Evidence-Based Complementary and Alternative Medicine
Volume 2018 (2018), Article ID 1073509, 9 pages
https://doi.org/10.1155/2018/1073509

Research Article

Preclinical Evaluation of In Vitro and In Vivo Antiviral Activities of KCT-01, a New Herbal Formula against Hepatitis B Virus

Hong Kim,¹ Eungyeong Jang,2,3 So-Young Kim,⁴ Ji-Yoon Choi,⁴ Na-Rae Lee,⁴ Dae-Sung Kim,⁵ Kyung-Tae Lee,6,7 Kyung-Soo Inn,⁴ Bum-Joon Kim,¹ and Jang-Hoon Lee²

¹Department of Microbiology and Immunology, Liver Research Institute, Cancer Research Institute and SNUMRC, College of Medicine, Seoul National University, 103 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea
²Department of Internal Medicine, College of Korean Medicine, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea
³Department of Internal Medicine, Kyung Hee University Korean Medicine Hospital, 23 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea
⁴Department of Fundamental Pharmaceutical Science, Graduate School, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea
⁵Hanpoon Pharmacy Company Limited, 301, Wanjusandan 6-ro, Bongdong-eup, Wanju Gun, Jeollabuk-do 55316, Republic of Korea
⁶Department of Pharmaceutical Biochemistry, College of Pharmacy, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea
⁷Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 02447, Republic of Korea

Correspondence should be addressed to Kyung-Soo Inn; innks@khu.ac.kr, Bum-Joon Kim; kbumjoon@snu.ac.kr, and Jang-Hoon Lee; komclive@khmc.or.kr

Received 7 February 2018; Accepted 12 June 2018; Published 4 July 2018

Academic Editor: Jae Youl Cho

Copyright © 2018 Hong Kim 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.

Abstract.

Hepatitis B virus (HBV) infectious diseases currently remain incurable due to limitations of conventional antivirals such as incapability of eradicating HBV DNA, prolonged use, drug resistance, and virological relapse. KCT-01, a 30% ethanol extract consisting of Artemisia capillaris, Sanguisorba officinalis, and Curcuma longa, was newly developed. The objective of this study was to investigate pharmacological activities of KCT-01 against HBV using HepG2.2.15 cells and a hydrodynamic injection model. KCT-01 significantly lowered antigen secretion, virion production, and pgRNA synthesis in HepG2.2.15 cells without affecting cell viability. KCT-01 administration also resulted in significant decrease of serum virion production, liver covalently closed circular (ccc) DNA levels, and mRNA synthesis of cytokines in the liver of mice injected with HBV DNA hydrodynamically. Interestingly, coadministration of KCT-01 with entecavir enhanced its in vitro and in vivo antiviral activities. Moreover, safety of KCT-01 was assured up to 5000 mg/kg in rats in both single and repeated-dose preclinical studies. Taken together, our findings demonstrate that KCT-01 is capable of suppressing HBV replication and inflammatory cytokine production in in vitro and in vivo models without showing toxicity, suggesting the potential of using KCT-01 alone or in combination with entecavir as antiviral agent.

1. Introduction

Hepatitis B virus (HBV), a major pathogen that causes chronic infection of the liver, is a serious global health burden [1]. Approximately 350 million people are suffering from chronic hepatitis B (CHB) worldwide. It has been estimated that 500,000 to 1,000,000 people die of HBV-related liver diseases annually [2]. Approximately 15-40% of CHB patients may develop exacerbated liver conditions such as cirrhosis, liver failure, and hepatocellular carcinoma (HCC) [3]. Current treatment of CHB depends on several oral nucleos(t)ide analogs (lamivudine, adefovir, telbivudine, entecavir (ETV), and tenofovir) and interferon therapy [4]. Although these therapeutic strategies over the past decade have been very potent in suppressing viral replication, 30-76% of patients treated with lamivudine or adefovir have shown drug resistance and virological breakthrough due to viral mutation after long-term use for 5 years or more. ETV or tenofovir has yet to be definitely investigated on its relevance with renal toxicity or undesirable side effects after long-term oral administration [5]. These shortcomings of current conventional anti-HBV agents expose patients with CHB to a high risk of developing liver cirrhotic or hepatocarcinogenic change [6].

