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Lipid profiling of the therapeutic effects of berberine in patients with nonalcoholic fatty liver disease
Journal of Translational Medicine volume 14, Article number: 266 (2016)
We recently demonstrated a positive effect of berberine on nonalcoholic fatty liver disease patients after 16 weeks of treatment by comparing mere lifestyle intervention in type 2 diabetes patients with berberine treatment, which decreased the content of hepatic fat. However, the potential mechanisms of the clinical effects are unclear. We used a lipidomic approach to characterize the state of lipid metabolism as reflected in the circulation of subjects with nonalcoholic fatty liver disease (NAFLD) before and after berberine treatment.
Liquid chromatography–mass spectrometry evaluated the various lipid metabolites in serum samples obtained from the participants (41 patients in the berberine group and 39 patients in the mere lifestyle intervention group) before and after treatment.
A total of 256 serum lipid molecular species were identified and quantified. Both treatments regulated various types of lipids in metabolic pathways, such as free fatty acids, phosphoglycerides and glycerides, in metabolic pathways, but berberine induced a substantially greater change in serum lipid species compared with mere lifestyle intervention after treatment. Berberine also caused obvious differences on ceramides. Berberine treatment markedly decreased serum levels of ceramide and ceramide-1-phosphate.
Berberine altered circulating ceramides, which may underlie the improvement in fatty liver disease.
ClinicalTrials.gov NCT00633282, Registered March 3, 2008
Berberine (BBR) is an alkaloid that was originally isolated from Huanglian (Coptischinensis). BBR is used as antimicrobial in China. Recent studies have demonstrated beneficial effects of BBR on serum lipids and glucose metabolism [1–3]. BBR exerted an anti-hyperlipidemia effect of lowering total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-c) levels in patients . The cholesterol-lowering mechanism of BBR was different from that of statins. Berberine elevated the LDLR expression by stabilizing LDLR message ribonucleic acid(mRNA)  and blocking proprotein convertase subtilisin/kexin type 9 (PCSK9) transcription [4, 5], but statins upregulated PSCK9 gene expression . BBR is also an effective anti-diabetes agent.BBR significantly lowered fasting blood glucose (FBG), hemoglobin A1C, triglyceride, and insulin levels in patients with type 2 diabetes mellitus (T2DM) in the clinical study .
The liver plays a vital role in lipid metabolism and glucose homeostasis. Nonalcoholic fatty liver disease (NAFLD) is associated with insulin resistance and the development of type 2 diabetes . The effect of BBR on regulating serum cholesterol and triglyceride suggested that BBR played a central role in decreasing hepatic fat content. Our previous study  demonstrated that BBR decreased hepatic fat content by 57.2 %, and reduced serum lipids and liver enzymes, which indirectly indicated that BBR improved liver inflammation. However, the mechanism of reducing hepatic fat content is not known.
Increased TG accumulation in the liver is the pathophysiological hallmark of NAFLD. Some studies suggest that the lipid metabolism perturbations in NAFLD are more complex. A comprehensive lipidomics study demonstrated that substantial changes in other lipid classes, such as cholesterol and specific phospholipids in the liver may play a role in the pathogenesis of NAFLD and the development of NASH . NAFLD is also associated with several changes in circulating lipidomics, such as an increase in the ratio of monounsaturated fatty acids: vs saturated fatty acids and a significant decrease in circulating levels of the essential fatty acids linoleic acid (18:2 n6) and alpha-linolenic acid (18:3 n3) across multiple lipid classes. The lipogenic activity levels off or declines modestly with progression to nonalcoholic steatohepatitis (NASH), but lipoxygenase (LOX) activity increases . Therefore, circulating lipidomics are closely associated with fat deposits in hepatocytes. Whether the compositions of the lipids are harmful and whether the changes of serum lipidomics are related with berberine treatment effect are not well identified. This study used a comprehensive lipidomic approach: (1) to quantify the absolute and relative amounts of free fattyacids (FFAs), glycerolipids (GL), glycerophospholipids (GP) and sphingolipids (SP) in subjects with NAFLD before and after berberine treatment and lifestyle intervention and (2) to compare the distribution of fatty acids within each of these classes in these groups of subjects.
