Fructose impairs glucose-induced hepatic triglyceride synthesis
© Huang et al; licensee BioMed Central Ltd. 2011
Received: 20 December 2010
Accepted: 24 January 2011
Published: 24 January 2011
Obesity, type 2 diabetes and hyperlipidemia frequently coexist and are associated with significantly increased morbidity and mortality. Consumption of refined carbohydrate and particularly fructose has increased significantly in recent years and has paralled the increased incidence of obesity and diabetes. Human and animal studies have demonstrated that high dietary fructose intake positively correlates with increased dyslipidemia, insulin resistance, and hypertension. Metabolism of fructose occurs primarily in the liver and high fructose flux leads to enhanced hepatic triglyceride accumulation (hepatic steatosis). This results in impaired glucose and lipid metabolism and increased proinflammatory cytokine expression. Here we demonstrate that fructose alters glucose-stimulated expression of activated acetyl CoA carboxylase (ACC), pSer hormone sensitive lipase (pSerHSL) and adipose triglyceride lipase (ATGL) in hepatic HepG2 or primary hepatic cell cultures in vitro. This was associated with increased de novo triglyceride synthesis in vitro and hepatic steatosis in vivo in fructose- versus glucose-fed and standard-diet fed mice. These studies provide novel insight into the mechanisms involved in fructose-mediated hepatic hypertriglyceridemia and identify fructose-uptake as a new potential therapeutic target for lipid-associated diseases.
Obesity, type 2 diabetes and hyperlipidemia frequently coexist and are associated with significantly increased morbidity and mortality . A significant increase in total refined carbohydrate intake and particularly fructose has paralled recent increased incidence of obesity and diabetes. Metabolism of sugars and particularly fructose occurs primarily in the liver and high fructose flux leads to enhanced hepatic triglyceride accumulation resulting in impaired glucose and lipid metabolism and increased proinflammatory cytokine expression [2–6].
The role that triglycerides play as an independent risk factor for CAD is still not well defined but a substantial number of individuals who maintain total plasma cholesterol concentrations within acceptable values (< 5.17 mmol/L or 200 mg/dL) still develop CAD [7, 8]. Some of these patients have low HDL -cholesterol concentrations (< 0.91 mmol/L or 35 mg/dL) [9, 10] and a decline in HDL-cholesterol often accompanies an increase in VLDL triglyceride, reflecting an interchange of cholesterol esters from HDL for triglyceride from VLDL [11–16]. In addition to lipid abnormalities, hyperinsulinemia also plays an important role in CAD risk and triglyceride concentrations are highly correlated to plasma insulin response to carbohydrate [17–22].
Given that dietary fructose has been associated with hypertriglyceridemia and insulin resistance, primarily of hepatic origin, the aim of this study was to evaluate the effects of fructose on hepatic intracellular triglyceride metabolism and gain some insight into the mechanisms by which fructose enhances hepatic lipogenesis. Here we demonstrate that addition of fructose to human hepatic HepG2 cells and primary murine hepatic cell cultures incubated in physiologic and diabetic-range glucose concentrations in vitro disrupts normal glucose metabolism and leads to hepatic triglyceride accumulation in association with reduced hepatic expression of phosphorylated acetyl CoA carboxylase (pSer479 ACC), phopshorylated hormone sensitive lipase (pSer660 HSL) and total adipose triglyceride lipase (ATGL) in comparison to glucose alone. Additionally fructose-fed athymic Nu/Nu mice exhibited increased hepatic steatosis in association with reduced hepatic ATGL expression in comparison to glucose- and standard defined diet-fed mice.
Materials and methods
Cell culture and hepatocyte isolation
Human hepatoma HepG2 cells purchased from ATCC were grown at 37°C in 5% CO2 in DMEM medium with 10% FBS, 500 mM Hepes, glutamine, penicillin (100 U/ml) and streptomycin (100 ug/ml) (Invitrogen). Hepatic tissue was harvested from 3-mth old male C57/Bl6 mice and primary hepatic cell culture performed as previously reported . At 30% confluence, HepG2 or primary hepatocyte cells were treated with glucose free DMEM with 5% FBS overnight and then incubated with glucose ( 5.5 and 11.1 mM) or fructose ( 0.55 mM) concentrations alone or fructose (0.55 mM) in combination with physiological glucose (5.5 mM) or high glucose (11.1 mM) for 72 hours. Tissue culture materials and other reagents were obtained from Sigma Chemical Co. (St. Louis, MO).