A variety of herbal medicines associated with treatment of liver diseases have been used as therapeutic alternatives for a long time. In China, 80% of patients with CHB receive herbal medicines [7]. It has been reported that herbal medicines generally have lower toxicity with better antiviral effects compared to lamivudine or interferon therapy [8]. In Korea, Injinchunggan-tang (IJCGT), a modified herbal decoction composed of 11 different medicinal herbs, has been prescribed for patients with viral hepatitis, liver cirrhosis, and HCC since the late 1990s. It has been revealed that Artemisia capillaris Thunberg (A. capillaris), a representative agent of IJCGT, can improve a wide spectrum of liver diseases, ranging from nonalcoholic steatohepatitis to HCC [9]. Sanguisorba officinalis Linné (S. officinalis) has been found to have potential antiviral effects against HBV [10–12]. Curcuma longa Linné (C. longa) has been used as traditional medicine for diverse diseases. C. longa and curcumin, its main constituents, have been shown to be able to inhibit the activation of hepatostellate cells and ameliorate liver fibrosis progression [13]. After extensive review and some basic screening tests to determine HBsAg secretion suppressive activities of herbal medicines, these three herbal medicines (A. capillaris, S. officinalis, and C. longa) were selected to produce a novel decoction KCT-01 to suppress HBV replication and HBV-related inflammatory responses in liver.

Due to limited host range of HBV infection, in vivo surrogate models are required to study HBV infectious liver diseases [14]. In particular, chimpanzees are the only known in vivo models adequate for investigating virologic response and the progression of HBV-related liver diseases [15, 16]. High expense, animal ethics, and availability difficulty of chimpanzees motivate the development of small mice models. However, there still exist challenges for inducing inflammatory cytokines and HBV infection in mice. Previous studies have demonstrated that HBV PreS1 mutation (W4P) plays a key role in the progression of CHB into cirrhosis or HCC. It contributes to male predominance in the prevalence of HCC. In addition, W4P mutations increase production of IL-6, an inflammatory cytokine critical for tumorigenesis. Male mice injected with HBV-W4P variants hydrodynamically have shown active virion production, HBsAg secretion, and high levels of IL-6 [17, 18]. This in vivo model might be appropriate to study antiviral and anti-inflammatory activities of KCT-01. Therefore, the objective of the current study was to determine the toxicity of KCT-01 and examine its antiviral activity against HBV and its inflammation suppressing activity using in vitro and in vivo W4P variant hydrodynamic injection models.

2. Materials and Methods

2.1. Preparation of KCT-01 and ETV

KCT-01 was produced and examined by Hanpoong Pharm. Co., Ltd (Jeollabuk-do, South Korea) under conditions and practices required by Korea Good Manufacturing Practice (KGMP). Briefly, raw herbal mixture of A. capillaris (12 kg), S. officinalis (4 kg), and C. longa (4 kg) was purchased from Kyung Hee Herb Pharm (Wonju, South Korea), cut, and pulverized with a pulverizer (30 mm) followed by extraction with a 10-fold volume of 30% EtOH (80-90°C, 3 h). After the first filtration with 5 μm microfilter, the same process of extraction and filtration was then repeated. KCT-01 (3.74-4.56 kg) of freeze-dried extract powder was prepared by vacuum evaporation of filtrates at temperature under 60°C (average extraction yield: about 20.75%). ETV was purchased from Lianyungang Guike Pharmaceutical Co., Ltd (Jiangsu, China). Its purity was 99.9% and its water content was 0.4%. It was white or offwhite powder in appearance.

2.2. Analysis of KCT-01

Curcumin (C₂₁H₂₀O₆) and 6,7-dimethylesculetin (98%, C₁₁H₁₀O₄) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Ziyuglycoside I (98%, C₄₁H₆₆O₁₃) was purchased from Wuhan ChemFaces Biochemical Company (Hubei, China). To set reference content of these three compounds in KCT-01, test solutions of A. capillaris, S. officinalis, and C. longa were produced through a series of processes of weighing, methanol addition, extraction, and filtration. To prepare standard solutions, 6,7-dimethylesculetin, ziyuglycoside I, and curcumin were diluted with methanol solution. All test solutions and standard solutions (10 μL each) were subjected to liquid chromatography. Their peak areas were measured under established conditions for standardization.

2.3. Cells

HepG2 (ATCC HB-8065) and HepG2.2.15 human hepatocellular carcinoma cells [19] were maintained in Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS) and penicillin/streptomycin (100 U/ml).

2.4. Cell Cytotoxicity Assay

Effects of KCT-01 on cell viability were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Briefly, HepG2 and HepG2.2.15 cells were treated with increasing concentrations of KCT-01 for 24 h and 48 h. After further incubation with MTT-containing medium for 4 hours, cells were lysed with dimethyl sulfoxide. Absorbance of cell lysate was determined at wavelength of 570 nm using a microplate reader (BMG LABTECH, Ortenberg, Germany).

