Anti-lipoapoptotic effects of Alisma orientalis extract on non-esterified fatty acid-induced HepG2 cells
- Hyeon-Soo Jeong†1,
- Young-Hwan Cho†1,
- Kang-Hoon Kim†1,
- Yumi Kim1, 2,
- Ki-Suk Kim1,
- Yun-Cheol Na2,
- Jiyoung Park1,
- In-Seung Lee1,
- Jang-Hoon Lee1Email author and
- Hyeung-Jin Jang1Email author
© The Author(s). 2016
Received: 29 October 2015
Accepted: 14 June 2016
Published: 25 July 2016
Liver steatosis was caused by lipid accumulation in the liver. Alisma orientale (AO) is recognized as a promising candidate with therapeutic efficacy for the treatment of nonalcoholic fatty liver disease (NAFLD). HepG2 hepatocyte cell line is commonly used for liver disease cell model.
The HepG2 cells were cultured with the NEFAs mixture (oleic and palmitic acids, 2:1 ratio) for 24 h to induce hepatic steatosis. Then different doses of Alisma orientale extract (AOE) was treated to HepG2 for 24 h. Incubated cells were used for further experiments.
The AOE showed inhibitory effects on lipid accumulation in the Oil Red O staining and Nile red staining tests with no cytotoxicity at a concentration of 300 μg/mL. Fatty acid synthase (FASN) and acetyl-CoA carboxylase 1 (ACC1) mRNA and protein expression level were down-regulated after AOE treatment. Bcl-2 associated X protein (Bax) and c-Jun N-terminal kinase (JNK) mRNA expression level were decreased as well as p-JNK (activated form of JNK), Bax, cleaved caspase-9, caspase-3 protein expression level. Anti-apopototic B-cell lymphoma 2 (Bcl-2) protein level increased after AOE treatment. In addition, inflammatory protein expression including p-p65, p65, COX-2 and iNOS were inhibited by AOE treatment.
The results suggest that AOE has anti-steatosis effects that involve lipogenesis, anti-lipoapoptosis, and anti-inflammation in the NEFA-induced NAFLD pathological cell model.
KeywordsAlisma orientale HepG2 Nonalcoholic fatty liver disease De novo lipogenesis Lipoapoptosis Inflammation
Hepatic steatosis has been defined chemically as an intrahepatic triglyceride (TG) content that is more than 5 % of the liver volume or weight, and histologically as more than 5 % of the hepatocytes containing visible intracellular TG [1, 2]. Nonalcoholic fatty liver disease (NAFLD) stands for a spectrum of diseases ranging from simple steatosis to steatohepatitis through to fibrosis and cirrhosis . Although the prevalence of NAFLD varied between different regions an countries, the accepted global prevalence is 20–30 % for NAFLD and 2–3 % for nonalcoholic steatohepatitis (NASH) . In Korea, according to a study using sonography surveys, it is estimated that 28.1 % of the Korean nondiabetic population suffers from NAFLD . The reported risk factors for NAFLD include obesity, insulin resistance, hyperlipidemia, and hyperglycemia  and the increasing prevalence of obesity makes NAFLD a potential emerging pandemic .
Lipoapoptosis is a term representing a pathogenic phenomenon induced when non-esterified fatty acids (NEFAs) overwhelm the esterifying capacity of the liver. Excessive NEFAs may induce lipotoxicity including the promotion of apoptosis and, therefore, the phenomenon is termed lipoapoptosis [8, 9].
Hepatic steatosis develops when the rate of fatty acid (FA) input outweighs the output. de novo lipogenesis (DNL), one of the FA input components, is concerned with the FA synthesis mechanism of the liver . And fatty acid synthase (FASN) and acetyl-CoA carboxylase 1 (ACC1) are the key genes associated with DNL .
Saturated NEFA causes cell death via sustained activation of the c-Jun N-terminal kinase (JNK). Through several complex processes, activated JNK activates Bcl-2-associated X protein (BAX), a multidomain proapoptotic member of the B-cell lymphoma 2 (Bcl-2) family, which then translocates to the mitochondria, causing its dysfunction and caspase-dependent cell death .
Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB), which is a key transcription factor that regulates the genes related to the immune response and inflammation is activated by NEFA induction. Dysregulation of the NF-kB pathway plays an essential role in many diseases such as inflammatory diseases, cancer, and atherosclerosis [12, 13].
