Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2018 / Article

Research Article | Open Access

Volume 2018 |Article ID 3523126 | 10 pages | https://doi.org/10.1155/2018/3523126

The Investigation of the Effect and Mechanism of Sophora moorcroftiana Alkaloids in Combination with Albendazole on Echinococcosis in an Experimental Rats Model

Academic Editor: Vincenzo De Feo
Received10 Oct 2017
Revised24 Jan 2018
Accepted14 Feb 2018
Published28 Mar 2018

Abstract

Echinococcosis is a worldwide anthropozoonosis which is highly endemic over large animal husbandry areas in northwestern China. The current clinical therapeutic medicine against echinococcosis is albendazole, although it caused serious side effects in patients. The component in traditional Chinese herb medicine, Sophora moorcroftiana alkaloids (SA), is thought to be a potential drug to treat echinococcosis. In order to explore the effect and mechanism of SA treatment against echinococcosis, we established animal echinococcosis model and treated rats with albendazole alone, alkaloids alone, and combined therapy. The combined treatment showed effective inhibition against parasite infection due to induction of host response and alleviated liver injury; meanwhile albendazole caused serious liver problem. The proteomics study revealed that the combined therapy might induce complement activation through C3, C4, C5, SERPINA1, and SERPINC1 proteins and cell adhesion by ANXA2, EZR, YWHAB, HSP90AN1, and PRKAR2A proteins, while albendazole treatment could induce liver injury through CRYAB, YWHAZ, SLC25A24, and HSPA1B proteins that were involved in cell death. In all, we consider that the combinational treatment displayed better therapeutic effects against liver echinococcosis as well as alleviated liver injury, which could be considered as an effective strategy to treat echinococcosis clinically.

1. Introduction

Echinococcosis is a worldwide anthropozoonosis which is caused by Echinococcus granulosus [1]. In China, it is highly endemic over large animal husbandry areas in northwestern provinces. As estimated, approximately one percent of the farmer population in these areas was infected by Echinococcus granulosus. In humans, ingested eggs can be mainly distributed to liver and lung, leading to cystic echinococcosis (CE) and alveolar echinococcosis (AE). CE infection is the leading consequence, which is responsible for over 98 percent of all echinococcosis cases [2]. The current clinical treatment strategies against echinococcosis are surgery and chemotherapy; other approaches including gamma-ray treatment are still limited to bench level [2, 3]. However, surgery is prone to cause parasite lesion residual or unfortunate parasite dissemination by inappropriate operation, leading to disease relapse. Meanwhile, the use of chemotherapy also does not achieve desirable effect. Albendazole is the most common clinical drug to treat echinococcosis [4]. But it showed poor solubility in gastrointestinal (GI) tract, causing low drug concentration in liver. Albendazole also causes serious adverse side effects in patients such as encephalitis syndrome, influenza-like syndrome, allergic purpura, and drug rash. Furthermore, it has been reported that Echinococcus granulosus protoscolices have developed resistance to albendazole [46]. Thus, it is urgent to develop new therapeutic strategies against echinococcosis.

Sophora moorcroftiana, also known as Tibet S. viciifolia, thorn firewood, is an endemic leguminous shrub widespread in valleys of Tibet plateau in China. The decoction of its seeds has been commonly used in folk medicine to treat parasitosis by local people for years. The main composition of alkaloids in the seed decoction includes oxymatrine, sophora, sophorine, and matrine, which was also used as an emetic, detoxicant, and antiphlogistic and in verminosis in traditional Chinese medicine [7, 8]. Clinically, its seeds decoction is combined with albendazole to treat echinococcosis [9]. It was reported that the alkaloids from Sophora moorcroftiana is the potential active ingredient in this folk medicine [7, 10]. In the present study, we not only investigated the therapeutic effect of the combinational treatment of Sophora moorcroftiana alkaloids and albendazole against echinococcosis in an experimental rats model, but also explored the underlying molecular mechanism of this strategy by proteomics. First, we evaluated the effect of combination therapy by measuring several blood biochemical indicators and histological observation; then, we employed quantitative proteomic assays using isobaric tags for relative and absolute quantitation (iTRAQ), combined with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), to detect proteome alteration in different treatment. Additional bioinformatics analyses were used to analyze the differential proteins (DPs) to investigate the key pathways underlying the mechanism of combinational treatment. The results showed that the combination therapy was effective in treating echinococcosis in animal model. More importantly, it was found that the combination therapy leads to complement activation and elevated cell adhesion, while the treatment with albendazole alone induced cell death which might cause hepatic injury.

