Prevention mechanism of 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-D-glucoside on lipid accumulation in steatosis hepatic L-02 cell
Pei Lin1, Jian-Mei Lu2, Yan-Fang Wang2, Wen Gu2, Rong-Hua Zhao2, Jie Yu2
1 Department of Pharmacy, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan, China; Department of Oriental Medicinal Material and Processing, College of Life Science, Kyung Hee University, Yongin, South Korea
2 Department of Pharmacy, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan, China
|Date of Submission||23-Oct-2015|
|Date of Acceptance||25-Jan-2016|
|Date of Web Publication||18-Apr-2017|
Dr. Jie Yu
Department of Pharmacy, Yunnan University of Traditional Chinese Medicine, Kunming, Yunnan
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Aim: 2,3,5,4'-Tetrahydroxy-stilbene-2-O-β-d-glucoside (TSG), a natural stilbene, shows great activities in hepatic lipid regulation, especially for hepatic triglyceride lowering. However, information about its mechanisms on biosynthesis and degradation of triglyceride is still limited. This research pays close attention to clarify the mechanism of TSG on prevention of hepatic lipid accumulation. Materials and Methods: TSG was given to steatosis hepatocyte L-02 cell induced by fat emulsion incubation. The contents of free fatty acid, triglyceride, rate-controlling enzymes, and transcriptional regulatory factors, which play key role in biosynthesis and decomposition of triglyceride, were determined with or without TSG exposure. Results: TSG could reduce the free fatty acid material supply for the synthesis of endogenous triglyceride and it did so by reducing the expression of liver type fatty acid binding protein and fatty acid transport protein 4. TS Ginhibited the expression of sterol regulatory element-binding protein 1c, and then reduce the contents of acetyl-CoA carboxylase 1 and fatty acid synthase. Therefore,TSG prevented biosynthesis of triglyceride. Mean while, TSG also promoted the decomposition of triglyceride by the activation of peroxisome proliferators activator receptors alpha. Conclusion: TSG could effective intervene the accumulation of triglyceride in hepatic cell. Thus, TSG could be considered as a promising drug candidate in prevention and treatment of lipid metabolic disorders, especially nonalcoholic fatty liver disease.
Abbreviations used: ACACA: Acetyl-CoA carboxylase 1, Apo-B100: Apo lipoprotein B100, FASN: Fatty acid synthase, FATP4: Fatty acid transport protein 4, FBS: Fetal bovine serum; FEN: Fenofibrate, FFA: Free fatty acid, L-FABP: Liver type fatty acid binding protein, LPL: Lipoprotein lipase, MTTP: Microsomal triglyceride transfer protein, NAFLD: Non-alcoholic fatty liver disease, PBS: Phosphate buffer saline, PPAR-α: Peroxisome proliferators activator receptors alpha, RPMI: Roswell Park Memorial Institute, SIM: Simvastatin, SREBF1c: Sterol regulatory element-binding protein 1c, TG: Triglyceride, TSG: 2, 3, 5, 4-tetrahydroxy-stilbene-2-O-β-Dglucoside, VLDL: Very low density lipoprotein
Keywords: Decomposition, lipid accumulation, Polygonum multiflorum, 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-d-glucoside, triglyceride biosynthesis
|How to cite this article:|
Lin P, Lu JM, Wang YF, Gu W, Zhao RH, Yu J. Prevention mechanism of 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-D-glucoside on lipid accumulation in steatosis hepatic L-02 cell. Phcog Mag 2017;13:245-53
|How to cite this URL:|
Lin P, Lu JM, Wang YF, Gu W, Zhao RH, Yu J. Prevention mechanism of 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-D-glucoside on lipid accumulation in steatosis hepatic L-02 cell. Phcog Mag [serial online] 2017 [cited 2021 Jun 13];13:245-53. Available from: http://www.phcog.com/text.asp?2017/13/50/245/204563
| Introduction|| |
With the rapid improvement of living standards and huge changes of lifestyle, lipid metabolism abnormality and related diseases have extremely high prevalence all around the world. Nonalcoholic fatty liver disease (NAFLD) is a major disease endangering human health, which is used to describe a condition of lipid accumulation in the liver. NAFLD is usually accompanied by diabetes, hyperlipidemia, and insulin resistance, a cluster of diseases collectively known as metabolic syndrome. Almost 20–30% of adults in developed countries are suffering from NAFLD. NAFLD used to be considered a disease mainly affecting middle-aged people; however, the diagnosis of NAFLD is increasingly more frequent during adolescence, and it has been shown to affect both sexes equally after adolescence., More disappointing is that one in five of those with NAFLD will not survive more than 15 years.