Alisma orientale (AO) has been known to have anti-inflammatory and diuretic effects in traditional medicine  and is prescribed to treat diseases including inhibited urination, edema, strangury disease, disease associated with fluid retention . Several previous studies have reported the therapeutic efficacy of AO in NAFLD. The aqueous extract of AO showed anti-apoptotic and inhibitory effects against cellular steatosis and reactive oxygen species (ROS) production in a palmitate-induced cellular model [15, 16]. The 80 % ethanol extract of AO had been reported to show hepatocellular protective effects mediated by the regulation of apoptosis-related proteins .
In this study, additional attempt was made to reveal effects against pathological mechanisms including lipid accumulation, lipoapoptosis and inflammation induced by NEFA. HepG2 cells were treated with the 30 % ethanol Alisma orientale extract (AOE) and a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed to determine the safe concentration. In addition, Oil Red O staining and Nile red staining were performed to visually assess the effect of AOE against hepatocyte lipid accumulation. Furthermore, mRNA real-time quantitative polymerase chain reaction (qPCR) and western blot analysis were performed to evaluate NAFLD related factors including ACC1 and FASN markers including DNL, Bcl-2, BAX, JNK, caspase-3, and −9 and key molecules of inflammation associated with p-65, COX-2, and iNOS.
Dulbecco’s modified Eagle’s medium (DMEM), and fetal bovine serum (FBS) were purchased from Lonza (Walkersville, MD, USA). Bovine serum albumin (BSA) was purchased from RMBIO (6015 Greg`s Way Missoula, MT, USA, Cat# : BSA-BLP-1XG). Oil Red O, oleic and palmitic acids (Cat# : O0625-25G), Nile red (Cat# : N3013-100MG), and the MTT (Cat# : M2003-1G) were purchased from Sigma-Aldrich (Saint Louis, MO, USA). The total RNA isolation and cDNA synthesis kits were purchased from GeneAll Bioscience (Seoul, Korea, Cat# : 305–101). The SYBR green master mix was purchased from Life Technologies (Carlsbad, CA, USA, Cat# : 43676569). BAX (Cat# : ab10813) and Bcl-2 (Cat# : ab59348) antibodies were purchased from Abcam (Cambridge, UK). JNK (Cat# : 9252), p-JNK (Cat# : 9251), caspase-9 (Cat# : 9502), cleaved caspase-9 (Cat# : 9501), caspase-3 (Cat# : 9665), and cleaved caspase-3 (Cat# : 9661) antibodies were purchased from Cell Signaling Technology (Danvers, MA, USA). β-actin (Cat# : sc-47778) and FASN (Cat# : 55580) antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). The enhanced chemiluminescence (ECL) solution (Luminata™ crescendo western horseradish peroxidase, HRP substrate, Cat# : WBLUR0100) was purchased from Merck Millipore (Jeffrey, NH, USA).
The Alisma orientale was obtained from the Kyung Hee Oriental Herbal Medicine Research Center (Seoul, Korea) . Alisma orientale was purchased by Omniherb (Yeoncheon, South Korea), which had sale as a nationally authorized distribution enterprise of herbal medicine. The product number of Alisma orientale was #: DH1602025041K. The preparation of the samples is described in the cited references excluding the solvent composition [19, 20]. Alisma orientale was ground to the appropriate particle size and extracted in 30 % ethanol. Then, ultrasound-assisted extraction was performed twice at 40 °C for 3 h. The extracted Alisma orientale sample was filtered, and continuously evaporated using a rotary evaporator. The dried Alisma orientale extracts powder was used in this experiment.
HepG2 cells were obtained from the Korea Cell Line Bank (Seoul, Korea). The cells were maintained in DMEM supplement with 10 % FBS, 1 % antibiotics and antimycotic (ABAM) solution, and then incubated at 37 °C in a 5 % CO2 humidified atmosphere . For the experiments, the cells were seeded in a 24-well cell culture plate at a density of 5 × 105 cells per well and incubated for 16 h, and then washed with PBS and incubated with low glucose DMEM for 12 h for serum starvation. Then, the medium was changed to DMEM with 0.5 mM NEFA (0.33 mM oleic acid and 0.17 mM palmitic acid) (with 1 % BSA), and the cells were incubated further for 24 h to induce the hepatosteatotic condition. Then, the medium was changed to DMEM containing 10 % FBS, 1 % ABAM, and appropriate doses of the drugs and cells were incubated further for 24 h.