2. Materials and Methods

2.1. Materials

Sophora moorcroftiana used in this study was purchased from Linzhi, Tibet. Alkaloids (purity > 90%) were extracted from S. moorcroftiana seeds in our laboratory and prepared for use as described previously [9]. Albendazole was purchased from Zhejiang Wanma Pharma Ltd. Co., Hangzhou, China. The RPMI medium, IL-2, IL-6, IL-10, IgE, and TNF-α  ELISA detection kits were purchased from Invitrogen, USA. The aspartate aminotransferase (AST) activity assay kit and the alanine transaminase (ALT) activity assay kit were obtained from Sigma-Aldrich, USA.

2.2. Protoscolex Collection

Echinococcus granulosus protoscolices were kindly provided by Qinghai Institute for Endemic Disease Prevention and Control, China. The protoscolices were aseptically removed from liver hydatid cysts obtained from cattle and washed several times with saline containing 1500 U/mL penicillin and 1000 U/mL streptomycin [11]. The survival rate of the protoscolices exceeded 95% after these procedures.

2.3. Animal Study

The experimental animal protocols were approved by the Experimental Animal Care and Ethics Committees of Qinghai University. 54 female Sprague-Dawley rats were purchased from Research Laboratory Center of Gansu University of Traditional Chinese Medicine (Gansu, China). All rats were 10 weeks old with a body weight between 180 g and 200 g (certification number: SCXK (gan) 2011-0001). All rats were randomly divided into two groups, 64 rats in experiment group and 10 rats in normal group. The rats in experiment group were inoculated intraperitoneally with 4,500 viable protoscolices in 0.3 mL RPMI medium, while the rats in normal group were injected intraperitoneally with 0.3 mL normal saline. The rats were housed under standard conditions (temperature: 18–22°C, humidity: 50–60%) with free access to food and water. After 30 days (12), four rats from experiment group were randomly sacrificed for histological observation, in order to ensure successful establishment of echinococcosis animal model.

The 40 infected rats were divided into four groups (10 rats per group). Rats were administered with Sophora moorcroftiana alkaloids (SA) alone (SAT group, 8 mg/kg per day, once a day), albendazole (A) alone (AT group, 20 mg/kg per day, once a day), and combined treatment ( SAT + AT group, 8 mg/kg per day SA + 10 mg/kg A per day, once a day) by gavage, respectively. The rats in model group (M group) were given equivalent volume of normal saline. The normal group (N group) of 10 uninfected rats was also treated with normal saline.

All rats were anesthetized and sacrificed under the experimental protocols described above and all efforts were made to minimize animal suffering.

2.4. Blood Indicators Examination

Thirty days after treatment, rats were sacrificed and blood was collected. Serum was obtained by centrifugation. The level of IL-2, IL-6, IL-10, IgE, and TNF-α was measured by a microplate reader (BioRad, xMark-10483) using ELISA detection kits (Invitrogen, USA). The AST and ALT level in serum were also detected by Sigma-Aldrich kits (USA).

2.5. Pathologic Histology Analysis

For pathological analysis, rats were sacrificed and the hydatid cysts were harvested from peritoneal cavity and liver. The thymus and spleen were also collected. The weight of the hydatid cysts, thymus, and spleen was measured, respectively. Thymus index, spleen index, and inhibition rate of cysts were calculated as follows: thymus index = (thymus weight/body weight) × 10; spleen index = (spleen weight/body weight) × 10; inhibition rate of cysts = (the weight of cysts in model group − the weight of cysts in experiment group)/the weight of cysts in model group × 100%.

To observe histological changes after treatment, liver and spleen were collected, sectioned, and stained with hematoxylin-eosin (H&E) staining. Observation was performed under microscope.

2.6. Proteomic Analysis

In order to study the molecular mechanism of SA plus albendazole combination therapy treating liver echinococcosis, we performed proteomic analysis on animal samples from five experiment groups (SAT-L group, AT group, SA + AT group, model group, and normal group). One gram of rats liver from each group (0.1 g per rat) was collected for protein extraction. Then, the protein (100 ug) was digested with trypsin for 12 h at 37 °C (protein/enzyme = 100/3.3). After iTRAQ (AB Science) labeling, equal amounts of labeled peptides from each group were mixed and resolved into 15 fractions by high performance liquid chromatography (HPLC), followed by Q Exactive mass spectrometry (Thermo Fisher Scientific). The resulting MS/MS data were qualitatively and quantitatively analyzed by Mascot 2.3.01 with the following parameters: protein identification using nonredundant International Protein Index rat protein database (version 3.72), full trypsin digest with maximum 1 missed cleavage, peptide tol., and MS/MS tol. were 0.05 Da. Scaffold software was used to identify the differential proteins (DPs). Proteins with and fold change higher than 1.2 or lower than 0.833 were DPs.