The detailed design of this study was previously published . Briefly, a randomized, parallel-controlled, open-label clinical trial was conducted in three medical centers for the treatment of NAFLD patients with impaired glucose regulation (IGR) or T2DM with lifestyle intervention (LSI) with or without BBR (NIH Registration number: NCT00633282). The trial design conformed to the revised CONSORT standards for the reporting of randomized trials. Eligible adults were identified and recruited from unsolicited referrals to the three participating clinical centers from March 2008 to August 2011. Hepatic fat content (HFC) was assessed using proton magnetic resonance spectroscopy (1H MRS). Subjects who met all enrollment criteria were randomly assigned to one of the two groups for the 16-week clinical trial, Group A- LSI or Group B-LSI plus BBR (0.5 g, t.i.d.). BBR (berberine®, Huashi Pharmaceuticals Shanghai, China, Inc.) was administered orally at a 0.5 g dose 30 min before meals, three times daily (according to the Chinese Pharmacopeia . LSI (including dietary modification and exercise) was performed following standardized recommendations . All participants were required to fast overnight (12 h) before participating in a physical examination by trained staff and physicians using standard protocols. Blood samples were drawn after an overnight fast and immediately centrifuged. The samples were frozen immediately and stored at −80 °C until assayed. These samples were used for the final lipidomics analysis. Table 1 summarizes the detailed characteristics of these 80 patients at baseline and at the end of follow-up. The following main reasons determined the exclusion of the original participants from the present analysis: (1) incomplete information and (2) insufficient blood samples. The ethics committee of Zhongshan Hospital, Fudan University approved the study, which was conducted in accordance with the guidelines of the Declaration of Helsinki. Written informed consent was obtained from each patient.
All lipid standards were purchased from Avanti Polar Lipids (Alabaster, AL, USA). Organic residue grade methanol, MS grade acetonitrile and HPLC grade methyl-tert-butyl ether (MTBE) were purchased from Mallinckrodt BakerInc. (Phillipsburg, NJ, USA). HPLC grade isopropyl alcohol and chloroform were purchased from Honeywell Inc. (Muskegon, MI, USA). Formic acid of analytical grade was obtained from TEDIA Company, Inc. (Fairfield, OH, USA). Ammonium formate and ammonium acetate (purity 99.99 %) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Ultra-pure water was prepared using a Milli-Q purification system (Millipore, Bedford, MA, USA).
Method of lipid profiling
Free fatty acids were determined according to our previous study . Samples were first extracted using reverse phase SPE and analyzed in an Agilent 6410B Triple Quadrupole LC–MS after pre-column derivatization.
Sphingolipids, phosphoglycerides and glycerides were determined in our lipid profiling platform  with a slight modification Plasma (0.1 mL) was transferred into a glass tube containing 20 μL of sphingolipid internal standards. Methanol (1.5 mL) was added to the tube, and the sample was vortexed for 10 s. Methyl-tert-butyl ether (MTBE) (5 mL) was added, and the sample was vortexed again for 15 min. Phase separation was induced by the addition of 1.5 mL of MS-grade water. Samples were incubated for 10 min at room temperature, and the tube was centrifuged at 4500 r/min for 10 min. The organic supernatant was collected, and the lower phase was re-extracted with 2 mL of the solvent mixture (MTBE:methanol:water, 10:3:2.5). The pooled organic supernatant was collected and dried under a gentle nitrogen stream. The dried extracts were re-dissolved in 100 μL of methanol/chloroform (1:1, v/v) containing internal standards of phosphoglycerides, glycerides and sphingomyelins for analysis. A 50-μL aliquot was used for Agilent 6410B Triple Quadrupole LC–MS testing to analyzes phingolipids, and another 50 μL were used for Thermo Scientific HPLC-LTQ/FTICRMS testing to analyze phosphoglycerides, glycerides and sphingomyelins.
Chromatographic separation was performed for sphingolipids testing using a SpectraC8SR column (150 × 3.0 mm; 3 μm particle size; Peeke Scientific, Redwood City, CA, USA). The column temperature was 40 °C. Mobile phase A was comprised of 1 mM ammonium formate in water containing 0.1 % formic acid. Mobile phase B was comprised of 1 mM ammonium formate in methanol containing 0.1 % formic acid. The gradient was programmed as follows: 0–10 min, 80–100 % B; 10–18 min, 100 % B; 18–18.1 min, 100–80 % B; and 18.1–25 min, 80 % B. The flow rate was 0.5 mL/min. The injection volume was 3 μL. The parameters for electrospray ionization tandem MS in positive ion mode were as follows: gas temperature, 350 °C; gas flow rate, 10 L/min; nebulizer, 30 psi; and capillary voltage, 4000 V. Multiple reaction monitoring was performed using the characteristic precursor-to-production transitions, optimized fragmentor voltages, and collision energies.
