibrosis in vivo and vitro . Zhou’s study found that PNS protected liver against hepatotoxicity induced by Triptolide . The protective effect of PNS against liver injuries in mice induced by ethanol has been verified in previous study . Hepatic hemodynamics changed obviously and oxidative stress were increased after partial hepatoectomy (PH) and a quick recover of blood supply and relieved oxidative stress in liver would be beneficial for liver regeneration . It is reasonable to predict that PNS may have protective effects against injuries induced by PH. However, the effect of PNS on the injury induced by PH has never been studied.
The phosphatidylinositol-3-kinase (PI3K)-Protein kinase B(AKT) signaling pathway has long been confirmed as an important pathway regulating cell proliferation. Phosphorylated AKT acts on its downstream targets and participates in the regulation of the cell cycle and growth . It has been reported that PNS activated the PI3K/AKT/mammalian target of rapamycin(mTOR) signaling pathway in anterior cruciate ligament fibroblasts . However, whether the PI3K/AKT signaling pathway in primary hepatocytes is activated upon treatment with PNS is unknown.
The present study examined the effect of PNS on 70% liver resection of liver regeneration (LR) mouse models and studied the underlying mechanism.
Male C57BL/6 mice that weighed 19–23 g and were 8–10 weeks of age were purchased from the Experimental Animal Center of Chongqing Medical University (Chongqing, China). Animals were housed in sterile polycarbonate cages with free access to water and food in a specific pathogen-free (SPF) barrier. All animal care and experimental protocols were in compliance with the Animal Management Rules of the Ministry of Health of the People’s Republic of China.
PNS were purchased from Kunming Pharmaceutical Corporation(China Food and Drug Administration (CFDA) approval number: Z20026438, KPC Pharmaceuticals, Inc., Kunming, China). Seven days before PH, mice were divided into two groups that were administered saline (normal control, NC) or PNS (200 mg/kg, intraperitoneal injection) at 8:00 am everyday . The treatment is maintained during the whole experiment. The same surgical procedure were performed in both NC and PNS group. Before PH, mice were subjected to adequate anesthesia by sodium pentobarbital (50 mg/kg) intraperitoneal injection while the body temperature was sustained by a heating pad at around 36 °C. Two-thirds of the liver (median and left lobes) was removed . All surgeries were performed at 9:00–11:00 AM to rule out the influence of diurnal variations on regeneration. Then, the mice were divided into 3 groups (n = 6 animals per group): PH 2 d, 7 d and sham-operation (sham) groups. The same surgical procedure was performed on the sham groups without conducting PH. The mice were anaesthetized by sodium pentobarbital (50 mg/kg) intraperitoneal injection and sacrificed by cervical dislocation, and the remnant liver tissues were harvested at different time points: 2 and 7 days (s). The regenerative remnant lobe was snap-frozen in liquid nitrogen and stored at − 80 °C for further analysis.
Isolation of primary hepatocytes and cell culture
Primary hepatocytes were isolated according to a method introduced by Edwards M et al. . Briefly, under adequate anesthesia, the inferior vena cava (IVC) was exposed. The IVC was infused with buffer 1 (Ca2+- and Mg2+-free Hanks balanced salt solution (HBSS)) after it was blocked just below the heart. The infusion was changed to buffer 2 (Ca2 + − and Mg2 + −containing HBSS to a final concentration of 0.08 U/mL) and the perfusion was continued for approximately 8–10 min after perfusing buffer 1 for 8 min (5 mL/min). The liver was then placed in a 100-mm cell-culture plate for further hepatocyte isolation. Finally, 1 mL (5 × 106 hepatocytes/mL) of the suspension was dispensed into each well of 12-well culture plates and incubated at 37 °C with 5% CO2 for later use. Hypoxia was simulated according to the study design by Hong et al. . Hepatocytes were preincubated with 10 μM LY294002 for 1 h and were then treated with PNS (0.12 mg/ml) for 24 h. Six hours after the addition of PNS (0.12 mg/ml), the cells were subjected to hypoxia for 24 h.