2.7. Statistical Analysis and Data Preprocessing

The data are presented as mean ± standard deviation (SD). Statistical comparisons among experimental groups were made by Student’s -tests using SPSS 22.0 software. Difference was considered significant when . The GO and KEGG pathway enrichment analysis of DPs were performed using the Database for Annotation, Visualization, and Integrated Discovery (DAVID) [12].

3. Results

3.1. Blood Indicators Examination

As seen in Table 1, the level of IL-2 increased when SA was given to rats. The IL-2 level in SAT + AT group was significantly higher than that in model group, while no obvious difference was observed between each treatment group and normal group. For IL-6, its amount in SAT group showed significant difference compared with model group, but there is no significant difference among other groups. The level of IL-10 was also increased when albendazole was administered to rats. When combined with SA treatment, the combinational treatment induced the highest IL-10 expression, which was significantly higher than that in model group yet not significantly different from that in normal group. The IgE expression in treatment group was obviously lower than that in model group (), but showed no difference compared with normal group. In addition, the level of TNF-α among all groups displayed no significant difference.


GroupIL-2 (pg⋅ml−1)IL-6 (pg⋅ml−1)IL-10 (pg⋅ml−1)IgE (pg⋅ml−1)TNF-α (pg⋅ml−1)

SAT group (8 mg/kg⋅d)10750.93 ± 35.08▼1581.27 ± 8.97#2■2182.23 ± 33.07▼2■2539.83 ± 48.66
AT group (20 mg/kg⋅d)10513.42 ± 54.86▼1765.80 ± 48.11▼2606.40 ± 13.12▼2195.71 ± 22.52567.21 ± 12.04
SAT + AT group (8 mg/kg⋅d SA + 20 mg/kg⋅d A)10488.45 ± 28.10▼1763.58 ± 33.80▼2606.00 ± 15.49▼1198.19 ± 36.97▼2560.34 ± 17.15
Model group10406815..88557.78 ± 17.11
Normal group10781.51 ± 33.92609.28 ± 21.24183.81 ± 44.32546.68 ± 25.49

value8.95383.89245.56372.89671.6086
  value0.00000.00850.00100.03240.1886

Data were expressed as mean ± SD; mpared with normal group; compared with model group; compared with AT group; #compared with SAT + AT group. 1; 2.
3.2. Pathologic Histology Analysis

As shown in Table 2, the thymus index was increased when SA was administered to rats, but there was no significant difference compared with model group. Similarly, the spleen index was also elevated when SA was given. However, the combinational therapy group displayed significant higher spleen index value than model group, while no obvious difference was observed between each treatment group and normal group. Besides, we detected that the cyst weight in treatment group was significantly lower than that in model group. Moreover, the combined treatment group showed significantly lower cysts weight and higher inhibition rate of cysts than SA alone-treated groups.


GroupThymus index (mg⋅g−1)Spleen index (mg⋅g−1)Cysts weight (g)Inhibition rate of cysts (%)

SAT group (8 mg/kg⋅d)101.99 ± 1.55▼234.93 ± 8.94■2
AT group (20 mg/kg⋅d)104.45 ± 1.45#21.40 ± 1.20▼166.78 ± 15.42
SAT + AT group (8 mg/kg⋅d SA + 10 mg/kg⋅d A)100.73 ± 0.60▼180.39 ± 39.87■1
Model group104.52 ± 2.04-
Normal group103.44 ± 1.46--

value3.80616.18158.5625
value0.00950.00170.0013

Data were expressed as mean ± SD; compared with model group; compared with AT group; #compared with SAT + AT group. 1; 2.

We also investigated histological changes in hydatid cysts, liver, and spleen tissues after treatment. As shown in Figure 1, the tissues of the hydatid in model group were well developed, and the protoscolex and the intact brood capsule could be found. In SAT group, the structure of the brood capsule was shrinking and collapsing, indicating the therapeutic effect of SAT. In the AT and SAT + AT group, we observed that the nuclear germinal layer cells shrink, dissolved, and even disappeared; no protoscolex structure was detected. Meanwhile, necrosis was observed in the surrounding tissues.

As shown in Figure 2, obvious deposition could be observed in both liver and spleen tissue from AT group; meanwhile such deposition was alleviated in other treatment groups. However, a fair number of monocytes filtrated in spleen tissue and a few polykaryocytes could also be detected in spleen tissue in all treatment groups.

3.3. Liver Function Evaluation

With the administration of SA or albendazole, the AST level of rats increased (Table 3). Thereinto, SAT + AT group induced lowest AST expression, but still obviously higher than normal group. It is clear that all treatments caused hepatic injury. As for ALT level, the difference among all groups was not significant. However, the ALT level in combinational therapy group was lowest.