The surveyor HPLC system was equipped with an X terra MS C8 column (100 × 2.1 mm; 3.5-μm particle size; Waters, Milford, MA, USA) for phosphoglycerides, glycerides and sphingomyelins testing. Mobile phase A was comprised of 0.1 % formic acid in water containing 2 mM ammonium acetate. Mobile phase B was comprised of 2-propanol/acetonitrile (2:5, v/v) containing 2 mM ammonium acetate and 0.1 % formic acid. The flow rate was 0.35 mL/min. The gradient was programmed consecutively as follows: 0–1 min, 10 % B; 1–2 min, 10–30 % B2-4 min, 30–50 % B; 4–8 min, 50–70 % B; 8–12 min, 70–100 % B; and 12–24 min, 100 % B. The oven temperature was 40 °C. The injection volume was 10 μL. The LTQ-FT was run in full-scan mode at 100,000 resolution ranging from m/z 50–1200 with the following MS parameters: sheath gas flow rate, 50 arb; aux gas flow rate, 20 arb; sweep gas flow rate, 3 arb; and capillary temperature, 275 °C in positive and negative mode. The positive mode used a spray voltage of 4.5 kV, capillary voltage of 35.0 V, and tube lens of 120 V. The negative mode used a spray voltage of −4.0 kV, capillary voltage of −35.0 V, and tube lens of −120 V.
Sphingolipids were identified based on retention time using authentic standards and quantified using standard curve samples. The identification and quantitation of other lipids was performed using the lipid data analyzer (LDA) software package (Graz University of Technology, Graz, Austria).
Variables are expressed as the means ± SD or medians (quartile). Differences between groups were analyzed using Student’s t test (for data that were normally distributed) or the Mann–Whitney test (for data that were not normally distributed) using SPSS 18.0 software (SPSS Inc., Chicago, IL, USA). A P value less than 0.05 was considered significant. Orthogonal partial least squares discriminant analysis (OPLS-DA) was used to visually discriminate between groups. Lipid profiling data were mean-centered and Pareto-scaled using Simca P + 12.0.1 (Umetrics, Umeå, Sweden) to reduce noise and artifacts. The quality and predictability of each OPLS-DA model was evaluated using R2Y (cum) and Q2 (cum) values, respectively. The following criteria for each potential biomarker were used: (1) A variable importance in projection greater than one; (2) The jack-knife uncertainty bar excluded zero; and (3) The absolute value of P corr in the S-plot was greater than 0.58 .
The general characteristics of the subjects at baseline
Serum samples, which were subjected to the lipidomics analyses, were obtained from 41 BBR-treated patients and 39 LSI patients at baseline and at the end of treatment. Table 1 summarizes the detailed characteristics of the 80 patients at baseline. There were no significant differences in the clinical characteristics between groups at baseline, which suggests that the two groups were well matched in demographic profiles, HFC and other baseline characteristics (Table 1).
Berberine significantly influenced hepatic fat content and energy metabolism
After 16 w treatment, HFC decreased by 55.1 % in the BBR group (P = 0.00) and by 29.3 % in the LSI group (P < 0.05; Table 1). BBR caused a greater reduction in HFC as compared to that with LSI alone (P = 0.021; Additional file 1: Table S1). Liver enzymes, such as ALT, AST and γ-GT were not significantly different between BBR and LSI groups at the 16th week (Additional file 1: Table S1).
Body weight, waist, body mass index (BMI), HFC, blood glucose, HbA1c, ΔI30/ΔG30, serum cholesterol, triglyceride, LDL-c, apoA/B, LP(a) and liver enzymes were significantly decreased after 16 weeks of BBR treatment (P < 0.05) (Table 1). BBR exhibited greater decreases in body weight, BMI, waist, HFC, serum cholesterol and triglycerides compared with LSI alone (Additional file 1: Table S1), which demonstrates a clearly significant benefit of BBR on metabolism. Additional file 2: Figure S1 shows the line graph of the glucose tolerance test (0–3 h). BBR reduced the area under the OGTT curve [−5.9(−6.9 to −4.8) vs. −4.0(−4.6 to −1.9), P = 0.041] more than lifestyle intervention alone.
