Uridine prevents tamoxifen-induced liver lipid droplet accumulation
© Le et al.; licensee BioMed Central Ltd. 2014
Received: 24 January 2014
Accepted: 30 April 2014
Published: 23 May 2014
Tamoxifen, an agonist of estrogen receptor, is widely prescribed for the prevention and long-term treatment of breast cancer. A side effect of tamoxifen is fatty liver, which increases the risk for non-alcoholic fatty liver disease. Prevention of tamoxifen-induced fatty liver has the potential to improve the safety of long-term tamoxifen usage.
Uridine, a pyrimidine nucleoside with reported protective effects against drug-induced fatty liver, was co-administered with tamoxifen in C57BL/6J mice. Liver lipid levels were evaluated with lipid visualization using coherent anti-Stokes Raman scatting (CARS) microscopy, biochemical assay measurement of triacylglyceride (TAG), and liquid chromatography coupled with mass spectrometry (LC-MS) measurement of membrane phospholipid. Blood TAG and cholesterol levels were measured. Mitochondrial respiration of primary hepatocytes in the presence of tamoxifen and/or uridine was evaluated by measuring oxygen consumption rate with an extracellular flux analyzer. Liver protein lysine acetylation profiles were evaluated with 1D and 2D Western blots. In addition, the relationship between endogenous uridine levels, fatty liver, and tamoxifen administration was evaluated in transgenic mice UPase1 −/−and UPase1-TG.
Uridine co-administration prevented tamoxifen-induced liver lipid droplet accumulation in mice. The most prominent effect of uridine co-administration with tamoxifen was the stimulation of liver membrane phospholipid biosynthesis. Uridine had no protective effect against tamoxifen-induced impairment to mitochondrial respiration of primary hepatocytes or liver TAG and cholesterol export. Uridine had no effect on tamoxifen-induced changes to liver protein acetylation profile. Transgenic mice UPase1 −/−with increased pyrimidine salvage activity were protected against tamoxifen-induced liver lipid droplet accumulation. In contrast, UPase1-TG mice with increased pyrimidine catabolism activity had intrinsic liver lipid droplet accumulation, which was aggravated following tamoxifen administration.
Uridine co-administration was effective at preventing tamoxifen-induced liver lipid droplet accumulation. The ability of uridine to prevent tamoxifen-induced fatty liver appeared to depend on the pyrimidine salvage pathway, which promotes biosynthesis of membrane phospholipid.
KeywordsCoherent anti-Stokes Raman scattering microscopy Drug-induced fatty liver Lipidomics Membrane phospholipid Mitochondrial respiration Protein lysine acetylation Pyrimidine Tamoxifen Triacylglyceride Uridine phosphorylase
Tamoxifen is an effective drug widely used for the treatment of estrogen receptor-positive breast cancer . Women taking tamoxifen from 5 to 10 years exhibit reduced risks of breast cancer recurrence and mortality [2, 3]. While generally well-tolerated, tamoxifen is known to induce fatty liver in 43% of women within the first 2 years of treatment [4–6]. Fatty liver is an established risk factor for non-alcoholic fatty liver disease (NAFLD) . Prolonged tamoxifen treatment increases the risk of NAFLD, particularly in women with pre-existing metabolic condition .
The mechanism underlying tamoxifen-induced fatty liver is a topic of active investigation. Evidence from several independent research groups supports tamoxifen-induced impairment of mitochondrial fatty acid oxidation (FAO) as a primary cause of lipid accumulation in the liver [9–11]. Co-administration of tetradecylthioacetic acid, which improves mitochondrial and peroxisomal FAO, prevents tamoxifen-induced fatty liver . Tamoxifen also inhibits hepatic triacylglyceride secretion leading to liver lipid accumulation [10, 11]. Therapeutic intervention to prevent tamoxifen-induced fatty liver condition has the potential to improve the safety of long-term tamoxifen usage for breast cancer treatment.