2.5. In Vivo Toxicology Study

Preclinical toxicology test of KCT-01 was performed in ChemOn Inc (Gyeonggi-Do, South Korea), a private contract research organization (CRO) in Korea for nonclinical area certified with Korea Good Laboratory Practice (KGLP). Single dose toxicity and repeated dose toxicity studies were performed according to “Guidelines for toxicity tests for drugs and related materials, #2015-82” and “Guidelines for preclinical trials of herbal medicine, #B1-2014-3-014” prepared by the Korean Ministry of Food and Drug Safety. A total of 40 Crl:CD SD rats of each sex (males: 20, females: 20) at 8 weeks old were divided into four groups (KCT-01 1250, 2500, and 5000 mg/kg/day groups and a vehicle control group) to evaluate the approximate lethal dose (ALD) in the single dose toxicity test (study no. 17-RA-0037). For a 2-week-repeated-oral-dose study of KCT-01, a total of 80 healthy rats were randomly assigned into four groups (KCT-01 1250, 2500, and 5000 mg/kg/day groups, and a vehicle control group, and 20 rats (males: 10, females: 10) per group). Clinical signs, serum/urine analysis, and histological analysis were performed to evaluate no-observed-adverse-effect level (NOAEL) (study no. 17-RR-0038).

2.6. Analysis of HBsAg and HBeAg Secretion by Enzyme-Linked Immunosorbent Assay (ELISA)

HepG2.2.15 cells were treated with ETV or KCT-01 to detect the secretion of HBsAg and HBeAg for 24 h and 48 h, respectively. Levels of HBsAg and HBeAg secreted from HepG2.2.15 cells were determined by ELISA using HBsAg detection kits (Shanghai Shiye Kehua Company, Shanghai, China) and HBeAg detection kits (DIAsource ImmunoAssays SA, Louvain-la-Neuve, Belgium) according to manufacturers’ instructions.

2.7. Determination of Virion Particle Production and Viral Pregenomic RNA (pgRNA) Levels by Quantitative PCR

HepG2.2.15 cells were treated with ETV or KCT-01 for 48 h. HBV DNAs and total pgRNAs were extracted from culture supernatants using Viral Gene-Spin Kit (Intron, Gyeonggi-do, South Korea) and RNA extraction Kit (Geneall, Seoul, South Korea) according to manufacturers’ instructions, respectively. PCR amplifications were performed using a set of real-time PCR primers listed in Table 1.

Table 1: Primers used to analyze mice liver tissue mRNAs.

Forward
Reverse
Remarks

1
mTNF-
AGGGTCTGGGCC
ATAGAACT
CCACCACGCTCTT
CTGTCTAC

2
mIL-6
GACAACTTTGGC
ATTGTGG
ATGCAGGGATGA
TGTTCTG

3
mMCP
ATTGGGATCATCT
TGCTGGT
CCTGCTGTTCACA
GTTGCC

4
mIFN-
AGCTCCAAGAAA
GGACGAAC
GCCCTGTAGGTG
AGGTTGAT

5
3.5 kb/pg RNA
GGTCCCCTAGAA
GAAGAACTCCCT
CATTGAGATTCCC
GAGATTGAGAT

6
cccDNA level
CCGTCTGTGCCTT
CTCAT
CACAGCTTGGAG
GCTTGAAC
PROBE:
CGTGTGCACTTCG
CTTCACCTCTGC

7
small S
TTGACAAGAATC
CTCACAATACC
GGAGGTTGGGGA
CTGCGAAT
Real-SF (positions 218-240)
Real-SR (positions 309-328)

8
HBV virion particle
TTAACAAGAATC
CTCACAATA
GGAGGTTGGGGA
CTGCGAAT

9
18S rRNA
AGTCCCTGCCCTT
TGTACACA
CGATCCGAGGGC
CTCACTA

2.8. Animals

C57BL/6 male mice (Specific-pathogen-free, 8-week old, 20-25 g) were obtained from Orientalbio (Seoul, South Korea). These animals were cared under standard conditions with water and food provided ad libitum following NIH guidelines for housing and care of laboratory animals in the Animal Facility of College of Medicine, Seoul National University (Seoul, South Korea). All animal experiments were conducted following the protocol approved by Institutional Animal Care and Use Committee (IAUAC) of Seoul National University College of Medicine (protocol no. SNU150609).

2.9. Hydrodynamic Injection

To determine in vivo antiviral activities of KCT-01 against HBV, hydrodynamic injection of pHBV-1.2X-W4P harboring HBV variant full genome was performed. For systemic hydrodynamic injection of pHBV-1.2X-W4P /HBV in vivo, a total of 10 µg of plasmids in PBS was injected into the tail vein within 5–8 seconds. The injected volume was 8% of the mouse’s body mass (e.g., 1.6 ml for a mouse of 20 g). Mice were housed in a biohazard facility until sacrifice. A reporter plasmid pIRES2-Luci expressing Renilla luciferase was also included in the injection mixture as an internal control to evaluate the delivering efficiency.