75% confluent cultures of HepG2 cells (3 × 106) were incubated for 72 h in 5.5 mM glucose, 11.1 mM glucose alone or 5.5 mM glucose in combination with 5.5 mM fructose, all of which contained a 10% solution of 13C tracer - [1,2-13C2] D-glucose (> 99% purity, and 99% isotope enrichment for each carbon position) (Cambridge Isotope Labs, Massachusetts) in T75 culture flasks. Following the glucose- or combination glucose/fructose treatment, culture medium was collected and cells were washed twice in PBS. Cell pellets were then harvested and palmitate, and oleate were extracted after saponification of cell pellets in 30% KOH and 100% ethanol using petroleum ether. Fatty acids were then converted to their methylated derivative using 0.5N methanolic-HCL and mass spectral data then obtained on a HP5973 mass selective detector connected to an HP6890 gas chromatograph. Palmitate and oleate were monitored at m/z 270 and m/z 264, respectively, with the enrichment of 13C labeled acetyl units to reflect synthesis, elongation and desaturation of the new lipid fraction as determined by mass isotopomer distribution analysis (MIDA) .
Cell lysates or homogenized frozen hepatic tissue (100-120 mg) were solubilized in buffer. Lysates were cleared by centrifugation and total protein concentration determined using a BioRad DC kit. 30 ug of the proteins were separated by 10% SDS-PAGE and transferred to nitrocellulose membranes, followed by immunoblotting using specific primary and secondary antibodies and visualized using SuperSignal Chemiluminescence Assay kit (Pierce Inc., Rockville, MD). Antibodies to pSer79 ACC, total ACC, pSer660 HSL, total HSL and ATGL were from Cell Signaling Technology (Danvers, MA) and β-actin was from Santa Cruz Biotechnology (Santa Cruz, CA).
Animals and Diet
All procedures were approved by the UCLA Animal Research Committee. Three-month old male athymic Nu/Nu mice purchased from Jackson Labs were housed individually in open-topped cages undera 12-hour light and 12-hour dark regimen and groups of six mice fed isocaloric (3675 kcal./kg) defined diets; standard (STD)diet (10% sucrose, 47% cornstarch), high glucose (HG, 60% glucose) or high fructose (HF, 60% fructose) diets [Dyets Inc, Pennsylvania, USA] for 12 weeks. Food intake and body weights were determined weekly. For intraperitoneal glucose tolerance tests (IPGT), mice were fasted overnight and retro-orbital blood glucose monitored at baseline (0), 15, 30, 60 and 120 minutes using a glucometer (Lifescan) after intraperitoneal glucose loading (1 g glucose per kg body weight) and area under the curve (AOC, mg/dl × min) for glucose levels during IPGT's was calculated for each group as previously described. All assays were carried out in triplicate and expressed asmean ± SEM. Insulin was measured in plasma samples by RIA (Linco, St. Charles, Missouri). Histological analysis was performed on paraffin-embedded hepatic tissues using consecutive 5-μm sections stained with hematoxylin and eosin. Briefly, 1/3 of the left posterior lobe of the liver was fixed in 10% neutral-buffered formalin for 24h, processed though graded alcohols and xylene and embedded in paraffin. 5-μm sections were deparaffinized and stained with hematoxylin and eosin (HE) using routine methods. Fat deposition was also analyzed in 8-μm frozen liver sections stained with 0.18% oil red O (Sigma-Aldrich) with 60% 2-propanol (Sigma-Aldrich) for 20 minutes at 37° and counterstained with hematoxylin. Fat accumulation stained with oil red O was quantified using an Image-Pro Plus Analyzer (Media Cybernetics, Inc., Bethesda, MD) by a pathologist (W. Yong). To quantify hepatic triglyceride content, liver tissues (100 mg) were homogenized in ice-cold 20 mmol/L Tris-HCl, 150 mmol/L NaCl, 2 mmol/L EDTA, and 1% Triton X-100, pH 7.5, triglycerides extracted with chloroform/methanol (2:1) and triglycerides quantitated using a commercially available kit (Infinity Triglycerides Stable Reagent, Thermo Electron) and correlated to total hepatic protein content. Oil Red O-staining was used to measure cellular neutral lipid droplet accumulation in vitro in the HepG2cells .