Lipid profiling of berberine treatment and lifestyle intervention alone
Sixty-one free fatty acids, 54 sphingolipids, 86 phosphoglycerides and 55 glycerides were successfully identified and quantified. Subsequent comprehensive statistical analyses identified lipid variations between the groups. Table 2 shows lipids with significant differences between groups after Student’s t test and Mann–Whitney tests. Figure 1 shows the effect of berberine and lifestyle intervention on lipid metabolic pathways. Berberine altered lipid metabolism, and this effect was related to a variety of lipid types.
More lipids were significantly changed after berberine treatment compared with lifestyle intervention. Nineteen free fatty acids [FA(15:1), FA(16:1), FA(16:2), FA(16:3), FA(18:1), FA(18:2), FA(20:2), FA(20:3), FA(20:4), FA(20:5), FA(22:4), FA(22:5), FA(22:6), FA3, FA40, FA48, FA51, FA(α-18:3), FA(γ-18:3)] were markedly decreased in the BBR group, and 8 of these free fatty acids were also altered after lifestyle intervention. Levels of Cer(d18:1/18:0), Cer(d18:1/20:0) and Cer(d18:1/18:0)-1P sphingolipids were significantly decreased. The sphingomyelin (SM) SM(d18:1/16:1) was significantly decreased, and SM(d18:1/24:4) was elevated. Levels of LPE(18:0), LPE(O-20:0), PC(O-36:3), PC(P-38:5), PC(40:8), PS(P-36:1), 5 lysophosphatidylcholine [LPC(14:0), LPC(16:1), LPC(18:0), LPC(18:3), LPC(20:0)], 3 phosphatidylinositol [PI(34:2), PI(40:6), PS(P-36:1)] and TG(52:7) were markedly decreased, and LPI(18:0), LPI(20:4), PC(P-38:5) and 4 lysophosphatidylcholines [LPC(18:2), LPC(20:2), LPC(20:4), LPC(20:5), LPC(22:6)] were significantly elevated (Table 2).
Table 2 shows that most lipids were markedly decreased after LSI. Levels of 8 free fatty acids [FA(16:1), FA(16:2), FA(18:2), FA(20:2), FA(20:3), FA27, FA51, FA(α-18:3)] were significantly decreased. The levels of LPC(16:1), LPC(18:3), LPE(18:0), LPS(O-18:0), PC(O-36:3), PC(P-38:5) and 6 phosphatidylinositols [PI(34:2), PI(36:2), PI(36:3), PI(38:4), PI(38:6), PI(40:6)], PS(P-36:1) were significantly decreased, and LPI(18:0), LPI(20:4) and 7 lysophosphatidylcholine [LPC(18:1), LPC(18:2), LPC(20:2), LPC(20:3), LPC(20:4), LPC(20:5), LPC(22:6)] levels were markedly elevated. The TG (46:11) level was also significantly decreased.
Only 5 lipids were significantly different before BBR treatment or LSI: LPE (16:0), PC(34:0), PC(38:4), PC(40:5) and SM(d18:1/12:0). However, 10 lipids were markedly different after the two interventions. Levels of Cer(d18:1/28:0)-1-P, LPC(14:0), LPC(20:3) and 4 triglycerides [TG(48:0), TG(P-52:1), TG(52:7), TG(54:8)] in the berberine treatment group were significantly lower than the lifestyle intervention group. Levels of SM(d18:1/24:4), PC(36:4) and PC(40:9) in the berberine treatment group were significantly higher than the lifestyle intervention group.
These results demonstrated that the lipid-lowering effect of berberine was similar with lifestyle intervention. Both treatments regulated various types of lipids in metabolic pathways. The two interventions similarly regulated free fatty acids, phosphoglycerides and glycerides, but there were obvious differences in regulation for sphingolipids. Ceramide and ceramide-1-phosphate levels decreased markedly after BBR treatment, and sphingomyelin levels were slightly elevated. The lifestyle intervention only significantly decreased sphingosine levels. These data suggest that berberine participates in phospholipid metabolism.
Orthogonal partial least squares discriminant analysis (OPLS-DA) was used to further study the subtle differences between groups. Figure 2 shows the score plots obtained from OPLS-DA. Patient groups before and after lifestyle intervention exhibited a reliable discrimination, which means lifestyle intervention obviously affected lipid metabolic pathways. OPLS-DA analysis detected four biomarkers that reflected the therapeutic effect of lifestyle intervention (Table 3).