In this study, we examine the effects of uridine co-administration with tamoxifen on liver lipid content in control C57BL/6J and transgenic UPase1 −/−and UPase1-TG mice. Specifically, we examine the contribution of pyrimidine salvage and catabolism pathways to the biological activity of uridine. We aim to explore therapeutic potential of uridine for the prevention of drug-induced fatty liver and biological action of uridine on liver lipid metabolism.
All animal studies were performed with the ethical approval of the Animal Care and Use Committees at Nevada Cancer Institute, Desert Research Institute, and Touro University Nevada. All experiments conducted on animals were in compliance with the guidelines of the U.S. Office of Laboratory Animal Welfare of the National Institutes of Health and the Public Health Service Policy on Humane Care and Use of Laboratory Animals.
Three mice strains were used, C57BL/6J or wildtype mice (Jackson Laboratories, Bar Harbor, ME), UPase1-TG mice with ubiquitous genetic knock-in of uridine phosphorylase 1 , and UPase1 −/−mice with ubiquitous genetic knock-out of uridine phosphorylase 1 . Transgenic mice described in this study have been deposited into the Mutant Mouse Regional Resource Centers supported by the National Institutes of Health. The MMRRC strains are now known as B6;129-Upp1 tm1Gp /Mmucd (037119-UCD) for UPase1 −/−mice and B6; FVB-Gt (ROSA) 26Sor tm1.1(CAG-Upp1)Gp /Mmucd (037120-UCD) for UPase1-TG mice. All mice used were female at 10–12 weeks of age with average bodyweight of approximately 20 grams.
All mice were randomly divided into groups of 4 or 5 mice per cage and housed in a controlled environment with an average temperature of 22°C, a 12 hours of light and 12 hours of dark cycle, and with ad libitum access to food and water. For control C57BL/6J mice, 36 mice were randomly divided into 4 experimental groups of 9 mice per group: control diet (C57BL/6J), diet supplemented with uridine (C57BL/6J + U), diet supplemented with tamoxifen (C57BL/6J + Tmx), and diet supplemented with both tamoxifen and uridine (C57BL/6J + Tmx + U). For transgenic UPase1 −/−and UPase1-TG mice, 18 mice per strain were randomly divided into the following 4 experimental groups of 9 mice per group: UPase1 −/−mice on control diet (UPase1 −/−), UPase1 −/−mice on tamoxifen-supplemented diet, UPase1-TG mice on control diet (UPase1-TG), and UPase1-TG mice on tamoxifen-supplemented diet. In addition, 6 C57BL/6J mice were used for primary hepatocyte collection for bioenergetics experiments. The number of mice per experimental group was chosen to ensure that data obtained were statistically significant.
Control mice were fed with PicoLab Mouse Diet ground pellets (Cat. No. 5058, LabDiet, Brentwood, MO) that provide 4.6 kcal/g and consist of 22% protein and 9% fat. The lipid composition includes cholesterol (200 ppm), linoleic acid (2.32%), linolenic acid (0.21%), arachidonic acid (0.02%), and omega-3 fatty acid (0.32%). The total saturated and monounsaturated fatty acids are 2.72% and 2.88%, respectively. For mice receiving uridine supplementation alone, uridine was thoroughly mixed with ground pellets with a dosage of 400 mg/kg/day. For mice receiving tamoxifen treatment alone, tamoxifen was thoroughly mixed with ground pellets with a dosage of 200 mg/kg/day. For mice receiving both uridine and tamoxifen, uridine and tamoxifen were thoroughly mixed with ground pellets with a dosage of 400 mg/kg/day and 200 mg/kg/day, respectively. Mice were placed on control or supplemented diets for 5 days prior to terminal liver and blood samples collection. All samples were collected in early mornings. Blood samples were collected via the tail veins while mice were under anesthesia with isoflurane. Liver tissues were collected following cardiac perfusion under deep anesthesia with isoflurane. Cardiac perfusion was necessary to ensure collection of pure liver tissues devoid of blood and plasma contaminants. Mice were anaesthetized and incisions were made from the abdomen up to the torso. Diaphragms were severed and 22 gauge needles were inserted into the left ventricles. Phosphate buffered saline (PBS) was used as the perfusate. Approximately 50–100 ml of PBS was flushed through each mouse from the left ventricle and exited through the incision made to the right atrium. Following the perfusion procedure, liver tissues were collected for immediate usage or frozen in liquid nitrogen for future usage.