In the development of NAFLD, the accumulation of lipid within hepatic cells, especially triglycerides, has been confirmed by numerous researches.,,, In healthy human liver, the mean contents of total cholesterol and triglyceride are 3.9 and 19.5 mg/g wet weight, respectively. However, liver fat content increased to more than 50 mg/g (5% by wet weight) in fatty liver., This hepatic lipid accumulation results from an imbalance between lipid availability and lipid disposal. In general, the dietary triglyceride and carbohydrates will be oxidatively decomposed into free fatty acid (FFA), and then transported to the liver for triglyceride bio-synthetization or stored in adipose tissues. Lipid accumulation in hepatic cells is usually occurring under these following conditions: FFA absorption from peripheral adipose tissue or nutrient is increased; the endogenous synthesis of FFA is increased; decomposition of fatty acid is reduced; the function of very low-density lipoprotein or other Apo lipoprotein is inhibited, and so on.
Therefore, regulations of triglyceride and FFA (raw material for triglyceride bio-synthetization) in hepatic cells will be an effective prevention and treatment of NAFLD. Drug treatment is still an important part of addressing these issues. However, there is still no specific drug in prevention and treatment of NAFLD, Most patients were treated with no-specific drugs, such as insulin sensitizers (metformin and thiazolidinediones), vitamin E, and statins. Finding natural products in the traditional medicines seems to be a promising way.
The naturally occurring stilbenoid, 2, 3, 5, 4'-tetrahydroxy-stilbene-2-O-β-D-glucoside (TSG) is mainly distributed in Polygonum multiflorum Thunb. TSG and extractions of P. multiflorum show great lipid regulation effects in our previous studies.,, TSG also interacts with multiple targets in a variety of disease models to exert protective effects on human health.,, However, information about its mechanisms of regulation in biosynthesis and degradation of triglycerideis still limited. In this study, prevention mechanisms of TSG on hepatic lipid accumulation were evaluated by in vitro steatosis hepatic L-02 cell.
| Materials and Methods|| |
The whole research was carried out by L-02 cells, which were purchased from Cell Bank, Kunming Institute of Zoology, Chinese Academic of Science. Cells were grown in RPMI-1640 medium (Gibco Invitrogen Corporation, USA) supplemented with 10% fetal bovine serum (FBS; Hyclone, USA). Cultures were maintained in a humidified incubator (Series II water jacketed CO2 Incubator Model 3111; Thermo Electron Corporation, USA) with 5% carbon dioxide 95% air at 37°C.
Five groups were involved: normal group (CON), model group (MOD), the TSG group (TSG powder, purity higher than 98%, was purchased from Nanjing Jingzhu Bio-technology Co., Ltd., and stored in a dry and cool dark place), Simvastatin (SIM; Hangzhou MSD Pharmaceutical Co., Ltd., China), and Fenofibrate (FEN; Laboratories Fournier S.A., France). The concentration of TSG (150 μmol/L) was optimized and selected from our previous research., Both SIM and FEN were considered as positive control.
L-02 cells were seeded in six-well plates (Corning, USA) at a cell density of 3×105 in 2 mL/well and incubated till 80–90% confluence with 10% FBS-RPMI 1640 medium. Then the cell synchronization was routinely accomplished by incubating cells in G0 medium (0.2% FBS-RPMI 1640 medium) for 12 h before test.