Cell viability assay
Cell viability was measured using the MTT assay. The cells were seeded (10 × 103 cells/well) in a 96-well cell culture plate, incubated for 48 h, and then treated with different concentrations of AOE (1, 10, 50, 100, 300, 500, 1000 μg/mL) for 24 h. The MTT was dissolved at 1 mg/mL in phosphate-buffered saline (PBS). After incubation, the medium was discarded, and the cells were treated with 100 μL of MTT solution for 1 h. Then the solution was removed, and dimethyl sulfoxide (DMSO) was added to dissolve the insoluble formazan crystal, which were measured at an absorbance of 570 nm using a Bio-Rad model 680 microplate reader .
Oil red O staining
The steatosis-induced HepG2 cells were washed with ice-cold PBS to remove unbound stain, and then fixed in ice-cold 10 % formalin for 30 min. The cells were then washed with distilled water, and stained for 30 min with 0.3 % Oil Red O solution (in 60 % isopropanol) at room temperature for the stain lipid droplets to form. The stained cells were washed with running tap water for 2 min, and immediately counterstained with Harris’s hematoxylin before cell drying. The cells were observed and photographed using an optical microscope (Olympus IX71).
Nile red staining
The cells were washed with ice-cold PBS, fixed for 30 min in ice-cold 10 % formalin, washed with PBS, then stained with 0.3 nM Nile red solution (in PBS) for 15 min in a dark room. After staining, the Nile red solution was removed, and the cells were washed with PBS, suspended in PBS, and collected in a polystyrene flow cytometry sample tube. The stained cell lipid was determined by measuring the fluorescence using the FACScalibur flow cytometer (BD Bioscience) and analyzed using the Cellquestpro (BD Bioscience).
Real-time quantitative PCR
List of real time PCR primer sequence
GCCAC ATCGC TCAGA CACC
CCCAA TACGA CCAAA TCCGT
CACCA AGGTG CCGGA ACT
TCCCG GAGGA AGTCC AATG
CATGT GTGTG GAGAG CGTCA A
GCCGG TTCAG GTACT CAGTC A
TGGTC AGCAG GGTGT CACA
TCGCA GAGGG AGAAA AGCAA
GGCTT ACATC CTGAG CATGG A
CGGCA GAAGT TCACA TTGTT GA
CGCTC GGCAT GGCTA TCT
CTCGT TGAAG AACGC ATCCA
GGATG GTGTT CACTC GGTAA TAGA
GGGTG ATATG TGCTG CGTCA T
The cells were washed, scraped into ice-cold PBS, and then incubated in radioimmunoprecipitation (RIPA) assay buffer with NP-40 and protease inhibitor cocktail for 1 h on ice for cell lysis. After lysis, a Bradford assay was performed to ensure the cell lysates contained the same protein quantities. Each protein (10 μg samples) was separated according to size using 10 % sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE), and then transferred to a polyvinylidene fluoride (PVDF) membrane. The membrane was incubated with primary antibodies diluted 1:3000 in Tris-buffered saline-Tween (TBS-T) and the secondary antibody (1:10000 in TBS-T) in that order . The protein blot was detected with the ECL solution using a Davinci-chemi chemiluminescence system (Davinch-K). The intensity of the protein blot was measured and calculated using the ImageJ software (NIH).
Identification of AO30 compound
The analysis was performed in the Korea Basic Science Institute (Seoul, Korea). The system consisted of an Infinity 1290 ultra-performance liquid chromatography (UPLC) system and an electrospray ionization (ESI) quadruple time-of-flight (QTOF) mass spectrometer (MaS) (G6550A, Agilent, CA, USA). A supelco ascientis express c18 column (1.7 μm, 150 mm × 2.1 mm i.d.) was used as an analytical column. The column was maintained at 40 °C. The total running time, including the conditioning of the column to the initial conditions, was 50 min. The injection volume was 1 μL. The ESI-QTOF-MaS instrument was operated in the positive and negative ion mode using a dual agilent jetstream electrospray ionization source. The desolvation gas was set to a flow rate of 720 L/h at a temperature of 350 °C. The source temperature was set to 100 °C. The capillary voltage was set to 4000 V.
