Open Access

Liver X receptor agonist treatment attenuates cardiac dysfunction in type 2 diabetic db/db mice

  • Qing He1,
  • Jun Pu1Email author,
  • Ancai Yuan1,
  • Tianbao Yao1,
  • Xiaoying Ying1,
  • Yichao Zhao1,
  • Longwei Xu1,
  • Huan Tong1 and
  • Ben He1
Cardiovascular Diabetology201413:149

https://doi.org/10.1186/s12933-014-0149-0

Received: 27 May 2014

Accepted: 20 October 2014

Published: 22 November 2014

Abstract

Background

Liver X receptor (LXR) plays a critical regulatory role in metabolism and inflammation, and has been demonstrated to be involved in cardiovascular physiology/pathology. In the present study, we investigated the effect of GW3965, a potent LXR agonist, on diabetic cardiomyopathy (DCM) in type 2 diabetic db/db mice.

Methods and Results

Non-diabetic db/+ mice and diabetic db/db mice received either vehicle or LXR agonist GW3965 for 12 weeks. Systemic insulin resistance was evaluated by glucose tolerance test and homeostasis model assessment for insulin resistance. Endpoint cardiac function was assessed by echocardiography and catheterization. Ventricular tissue was collected for histology and gene/protein expression analysis. Untreated db/db diabetic mice exhibited diastolic dysfunction with adverse structural remodeling (including myocardial fibrosis and increased apoptosis). Treatment with GW3965 remarkably attenuated myocardial dysfunction and structural remodeling in diabetic db/db mice. Mechanistically, GW3965 restored Akt phosphorylation and inhibited MAP kinases phosphorylation, and reduced oxidative/nitrative stress and inflammation response in the diabetic myocardium.

Conclusions

Our data demonstrate that GW3965 exerts a cardioprotective effect against DCM by (at least in part) attenuating insulin resistance, modulating Akt and MAP kinases pathways, and reducing oxidative/nitrative stress and inflammatory response. These findings strongly suggest that LXR agonist may have therapeutic potential in treating DCM.

Keywords

Liver X receptor Diabetic cardiomyopathy Insulin resistance Antioxidant

Background

The incidence and prevalence of diabetes mellitus are growing rapidly in societies around the world. Type 2 diabetes mellitus (T2DM) accounts for 90-95% of all diagnosed diabetes in adults [1]. Growing evidence has shown that diabetes mellitus, independent from other risk factors such as coronary artery disease and hypertension, can affect cardiac structure and function, which supports the existence of diabetic cardiomyopathy (DCM) [2]. As an independent diabetic cardiac complication, DCM is defined as diabetes-caused pathologic abnormalities including myocardial metabolic disturbance, oxidative/nitrative stress, inflammation, cardiomyocyte apoptosis, left ventricular dysfunction and structural remodeling [3]. Although treatment for DCM including improving glycemic control and restoring cardiovascular function is currently available to diabetic patients in clinical practice, therapeutic outcomes are far from satisfactory and the incidence of diabetes-induced cardiac dysfunction continues to escalate [3],[4]. Thus, there is a great medical need to develop novel pharmacological or molecular interventions to treat left ventricular dysfunction and remodeling in DCM.

Liver X receptors (LXRs), including two different but highly homologous LXR isoforms (LXRα and LXRβ), are ligand-activated transcriptional factors belonging to the nuclear receptor superfamily [5]. LXRα is highly expressed in metabolically active tissues, such as liver, kidney, adipose, and intestines. LXRβ is ubiquitously expressed throughout the body [5]. Recently, by regulating metabolic and inflammatory pathways, LXR has been considered as a potential pharmacological target in the pathogenesis of cardiovascular and metabolic diseases [6]. Two synthetic LXR agonists, GW3965 and T0901317, have been reported to prevent atherosclerosis, inhibit inflammation, attenuate myocardial hypertrophy, and reduce ischemia/reperfusion injury [7]-[11]. Moreover, activation of LXR by T0901317 mitigates high glucose-induced oxidative stress, and apoptosis in cardiomyocytes in vitro[12]. However, the potential of LXR activation to attenuate the structural and functional defects caused by DCM in vivo have not been investigated. Therefore, the aims of the current study were to 1) investigate whether the LXR agonist GW3965 can protect the diabetic heart against adverse changes using the db/db mouse model of T2DM; and 2) clarify the downstream signaling mediating its effect in DCM.