2.10. Determination of In Vivo Anti-HBV Activity of KCT-01

To evaluate in vivo antiviral effects, ETV and KCT-01 were administered to mice injected with HBV genome hydrodynamically. Various dosages of ETV and KCT-01 were delivered into the stomach using an oral gavage needle in a volume of 0.1 ml. At 24 h after hydrodynamic injection, mice were administered with ETV at 0.2 mg/kg or KCT-01 at 250 or 500 mg/kg once daily for 14 days. Two other groups were administered with both ETV (0.2 mg/kg) and KCT-01 (250 or 500 mg/kg) to test the effect of coadministration. PBS was used as control. At 14 days after administration, blood samples were collected and sera were stored at −20°C before use. These mice were sacrificed and samples of liver tissues were collected. At least five mice were included in each group. HBV DNA was extracted from 30 μl of mouse serum sample collected at 14 days after administration and analyzed by qPCR as described in Section 2.7. Levels of covalently closed circular (ccc) DNA in liver tissue samples were quantified using a set of specific primers (Table 1) to amplify and detect cccDNA. Briefly, liver tissues were lysed with lysis buffer A (50 mM Tris-HCl, pH7.4, 1 mL EDTA, and 1% NP-40) and subjected to sonication (on ice, 1-2 pulses of 5 sec), centrifugation (10,000g, 25°C, 1 min), resuspension (lysis buffer B (10 mM Tris-HCl, 10 mM EDTA, 150 mM NaCl, 0.5% sodium dodecyl sulfate, and 0.5 mg/mL proteinase K), and incubation (37°C, 24 h). After purification using MEGA Quick Spin Kit, cccDNA was quantified by qPCR.

2.11. Isolation and Analysis of Mouse Liver Tissue mRNAs

Total RNAs were extracted from liver tissues using TRIzol Reagent (Life Technologies, Carlsbad, CA, USA). They were treated with ribonuclease-free deoxyribonuclease I (Roche, Mannheim, Germany) for 40 min at 37°C to eliminate residual DNA followed by phenol/chloroform extraction, ethanol precipitation, and resuspension with diethyl pyrocarbonate–treated water. Extracted RNAs from liver tissues were then subjected to reverse transcription and subsequent PCR reaction. The values were normalized to those of 18S rRNA. Primers used for qPCR are listed in Table 1. Cycling parameters were as follows: 1 cycle of 45°C for 10 min, 1 cycle of 95°C for 2 min, and 40 cycles of 95°C for 5 s and 60°C for 20 s.

2.12. Statistical Analysis

Both in vitro and in vivo data in this study are expressed as mean ± S.D. and analyzed using Student’s t-test with GraphPad Prism 5.01 software (GraphPad Software Inc., San Diego, CA, USA). Statistical significance was considered when p value was below 0.05.

3. Results and Discussion

3.1. Preparation and Standardization of KCT-01

To set criteria for contents of three major reference constituents (6,7-dimethylesculetin, ziyuglycoside I, and curcumin) from 1 g of KCT-01, dry material of KCT-01 manufactured in three LOTs (16001, 16002, and 16003) was repeatedly tested (three times) to obtain the content of each index component in a KGMP certified company. Values of over 90% of the average content of each compound were set as criteria for standardization. As shown in Table 2, quantitative analysis of KCT-01 revealed that 1.76 mg/g of 6,7-dimethylesculetin, 21.09 mg/g of ziyuglycoside I, and 0.61 mg/g of curcumin or more should be included in KCT-01 extract.

Table 2: Contents of three reference constituents from KCT-01.

Compounds
6,7-Dimethylesculetin
Ziyuglycoside I
Curcumin

LOT 16001
1.93
1.93
1.91
23.07
22.91
23.07
0.67
0.67
0.67

LOT 16002
2.00
1.97
1.98
24.56
24.53
24.80
0.71
0.67
0.67

LOT 16003
1.97
1.96
1.93
22.67
22.56
22.66
0.69
0.68
0.68

Average (mg/g)
1.95

23.43

0.68

90% of average (mg/g)
1.76

21.09

0.61

3.2. In Vitro and In Vivo Toxicological Study of KCT-01

In vitro cell cytotoxicity of KCT-01 was evaluated using HepG2 cells and HepG2.2.15 cells by MTT assays. As shown in Figures 1(a) and 1(b), treatment with KCT-01 at concentration up to 250 μg/ml for 24 or 48 hours did not induce any significant cell cytotoxicity of HepG2 or HepG2.2.15 cells.

(a)

(b)

Figure 1: Analysis of in vitro cell cytotoxicity of KCT-01 on HepG2 and HepG2.2.15 cells. (a-b) HepG2 and HepG2.2.15 cells were treated with increasing doses of KCT-01 for 24 h (a) or 48 h (b). Cell viability was determined by MTT assays. Error bars represent standard deviations from triplicated samples.