All data represent at least two separate experiments performed in triplicate. The significance of the data was analyzed using the Prism 5 software with a one-way analysis of variance (ANOVA), Bonferroni’s post hoc test, and Student’s t-test to compare each set of data. Bars show the means ± standard error of the means (SEM). Significance was denoted as follows, * p < 0.05, ** p < 0.01, and *** p < 0.001.
Effects of AOE on HepG2 cell viability
Effects of AOE and NEFA on HepG2 cell lipid accumulation
Effects of AOE on HepG2 cell lipogenesis related mRNA and protein expression
Down-regulation of cell lipoapoptosis-related mRNA and protein expression by AOE in HepG2 cells
Effects of AOE on inflammatory protein expression in HepG2 cells
High performance liquid chromatography (HPLC) of Alisma orientale extracts
This study was designed to investigate the anti-steatotic effects of AOE using NEFA-induced HepG2 cells as lipogenesis markers that contribute to lipid accumulation. In addition, the anti-lipoapoptotic and anti-inflammatory effects of AOE were also investigated in the same cell line model. To determine the cytotoxicity of AOE, the MTT assay was performed. In addition, the Oil Red O staining and Nile red staining were used to determine the inhibitory effects of AOE on hepatocyte lipid accumulation. Furthermore, we sought to determine if the pathway mediating the effects of AOE involves the reduction of hepatocyte lipid accumulation, lipoapoptosis, and inflammation as they relate to the progression from simple steatosis to NASH. NASH is characterized histologically by hepatic steatosis with evidence of liver cell inflammation and injury (ballooning degeneration) . Although the mechanisms underlying the progression from steatosis to NASH is still not fully elucidated, increasing evidence suggests that oxidative stress, which occurs when ROS are generated to certain levels and not appropriately removed, is a key driving force in triggering inflammatory signaling pathways that promote the progression of simple steatosis to NASH [26–32]. Therefore, mRNA qPCR and western blot were performed to evaluate the expression of the specific mRNA and proteins involved in these phenomena.
The MTT assay was used to determine the AOE concentrations that safe for use in this study. Concentration of AOE was up to 300 μg/mL showed no significant decrease in the viability of the treated HepG2 cells compared to the control group. However, higher doses of AOE (500 and 1000 μg/mL) significantly decreased the cell viability (Fig. 1). In previous studies using the 80 % ethanol AOE, 100 μg/mL had no significant cytotoxicity while concentrations of 500 and 1000 μg/mL of AOE caused a significant decrease in cell viability , similar to our result. Based on this result, a concentration of 300 μg/mL of AOE could be used in future experiments.
FAs are classified chemically as saturated and unsaturated (monounsaturated and polyunsaturated), and their structures affect their biological activity . Saturated fatty acids (SFAs) are known to induce lipotoxicity such as insulin resistance and cell death. Palmitic and oleic acids are a typical SFA and monounsaturated fatty acid (MUFA), respectively . In a study of the differential effects of these FAs on apoptosis and lipid accumulation in cultured hepatocytes, oleic acid was revealed to be more steatogenic but less apoptotic than palmitic acid was. Incubation with both FAs resulted in a higher amount of fat accumulation than with palmitic acid alone, but the apoptosis was lower, indicating a protective feature for oleic acid . A proper ratio of palmitic and oleic acids in a combination mixture leads to significant lipoapoptosis and intracellular lipid accumulation with minimal cellular damage [18, 19]. In one study, NEFAs composed of oleic and palmitic acids (2:1), maximized lipid accumulation without causing severe cellular toxicity  and a 0.5 mM mixture of NEFAs in the same ratio showed sufficient lipid accumulation in HepG2 cell in the Oil Red O and Nile red staining tests. Based on these results, the study design used a combination NEFA consisting of oleic acid and palmitic acid in a 2:1 molar ratio for developing the pathological cell model of NAFLD.
In the Oil Red O staining test, AOE reduced the 0.5 mM NEFA-induced cell lipid accumulation dose-dependently up to a concentration of 300 μg/mL (Fig. 2). The Nile red staining was performed using flow cytometry to quantify the cell lipid accumulation, and the relative fluorescence intensity showed that the cell lipid decreased significantly following treatment with 300 but not 50 or 100 μg/mL concentrations of AOE (Fig. 3). This result suggests that 300 μg/mL of AOE has an effect on lipid accumulation in HepG2 cells without any cell toxicity.