GroupAST (ng⋅ml−1)ALT (ng⋅ml−1)

SAT group (8 mg/kg⋅d)10
AT group (20 mg/kg⋅d)10
SA + AT group (8 mg/kg⋅d SA + 10 mg/kg⋅d AL)10
Model group10
Normal group10

value8.0028
value0.0001

Data were expressed as mean ± SD; , compared with normal group; , compared with normal group.
3.4. Proteomics Analysis

To explore the underlying molecular mechanism of combination treatment, the liver tissues from five groups were collected for proteomics analysis using an iTRAQ approach. A total of 711 proteins were identified. There were 156 DPs between model and normal group, 126 DPs between SAT group and model group, 123 DPs between AT group and model group, and 138 DPs between SAT + AT group and model group. As shown in Figure 3(a), 67 overlapping DPs were found between the comparison of DPs in control versus model and model versus SAT group, 57 overlapping DPs were found between the comparison of DPs in control versus model and model versus AT group, and 65 overlapping DPs were found between the comparison of DPs in control versus model and model versus SAT + AT group. Further analysis of these overlapping DPs revealed abnormal expression of proteins. There were 38 proteins abnormally expressed in model group and normalized in SAT group (named SAT-normalized DPs), of which 12 DPs were upregulated in model group and downregulated in SAT group and 26 DPs were downregulated in model group and upregulated in SAT group (Table 4). Further investigation of these DPs’ biological functions revealed that they were enriched in complement activation process (Table 5). There were 32 proteins abnormally expressed in model group and normalized in AT group (named AT-normalized DPs), of which 12 DPs were upregulated in model group and downregulated in AT group and 20 DPs were downregulated in model group and upregulated in AT group (Table 4). These DPs were found associated with cell adhesion and cell death (Table 5). There were 34 proteins abnormally expressed in model group and normalized in SAT + AT group (named SAT + AT-normalized DPs), of which 18 DPs were upregulated in model group and downregulated in SAT + AT group and 16 DPs were downregulated in model group and upregulated in SAT + AT group (Table 4). These DPs were found involved in complement activation and cell adhesion (Table 5).


Accession numberSymbolMolecular weight (kDa)Ratio (model/control)Ratio (treatment/model)

SAT + AT groupIPI00231139Tkt710.4061261981.231144413
IPI00326305Atp1a11130.4352752821.515716567
IPI00230837Ywhab280.4665164961.866065983
IPI00210542Gsta4260.51.414213562
IPI00210234Pls3710.5743491771.624504793
IPI00213036C4b1920.7071067811.741101127
IPI00470288Ckb430.7071067811.231144413
IPI00471584Hsp90ab1830.7071067811.515716567
IPI00213463Actn41050.7578582831.231144413
IPI00325146Anxa2390.7578582831.319507911
IPI00231136Nid11370.7578582831.741101127
IPI00191761Rab5c230.7578582831.231144413
IPI00327469Ahsg381.2311444130.757858283
IPI00230787Car2291.2311444130.812252396
IPI00200352Crip2231.2311444130.659753955
IPI00421517Des531.3195079110.812252396
IPI00231925Gnai2411.3195079110.535886731
IPI00189809Myh62241.3195079110.707106781
IPI00208061Atp1b3321.4142135620.615572207
IPI00190240Rps27a181.4142135620.757858283
IPI00200466Slc25a5331.4142135620.812252396
IPI00191444Capzb311.5157165670.812252396
IPI00188921Col1a21301.6245047930.659753955
IPI00231662Cyb5r3341.6245047930.757858283
IPI00324380Ttr161.7411011270.659753955
IPI00382098RT1-EC24220.466516496
IPI00886485Kng1491.8660659830.757858283
IPI00368550C51910.7578582831.231144413
IPI00480639C31860.6597539551.624504793
IPI00202651Fga881.6245047930.812252396
IPI00205389Fgb550.5743491771.319507911
IPI00554059Serpinc1670.5743491771.231144413
IPI00324019Serpina1461.2311444130.757858283
IPI00230783Nr1d2431.3195079110.707106781