Subsequently, all cells, except normal group, were exposed to 1% fat emulsion–10% FBS-RPMI-1640 medium for steatosis. Fat emulsion was purchased from Sichuan Guorui Pharmaceutical Co., Ltd., China. This fat emulsion (each 250 mL) contained 50 g of refined soybean oil, 5.5 g of glycerol, and 3 g of refined lecithin. In the same time, TSG, SIM, and FEN were synchronously given to these steatosis hepatic cells to intervene the steatosis procedure.
After treated with TSG, SIM, or FEN for 4, 8, 12, 18, 26, 36, 48, and 60 h, respectively, the cells were washed with 2 mL phosphate buffer saline (PBS) for two times. Then cells were fixed with 70% ethanol and further dehydrated with 100% propylene glycol. The cells were stained with Oil-Red O dye, and fat droplets in hepatocytes were stained red.
Assessment of free fatty acid, triglyceride, protein, and transcriptional regulatory factors levels
After treated with TSG, SIM, or FEN, the cells were washed with 2 mL PBS per well for two times. Cells were collected with cell scraper with 1 mL PBS and centrifuged for the removal of PBS at 6900 g for 10 min in 4°C. Then, the mixed suspension was blown with 50 μL iced PBS and lysed at 37°C after refrigerated for 30 min in 20°C. This freeze–thawing procedure was repeated for three times. Finally, cell lysis was collected after centrifugation at 6900 g for 20 min in 4°C.
Contents of FFA and triglyceride were measured by assay kits purchased from Bio Sino Bio-technology and Science Inc. and Nanjing Jiancheng Bioengineering Co., Ltd., China. The liver type fatty acid binding protein (L-FABP), fatty acid transport protein 4 (FATP4), microsomal triglyceride transfer protein (MTTP), Apo lipoprotein B100, acetyl-CoA carboxylase 1 (ACACA), fatty acid synthase (FASN), peroxisome proliferators activator receptors alpha (PPAR-α), sterol regulatory element-binding protein 1c (SREBP-1c), and lipoprotein lipase (LPL) contents were tested by ELISA assay kits purchased from Cusabio Biotech Co., Ltd., China.
All data in this study were expressed in the form of mean ± SD. The data were evaluated by one-way analysis of variance with a significance level The significance level of P < 0.05, P < 0.01, and P < 0.001.
Relationships between FFA, triglyceride, and key enzymes and transcriptional regulatory factors were assessed by Pearson's correlation coefficient. Results were classified into two significance levels using the P values of 0.05 and 0.01.
| Results|| |
TSG inhibited the formation of lipid droplets and suppressed free fatty acids supply
Oil-Red O staining [Figure 1] showed that the amounts of stained lipid drops in model group were increased in a time-dependent manger. Lipid droplets merged with each other inside the cell obviously after induced for 48 h by 1% fat emulsion–10% FBS-RPMI-1640 medium. Compared with normal cells [Table 1], the intracellular content of triglyceride in model group (3.06 ± 0.01 mmol/L) increased almost two times than the control group (1.61 ± 0.02mmol/L).
|Figure 1: Morphological observations in model group (MOD) and TSG group (TSG) at each time point (10×40). Oil-Red O dye stained fat droplets in steatosis (MOD) and TSG treated (TSG) hepatocytes from 4 to 60 h|
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|Table 1: Contents of TG and FFA in steatosis L-02 cells at each time point (x ± s , n=3)|
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However, intracellular FFA content remained at about 70 ng/mL in steatosis hepatic cells. We speculated that more FFA was absorbed from 1% fat emulsion for the synthesis of endogenous triglyceride. Further investigation on L-FABP and FATP4 expressions were conducted to confirm our speculation. As shown in [Figure 2], the expressions of L-FABPand FATP4 in model cells were raising continuously. L-FABP content increased to about four times in the normal cells after induction for 36–48 h. L-FABP and FATP4 were responsible for the transport and absorption of fatty acids., Therefore, high level of extracellular FFA content promoted hepatic L-FABP and FATP4 expressions, which provided more FFA material supply for the synthesis of endogenous triglyceride.