The berberine treatment group also exhibited an obvious discrimination, which means that berberine markedly regulated the lipid metabolic pathways. Six biomarkers that reflected the therapeutic effect of berberine were detected (Table 3).
The two groups of patients could not be discriminated before intervention. The two groups only achieved incomplete discrimination after intervention. Only two biomarkers were detected that discriminated these two types of intervention (Table 3).
In the present study, BBR treatment for 16 weeks reduced more hepatic fat content in NAFLD patients, which was paralleled with a global metabolic benefit, as reflected in reduced body weight and improved glucose and lipid profiles compared with lifestyle intervention alone. Lipidomics analyses demonstrated that berberine and lifestyle intervention alone regulated various types of lipids in lipid metabolic pathways comprehensively. Notably, berberine exerted a special effect on sphingolipids, including a down-regulation of ceramides, which play an important role in the pathogenesis of nonalcoholic fatty liver disease. However, lifestyle intervention alone had no effect on ceramides.
Patients treated with berberine lost significantly more liver fat content and exhibited greater reductions in blood glucose, triglycerides and cholesterol than the LSI group, which is consistent with previous studies [1, 2, 7]. BBR was absorbable after oral administration in our previous study , which demonstrated that BBR directly affected hepatic lipid metabolism.
Previous studies indicated that fat deposit in hepatocytes was associated with several changes in circulating lipidomes . Lipids are the fundamental components of cellular membranes, and they are essential because they represent the biochemical activity signature during lipid metabolism. Therefore, lipids are closely related to observable phenotypes. Lipidomics is the process of defining multivariate lipid metabolic trajectories that represent the systemic response (i.e., holistic lipid metabolic changes) of a living system to pharmaceutical interventions over time.
Berberine plus lifestyle intervention and lifestyle interventional one exhibited a substantially greater effect on serum lipid metabolism, which primarily included FA, LPC, LPI, LPE, PC and PI (Table 2). Only berberine plus lifestyle intervention altered serum sphingolipids, including decreasing serum sph(d18:1), Cer(d18:1/18:0), Cer(d18:1/18:0)-1-p, and Cer(d18:1/20:0) levels, which was not achieved by exercise with diet control alone. This effect may be a special mechanism of berberine.
Ceramides are important members of the sphingolipid family, and they are essential precursors for complex sphingolipids. Ceramide and ceramide-derived sphingolipids are structural components of membranes, and these components are associated with insulin resistance, oxidative stress, and inflammation [17–19], which suggest that they play a role in the development of liver steatosis [20, 21]. Ceramides (Cer) may inhibit several mediators of the insulin signaling pathway, including insulin receptor substrate 1 (IRS1), phosphatidylinositol 3-kinase (PI-3 K) and AKt/PKB . Previous studies indicated that inhibition of ceramide synthesis, including ceramide-1-phosphate and glucosylceramide, inhibited several underlying causes of insulin resistance and improved insulin sensitivity in tissues [23–26]. A recent report suggested that the liver is a major contributor of circulating ceramide species . Plasma levels of total ceramide and all ceramide species in western-diet induced NAFLD were elevated, and major changes were observed in Cer(d18:1/16:0), Cer(d18:1/22:0), Cer(d18:1/24:0) and Cer(d18:1/24:1). A study in animals demonstrated that inhibition of ceramide biosynthesis reduced hepatic and plasma ceramides and sphingomyelin, improved insulin sensitivity and reduced hepatic fat accumulation [27, 28]. Berberine significantly decreased the level of ceramides in the present study, with major changes in Cer(d18:1/18:0), Cer(d18:1/20:0) and Cer(d18:1/18:0)-1P, which demonstrates that the improving effects of BBR in liver steatosis related to ceramide reduction.
Berberine also reduced blood glucose levels in the oral glucose tolerance test (OGTT), which is consistent with previous studies . Some studies suggested that berberine decreased blood glucose by improving insulin resistance . A recent report suggested that overexpression of acid ceramidase in the liver reduced hepatic ceramide levels and improved hepatic and adipose insulin sensitivity . Plasma ceramide levels reflected changes in hepatic ceramide levels. The present study found that berberine reduced circulating ceramide levels, which may be related to decreasing serum glucose.