The possible sources of the fats that are responsible for hepatic steatosis are peripheral fats contained in adipose tissue, which flow to the liver via the plasma NEFA pool, FAs newly formed in the liver by DNL, and dietary FAs. DNL is an endogenous pathway, which converts carbohydrates and proteins to NEFAs . Furthermore, in the fasting state, roughly one-fourth of all the FAs are newly made via DNL . FASN and ACC1 are key genes associated with DNL  and regulated by sterol regulatory element-binding protein (SREBP)-1c. ACC1 forms the malonyl-CoA that is used by FASN to synthesize palmitic acid, and it is possible to synthesize oleic acid by successive elongation and desaturation processes [32–37]. We investigated the inhibitory effects of AOE on the mechanism of DNL-mediated lipid accumulation using qPCR and western blotting to determine mRNA and protein levels. The NEFA-treated group showed a higher increased in the expression of FASN and ACC1 than the control group did. And the AOE-treated group showed higher down-regulation of FASN and ACC1 protein expression than the 0.5 mM NEFA-treated group did (Figs. 4 and 5). This result suggests that the effect of AOE on lipid accumulation is associated with the DNL process.
Factors related to lipoapoptosis, the pathological phenomenon induced by lipid accumulation were determined following the treatment of HepG2 cells with 0.5 mM NEFA and 300 μg/mL of AOE. When NEFAs penetrate cells, JNK is activated and the JNK protein, which is the central mediator of saturated NEFA induced hepatocyte apoptosis , and can causes potential cellular damage via the cellular apoptosis pathway [19, 28]. The JNK signaling pathway has been reported to affect members of the Bcl-2 family. Specifically, JNK can activate the mitochondrial translocation of BAX and inactivate anti-apoptotic Bcl-2 proteins [24–29]. BAX translocates to the mitochondria and thereby facilitates the release of the mitochondrial cytochrome C protein into the cytosol, which then interacts with procaspase-9, switching on caspase-3, to induce apoptosis [24–29, 34–39]. At the mRNA level, the AOE-treated group showed a more significant inhibition of BAX and MAPK8 expression but not caspase-9 than the 0.5 mM NEFA-treated group did. Protein expression levels of p-JNK (activated form of JNK), BAX, as well as cleaved caspase-9 and caspase-3 were more decreased in the AOE-treated HepG2 cells than they were in the 0.5 mM NEFA-treated cells, which corresponds to a previous study using 100 μg/mL of 80 % ethanol AOE and 1 mM mixed NEFAs in the same ratio . The AOE treatment significantly affected Bcl-2 and caspase-9 protein expression levels (Figs. 6 and 7). Based on these result, the anti-lipoapoptosis was mediated via the JNK signaling pathway on HepG2 cell line treated with AOE.
NF-kB is known to play a critical role in the regulation of cell survival genes and coordination of pro-inflammatory mediators. NF-kB regulates the expression of iNOS, a pro-inflammatory enzyme that is involved in the production of nitric oxide (NO) at the transcriptional level [40, 41]. NF-kB also regulates COX-2, the key enzyme regulating the production of prostaglandins, which are central mediators of inflammation . The p-p65 and COX-2 protein expression was more highly increased in the NEFA group than the control group. But, exposing the group treated with AOE showed remarkably decrease in their inflammatory protein expression. In summary, AOE was revealed to have anti-inflammatory effects in HepG2 cells.
From the result presented, AOE showed anti-steatosis effects mediate via lipogenesis, anti-lipoapoptosis, and anti-inflammatory mechanisms in the NEFA-induced NAFLD pathological cell model. We observed that AOE contributed not only to inhibiting simple steatosis, but also NASH based on the experiments involving lipoapoptosis and inflammation, which are factors involved in the progression of NAFLD. The described effects of AOE derived from Alisol A, Alisol acetate, Alisol B, and Alisol B acetate. Using the components of AOE, Alisol A, Alisol acetate, Alisol B, and Alisol B acetate need to discovery an individual pharmacological capacity in lipoapoptosis and anti-inflammation reageant.
AOE concentrations of up to 300 μg/mL caused no significant decrease in the viability of HepG2 cells compared to the control group.