Results are expressed as mean ± SEM (metabolomic experiments mean +/- SD) and analysis performed by ANOVA with Bonferroni comparison tests or nonparametric t- test (one tailed/unpaired) as indicated. P values < 0.05 were considered significant.
Fructose increases in vitro hepatic triglyceride storage and secretion
Fructose impairs glucose-induced hepatic triglyceride synthesis and hydrolysis
As our metabolomic studies had demonstrated increased de novo triglyceride synthesis and secretion in hepatic cells cultured in 11 mM glucose co-treated with low concentration fructose, we next sought to explore the mechanism(s) by which fructose resulted in increased hepatic triglycerides. Hepatic triglyceride synthesis involves multiple metabolic pathways, including glycolysis and pyruvate oxidation which generate acetyl-CoA. Acetyl CoA is then converted to malonyl-CoA by the enzyme acetyl CoA carboxylase before conversion to palmitate by fatty acid synthase .
Fructose impairs murine hepatic triglyceride synthesis in vitro
Dietary fructose impairs glucose disposal and glucose-stimulated insulin release
Refined carbohydrate induces hepatic steatosis and elevated hepatic triglyceride levels in vivo
Several human and animal studies have demonstrated that dietary fructose intake increases triglyceride levels [27–34]. In humans, these lipid alterations occur quite quickly as evidenced by a 10 week study in 32 men & women who ate a 15% protein, 30% fat and 55% carbohydrate diet where 25% of calories were replaced with a glucose- or fructose-containing drink. De novo hepatic lipogenesis, markers of altered lipid metabolism and lipoprotein remodeling, including fasting apoB, LDL, small dense LDL and oxidized LDL all increased . The postprandial triglyceride response in particular increased 10% in the fructose-treated group in comparison to glucose, emphasizing the role of the hepatic response to fructose loads . However, the molecular mechanisms by which high fructose diets induce abnormalities in liver triglyceride metabolism are not fully understood [35–37].
Synthesis of hepatic TGs involves multiple metabolic pathways, including glycolysis and pyruvate oxidation to generate acetyl-CoA. Our 13C glucose tracer studies demonstrate increased intracellular palmitate and extracellular oleate concentration in fructose and glucose-cotreated cells compared to glucose-treated cells in keeping with increased "de novo" fatty acid synthesis . Our molecular in vitro studies demonstrate that addition of fructose to glucose-treated hepatic cells leads to reduced serine-phosphorylated ACC, HSL and ATGL . Therefore, in addition to serving as a substrate for enhanced de-novo fatty acid synthesis, fructose and or its intermediate metabolites may also alter expression of several enzymes involved in hepatic lipid synthesis and hydrolysis pathways.
As we observed increased extracellular oleate concentrations in the fructose-treated liver cells, this study indicates that in addition to increasing de novo hepatic fatty acid synthesis, fructose-treatment also leads to enhanced triglyceride secretion, as when triglycerides are assembled for release, they require oleate to provide fluidity. The combination of increased fatty acid synthesis and triglyceride release provides novel insight into the hepatic steatosis that has been demonstrated in animal models following dietary fructose and in humans where fructose intake correlates with prevalence of fatty liver [27, 28, 34, 39].