CARS imaging of liver tissues
A home-built CARS microscope was used to image lipid using CH2 vibrational frequency at 2851 cm−1 as described previously . Approximately 31 frames were taken along the vertical axis at 1-micron increment for volumetric evaluation of liver lipid content. Liver lipid level was the square root of resonant CARS signal intensity, which is the difference between total CARS signal intensity and CARS signal intensity arising from cellular membrane and non-resonant signal [21–23]. Liver lipid level was normalized to 1 for control wildtype mice and respectively for other mice strains or treatment conditions. Quantitative analysis of liver lipid level was performed using the NIH ImageJ software. Liver was perfused with PBS prior to collection. Liver tissues were sliced into 200-micron thick sections, transferred into glass-bottom chambered slides, overlaid with 200 microliter of 1% agarose, and imaged with CARS microscopy. On average, 9 imaging volumes were analyzed with CARS microscopy per liver sample. The xyz dimensions of each analysis volume were 167 μm × 167 μm × 30 μm. Nine liver samples from nine mice were used for CARS imaging analysis per animal group.
Biochemical measurement of liver triacylglyceride (TAG)
Liver samples of equal weight were used for chloroform/methanol total lipid extraction. TAG was determined using the commercial TAG quantitation kit (Cat. No. 10010303, Cayman Chemical, Ann Arbor, MI) according to manufacturer’s protocol and normalized with liver tissue weight. Nine liver samples from nine mice were used for biochemical TAG measurement per animal group.
1D Western blots
Total liver protein extracts were separated on 10% SDS-PAGE gels, transferred to nitrocellulose membranes, incubated first with primary antibodies against proteins of interest and then with secondary antibodies conjugated with horseradish peroxidase (Cat. No. 31460, Thermo Scientific, Rockford, IL). Membrane was developed with enhanced chemiluminescence reagents (Cat. No. 34075, Thermo Scientific), stripped, and re-incubated with antibodies against β-actin for evaluation of loading controls. Primary antibodies against acetylated lysine and β-actin were from Cell Signaling (Cat. No. 9441 & 4967, Danvers, MA).
2D Western blots
2D Western blots were performed by Kendrick Laboratories (Madison, WI). Approximately 500 μg of protein from each liver tissue was loaded per gel. Proteins were separated using isoelectric focusing (IEF) in the first dimension and SDS polyacrylamide gel electrophoresis (SDS-PAGE) in the second dimension. Primary and secondary antibodies were the same as in 1D Western blot. Molecular weight standards were: myosin (220,000), phosphorylase A (94,000), catalase (60,000), actin (43,000) carbonic anhydrase (29,000) and lysozyme (14,000) (Sigma Chemical Co., St. Louis, MO).
Bioenergetics of primary hepatocytes
Immediately after isolation, primary hepatocytes were plated into 24-well plates at a density of 1 × 105 cell per well. Plating media was consisted of DMEM with 25 mM glucose, 2 mM glutamine, 10% FBS, 0.1 mM sodium pyruvate, 1% Pen/Strep, and 1 mM HEPES at pH 7.4. At 4 hours after plating, primary hepatocytes were incubated for 24 hours with either uridine alone, tamoxifen alone, or a combination of tamoxifen and uridine depending on the treatment condition. The final concentration used for uridine was 100 μM and tamoxifen was 10 μM. At 90 minutes prior to assaying, plating media was replaced with Cellular Assay Solution consisting of DMEM, 25 mM glucose, 2 mM glutamine, 1 mM sodium pyruvate and adjusted to pH 7.2 with 25 mM of MOPS. Bioenergetics of primary hepatocytes were determined using the XF Cell Mito Stress Test Kit and a XF24-3 Analyzer (Seahorse Bioscience, North Billerica, MA) following manufacturer’s suggested protocols and published protocols . Bioenergetics experiments were performed at the UCLA’s Cellular Bioenergetics Core Facilities. At least 24 repeated measurements were performed per experimental condition. Final concentrations of oligomycin, FCCP, rotenone, and myxothiazol were 1 μg/ml, 1 μM, 0.1 μM, and 2 μM, respectively. Oxygen consumption rates were reported as absolute values (pmol O2 consumed per minute) on a per-unit of protein basis, where average protein concentration per well was normalized to 1.