|Figure 2: Contents of L-FABP and FATP4 in treated steatosis L-02 cells (x ± s, n = 3). Intracellular L-FABP and FATP4 contents were tested by ELISA assay kits from 4 to 60 h, mean ± SD were calculated and presented as bar graphs. For the statistical analysis, the * indicates a significant difference compared with control group, * P < 0.05, ** P < 0.01, *** P < 0.001; the # indicates a significant difference compared with model group, # P < 0.05, ## P < 0.01, ### P < 0.001|
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On the one hand, TSG partly suppressed the expressions of L-FABP and FATP4 in steatosis hepatic cells [Figure 2], and TSG stored similar contents intracellular FFA as normal group; however, FFA content in TSG group had a slight increase compared with model group [Table 1].On the other hand, TSG relieved a certain degree of lipid droplets formation [Figure 1] and the elevation of triglyceride was also alleviated by TSG after 18 hinduction (P < 0.01). These indicated TSG may also prevent triglyceride biosynthesis from intracellular FFA.
TSG prevented triglyceride biosynthesis
To clearly illustrate how TSG prevent triglyceride biosynthesis, we measured the influence of TSG on several triglyceride synthases. ACACA and FASN genescoded two rate-controlling enzymes in the triglyceride synthesis pathway. ACACA was in charge of transform Acetyl-CoA to Malonyl-CoA, where as FASN was in charge of transform Malonyl-CoA to Fatty Acyl-CoA.
After 8 h induction by fat emulsions [Table 3], the content of ACACA in model group raised about 50% than the normal group (P < 0.001). TSG effectively prevented ACACA content from increasing; however, the regulation activity of TSG was still weaker than FEN and SIM. Both FEN and SIM could keep the ACACA content similar with that in normal group.
The content of FASN also showed significantly increasing during the process of steatosis [Table 3]. TSG intervention could also decrease FASN content significantly.
As TSG effectively inhibited ACACA and FASN expressions, both of which were rate control enzymes of triglyceride synthesis, we considered that triglyceride accumulation prevention effect of TSG was not only contributed by reducing of external FFA absorbing but also by inhibition of triglyceride biosynthesis from FFA.
TSG-regulated triglyceride transportation
MTTP, an important lipid transfer protein in endoplasmic reticulum, took part in triglyceride transportation and very low-density lipoprotein assembly. Fat emulsion induction suppressed the MTTP expression in model group, whereas TSG and positive drugs could enhance the expression of MTTP within 48 and 60 h. TSG gave out better up regulation effect on MTTP expression than FEN and SIM [Table 2]. MTTP expression in TSG group (133.3 ± 0.84 pg/mL) returned to about 83% of normal group (159.8 ± 0.01 pg/mL). However, we noticed that neither steatosis process nor TSG treatment altered Apo lipoprotein B100 expression significantly. Therefore, TSG regulated triglyceride transportation mainly through MTTP expression adjustment.
|Table 2: Contents of MTTP and Apo-B100 in steatosis L-02 cells at each time point ( x ± s, n=3)|
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|Table 3: Contents of ACACA and FASN in steatosis L-02 cells at each time point ( x ± s, n=3)|
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TSG promoted triglyceride decomposition
LPL was in charge of hydrolyzing triglycerides in lipoproteins into FFAs and monoacyl glycerol molecule. In our research, LPL expression decreased significantly from 26 h after fat emulsion induction. We found TSG could obviously reverse this decreasing [Figure 4] and increase the content of LPL from 260.32 ± 9.07pg/mL to 476.03 ± 35.07 pg/mL at 48 h. TSG exhibited even better LPL regulation activity than SIM and FEN at the end of the research. Promotion of triglyceride decomposition by TSG also helped to alleviate thetriglyceride accumulation in liver cells.
TSG suppressed activation factors in lipid metabolism
Transcriptional regulatory factors, such as SREBP-1c and PPAR-α, also play key role in triglyceride synthesis and transportation. SREBP-1c acted as a critical connection point in the network of lipid regulation and activated almost all genes in the synthesis of fatty acid and triglyceride in liver. Activation of PPAR-α would promote -oxidation of fatty acid and triglyceride decomposition, reduce lipid accumulation, and increase LPL content. The expression of LPL, regulated by PPAR-α, was critical to lipid metabolism. Activation of PPAR-α would result in increased LPL activity in the liver and skeletal muscle leading to higher triglyceride clearance.