IPI00421539Aco2850.4665164961.319507911
IPI00213463Actn41050.7578582831.414213562
IPI00327469Ahsg381.2311444130.812252396
IPI00325146Anxa2390.7578582831.515716567
IPI00207390Anxa3360.6597539551.414213562
IPI00192310Bcam681.2311444130.707106781
IPI00213036C4b1920.7071067811.624504793
IPI00191444Capzb311.5157165670.812252396
IPI00470288Ckb430.7071067811.624504793
IPI00189503Clic5280.7071067811.319507911
IPI00205332Etfa350.8122523961.231144413
IPI00470254Ezr690.8122523961.515716567
IPI00205389Fgb540.8122523961.414213562
IPI00231925Gnai2411.3195079110.707106781
IPI00212969Hnrnpa2b1341.4142135620.707106781
IPI00210566Hsp90aa1850.5358867311.231144413
IPI00231136Nid11370.7578582831.319507911
IPI00209000Plec5340.7578582831.319507911
IPI00210234Pls3710.5743491771.741101127
SAT groupIPI00196684Prkar2a460.5743491771.414213562
IPI00191761Rab5c230.7578582831.414213562
IPI00382098RT1-EC24220.574349177
IPI00205135Tgm2771.2311444130.812252396
IPI00231139Tkt710.4061261981.866065983
IPI00187731Tpm2330.8122523961.624504793
IPI00231368Txn1120.8122523961.319507911
IPI00212014Vcp891.3195079110.812252396
IPI00230837Ywhab280.4665164961.866065983
IPI00886485Kng1491.5157165670.757858283
IPI00368550C51910.8122523961.414213562
IPI00480639C31860.7578582831.515716567
IPI00554059Serpinc1670.3535533911.414213562
IPI00324019Serpina1460.8122523961.231144413
IPI00230783Nr1d2431.3195079110.615572207
IPI00914765Zyx622.1435469250.574349177
IPI01016329Ager141.3195079110.757858283
IPI00212523Park7200.6597539551.319507911
IPI00327469Ahsg390.7071067811.624504793

AT groupIPI00207390Anxa3360.6597539551.624504793
IPI00326305Atp1a11130.4352752821.624504793
IPI00213036C4b1920.7071067812.143546925
IPI00768626Cdh5870.7071067811.414213562
IPI00470288Ckb430.7071067811.515716567
IPI00189503Clic5280.7071067811.741101127
IPI00200352Crip2231.2311444130.757858283
IPI00421517Des531.3195079110.812252396
IPI00205332Etfa350.8122523961.231144413
IPI00210542Gsta4260.52
IPI00557598LOC100363606391.2311444130.535886731
IPI00210234Pls3710.5743491771.515716567
IPI00211779Prdx1221.3195079110.435275282
IPI00324019Serpina1461.3195079110.535886731
IPI00324380Ttr161.7411011270.5
IPI00196684Prkar2a460.5743491771.414213562
IPI00470254Ezr690.8122523961.515716567
IPI00213463Actn41050.7578582831.414213562
IPI00230837Ywhab280.4665164961.866065983
IPI00205135Tgm2771.2311444130.812252396
IPI00209000Plec5340.7578582831.319507911
IPI00325146Anxa2390.7578582831.515716567
IPI00324893Ywhaz281.5157165670.707106781
IPI00215465Cryab200.7071067811.515716567
IPI00896184Slc25a24530.7578582831.231144413
IPI00196751Hspa1b701.2311444130.659753955
IPI00231368Txn1121.2311444130.757858283
IPI00212523Park7201.3195079110.574349177
IPI00949898Hspa8710.6597539551.414213562
IPI00190701Apoe361.4142135620.812252396
IPI00190290Rras2240.7578582831.319507911
IPI00198667Clu520.5743491771.231144413


DatabaseDescriptionProtein number value

SAT + AT groupGOCell-cell adhesion30.036057
GOCadherin binding involved in cell-cell adhesion30.042721
GOCell-cell adherens junction30.047327
KEGGComplement and coagulation cascades80.004562
GOComplement activation30.014568

SAT groupGOActin filament binding6
GOActin binding40.007415
KEGGComplement and coagulation cascades60.024352
GOComplement activation30.014568
GORegulation of inflammatory response40.087112

AT groupGORegulation of cell death40.006309
GONegative regulation of hydrogen peroxide-induced cell death30.049772
GOFocal adhesion6
GOCadherin binding involved in cell-cell adhesion40.005268
GOCell-cell adherens junction40.006171
GOProtein complex binding40.021302
GOCell-cell adhesion30.041535

We investigated the associated function and potential relationship of the enriched normalized DPs. As shown in Figure 3(b), there were three groups of DPs. C3, C4, C5, SERPINA1, and SERPINC1 and their interaction were found to be involved in complement activation procedure; all of them were downregulated in model group and upregulated in SAT and SAT + AT group. ANXA2, EZR, YWHAB, HSP90AN1, PRKAR2A, and their interactions were also found to be involved in cell adhesion; they were downregulated in model group and upregulated in AT and/or SAT + AT group. Meanwhile, CRYAB, YWHAZ, SLC25A24, and HSPA1B were found associated with cell death; they were downregulated in model group and upregulated in AT group.