For in vivo preclinical safety evaluation of KCT-01, single-dose and 2-week repeated-dose toxicity studies were performed by a CRO (ChemOn Inc., South Korea) in accordance with Korea Good Laboratory Practice (KGLP). No deaths were observed in either study (single-dose study and repeated-dose study) during the observation period for two weeks. Consistent with results from the single-dose oral toxicity study, no toxic influence of KCT-01 administration (1250, 2500, and 5000 mg/kg/day) was observed based on results of body weight, food intake, hematological examination, autopsy findings, and histopathological examination in the 2-week repeated-dose study. Test substance-colored stool, drooling, reduced water intake, increased ketone, protein, and pH in urine analysis, decreased urine volume, increased albumin/globulin ratio and K⁺ levels in biochemistry analysis were observed during the 2-week administration period. However, these occurrences were judged to be caused by the influence of the test substance. They were not toxicologically harmful changes based on histopathological results. As a result of a single oral administration of KCT-01, ALD was found to exceed 5000 mg/kg/day regardless of sex. NOAEL of KCT-01 was determined to be up to 5000 mg/kg/day in both female and male rats.

3.3. Suppression of HBsAg and HBeAg Production in HepG2.2.15 Cells by KCT-01

The three herbal medicines (A. capillaris, S. officinalis, and C. longa) as components of KCT-01 have been implicated to have efficacy for HBV-related liver diseases and hepatitis. To examine the antiviral function of KCT-01 against HBV, its ability to suppress secretion of HBsAg and HBeAg in HepG2.2.15 stably transfected with HBV genome was determined. Treatment with KCT-01 resulted in decreased secretion of HBsAg and HBeAg in HepG2.2.15 cells in a dose-dependent manner (Figures 2(a) and 2(b)). KCT-01 at 250 μg/ml was sufficient to reduce secretion of both HBsAg and HBeAg to less than 50% compared to mock-treated control. KCT-01 at 62.5 μg/ml was also able to suppress secretion of HBeAg to less than 50% of the control. These results demonstrate that KCT-01 can inhibit the production of HBV antigens from HBV genomes existing in cells.

Figure 2: Suppression of HBsAg and HBeAg secretion by KCT-01 in HepG2.2.15 cells. (a-b) HepG2.2.15 cells were treated with increasing amounts of KCT-01 for 48 h. Amounts of HBsAg (a) and HBeAg (b) in culture supernatants were analyzed by ELISA. (c-d) HepG2.2.15 cells were treated with different concentrations of KCT-01 with ETV. Secreted amounts of HBsAg (c) and HBeAg (d) were analyzed by ELISA. Values are provided as mean ± S.D. of triplicated experiments. Statistical significance was processed using Student’s t-test. p < 0.01 and p < 0.001 compared to control conditions; p < 0.05 and p < 0.001 compared to ETV (25 μg/ml-) treated group; p < 0.01 and p < 0.001 compared to ETV (100 μg/ml-) treated group.

Next, we examined the effect of KCT-01 on secretion of HBV antigens when it was cotreated with ETV. As depicted in Figure 2(c), 25 μg/ml of KCT-01 reduced the secretion of HBsAg to approximately 40% of section in mock-treated control when it was treated together with ETV. Suppressive effect of ETV on HBsAg secretion was enhanced by cotreatment with KCT-01 in a dose-dependent manner (Figure 2(c)). These results indicate that KCT-01 cotreatment with ETV does not interfere with the action of ETV. Antiviral effects of KCT-01 and ETV can be augmented by such combined treatment. In case of HBeAg, ETV alone did not induce significant reduction of HBeAg. Cotreatment and KCT-01 treatment alone showed similar results (Figure 2(d)). Since ETV exerts its antiviral activity through inhibiting HBV replication, it may not be able to suppress HBeAg production from HepG2.2.15 cells stably presenting the HBV genome. The discrepancy between effects of ETV on HBsAg and HBeAg production in HepG2.2.15 cells remains elusive. Nonetheless, the suppressive effect of KCT-01 on HBeAg production was not affected by ETV, suggesting that combined treatment of KCT-01 and ETV might be used as a possible therapeutic strategy against HBV chronic infection.

3.4. Inhibition of HBV Virion Particle Production and pgRNA Synthesis by KCT-01

To further confirm the antiviral activity of KCT-01, its effect on viral pgRNA production in HepG2.2.15 cells was examined. As shown in Figure 3(a), 3.5 kb pgRNA levels in HepG2.2.15 cells treated by KCT-01 at 25 and 250 μg/ml were significantly (p < 0.001) reduced compared to those in the control group in a dose-dependent manner. However, they were not significantly affected by ETV. Thus, KCT-01 might exert its antiviral activity against HBV through mechanism distinct from ETV. The reduction of pgRNA synthesis by KCT-01 indicates that KCT-01 is capable of suppressing viral replication and virion production of HBV. Indeed, levels of virion particles in culture supernatants of KCT-01-treated HepG2.2.15 cells were reduced. Treatment with 250 μg/ml of KCT-01 for 48 h resulted in significant (p < 0.05) reduction of virion particle production in HepG2.2.15 cells. Such effect was comparable to that of treatment with 100 μM ETV (Figure 3(b)). These results indicate that the antiviral effect of KCT-01 is not only due to suppression of viral antigen production, but also due to suppression of viral particle production.