Lipid microdomains or caveolae, which are small invaginations of plasma membrane, emerged as important elements for lipid uptake, including triglycerides (TG) and fatty acids . Sphingomyelin (SM) is a major phospholipid of lipid microdomains. The conversion of SM to Cer is also necessary to maintain the homeostasis of these domains . Sphingomyelin synthase (SMS) converts Cer to SM in the plasma membrane, and a deficiency of SMS may affect the metabolism of ceramide, sphingosine and sphingosine 1-phosphate. The present study found that berberine also altered plasma levels of SM, as characterized by a significant decrease in SM(d18:1/16:1) and elevated SM(d18:1/12:0) and SM(d18:1/24:4).BBR also reduced the level of ceramides. However, how these changes affect hepatic fat deposit requires investigation.
PC combats fatty liver and blood lipid disorders due to obesity [31, 32], promotes the absorption and utilization of lipid, removes cholesterol from vessel walls, reduces HDL-cholesterol and promotes hydrolysis of atherosclerotic plaques . The content ratio of PC and PE is closely related to the accumulation of TG in liver . Berberine treatment and lifestyle intervention regulated the level of PC in plasma. Two PCs containing polyunsaturated fatty acids [PC(36:4) and PC(40:9)] were biomarkers that discriminated between these two interventions, and the levels of these PCs in the berberine group were significantly higher than the lifestyle intervention.
Lysophosphatidylcholine (LPC) has been reported to be closely related to many inflammatory diseases, such as T2DM, obesity, and atherosclerosis . Several LPC biomarkers [LPC(18:2), LPC(20:4), LPC(20:5), and LPC(22:6)] were significantly elevated after BBR treatment, and other LPCs [LPC(14:0), LPC(16:1), LPC(18:0), LPC(18:3), and LPC(20:0)] were reduced. Lifestyle intervention also caused similar changes. The levels of 2 lysophosphatidylinositol (LPI) biomarkers [LPI(18:0) and LPI(20:4)] also markedly increased after berberine and lifestyle intervention alone treatments. The role of this lipid type has not been reported in type 2 diabetes or nonalcoholic fatty liver disease.
Further studies are needed to elucidate the biological mechanisms accounting for the link between berberine, serum lipid profile, especially ceramides, and fatty liver, but these findings indicate that the systematic analysis of serum lipid species, rather than lipid classes as a whole, may reveal the beneficial effects of berberine on fatty liver beyond improvements in clinical biomarkers.
One limitation of the present study is the cross-sectional nature of the study, and no patients were examined using liver biopsy because of ethical concerns. Therefore, the effects of BBR on human hepatic lipid profile and the genes related to lipid metabolism require further study.
The application of LC-MS-based lipidomics and measurement of biochemical parameters revealed the differential therapeutic effects of berberine and mere lifestyle intervention on serum lipid profile, which were comparable with their differential effects on hepatic fat content, serum lipid and glucose metabolism. Berberine more substantially altered serum lipid species compared with mere lifestyle intervention. The altering of sphingolipid metabolism by BBR, including a decrease in serum ceramides, was a novel mechanism. These findings suggest that a lipidomics approaches useful for the elucidation of the complex mechanism of action of particular drugs and a novel tool to probe the mechanisms of NAFLD progression. Future studies are required to precisely evaluate the predictive findings in additional cohorts and confirm whether we identified an early marker of NAFLD and its associated therapeutics.
nonalcoholic fatty liver disease
polyunsaturated fatty acids
impaired glucose regulation
hepatic fat content
body mass index
Yin J, Xing H, Ye J. Efficacy of berberine in patients with type 2 diabetes mellitus. Metabolism. 2008;57:712–7.
Kong W, Wei J, Abidi P, Lin M, Inaba S, Li C, et al. Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. Nat Med. 2004;10:1344–51.
Lu SS, Yu YL, Zhu HJ, Liu XD, Liu L, Liu YW, et al. Berberine promotes glucagon-like peptide-1 (7-36) amide secretion in streptozotocin-induced diabetic rats. J Endocrinol. 2009;200:159–65.
Li H, Dong B, Park SW, Lee HS, Chen W, Liu J. Hepatocyte nuclear factor 1—plays a critical role in PCSK9 gene transcription and regulation by the natural hypocholesterolemic compound berberine. J Biol Chem. 2009;284:28885–95.
Cameron J, Ranheim T, Kulseth MA, Leren TP, Berge KE. Berberine decreases PCSK9 expression in HepG2cells. Atherosclerosis. 2008;201:266–73.