Our results [Figure 3] showed that fat emulsion induction reduced PPAR-α expression where as increased the content of SREBP-1c. Fortunately, these alternations induced by steatosis process were prevention by TSG. SREBP-1c increasing was effectively inhibited after treatment with TSG for 36 h. The expression of PPAR-α returned to normal level after treated with TSG for 2 days.
|Figure 3: Contents of SREBF-1c and PPAR- α in treated steatosis L-02 cells (x ± s, n = 3). Intracellular SREBF-1c and PPAR-α contents were tested by ELISA assay kits from 4 to 60 h, mean ± SD were calculated and presented as bar graphs. For the statistical analysis, the * indicates a significant difference compared with control group, * P < 0.05, ** P < 0.01, *** P < 0.001; the # indicates a significant difference compared with model group, # P < 0.05, ## P < 0.01, ### P < 0.001|
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|Figure 4: Contents of LPL in treated steatosis L-02 cells (x ± s, n = 3). Intracellular LPL contents were tested by ELISA assay kits from 4 to 60 h, mean ± SD were calculated and presented as bar graphs. For the statistical analysis, the * indicates a significant difference compared with control group, * P < 0.05, ** P < 0.01, *** P < 0.001; the # indicates a significant difference compared with model group, # P < 0.05, ## P < 0.01, ### P < 0.001|
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| Discussion|| |
Regulation of lipid accumulation was a complicated biological process involving regulation of membrane transport proteins and cellular enzymes. Finding natural products in the traditional medicine system seemed to be a promising way in the prevention and treatment of NAFLD.
In this research, activities and mechanisms of TSG on biosynthesis and decomposition were investigated on this steatosis hepatic cell.
Judging from Pearson's correlation coefficient between FFA, triglyceride, and key enzymes and transcriptional regulatory factors [Table 4], the intracellular FFA content was mainly highly negative correlated with SREBP-1c expression from 8 to 18 h. In the beginning of the steatosis process, excess intracellular FFA was synthesis to triglyceride mainly under adjustment of SREBP-1c. Therefore, high SREBP-1c expression was negative correlated with intracellular FFA content.
|Table 4: Pearson correlation analysis between FFA, TG and key enzymes or proteins|
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The intracellular triglyceride content was correlated with several factors, L-FABP, FATP4, FASN, MTTP, and SREBP-1c. Expression of SREBP-1c was inhibited after TSG treatment. As consequences, less FFA were brought into hepatic cell though L-FABP and FATP4, less triglyceride was synthesized under FASN control. However, TSG activated PPAR-α expression and then increased the LPL content, promoted β-oxidation of fatty acid. Stilbenes other than TSG, such as resveratrol and amorphastilbol, also could bind to and activate PPAR-α. These agonists of the nuclear receptor PPAR were therapeutically used to combat hyperglycemia associated with the metabolic syndrome and type II diabetes and may be also beneficial for the NAFLD patients.
Our latest in-vivo research has confirmed these benefits, TSG as a natural stilbene significantly inhibited the accumulation of FFA in liver, which cuts off the supply of raw triglyceride materials for endogenous synthesis, possibly mediated by the decrease in L-FABP and FATP4 expression.