Materials and methods

Reagents and antibodies

Synthetic LXR ligand 3-[3-[N-(2-Chloro-3-trifluoromethylbenzyl)-(2,2-diphenylethyl) amino] propyloxy] phenylacetic acid hydrochloride (GW3965) was kindly donated by Jon Collins (GlaxoSmithKline, Research Triangle Park, NC). Dihydroethidium (DHE) and TRIzol Reagent were from Life Technologies (Carlsbad, CA). Mouse monoclonal antibody against LXRα (ab41902) and rabbit polyclonal antibody against LXRβ (ab28479) were from Abcam (Cambridge, UK); Rabbit anti-mouse nitrotyrosine antibody (06-284) was from Millipore (Billerica, MA); rabbit anti-cleaved caspase-3 (5A1E, #9664), rabbit anti-nuclear factor kappa-light-chain-enhancer of activated B cell p65 (NF-κB p65, C22B4; #4764), rabbit anti-Akt (#9272), rabbit anti-phospho-Akt (D9E, Ser473, #4060), rabbit anti-p38 mitogen-activated protein kinase (p38 MAPK, #9212), rabbit anti-phospho-p38 MAPK (D3F9, Thr180/Tyr182, #4511), rabbit anti-c-Jun N-terminal kinase (JNK, 56G8, #9258), rabbit anti-phospho-JNK (81E11, Thr183/Tyr185, #4668), rabbit anti-Histone H3 (#9715) and rabbit anti-glyceraldehyde-3-phosphate dehydrogenase (GAPDH, 14C10, #2118) were from Cell Signaling Technology (Beverly, MA). IRDye 800CW goat anti-mouse (926-32210) and anti-rabbit IgG (926-32211) secondary antibodies were from LI-COR Biosciences (Lincoln, NE).

Animals and treatment

Experimental protocols complied with the National Institutes of Health Guidelines on the Use of Laboratory Animals, and were approved by the Institute’s Animal Ethics Committee. Male diabetic (db/db) mice and their non-diabetic littermates (db/+) were obtained from the SLAC Experimental Animal Center (Shanghai, China) and were housed at 22 ±  ± 1°C, adherent to a 12 hour light-dark cycle. All the animals were provided with food and water ad libitum. At 8 weeks of age, the db/+ and db/db mice were randomized into four groups: (1) control db/+ mice (db/+); (2) db/+ mice + GW3965 (db/+ GW); (3) db/db mice (db/db); (4) db/db mice + GW3965 (db/db GW). The mice were treated with GW3965 (20 mg/kg intraperitoneally) or vehicle daily for 12 weeks prior to sacrifice and tissue collection. GW3965 at this dose, which was chosen based upon our pilot study data and the published literature [11],[13],[14], GW3965 at this dose effectively invokes LXR activity without inducing observable hemodynamic changes in animal studies [11],[13],[14]. After 12 weeks, animals were subjected to hemodynamic measurements (described below), and hearts were excised and snap-frozen in liquid nitrogen for biochemical determinations, or fixed in formalin for histological evaluations. At the endpoint, mice were fasted overnight and serum samples were collected. Plasma glucose, total cholesterol (TC), and serum triglyceride (TG) were determined by an auto-biochemical analysis system (Chemix-180, Sysmex, Japan).

Western blot analysis

Proteins were prepared per standard protocol, and protein lysate concentrations were determined via Pierce BCA Protein Assay Kit (Thermo Scientific, Rockford, IL). To prepare the nuclear or cytosolic fractions, protein lysate was collected via NE-PER Nuclear Protein Extraction Kit (Thermo Scientific). Equal quantities of proteins (30-50 μg/lane) were subjected to 10 or 12% SDS-PAGE, dependent upon the target proteins, electrotransferred onto nitrocellulose membranes, and incubated with primary antibodies against LXRα (1:1000), LXRβ (1:1000), cleaved caspase-3 (1:1000), NF-κB p65 (1:1000), Akt (1:1000), phospho-Akt (1:1000), p38 MAPK (1:1000), phospho-p38 MAPK (1:1000), JNK (1:1000) and phospho-JNK (1:1000). GAPDH and Histone levels were utilized as loading controls for total and nuclear protein expression, respectively. After incubation with the corresponding secondary antibodies, protein bands were detected by an Odyssey® IR scanner (LI-COR Biosciences, Lincoln, NE). Quantitation was performed via Quantity One 4.4.0 software (Bio-Rad, Hercules, CA).