Our studies have focused on the liver as approximately 40% of ingested fructose is extracted and metabolized in the liver. Adipose tissue serves as the main TG store but they are also stored in non-adipose tissues including muscle and liver where they can provide fatty acid substrate for metabolic processes . Additionally, studies have shown that fructose plays a specific role in the pathogenesis of hepatic steatosis and metabolic syndrome due to differential hepatic fructose metabolism. Unlike most tissues which contain only hexokinase that competitively phosphorylates glucose or fructose at the sixth carbon , hepatocytes also express fructokinase-1 that phosphorylates fructose on 1C to generate fructose 1- phosphate. Fructose-1-phosphate can then be metabolized into dihydroxyacetone phosphate and glyceraldehydes entering the latter steps of the Embden-Meyerhof pathway to generate triacylglycerol. As this entry point is distal to the glycolysis rate limiting enzyme phospho fructokinase-1, unlike glucose, fructose can serve as a relatively unregulated source of acetyl-CoA . However, the contribution of glycolysis to de-novo hepatic fatty acid synthesis is small (< 10%) as supported by our metabolomic studies. Therefore, other mechanisms to increase fatty acid synthesis are likely more important including, fructose 1, 6 bis-phosphate which is a potent regulator of fatty acid synthesis by directly activating fatty acid synthase.
Although dietary carbohydrate induces insulin resistance in rats and hamsters, most commonly employed mice strains such as C57Bl/6 appear to be relatively resistant to CHO-induced metabolic syndrome . The athymic Nu/Nu mouse represents a model of non obese non-immune non-insulin-dependent diabetes [43, 44] and has been used to delineate immune-mediated pancreatic islet effects in insulin-dependent diabetes mellitus [45, 46]. Our studies demonstrate that unlike the C57Bl/6 mouse, increased CHO feeding to Nu/Nu mice results in development of a metabolic syndrome phenotype with modestly impaired peripheral glucose disposal. In contrast to our in vitro finding of reduced pS79ACC levels following fructose, we did not see changes in in vivo hepatic pS79ACC, ACC and/or pSer660 HSL or total HSL expression . This is unusual, given that ACC is the rate-limiting enzyme in lipogenesis but may be due to other actions of the sugars to alter ACC aggregation or other longer chain CoA. Given that glucose-stimulated insulin levels were attenuated in the fructose-fed mice in comparison to glucose- and standard-diet fed mice, our studies also suggest that fructose-fed mice may exhibit a degree of beta-cell impairment and this is an area that we are currently investigating.
It is important to acknowledge that our animal in vivo studies employed higher refined carbohydrate content (60% of energy) than would be consumed in a typical western diet (7.5-20% of energy) and the relevance of in vivo findings in these stylized animal models to humans can reasonably be questioned. However, our in vitro study fructose concentrations (0.5 mM) are easily attainable in the peripheral human circulation and fructose concentrations can be predicted to be higher in post-prandial portal venous blood in subjects consuming average Western diets containing 10-15% refined carbohydrate .
It is widely appreciated that increases in triglycerides are typically more pronounced in obese patients with insulin resistance. Our studies demonstrating that the fructose effect to interfere with hepatic lipid metabolism is more marked in hyperglycemic conditions is of importance to diabetic patients as they suggest that fructose consumption may exacerbate an already existing adverse metabolic profile especially in diabetic patients who have poor glycemic control. However, the adverse effects of fructose on hepatic lipid metabolism are not restricted to poorly controlled diabetic patients as our in vitro experiments demonstrate that even low concentrations of fructose can disrupt normal hepatic glucose metabolism.
In summary, our studies provide novel insight into the mechanism of fructose-induced hepatic hypertriglyceridemia and show that fructose, a component of sucrose (table sugar) and high fructose corn syrup, leads to increased de novo hepatic fatty acid synthesis and release of triglycerides in comparison to glucose. This not only entails differential utilization of fructose as a substrate for de novo fatty acid synthesis but may also involve alterations in the levels of key enzymes involved with fatty acid synthesis and hydrolysis including ACC-, ATGL- and HSL. Furthermore, they support the contention that fructose-containing foods can have detrimental effects on hepatic lipid synthesis with potentially adverse consequences on cardiovascular risk. They have important clinical implications given the increase in obesity rates and its associated complications, including diabetes.
This research was supported by NIH/NIDDK P30 DK063491-07 P & F grant (A.P.H.).
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