AOE inhibited lipid accumulation in the Oil red O staining test and moreover, the Nile red staining test, which particularly enabled the quantification of cell lipid using flow cytometry, showed that cell lipid was decreased significantly following AOE treatment only at a concentration of 300 μg/mL.
AOE treatment down-regulated FASN and ACC1 protein expressions more than treatment with 0.5 mM NEFA did, and NEFA-treated cells showed a higher increase in the mRNA and protein expression levels of FASN and ACC1 than the control group cells.
AOE-treated HepG2 cells showed a significant inhibition of BAX and MAPK8 mRNA expression levels and of p-JNK (activated form of JNK) and BAX as well as cleaved caspase-9 and caspase-3 protein levels. Bcl-2 and caspase-9 protein but not mRNA expression levels were significantly affected by AOE treatment.
AOE- treated HepG2 cells showed decreased inflammatory protein expression including p-p65, COX-2, p65, and iNOS.
AOE was analyzed including in Alisol A, Alisol A acetate, Alisol B, Alisol B acetate by high performance liquid chromatography.
Based on these results, AOE is considered to have anti-steatosis effects, which involve lipogenesis, anti-lipoapoptosis, and anti-inflammation mechanisms in the NEFA-induced NAFLD pathological cell model. In the present study, AOE inhibited not only simple steatosis, but also the progression of the disease as evidenced by the results of the experiment involving lipoapoptosis and inflammation. Therefore, AO appears to be a potential candidate for development as a therapeutic option for the treatment of NAFLD, as well as NASH, which are induced by lipoapoptosis and inflammation.
ABAM, antibiotics and antimycotic; ACC, acetyl CoA carboxylase; ANOVA, one-way analysis of variance; AOE, Alisma orientalis extract; Bax, Bcl-2 associated X protein; Bcl-2, beta cell lymphoma 2; BSA, bovine serum albumin; COX-2, cyclooxygenase 2; DMEM, Dulbecco’s modified Eagle’s medium; DMSO, dimethylsulfoxide; DNL, de novo lipogenesis; ECL, enhanced ehmiluminescence; FASN, fatty acid synthase; FBS, fetal bovine serum; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; HCC, hepatocellular carcinoma; iNOS, inducible nitric oxide synthase; MAPK, mitogen-activated protein kinase; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; MUFA, monounsaturated fatty acid; NAFLD, non-alcoholic fatty liver disease; NASH, non-alcoholic steatohepatitis; NEFA, non-esterified fatty acid; NF-kB, nuclear factor kappa-light-chain-enhancer of activated B cells; NO, nitric oxide; PBS, phosphate buffer saline; p-JNK, phosphorylated jun-c-N-terminal kinase; PVDF, polyvinylidene fluoride; qPCR, quantitative polymerase chain reaction; RIPA, radioimmunoprecipitaion assay; ROS, reactive oxygen species; SDS, sodium dodecyl sulfate; SFA, saturated fatty acid; SREBP, sterol regulatory element-binding protein; TBS-T, tris-buffered saline-tween; TG, triglyceride
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 Number: HI13C22960000).
The Korea Health technology R&D Project through the Korea Health Industry Development Institute (KHIDI) and the Ministry of Health & Welfare, Republic of Korea. (Grant Number: HI13C22960000).
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article.
HSJ and YHC designed Anti-lioapoptotic effects study, performed the experiments of in vivo and in vitro, and wrote manuscripts. KSK participated manuscript’s design. YK contributed to blood isolation on db/db mice. YCN analzed an identification of AO30 extracts. JP and ISL performed qPCR and western blotting. KHK participated in vivo experiments and final revision of manuscripts. JHL isolated AO30. HJJang conducted academic plan of all experiments and revised final manuscript. All authors read and approved the final manuscript.
HS Jeong is a master of science. KH Kim, IS Lee, J Park, and Y Kim are studying at College of Korean Medicine, Institute of Korean Medicine, Kyung Hee University as Ph.D candidate. YH Cho is a master of science and a doctor of Korean medicine. KS Kim and YC Na are a doctor of philosophy. JH Lee and HJ Jang are professor at College of Korean Medicine, Institute of Korean Medicine, Kyung Hee University.
The authors declare that they have no competing interests.
Consent for publication
Not applicable in this section.
Ethics approval and consent to participate
Not applicable in this section. In this article, there are no clinical study involving human participants or animal study.
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