Clinical blood lipid analysis
Analysis of blood lipid level (TAG, cholesterol, HDL, and LDL) were performed by Research Animal Diagnostic Laboratory (RADIL, Columbia, MO) on terminally collected blood samples of 6 mice per animal group. HDL and LDL were determined via direct measurement.
Measurement of phospholipid with LC-MS
Total liver lipid extracts of 6 mice per animal group were sent to Kansas Lipidomics Research Center (Kansas State University, Manhattan, KS) for LC-MS analysis of phospholipid species. Concentrations of phospholipid are expressed as nmol per mg of dried liver lipid weight.
Data were presented as average values ± standard deviations. Statistical analysis was performed using Excel’s paired Student’s t-test and analysis of variance (ANOVA) functions. Statistical significance was set at p ≤ 0.05.
Results and discussion
Tamoxifen treatment is associated with reduced liver secretion of TAG and cholesterol [10, 11]. To determine if uridine co-administration with tamoxifen could improve liver secretion of TAG and cholesterol, blood lipid profiles were evaluated (Figure 4B). Consistent with the literature, tamoxifen treatment caused reduction of blood TAG and cholesterol levels. Uridine treatment by itself had no effect on blood TAG and cholesterol levels. Neither could uridine co-administration prevent tamoxifen-induced reduction of blood TAG and cholesterol levels. Thus, there was no evidence to support a role of uridine in reversing tamoxifen-induced suppression of liver secretion of TAG and cholesterol.
Liver phospholipid species quantified with LC-MS
Phospholipid species (nmol/mg)
C57BL/6J + U
C57BL/6J + Tmx
C57BL/6J + Tmx + U
6.7 ± 0.7
7.1 ± 0.3
7.4 ± 0.4
8.6 ± 0.8*
380.5 ± 51
486.8 ± 20*
421.9 ± 30.6
495.1 ± 39.6*
Sphingomyelin & dihydrosphingomyelin
29.1 ± 3.7
40.0 ± 2.8*
50.3 ± 3.9*
50.2 ± 3.7*
18.9 ± 2.2
18.5 ± 0.6
21.2 ± 1.4
22.5 ± 2.1
1.9 ± 0.1
2.3 ± 0.26
2.1 ± 0.2
2.6 ± 2.1
105.5 ± 8.9
140.1 ± 8.8*
149.2 ± 8.3*
165.6 ± 8.9*
0.01 ± 0.01
0.01 ± 0.01
0.016 ± 0.005
0.027 ± 0.013
4.0 ± 0.4
4.5 ± 0.3
4.5 ± 0.3
5.6 ± 0.4*
51.2 ± 6.9
60.0 ± 7.1
46.9 ± 3.7
58.4 ± 6.2
15.4 ± 0.8
22.3 ± 1.1*
25.4 ± 1.3*
28.2 ± 1.3*
0.2 ± 0.03
0.3 ± 0.03*
0.36 ± 0.017*
0.4 ± 0.04*
19.9 ± 2.3
23.2 ± 2.4
15.2 ± 1.7
21.2 ± 1.4
27.2 ± 3.1
29.9 ± 2.7
33.0 ± 2.1
29.7 ± 2.2
In this study, we report that uridine co-administration is effective at completely preventing intracellular lipid droplet accumulation in the liver tissues of mice treated with tamoxifen. To examine the roles of uridine in the prevention of tamoxifen-induced fatty liver, several aspects of liver energy metabolism perturbed by tamoxifen were evaluated. Tamoxifen administration was associated with an increased in acetylation of a protein band at 80 kD and impaired mitochondrial respiration; however, both of these tamoxifen-induced effects could not be reversed by uridine co-administration. Neither could uridine prevent tamoxifen-induced reduction in blood TAG and cholesterol levels. Surprisingly, both uridine and tamoxifen when administered alone and together increased membrane phospholipid biosynthesis. The synthesis of phosphatidylcholine (PC), the key component of phospholipid, was dependent on the availability of diacylglycerol (DAG) and cytidine diphosphocholine (CDPC) (Figure 1) . It is possible that tamoxifen-induced lipid accumulation in liver tissues made TAG and DAG to be readily available for PC synthesis. Uridine salvage into CTP promoted CDPC synthesis, which together with DAG availability stimulated PC synthesis. Transgenic mice UPase1 −/−with increased uridine salvage into CTP were protected against tamoxifen-induced fatty liver. In contrast, UPase1-TG mice with overt catabolism of uridine