4. Discussion

Echinococcosis is a widespread zoonosis caused by Echinococcus granulosus, which is a very popular disease in large western region of China [1, 7]. Clinically, albendazole was normally used to treat echinococcosis. However, its poor solubility and severe side effects limit its application. In animal husbandry areas of Tibet and some other western provinces of China, people have used decoction of Sophora moorcroftiana to treat echinococcosis patients for years. But the mechanism of this Chinese traditional medicine has not been investigated so far. Previous study indicated alkaloids extracted from Sophora moorcroftiana were the most effective active ingredients [7, 9]. Thus, it might be a potential way to treat echinococcosis by using Sophora moorcroftiana alkaloids in treatment.

In present study, we treated experimental echinococcosis animal model with Sophora moorcroftiana alkaloids and also with Sophora moorcroftiana alkaloids combined with the clinical medicine albendazole. Compared with albendazole-alone treatment, Sophora moorcroftiana alkaloids alone or the combined treatment with albendazole showed obvious therapeutic effects against echinococcosis in infected rats. In in vivo study, SAT treated animals showed inhibited cysts development compared with model rats. The cysts weight was significantly reduced by SAT and the inhibition rate was between 30% and 40%. The clinical medicine albendazole had greater effective inhibitory efficacy against echinococcosis infection. The inhibition rate of cysts even achieved 80%. However, the combined treatment was the most potent therapeutic strategy. The rats treated with SAT plus AT showed the lowest cysts weight and the highest inhibition against echinococcosis. In histological observation, we found that echinococcosis infection induced deposition in liver cells, resulting in cells swelling and alveolar wall thickening. When treated with AT alone, this situation was not changed obviously. In contrast, it was attenuated by SAT or SAT + AT treatment. In spleen tissue, it was the same scenario. Large number of lymphocytes filtrated in liver and spleen tissue due to immune response to infection. It caused swelling of infected tissues and increased tissue volume. This result coincided with the comparison of spleen weight in all groups. It revealed that such histological change could be alleviated by SAT + AT therapy.

Cytokines play important roles in host response to infections. Thus we examined IL-2, IL-6, IL-10, IgE, and TNF-α level in rats serum. We did not detect significant difference in IL-6 and TNF-α expression among all groups. However, the expression of IL-2 in AT group and SAT + AT group was significantly higher than that in model group, while SAT-treated alone group did not show significant difference compared with model group. As an important mediator in inflammatory and immune response of several infectious diseases, IL-2 is able to enhance host immunity and inhibit growth of tumors and parasites [1315]. Once rats were infected by Echinococcus granulosus, the IL-2 receptors mIL-2R in target cells could be overexpressed. The IL-2 level in serum was reduced due to the binding of IL-2 to overexpressed mIL-2R, thus leading to suppression of immune activity of T cells and favoring the parasites survival. Therefore, the expression of IL-2 was increased after treatment, especially in SAT + AT group, which enhanced host immunity against infection, accelerated clearance of polypide, and inhibited parasite growth. IL-10 is a multifunctional cytokine synthesized by Th2 cell subpopulation, which is associated with humoral immunity regulation and host susceptibility to certain disease [16]. Overexpression of IL-10 revealed elevated humoral immunity and suppressed T cells activity, challenging survival of parasites. The IL-10 level in AT group and SAT + AT group was obviously greater than that in model group, but not significantly different compared to normal group. The result indicated that IL-10 played an important part in immune response to echinococcosis infection, although the regulatory mechanism was not clear. It was estimated that IL-10 was associated with Tc cells function, antibody-dependent and complement participative autoimmune response, although the detailed mechanism needs further investigation. Hydatid cysts secrete multiple antigens in host body during its growth and development, which will stimulate different variety of antibodies like Ig G, Ig M, IgA, and IgE. Our result showed that the level of specific antibody IgE in model group was apparently higher, while the IgE level in treated animals was decreased to normal level. It indicated that these treatment strategies exert therapeutic effect against hydatid cyst, which could be considered as an index for evaluating treatment efficacy and prognosis.

We also examined liver function of each group by testing AST and ALT concentration in serum. High level of AST and ALT indicated hepatic injury and liver dysfunction. The model group showed higher AST and ALT level compared to normal group. After treatment, the AST and ALT level in SAT + AT group was decreased while only ALT level in other treatment groups was attenuated. It suggested that echinococcosis infection induced hepatic dysfunction and SAT and AT treatment alone might aggravate hepatic injury (especially AT alone even induced highest AST and ALT concentration) while the combinational therapy ameliorated liver damage [17, 18].