(a)

(b)

Figure 3: Suppression of virion particle production and pgRNA synthesis by KCT-01 in HepG2.2.15 cells. (a-b) HepG2.2.15 cells were treated with KCT-01 (0, 25, or 250 μg/ml) or ETV (100 μM) for 48 h. Levels of 3.5 kb pgRNA (a) and viral DNAs (b) were quantified by qPCR. Values are provided as mean ± S.D.s of triplicated experiments. Statistical significance was processed using Student’s t-test. p < 0.05 and p < 0.001 compared to ETV-treated group.

3.5. In Vivo Anti-HBV Activity and Anti-Inflammatory Activity of KCT-01

To further confirm the antiviral role of KCT-01, its activity was examined using a mouse hydrodynamic injection model. Mice were injected with HBV full genome and orally administered with KCT-01 alone or in combination with ETV for 14 days. Previously, we have reported that HBV variant is implicated in increased risk of progression of liver diseases [17, 18]. Thus, we injected HBV-full-genome with W4P mutation as described in Materials and Methods [19]. As depicted in Figure 4(a), administration of KCT-01 reduced viral DNA levels in mice sera in a dose-dependent manner, indicating that KCT-01 effectively inhibited in vivo HBV virion production. In addition, suppression of HBV production by ETV was significantly augmented by coadministration with KCT-01.

(a)

(b)

Figure 4: In vivo antiviral activity of KCT-01 against HBV. (a-b) Levels of serum HBV DNA (a) and cccDNA from liver tissues (b) were quantified by qPCR assay. Values are provided as mean ± S.D. of triplicated experiments. Statistical significance was processed using Student’s t-test. p < 0.05, p < 0.01, and p < 0.001 compared to control conditions; p < 0.05 compared to ETV single administration group; p < 0.01 compared to KCT-01 single administration group.

Next, we examined levels of intracellular cccDNA in liver tissues. In line with previous results, both KCT-01 at 500 μg/kg and ETV at 200 μg/kg administration significantly reduced levels of cccDNA extracted from liver tissues compared to the control group. In particular, concurrent administration of ETV and KCT-01 exhibited more potent reduction in cccDNA levels than single administration of either ETV or KCT-01 (Figure 4(b)). Inhibition of cccDNA formation is an important mechanism for treating CHB because current antiviral strategies have some limitations to completely eradicate cccDNA. These results suggest that KCT-01 might have potential as a novel therapeutic agent against HBV infection because its antiviral action could affect cccDNA formation, the early stage of viral replication.

Chronic inflammatory response caused by HBV chronic infection is the main risk factor for liver cirrhosis and HCC [20]. Thus, we also examined the effect of KCT-01 on HBV-mediated inflammatory responses using liver tissues from the hydrodynamic injection model. Notably, mice liver tissues from 500 μg/ml of KCT-01-treated group showed significant reduction in TNF-α, IL-6, and MCP mRNA synthesis. However, ETV treatment did not cause any significant change in mRNA levels of these genes (Figures 5(a), 5(b), and 5(c)). These results indicate that KCT-01 is capable of suppressing HBV-mediated inflammatory responses in addition to its inhibitory effect on viral replication. Considering that ETV did not display any significant effect on inflammatory cytokine or chemokine production, the effect of KCT-01 on inflammatory cytokine and chemokine production was not due to its suppression of viral replication. Presumably, KCT-01 itself might have potent anti-inflammatory activities. This is supported by a preclinical in vitro and in vivo study showing that KCT-01 can regulate inflammatory cytokines via suppression of Janus kinase [21]/signal transducer and activator of transcription (STAT) signaling pathway [22]. Interestingly, interferon (IFN)-β production was not suppressed by KCT-01 administration (Figure 5(d)). In fact, it was increased by KCT-01. This indicates that IFN-β mediated innate antiviral immune response is not hampered by KCT-01, unlike other inflammatory cytokine responses. The underlying molecular mechanism remains elusive.

(a)

(b)

(c)

(d)

Figure 5: Suppression of HBV-mediated inflammatory responses by KCT-01 administration. (a-d) mRNA levels of TNF-α (a), IL-6 (b), MCP (c), and IFN-β (d) in liver tissues from mice injected with HBV genome were analyzed by qPCR assay. Values are provided as mean ± S.D. of triplicated experiments. Statistical significance was processed using Student’s t-test. p < 0.05, p < 0.01, and p < 0.001 compared to control conditions.