Primary mouse hepatocytes (6 × 103 cells/well) were treated with a variety of concentrations of PNS for 24 h in 96-well plates. Cell viability was determined by a Cell Counting Kit-8 (MCE, Prod# HY-K0301) according to the company’s protocol. The absorbance at 450 nm was measured by a microplate reader (xMark™ Microplate Absorbance Spectrophotometer, BIO-RAD). Values represent the mean ± SD of at least three independent experiments .
Serum was isolated from whole blood by centrifuging (5000 rpm, 20 mins) at room temperature after coagulation. An automatic biochemical meter (CX7, Beckman Coulter, USA) was used to detect serum alanine aminotransferase (ALT) and aspartate transaminase (AST) levels.
Briefly, the paraffin-embedded tissue sections were deparaffinized and dehydrated. A portion of 50 μl of TUNEL reaction mixture was added to tissue sections. Then, on each slide, 50 μl of conversion agent (POD) and 50–100 μl of substrate solution were added successively, and slides were incubated for 10 min at room temperature. Slides were then dehydrated, cleared and mounted for confocal microscopy observation. A positive signal was defined as the presence of distinct fluorescence staining within the nuclei 4′,6-diamidino-2-phenylindole (DAPI).
All tissues were fixed in 4% paraformaldehyde for 36 h immediately after surgical resection and were embedded in paraffin. The tissue sections (5 μm) were heated, dewaxed and rehydrated by immersion in dimethylbenzene and a graded ethanol series. For immunohistochemistry, an antigen-retrieval technique consisting of heating in a citrate water bath was performed before dewaxing and rehydration. Endogenous peroxidase activity was blocked by incubation with 3% hydrogen peroxide, and nonspecific binding was blocked using 5% bovine serum albumin (BSA) at room temperature. Finally, specimens were incubated overnight with antibodies against PCNA (CST, Prod# 13110S, 1:200), and the sections were stained with diaminobezidin(DAB) the next day.
Ethynyl-2′-deoxyuridine cell proliferation assays
Cell proliferation was assessed by the incorporation of 5-ethynyl-2′-deoxyuridine (Cell-Light™ EdU In Vitro Imaging Kit, Prod# C10310, RiboBio Co) into DNA according to the manufacturer’s instructions. Briefly, hepatocytes were administered with PNS as described, and EdU was added to the culture at a concentration of 100 nmol/L. According to the standard formaldehyde fixation protocol, the cells were permeabilized, fixed and incubated with the reaction cocktail for 30 min. The images of stained cells were captured by fluorescence microscopy. Values represent the mean ± SD of at least three independent experiments.
Total proteins were extracted from mouse liver and primary hepatocytes by RIPA Buffer (Abcam, Prod# ab156034) containing a protease inhibitor cocktail (Beyotime, Prod# P1005). A BCA Protein Assay Kit (CST, Prod#7780) was used to quantify the protein concentration in the supernatant, and lysates were then mixed and heated with Sample Loading Buffer (Beyotime, Prod# P0015A) at 100 °C for 10 min. Samples were separated by SDS-PAGE gels of different concentrations and were then transferred to a 0.2 μm PVDF membrane (ROCHE, Prod# 03010040001). The membranes were blocked with 5% nonfat milk (Bio-Rad, USA) for 60 min at room temperature and incubated overnight at 4 °C with primary antibodies against PI3K antibodies (cat. no. ab32089; 1:1000; Abcam Inc.); p-PI3K antibodies (cat. no. 4228; 1:1000; CST Inc.); AKT (cat. no. ab38449; 1:1000 dilution; Abcam Inc.); p-AKT (cat. no. ab38449; 1:1000; Abcam Inc.); mTOR (cat. no. ab2732; 1:1000; Abcam Inc.); mTOR (cat. no. ab109268; 1:1000; Abcam Inc.) GADPH (cat. no. ab8245; 1:1000 Abcam Inc.); Bad (cat. no. ab32445; 1:1000 Abcam Inc.); and p-Bad (cat. no. ab129192; 1:1000 Abcam Inc.), which was followed by incubation with horseradish peroxidase-conjugated secondary antibodies (ZSGB-BIO, Inc., China). Membranes were washed three times, incubated with HRP-conjugated secondary antibodies (ABclonal, Prod# AS003, AS014) at a dilution of 1:8000 for 60 min the next day and detected by a ChemiDoc™ system (Bio-Rad, USA) via Western-Bright ECL kit (Advansta, USA). β-actin was analyzed as a loading control.