Dubuc G, Chamberland A, Wassef H, Davignon J, Seidah NG, Bernier L, Prat A. Statins upregulate PCSK9, the gene encoding the proprotein convertase neural apoptosis-regulated convertase-1 implicated in familial hypercholesterolemia. Arterioscler Thromb Vasc Biol. 2004;24(8):1454–9.
Zhang Y, Li X, Zou D, Liu W, Yang J, Zhu N, et al. Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. J Clin Endocrinol Metab. 2008;93(7):2559–65.
Perry RJ, Samuel VT, Petersen KF, Shulman GI. The role of hepatic lipids in hepatic insulin resistance and type 2 diabetes. Nature. 2014;510(7503):84–91.
Yan HM, Xia MF, Wang Y, Chang XX, Yao XZ, Rao SX, et al. Efficacy of berberine in patients with nonalcoholic fatty liver disease. PLoS ONE. 2015;10(8):e0134172.
Puri P, Baillie RA, Wiest MM, Mirshahi F, Choudhury J, Cheung O, Sargeant C, et al. A lipidomic analysis of nonalcoholic fatty liver disease. Hepatology. 2007;46(4):1081–90.
Puri P, Wiest MM, Cheung O, Mirshahi F, Sargeant C, Min HK, et al. The plasma lipidomic signature of nonalcoholic steatohepatitis. Hepatology. 2009;50:1827–38.
Cho E. Berberine hydrochloridein. Pharmacop People’s Repub China. 1990;2:437–9.
Astrup A, Carraro R, Finer N, Harper A, Kunesova M, Lean ME, et al. Safety, tolerability and sustained weight loss over 2 years with the once-daily human GLP-1 analog, liraglutide. Int J Obes (Lond). 2012;36:843–54.
Tie Cai, Ting Hu, Zhang Xinxiang, Zhou Jiang, Zhang Jinlan. HPLC-MRM relative quantification analysis of fatty acids based on anovel derivatization strategy. Analyst. 2014;139:6154–9.
Feng Qu, Zheng Su-Jun, Cai-Sheng Wu, Jia Zhi-Xin, Zhang Jin-Lan, Duan Zhong-Ping. Lipidomic profiling of plasma in patients with chronic hepatitis C infection. Anal Bioanal Chem. 2014;406:555–64.
Feng Qu, Cai-Sheng Wu, Hou Jin-Feng, Jin Ying, Zhang Jin-Lan. Sphingolipids as new biomarkers for assessment of delayed-type hypersensitivity and response to triptolide. PLoS ONE. 2012;7:1–12.
Chavez JA, Siddique MM, Wang ST, Ching J, Shayman JA, Summers SA. Ceramides and glucosylceramides are independent antagonists of insulin signaling. J Biol Chem. 2014;289:723–34.
Bikman BT. A role for sphingolipids in the pathophysiology of obesity-induced inflammation. Cell Mol Life Sci. 2012;69:2135–46.
Maceyka M, Spiegel S. Sphingolipid metabolites in inflammatory disease. Nature. 2014;510:58–67.
Pagadala M, Kasumov T, McCullough AJ, Zein NN, Kirwan JP. Role of ceramides in nonalcoholic fatty liver disease. Trends Endocrinol Metab. 2012;23:365–71.
Xia JY, Holland WL, Kusminski CM, Sun K, Sharma AX, Pearson MJ, et al. Targeted induction of ceramide degradation leads to improved systemic metabolism and reduced hepatic steatosis. Cell Metab. 2015;22:1–13.
Summers SA. Sphingolipids and insulin resistance: the five Ws. Curr Opin Lipidol. 2010;21:128–35.
Holland WL, Summers SA. Sphingolipids, insulin resistance, and metabolic disease: new insights from in vivo manipulation of sphingolipid metabolism. Endocr Rev. 2008;29(4):381–402.
Holland WL, Knotts TA, Chavez JA, Wang L, Hoehn KL, Summers SA. Lipid mediators of insulin resistance. Nutr Rev. 2007;65(6, part 2):S39–46.
Stratford S, DeWald DB, Summers SA. Ceramide dissociates 3′-phosphoinositide production from pleckstrin homology domain translocation. Biochem J. 2001;354(part 2):359–68.
Salinas M, López-Valdaliso R, Martín D, Alvarez A, Cuadrado A. Inhibition of PKB/Akt1 by C2-ceramide involves activation of ceramide-activated protein phosphatase in PC12 cells. Mol Cell Neurosci. 2000;15(2):156–69.