had intrinsic fatty liver phenotype, which was aggravated following tamoxifen treatment. In summary, uridine co-administration was able to prevent tamoxifen-induced intracellular lipid droplet accumulation, but not able to prevent other side effects associated with tamoxifen treatment such as impaired mitochondrial respiration and reduced TAG and cholesterol export. A plausible means that uridine prevented tamoxifen-induced fatty liver was via the pyrimidine salvage pathway, which channeled neutral lipid into phospholipid biosynthesis and reduced cytoplasmic lipid accumulation.
A previous study on the anti-proliferative effect of tamoxifen in human MCF-7 breast cancer cells proposed that tamoxifen prevented DNA synthesis by blocking uridine transport, thus, inhibiting the pyrimidine salvage pathway . In our study, C57BL/6J mice with dietary uridine supplementation or UPase1 −/−mice with elevated endogenous uridine levels both had enhanced pyrimidine salvage activity . Both mice strains were resistant to tamoxifen-induced fatty liver; however, they exhibited weight loss following tamoxifen treatment. In addition, uridine supplementation in primary hepatocyte cultures could not prevent tamoxifen-induced impairment to mitochondrial respiration. Our observation indicates that tamoxifen exert inhibitory effects beyond the pyrimidine salvage pathway. Indeed, tamoxifen has been shown to directly intercalate mitochondrial DNA (mtDNA) and impair mtDNA synthesis and mitochondrial respiration . It is unlikely that uridine can prevent the interaction of cationic tamoxifen with mtDNA, hence, its inability to suppress the inhibitory effects of tamoxifen on mitochondrial function.
The balance between purine and pyrimidine nucleotides is critical for the maintenance of genomic stability and regulation. A surge in uridine concentration subsequently leads to a rise in pyrimidine nucleotides and perturbs the balance of the nucleotide pool . Therefore, an adaptive mechanism must be in place to cope with excessive uridine concentration. In rodents, most tissues rely on the plasma for uridine supply . The circulating uridine concentration is tightly regulated by the liver, where plasma uridine is cleared in a single pass and replaced with newly synthesized uridine . Hence, the liver effectively serves as a regulator of uridine homeostasis. Rapid clearance of uridine in the liver involves both uridine salvage and catabolism, where uridine metabolites affect other cellular processes in a non-specific manner. Multi-targeted effects are evident by the ability of uridine to prevent fatty liver caused by different drugs with vastly different acting mechanisms [13, 14]. Multi-targeted effects pose a challenge for precise therapeutic targeting using uridine. However, uridine homeostasis is regulated by uridine phosphorylase . The enzymatic activity of uridine phosphorylase has been modulated by pharmaceutical compounds to prevent toxicity associated with 5-fluorouracil treatment of cancer . Modulation of uridine phosphorylase enzymatic activity is a possible means to achieve precise therapeutic targeting of uridine for the prevention of drug-induced fatty liver.
Coherent anti-Stokes Raman scattering
Liquid chromatography coupled with mass spectrometry
Oxygen consumption rate
This work was partially supported by the Nevada INBRE Program of the National Center for Research Resources (P20RR-016464, TTL), the Vons Breast Cancer Research Award (GP & TTL) and the American Cancer Society (IRG-08-062-04, TTL). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors thank Laurent Vergnes (UCLA) and Robert Kirsh (DRI) for help with some experiments.
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