The underlying mechanism was also explored by proteomics analysis. To characterize the molecular mechanism of SAT or AT or SAT + AT treatment, a proteomics analysis was performed to investigate multitargets characteristics. All abnormal expression of DPs was normalized and analyzed, respectively. As shown in Figure 3(b), functional enrichment analysis indicated that these DPs took important part in complement activation, cell adhesion, and cell death. Thus, we explored how these DPs linked to physiological alterations in serum indicators and histological changes in animal tissues. At first, C3, C4, C5, SERPINA1, and SERPINC1 were downregulated in model group and upregulated in SAT and SAT + AT group, which were found to be involved in complement activation procedure. Therein, the three proteins C3, C4, and C5 are key components in complement system, whose activation enhances the ability of antibodies and phagocytic cells to clear antigens, promotes inflammation, and attacks the pathogen’s plasma membrane [19]. Alkaloids treatment (SAT group and SAT + AT group) significantly stimulated expression of these complement activation-associated proteins and enhanced host immune response against parasite infection by increasing IL-2 and IL-10 level in serum. Second, albendazole treatment (AT group and SAT + AT group) could upregulate expression of ANXA2, EZR, YWHAB, HSP90AB1, and PRKAR2A, all of which are involved in cell adhesion [20, 21]. The production of cell-adhesion molecules, as well as inflammatory cytokines, was activated by host’s macrophages [22]. It is estimated that albendazole treatment may be able to induce activation of macrophage, although the molecular mechanism needs further investigation. These results indicated that the combined treatment with SAT and AT could activate complement system and induce macrophage activation to produce cell-adhesive molecules, leading to improvement of hepatic echinococcosis. On the other side, albendazole treatment alone (AT group) also induced expression of CRYAB, YWHAZ, SLC25A24, and HSPA1B, which were found to be involved in cell death; meanwhile the expression of these proteins was not upregulated in combinational therapy group [23]. It might be able to explain why the liver injury in AT group was obviously more serious than that in SAT + AT group. Albendazole treatment upregulated the expression of these proteins associated with cell death, leading to hepatic injury and liver dysfunction (significantly high level of AST and ALT in AT group), while SAT was able to attenuate tissue damage and loss of liver function [18]. In this scenario, the combinational treatment displayed better therapeutic effects against liver echinococcosis as well as alleviated liver injury, which could be considered as an effective strategy to treat echinococcosis clinically.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

This study was supported by the Basic Research Plan Project of Qinghai Provincial Science & Technology Department, China (no. 2014-ZJ-716).