From these results we concluded that TSG displayed multi targets regulation effects on triglyceride accumulation in hepatic cell [Figure 5]. It could not only limit the raw materials supply of triglyceride synthesis by reducing L-FABP and FATP4 expressions, but also inhibit SREBP-1c expression, and then reduce the contents of ACACA and FASN. Therefore, TSG could prevent the biosynthesis of triglyceride. Mean while, TSG also activated PPAR-α and increased β-oxidation of fatty acid. Thus, the decomposition of triglyceride was promoted by treatment of TSG.
|Figure 5: The hypothetical mechanisms of TSG on the triglyceride accumulation in hepatic cells. Dotted lines indicate normal biochemical pathways; green lines and + indicate the acceleration effects of TSG; red lines and – indicate the inhibition effects of TSG. Schematic representation of the mechanism has shown that TSG prevents triglyceride accumulation in hepatic cells through the multi targets regulation in triglyceride biosynthesis and decomposition. TSG inhibited SREBP-1c, promoted PPAR- α, and regulated rate control enzymes in triglyceride metabolism, thereby causing pronounced suppression on triglyceride accumulation in hepatic cells|
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| Conclusion|| |
TSG obviously blocked the first hit of NAFLD in the process of the lipid accumulation and could be considered as a promising drug candidate in prevention and treatment of NAFLD. Further researches of TSG on the second hit of NAFLD are still under investigation.
Financial support and sponsorship
This research was financially supported by National Natural Science Foundation of China (Grant no. 81460623); the Science and Technology Planning Project Foundation of Yunnan Province (Grant no. 2014FA035; 2014FZ085); the Southern Medicine Collaborative And Innovation Center (30270100500) and Young and Middle-aged Academic and Technological Leader of Yunnan (2015HB053).
Conflicts of interest
There are no conflicts of interest
| References|| |
Bellentani S, Marino M. Epidemiology and natural history of non-alcoholic fatty liver disease (NAFLD). Ann Hepatol 2009;8:4-8.
Moller DE, Kaufman KD. Metabolic syndrome: a clinical and molecular perspective. Annu Rev Med. 2005;56:45-62.
Hu KC, Wang HY, Liu SC, Liu CC, Hung CL, Bair MJ. Nonalcoholic fatty liver disease: updates in noninvasive diagnosis and correlation with cardiovascular disease. World J Gastroenterol. 2014; 20: 7718.
Caballería L, Pera G, Auladell MA, Torán P, Muñoz L, Miranda D. Prevalence and factors associated with the presence of nonalcoholic fatty liver disease in an adult population in Spain. Eur J Gastroenterol Hepatol. 2010;22:24-32.
Matteoni CA, Younossi ZM, Gramlich T, Boparai N, Liu YC, McCullough AJ. Nonalcoholic fatty liver disease: a spectrum of clinical and pathological severity. Gastroenterology 1999;116:1413-9.
Wattacheril J, Chalasani N. Nonalcoholic fatty liver disease (NAFLD): is it really a serious condition? Hepatology 2012;56:1580-4.
Musso G, Gambino R, Cassader M. Recent insights into hepatic lipid metabolism in non-alcoholic fatty liver disease (NAFLD). Prog Lipid Res 2009;48:1-26.
Kwiterovich PO, Sloan HR, Fredrickson DS. Glycolipids and other lipid constituents of normal human liver. J Lipid Res 1970;11:322-30.
Szczepaniak LS, Nurenberg P, Leonard D, Browning JD. Reingold JS, Grundy S. Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am J Physiol Endocrinol Metab 2005;288:E462-8.
Chen M, Song AH, Cheng XJ, Dong YH. Progress of pathogenesis and treatment nonalcoholic fatty liver disease. J Pract Diabetol 2008;4:9-10.
Xia Q, Sun T. Progress of pathogenesis and treatment nonalcoholic fatty liver disease.J Naval General Hospital 2010;23:100-3.
Bugianesi E, Gentilcore E, Manini R, Natale S, Vanni E, Villanova N. A randomized controlled trial of metformin versus vitamin E or prescriptive diet in nonalcoholic fatty liver disease. Am J Gastroenterol 2005;100:1082-90.
Belfort R, Harrison SA, Brown K, Darland C, Finch J, Hardies J. A placebo-controlled trial of pioglitazone in subjects with nonalcoholic steatohepatitis. N Engl J Med 2006;355:2297-307.
Sanyal AJ, Chalasani N, Kowdley KV, McCullough A, Diehl AM, Bass NM. Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N Engl J Med. 2010;362:1675-85.