HBV is known to be a noncytopathogenic virus which replication itself does not cause direct hepatocellular toxicity, but its ongoing attack to hepatocytes involves variable inflammatory cytokines secretion, eventually contributing to the development of cirrhosis and cancer [23]. Therefore, regulating inflammatory cytokines play an important role in treating CHB as well as inhibiting HBV DNA polymerase replication. However, currently validated antivirals have little capacity in modulating inflammation and eradicating HBV DNA. In addition, some adverse effects including lactic acidosis, disease progression, low HBeAg seroconversion, and drug resistance have been emerged as new issues during antiviral agents therapy [24, 25]. Therefore, the antiviral benefits of KCT-01 including suppressions of cccDNA formation, inflammatory cytokines, and antigen secretion by HBV might help physicians to apply optimal therapeutic strategies to manage CHB patients and it could be a novel potent antiviral candidate as not only single treatment but also cotreatment with conventional antivirals without hampering the efficacy of ETV.

4. Conclusions

This study demonstrates that KCT-01, a novel herbal decoction manufactured and examined according to KGMP and KGLP, exerts robust antiviral activities against HBV using in vitro and in vivo systems. Anti-HBV activity of ETV, a clinically proven therapeutic agent, can be significantly enhanced by KCT-01, suggesting that a combination of the two could be used as a potential therapeutic strategy. Furthermore, KCT-01, but not ETV, possesses anti-inflammatory activity. Their combination can suppress both virus replication and virus induced hepatitis. Significant suppression of IL-6 mRNA levels by KCT-01 was increased in the liver of W4P variant hydrodynamic injection mice, strongly indicating its preventive role in the progression of liver cirrhosis or HCC. Taken together, our results indicate that KCT-01 can efficiently regulate inflammatory cytokines such as IL-6 and inhibit tumorigenesis of HCC in addition to its suppression effect on the virus. Our findings may partly provide preclinical evidence to develop KCT-01 as an effective therapeutic agent to treat CHB and prevent HCC not only by itself alone, but also in combination with other antiviral agents.

Abbreviations

CHB: | Chronic hepatitis B
HCC: | Hepatocellular carcinoma
ETV: | Entecavir
DMEM: | Dulbecco’s modified Eagle’s medium
FBS: | Fetal bovine serum
MTT: | 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide
CRO: | Contract research organization
ALD: | Approximate lethal dose
NOAEL: | No-observed-adverse-effect level
ELISA: | Enzyme-Linked Immunosorbent Assay
pgRNA: | Pregenomic RNA
cccDNA: | Covalently closed circular DNA.

Data Availability

The data that support the findings of this study are available from the corresponding author, [Lee JH, Kim BJ and Inn KS], upon reasonable request.

Conflicts of Interest

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

Authors’ Contributions

Hong Kim, Eungyeong Jang, and So-Young Kim equally contributed to this work.

Acknowledgments

This research was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare, Republic of Korea (Grant no. HI14C0955).

References

D. Lavanchy, “Worldwide epidemiology of HBV infection, disease burden, and vaccine prevention,” Journal of Clinical Virology, vol. 34, no. 1, pp. S1–S3, 2005.

C. W. Shepard, E. P. Simard, L. Finelli, A. E. Fiore, and B. P. Bell, “Hepatitis B virus infection: epidemiology and vaccination,” Epidemiologic Reviews, vol. 28, no. 1, pp. 112–125, 2006.

A. S. F. Lok, “Chronic hepatitis B,” The New England Journal of Medicine, vol. 346, no. 22, pp. 1682-1683, 2002.

G. V. Papatheodoridis, S. Manolakopoulos, G. Dusheiko, and A. J. Archimandritis, “Therapeutic strategies in the management of patients with chronic hepatitis B virus infection,” The Lancet Infectious Diseases, vol. 8, no. 3, pp. 167–178, 2008.

M. G. Ghany and E. C. Doo, “Antiviral resistance and hepatitis B therapy,” Hepatology, vol. 49, supplement 5, pp. S174–S184, 2009.

R. J. Fontana, “Side effects of long-term oral antiviral therapy for hepatitis B,” Hepatology, vol. 49, no. 5, pp. S185–S195, 2009.

L. Zhang, G. Wang, W. Hou, P. Li, A. Dulin, and H. L. Bonkovsky, “Contemporary clinical research of traditional Chinese medicines for chronic hepatitis B in China: an analytical review,” Hepatology, vol. 51, no. 2, pp. 690–698, 2010.

M. McCulloch, M. Broffman, J. Gao, and J. M. Colford, “Chinese herbal medicine and interferon in the treatment of chronic hepatitis B: A meta-analysis of randomized, controlled trials,” American Journal of Public Health, vol. 92, no. 10, pp. 1619–1627, 2002.