References

  1. F. Valour, S. Khenifer, N. Della-Schiava et al., “Unusual growth rate during cystic echinococcosis,” Parasitology International, vol. 63, no. 2, pp. 275–277, 2014. View at: Publisher Site | Google Scholar
  2. P. Kern, “Medical treatment of echinococcosis under the guidance of Good Clinical Practice (GCP/ICH),” Parasitology International, vol. 55, pp. S273–S282, 2006. View at: Publisher Site | Google Scholar
  3. Q. Yuan, B. Li, S. Jiang, Q. Zhao, J. Duo, and X. Huang, “Gamma-Ray Treatment of,” BioMed Research International, vol. 2016, pp. 1–9, 2016. View at: Publisher Site | Google Scholar
  4. F. Samuel, A. Degarege, and B. Erko, “Efficacy and side effects of albendazole currently in use against Ascaris, Trichuris and hookworm among school children in Wondo Genet, southern Ethiopia,” Parasitology International, vol. 63, no. 2, pp. 450–455, 2014. View at: Publisher Site | Google Scholar
  5. M. Jamshidi, M. Mohraz, M. Zangeneh, and A. Jamshidi, “The effect of combination therapy with albendazole and praziquantel on hydatid cyst treatment,” Parasitology Research, vol. 103, no. 1, pp. 195–199, 2008. View at: Publisher Site | Google Scholar
  6. S. Kaur, P. Singhi, S. Singhi, and N. Khandelwal, “Combination therapy with albendazole and praziquantel versus albendazole alone in children with seizures and single lesion neurocysticercosis: A randomized, placebo-controlled double blind trial,” The Pediatric Infectious Disease Journal, vol. 28, no. 5, pp. 403–406, 2009. View at: Publisher Site | Google Scholar
  7. G.-S. Bao, D.-Z. Shi, and X.-M. Ma, “Effect of alkaloids from Sophora moorcroftiana on Echinococcus granulosus in mice,” Chinese journal of parasitology & parasitic diseases, vol. 23, no. 6, pp. 471-472, 2005. View at: Google Scholar
  8. S.-Y. Wang, Z.-L. Sun, T. Liu, S. Gibbons, W.-J. Zhang, and M. Qing, “Flavonoids from Sophora moorcroftiana and their synergistic antibacterial effects on MRSA,” Phytotherapy Research, vol. 28, no. 7, pp. 1071–1076, 2014. View at: Publisher Site | Google Scholar
  9. X. M. Ma, G. S. Bao, J. M. Wan et al., “Therapeutic effects of Sophora moorcroftiana alkaloids in combination with albendazole in mice experimentally infected with protoscolices of Echinococcus granulosus,” Brazilian Journal of Medical and Biological Research, vol. 40, no. 10, pp. 1403–1408, 2007. View at: Publisher Site | Google Scholar
  10. G. Su, W. Yang, W. Meng et al., “Anti-proliferation effects of ethanolic extracts from Sophora moorcroftiana seeds on human hepatocarcinoma HepG2 cell line,” Natural Product Research (Formerly Natural Product Letters), pp. 1–4, 2017. View at: Publisher Site | Google Scholar
  11. A. A. A. El-Aal, N. S. M. El-Gebaly, A. S. Al-Antably, M. A. Hassan, and M. A. El-Dardiry, “Post-immunization immunohistochemical expression of caspase 3 and p53 apoptotic markers in experimental hydatidosis,” Revista Brasileira de Parasitologia Veterinária, vol. 25, no. 3, pp. 333–340, 2016. View at: Publisher Site | Google Scholar
  12. D. W. Huang, B. T. Sherman, and R. A. Lempicki, “Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources,” Nature Protocols, vol. 4, no. 1, pp. 44–57, 2009. View at: Publisher Site | Google Scholar
  13. L. A. Lieberman and G. C. Tsokos, “The IL-2 defect in systemic lupus erythematosus disease has an expansive effect on host immunity,” Journal of Biomedicine and Biotechnology, vol. 2010, Article ID 740619, 6 pages, 2010. View at: Publisher Site | Google Scholar
  14. G.-H. Jin, T. Hirano, and M. Murakami, “Combination treatment with IL-2 and anti-IL-2 mAbs reduces tumor metastasis via NK cell activation,” International Immunology, vol. 20, no. 6, pp. 783–789, 2008. View at: Publisher Site | Google Scholar
  15. E. Ishikawa, K. Tsuboi, S. Takano, E. Uchimura, T. Nose, and T. Ohno, “Intratumoral injection of IL-2-activated NK cells enhances the antitumor effect of intradermally injected paraformaldehyde-fixed tumor vaccine in a rat intracranial brain tumor model,” Cancer Science, vol. 95, no. 1, pp. 98–103, 2004. View at: Publisher Site | Google Scholar
  16. H. Ghasemi, T. Ghazanfari, R. Yaraee, P. Owlia, Z. M. Hassan, and S. Faghihzadeh, “Roles of IL-10 in ocular inflammations: a review,” Ocular Immunology and Inflammation, vol. 20, no. 6, pp. 406–418, 2012. View at: Publisher Site | Google Scholar
  17. K. Fukazawa, S. Nishida, and E. A. Pretto, “Peak Serum AST Is a Better Predictor of Acute Liver Graft Injury after Liver Transplantation When Adjusted for Donor/Recipient BSA Size Mismatch (ASTi),” Journal of Transplantation, vol. 2014, pp. 1–7, 2014. View at: Publisher Site | Google Scholar
  18. A. R. Srivastava, S. Kumar, G. G. Agarwal, and P. Ranjan, “Blunt abdominal injury: Serum ALT-A marker of liver injury and a guide to assessment of its severity,” Injury, vol. 38, no. 9, pp. 1069–1074, 2007. View at: Publisher Site | Google Scholar
  19. T. Mosca, M. C. S. De Menezes, P. C. L. Dionigi, R. Stirbulov, and W. C. N. Forte, “C3 and C4 complement system components as biomarkers in the intermittent atopic asthma diagnosis,” Jornal de Pediatria, vol. 87, no. 6, pp. 512–516, 2011. View at: Publisher Site | Google Scholar
  20. F. Zhang, Y. Liu, Z. Wang et al., “A novel Anxa2-interacting protein Ebp1 inhibits cancer proliferation and invasion by suppressing Anxa2 protein level,” Molecular and Cellular Endocrinology, vol. 411, pp. 75–85, 2015. View at: Publisher Site | Google Scholar
  21. M. Haase and G. Fitze, “HSP90AB1: Helping the good and the bad,” Gene, vol. 575, no. 2, pp. 171–186, 2016. View at: Publisher Site | Google Scholar
  22. Y. Pan, X. Zhang, and Y. Wang, “Targeting JNK by a new curcumin analog to inhibit NF-kB-mediated expression of cell adhesion molecules attenuates renal macrophage infiltration and injury in diabetic mice,” PLoS ONE, vol. 8, no. 11, Article ID e79084, 2013. View at: Publisher Site | Google Scholar
  23. B. Stoevring, J. L. Frederiksen, and M. Christiansen, “CRYAB promoter polymorphisms: Influence on multiple sclerosis susceptibility and clinical presentation,” Clinica Chimica Acta, vol. 375, no. 1-2, pp. 57–62, 2007. View at: Publisher Site | Google Scholar

Copyright © 2018 Fabin Zhang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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