Liver/body weight ratio
The liver/body weight ratio, also known as the liver regeneration index, was calculated by the equation: A/B, in which A stands for liver weight after regeneration, while B stands for body weight.
Annexin V-FITC/PI staining
We detected apoptosis in primary mouse hepatocytes by flow cytometry (FCM) using Annexin V-FITC/PI double staining. The cells were harvested and washed with PBS and incubated in binding buffer containing Annexin V-FITC and PI for 15 min at 37 °C in the dark. Cells were then analyzed using FCM (FACS CantoTM, BD, CA, USA). FlowJo software version 7.6.1 (Ashland, OR, USA) was used to count the number of apoptotic cells per sample.
All values are expressed as mean ± SD. Data were analyzed using an unpaired two-tailed Student’s t-test or one-way analysis of variance with a post-hoc test. SPSS 22.0 software was applied in all statistical analyses. A P value less than 0.05 was required for results to be considered statistically significant.
PNS promoted primary mouse hepatocyte proliferation in a dose-dependent manner and activated the PI3K/AKT/mTOR signaling pathway in primary mouse hepatocytes
To examine whether PNS could activate AKT/mTOR in primary mouse hepatocytes, we added the PI3K/AKT inhibitor LY294002 to PNS-treated hepatocytes. The EdU staining showed that the proliferative effect of PNS was inhibited by LY294002 (P < 0.05) (Fig. 1D-E). The phosphorylated and total protein levels of PI3K, AKT, and mTOR were examined in hepatocytes treated with 0.12 mg/ml PNS with or without LY294002 by Western blotting. The results showed that PNS increased the phosphorylation of PI3K, AKT, and mTOR in primary mouse hepatocytes, and this effect was blocked by LY294002 (P < 0.05) (Fig. 1F-I).
PNS promoted liver regeneration and activated the PI3K/AKT/mTOR signaling pathway in vivo
PNS inhibited hepatocellular apoptosis during LR in mice through AKT/bad signaling
PNS alleviated hypoxia-induced hepatocellular apoptosis through AKT/bad signaling in vitro
PNS is a species of the genus Panax and have extensive pharmacological activities in the treatment of various diseases, such as cardiovascular, nervous and anticancer, anti-atherosclerotic and other biological activities . PNS are active components with different dammarane-type saponins . Notoginsenoside R1 is a unique component in PNS, which contributed to the amelioration of myocardial cells apoptosis and myocardial ischemia/reperfusion injury via inhibiting the activation of TAK1/NF-κB pathways . Additionally, Notoginsenoside R1 exerts protective effects through the enhancement of beta-amyloid protein degradation and maybe is a potential candidate for AD treatment . For the effective treatment of cerebrovascular diseases and improves the cognitive and sensorimotor deficits, Ginsenoside Rb1 as also a major active component in PNS has the function on the modulation of the AKT/mTOR signaling pathway and down-regulation of caspase-3 in rats subjected to phototrombic stroke . It was indicated that the ginsenoside Rh4 could trigger apoptosis by activating the ROS/JNK/p53 pathway in colorectal cancer cells . In general, these components of PNS have various biological effects, such as antioxidant, anti-inflammatory, antiaging, neuroprotective, and anti-apoptosis and this prompted us to investigate the overall effects of PNS on LR and explore related molecular mechanisms. In the current study, we demonstrated that administration of PNS can promote LR and improve liver function after PH in mice through PI3K/AKT/mTOR pathway, thus such protective mechanism might mainly be induced by Ginsenoside Rb1. In our study, the results demonstrated that PNS at concentrations varying from 0.03 to 0.5 mg/ml promoted cell proliferation, which peaked at a concentration of 0.12 mg/ml in primary mouse hepatocytes; thus, we chose this concentration (0.12 mg/ml) for further study.