Kurek K, Piotrowska DM, Wiesiołek-Kurek P, Łukaszuk B, Chabowski A, Górski J, Zendzian-Piotrowska M. Inhibition of ceramide de novo synthesis reduces liver lipid accumulation in rats with nonalcoholic fatty liver disease. Liver Int. 2014;34:1074–83.
Kasumov T, Li L, Li M, Gulshan K, Kirwan JP, Liu X, et al. Ceramide as a mediator of non-alcoholic fatty liver disease and associated atherosclerosis. PLoS ONE. 2015;10(5):e0126910.
Summers SA, Nelson DH. A role for sphingolipids in producing the common features of type 2 diabetes, metabolic syndrome X, and Cushing’s syndrome. Diabetes. 2005;54:591–602.
Mitsutake S, Zama K, Yokota H, Yoshida T, Tanaka M, Mitsui M, et al. Dynamic modification of sphingomyelin in lipid microdomains controls development of obesity, fatty liver, and type 2 diabetes. J Biolchem. 2011;286(32):28544–55.
Shirouchi B, Nagao K, Inoue N, Ohkubo T, Hibino H, Yanagita T. Effect of dietary omega 3 phosphatidylcholine on obesity-related disorders in obese Otsuka long-evans Tokushima fatty rats. J Agric Food Chem. 2007;55:7170–6.
Buang Y, Wang YM, Cha JY, Nagao K, Yanagita T. Dietaryphosphatidylcholine alleviates fatty liver induced by oroticacid. Nutrition. 2005;21:867–73.
Wang M, Wang F, Wang Y, Ma X, Zhao M, Zhao C. Metabonomics study of the therapeutic mechanism of gynostemmapentaphyllum and atorvastatin for hyperlipidemia in rats. PLoS ONE. 2013;8:e78731.
Jacobs RL, van der Veen JN, Vance DE. Finding the balance: the role of S-adenosylmethionine and phosphatidylcholine metabolism in development of nonalcoholic fatty liver disease. Hepatology. 2013;58:1207–9.
Sato A, Kumagai T, Ebina K. A synthetic biotinylated peptide, BP21, inhibits the induction of mRNA expression of inflammatory substances by oxidized- and lyso-phosphatidylcholine. Drug Dev Res. 2014;75:246–56.
XXC, ZF and JLZ performed most of the experiments, participated in data analyses and drafted the manuscript. HYM, HB, MFX and HDL performed the experiments. XG and JDJ conceived of the study, participated in its design and coordination and helped draft the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
The study protocol was in agreement with the Helsinki Convention and the study was approved by the ethics committee of Zhongshan Hospital, Fudan University. The patients gave informed consent for the lipids analysis.
This work was supported by Grants from the National Key Basic Research Program of China (Grant No. 2012CB524906 to X. Gao), the Shanghai Municipal Health Project grant (Grant No. 2013ZYJB0802 to X. Gao), the Shanghai Health and Family Planning Commission Foundation (Grant Nos. 12GWZX0103 and 2013SY005 to X. Gao), and Science and Technology Commission of Shanghai Municipality (Grant No. 13441900303 to Hua Bian).
The National Key Basic Research Program of China (Grant No. 2012CB524906 to X. Gao) and the Shanghai Municipal Health Project grant (Grant No. 2013ZYJB0802 to X. Gao) supported the design and collection of the study. The Shanghai Health and Family Planning Commission Foundation (Grant Nos. 12GWZX0103 and 2013SY005 to X. Gao) and Science and Technology Commission of Shanghai Municipality (Grant No. 13441900303 to Hua Bian) supported the interpretation and analysis of the study.
Changes of clinical and biochemical parameters after treatment.
The line graph of the glucose tolerance test (0–3 h). Data were mean ± SD, LSI: lifestyle intervention, BBR plus LSI: berberine treatment plus lifestyle intervention. *P < 0.05 when comparing before and after berberine plus lifestyle intervention treatment, #P < 0.05 when comparing before and after lifestyle intervention alone treatment.
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Chang, X., Wang, Z., Zhang, J. et al. Lipid profiling of the therapeutic effects of berberine in patients with nonalcoholic fatty liver disease. J Transl Med 14, 266 (2016). https://doi.org/10.1186/s12967-016-0982-x
- Nonalcoholic fatty liver disease
- Lipidomic approach