Chalasani N, Younossi Z, Lavine JE, Diehl AM, Brunt EM, Cusi K. The diagnosis and management of non-alcoholic fatty liver disease: practice guideline by the American association for the study of liver diseases, American College of Gastroenterology, and the American Gastroenterological Association. Hepatology 2012;55:2005-23.
Wang WG, He YR, Lin P, Li YF, Sun RF, Gu W. In vitro
effects of active components of Polygonum multiflorum
radix on enzymes involved in the lipid metabolism. J Ethnopharmacol 2014;153:763-70.
Lin P, He YR, Lu JM, Li N, Wang WG, Gu W. In vivo
lipid regulation mechanism of Polygoni multiflori
radix in high-fat diet fed rats. Evid-Based Complement Alternat Med 2014; 1-8.
Yu J, Lin P, Lu JM, Wang WG, Gu W, Zhao RH. Effects of stilbeneglucoside on lipid synthesis, decomposition and transport in steatosis hepatocyte L-02. Chin Pharm J 2014;49:2077-82.
Zhang SH, Wang WQ, Wang JL. Protective effect of tetrahydroxystilbene glucoside on cardiotoxicity induced by doxorubicin in vitro
and in vivo
. Acta Pharmacol Sin 2009;30:1479-87.
Sun F, Zhang L, Zhang RY, Li L. Tetrahydroxystilbene glucoside protects human neuroblastoma SH-SY5Y cells against MPP+
-induced cytotoxicity. Eur J Pharmacol 2011;660:283-90.
Goldsmith JR, Sartor RB. The role of diet on intestinal microbiota metabolism: downstream impacts on host immune function and health, and therapeutic implications. J Gastroenterol 2014;49:785-98.
Yu J, Xie J, Mao XJ, Wang MJ, Li N, Wang J. Hepatoxicity of major constituents and extractions of radix Polygoni multiflori
and radix Polygoni multiflori
praeparata. J Ethnopharmacol 2011;137:1291-9.
Furuhashi M, Hotamisligil GS. Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discovery 2008;7:489-503.
Stahl A, Gimeno RE, Tartaglia LA, Lodish HF. Fatty acid transport proteins: a current view of a growing family. Trends Endocrinol Metab 2001;12:266-73.
Wang JC, Gray NE, Kuo T, Harris CA. Regulation of triglyceride metabolism by glucocorticoid receptor. Cell Biosci 2012;2:1206-13.
Namikawa C, Shu-Ping Z, Vyselaar JR, Nozaki Y, Nemoto Y, Ono M. Polymorphisms of microsomal triglyceride transfer protein gene and manganese superoxide dismutase gene in non-alcoholic steatohepatitis. J Hepatol 2004;40:781-6.
Goldberg IJ. Lipoprotein lipase and lipolysis: central roles in lipoprotein metabolism and atherogenesis. J Lipid Res 1996;37:693-707.
Sekiya M, Yahagi N, Matsuzaka T, Takeuchi Y, Nakagawa Y, Takahashi H. SREBP-1-independent regulation of lipogenic gene expression in adipocytes. J Lipid Res 2007;48:1581-91.
Seo YS, Kim JH, Jo NY, Choi KM, Baik SH, Park JJ. PPAR agonists treatment is effective in a nonalcoholic fatty liver disease animal model by modulating fatty-acid metabolic enzymes. J Gastroenterol Hepatol 2008;23:102-9.
Ruby MA, Goldenson B, Orasanu G, Johnston TP, Plutzky J, Krauss RM. VLDL hydrolysis by LPL activates PPAR-α through generation of unbound fatty acids. J Lipid Res 2010;51:2275-81.
Wang L, Waltenberger B, Pferschy-Wenzig EM, Blunder M, Liu X. Malainer C. Natural product agonists of peroxisome proliferator-activated receptor gamma (PPARγ): a review. Biochem Pharmacol 2014;92:73-89.
Lin P, Lu JM, Wang YF, Gu W, Yu J, Zhao RH. Naturally occurring stilbenoid TSG reverses non-alcoholic fatty liver diseases via gut-liver axis. PLoS ONE 2015; 10:e0140346.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3], [Table 4]