During LR, organisms developed complex protective mechanisms to survive in a challenging environment. Stress response proteins and pathways were involved in these mechanisms, including membrane transporters, protein chaperones, antioxidant enzymes, growth factors, and signaling pathways and transcriptional factors . PI3K/AKT has long been considered a major pathway that promotes cell proliferation and prevents cellular apoptosis . AKT phosphorylation initiates the expression of proteins involved in regulating proliferation and apoptosis in cells . Cell apoptosis and survival, protein synthesis, and autophagy were regulated by phosphorylated mTOR, which was initiated by AKT . In A KT knockout mice, LR was severely impaired and mortality increased due to the impairment of the proliferative capacity of hepatocytes [32, 33]. In our study, the results showed that PNS at a concentration of 0.12 mg/ml significantly increased the expression level of phosphorylated PI3K, AKT and mTOR. Administration of LY294002 blocked the proliferative effect of PNS and the PI3K/AKT/mTOR pathway, suggesting that PNS promoted cell proliferation in primary hepatocytes through the PI3K/AKT/mTOR pathway. In vivo, the results showed that PNS promoted LR. The regenerated remnant was larger than that of the NC group at 7 days after PH. The circulating levels of ALT and AST decreased with PNS treatment, indicating that PNS ameliorated liver injury induced by PH . PCNA staining showed that PNS administration promoted cellular proliferation in regenerated liver. In our study, the phosphorylated levels of PI3K, AKT and mTOR increased at 2 days after PH, which is in accordance with a previous study , and the PI3K/AKT/mTOR pathway was elevated with administration of PNS.
TUNEL staining showed that apoptosis of hepatocytes increased at 2 days after PH, which is consistent with a previous study . PNS significantly relieved cellular apoptosis after PH. Bad has been confirmed to be a downstream target of AKT in preventing cellular apoptosis . Bad, which is a member of the Bcl-2 family, is able to combine with antiapoptotic Bcl-2 or Bcl-xL to form a complex that promotes apoptosis . Previous studies have suggested that phosphorylation of Bad by AKT resulted in cell survival . In our study, the results showed that p-Bad increased while Bad decreased after PNS administration. In vitro, we cultured primary hepatocytes in a hypoxic incubator to simulate the hypoxic state that hepatocytes undergo during LR. A previous study showed that AKT/Bad was activated during hypoxia . Our results showed that PNS ameliorated the cellular apoptosis induced by hypoxia, and the AKT/Bad pathway was activated. However, these effects of PNS could be abolished by treatment with LY294002. In summary, the antiapoptotic effects of PNS during hypoxia were related to the activation of the AKT/Bad cell survival pathway.
YFC and WH designed the study and supervised the project; ZH and BH carried out most of the experimental work; WMH conducted the molecular cloning experiments; WJ conducted part of the animal experiments; MMY analyzed the data; ZH, BH and GJP wrote the manuscript; YFC and WH approved the final version of manuscript. All authors read and approved the final manuscript.
This study was supported by grants from the National Natural Science Foundation of China (NSFC: No.81670599; awarded to GJP and No. 81570569; awarded to MMY) administered by the the National Natural Science Fund Committee. Both funds facilitate the design of the study and collection of data.
Ethics approval and consent to participate
Ethical reviews of animal experiment were approved by the ethics committee of the Second Affiliated Hospital of Chongqing Medical university and all animals’ care and experimental protocols were in line with the Animal Management Rules of the Ministry of Health of the People’s Republic of China.
Consent for publication
All of the authors declare that there are no competing interests.
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