E. Jang, B.-J. Kim, K.-T. Lee, K.-S. Inn, and J.-H. Lee, “A survey of therapeutic effects of Artemisia capillaris in liver diseases,” Evidence-Based Complementary and Alternative Medicine, vol. 2015, Article ID 728137, 10 pages, 2015.

T. G. Kim, S. Y. Kang, K. K. Jung et al., “Antiviral activities of extracts isolated from Terminalis chebula Retz., Sanguisorba officinalis L., Rubus coreanus Miq. and Rheum palmatum L. against hepatitis B virus,” Phytotherapy Research, vol. 15, no. 8, pp. 718–720, 2001.

T. H. Chung, J. C. Kim, C. Y. Lee et al., “Potential antiviral effects of Terminalis chebula, Sanguisorba officinalis, Rubus coreanus and Rheum palmatum against duck hepatitis B virus (DHBV),” Phytotherapy Research, vol. 11, no. 3, pp. 179–182, 1997.

T. G. Kim, M. S. Park, and H. M. Han, “Inhibitory effects of Terminalia chebula, Sanguisorba officinalis, Rubus coreanus and Rheum palmatum on hepatitis B virus replication in HepG2 2.2. 15 cells,” Journal of pharmaceutical society of Korea, vol. 43, pp. 447–457, 1999.

Y. Cheng, J. Ping, and L.-M. Xu, “Effects of curcumin on peroxisome proliferator-activated receptor γ expression and nuclear translocation/redistribution in culture-activated rat hepatic stellate cells,” Chinese Medical Journal, vol. 120, no. 9, pp. 794–801, 2007.

B. Y. Winer, Q. Ding, J. M. Gaska, and A. Ploss, “In vivo models of hepatitis B and C virus infection,” FEBS Letters, pp. 1987–1999, 2016.

M. Rizzetto, M. G. Canese, J. L. Gerin, W. T. London, D. L. Sly, and R. H. Purcell, “Transmission of the hepatitis B virus-associated delta antigen to chimpazees,” The Journal of Infectious Diseases, vol. 141, no. 5, pp. 590–602, 1980.

S. Govindarajan, H. A. Fields, C. D. Humphrey, and H. S. Margolis, “Pathologic and ultrastructural changes of acute and chronic delta hepatitis in an experimentally infected chimpanzee,” The American Journal of Pathology, vol. 122, no. 2, pp. 315–322, 1986.

S.-A. Lee, K.-J. Kim, D.-W. Kim, and B.-J. Kim, “Male-specific W4P/R mutation in the pre-s1 region of hepatitis b virus, increasing the risk of progression of liver diseases in chronic patients,” Journal of Clinical Microbiology, vol. 51, no. 12, pp. 3928–3936, 2013.

S.-A. Lee, H. Kim, Y.-S. Won et al., “Male-specific hepatitis B virus large surface protein variant W4P potentiates tumorigenicity and induces gender disparity,” Molecular Cancer, vol. 14, no. 1, article 23, 2015.

S.-Y. Kim, H. Kim, S.-W. Kim et al., “An effective antiviral approach targeting hepatitis B virus with NJK14047, a novel and selective biphenyl amide p38 mitogen-activated protein kinase inhibitor,” Antimicrobial Agents and Chemotherapy, vol. 61, no. 8, pp. 214–217, 2017.

C. Xu, W. Zhou, Y. Wang, and L. Qiao, “Hepatitis B virus-induced hepatocellular carcinoma,” Cancer Letters, vol. 345, no. 2, pp. 216–222, 2014.

T. J. Liang, T. M. Block, B. J. McMahon et al., “Present and future therapies of hepatitis B: From discovery to cure,” Hepatology, vol. 62, no. 6, pp. 1893–1908, 2015.

H. Han, E. Jang, J. Shin et al., “Kyungheechunggan-Tang-01, a New Herbal Medication, Suppresses LPS-Induced Inflammatory Responses through JAK/STAT Signaling Pathway in RAW 264.7 Macrophages,” Evidence-Based Complementary and Alternative Medicine, vol. 2017, pp. 1–15, 2017.

A. Busca and A. Kumar, “Innate immune responses in hepatitis B virus (HBV) infection,” Virology Journal, vol. 22, pp. 1–8, 2014.

H. W. Lee, J.-C. Kwon, I. S. Oh et al., “Prolonged entecavir therapy is not effective for HBeAg seroconversion in treatment-naive chronic hepatitis B patients with a partial virological response,” Antimicrobial Agents and Chemotherapy, vol. 59, no. 9, pp. 5348–5356, 2015.

C. M. Lange, J. Bojunga, W. P. Hofmann et al., “Severe lactic acidosis during treatment of chronic hepatitis B with entecavir in patients with impaired liver function,” Hepatology, vol. 50, no. 6, pp. 2001–2006, 2009.