Real-time quantitative PCR

Total RNA was isolated from tissues with TRIzol Reagent and purified with Qiagen’s RNeasy Mini Kit (Qiagen, Hilden, Germany). Reverse transcription was performed by Omniscript RT Kit (Qiagen). The resultant cDNA was amplified by SYBR ® Premix Ex Taq ™ Perfect Real Time Kit (Takara BIO, Otsu, Japan). The PCR reaction was directly monitored by The LightCycler® 480 Real-Time PCR System (Roche Applied Science, Indianapolis, IN). Real-time PCR primers used were as follows: mouse LXRα (GenBank Accession No. NM001177730 and NM013839), forward 5′-GCTCATTGCCATCAGCATC-3′ and reverse 5′-AGCATCCGTGGGAACATCA-3′; mouse LXRβ (GenBank Accession No. NM009473 and XM_001002072), forward 5′-TGCCAGGGTTCTTGCAGTTG-3′ and reverse 5′-AACGTGATGCATTCTGTCTCGTG-3′; mouse transforming growth factor beta1 (TGF- β1) (GenBank Accession No. NM_011577), forward 5′-TACGGCAGTGGCTGAACCAA-3′ and reverse 5′-CGGTTCATGTCATGGATGGTG-3′; mouse collagen, type I, alpha 1 (collagen 1A1) (GenBank Accession No. NM_007742), forward 5′-CACCTACAGCACCCTTGTGG-3′ and reverse 5′-GGGAGGTCTTGGTGGTTTTG-3′; mouse nicotinamide adenine dinucleotide phosphate oxidase gp91phox subunit (NADPH oxidase gp91phox subunit) (GenBank Accession No. NM_007807), forward 5′-TGATCCTGCTGCCAGTGTGTC-3′ and reverse 5′-GTGAGGTTCCTGTCCAGTTGTCTTC-3′; mouse inducible nitric oxide synthase (iNOS) (GenBank Accession No. NM_010927), forward 5′-CAAGCTGAACTTGAGCGAGGA-3′ and reverse 5′-TTTACTCAGTGCCAGAAGCTGGA-3′; mouse GAPDH (GenBank Accession No. BC083149), forward 5′- TGGCACAGTCAAGGCTGAGA-3′ and reverse 5′-CTTCTGAGTGGCAGTGATGG-3′. Real-time PCR data were represented as Ct values, defined as the crossing threshold of PCR, obtained via LightCycler 480 Data Analysis software. The fold change in the sample gene expression was calculated after adjusting for GAPDH using the 2 –ΔΔCt method [15].

Glucose Tolerance Test (GTT) and Homeostasis Model Assessment for Insulin Resistance (HOMA-IR)

Briefly, mice were fasted overnight (14-16 h). GTT was performed as described previously [16],[17]. Glucose solution was administered via an intraperitoneal injection at a dose of 2 g/kg body weight, and the blood glucose level was measured from tail snipping at 0, 30, 60, 90, and 120 min after the initial glucose loading. Blood glucose level was determined using a One-Touch Profile portable blood glucose monitor (Roche, Mannheim, Germany). The area under the curve of the glucose concentrations (AUCg) was calculated. Serum insulin was measured by ELISA (Millipore, Billerica, MA) [18]. HOMA-IR was calculated using the following formula: HOMA-IR (mmol/L  ×  μ U/mL) = fasting glucose (mmol/L) × fasting insulin (μU/mL) /22.5 [18].

In situ detection of apoptosis in heart tissue

Myocardial apoptosis was determined by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) technique via an In Situ Cell Death Detection Kit (Roche Diagnostics) as described previously [19],[20]. Results were expressed as the percentage of apoptotic cells among the total cell population.

Detection of caspase-activity in heart tissue

Cardiac caspase-3 activity was measured via caspase-3 Colorimetric Assay Kit (Millipore, Billerica, MA) as previously described [15],[21],[22]. Briefly, 100 μg of total protein from tissues was loaded and incubated with 25 μg Ac-DEVD-pNA as a colorimetric-specific substrate at 37°C for 1.5 hours. Then, pNA cleaved from DEVD by caspase-3 was quantified by a microplate reader (BioTek, Winooski, VT) at 405 nm. Changes of caspase-3 activity in db/db tissue samples were calculated and compared with the mean value from control db/+ mice tissue. Data were expressed as nmol pNA /h /mg protein.

Hemodynamic measurements

Left ventricular hemodynamics was evaluated after 12 weeks by catheterization as previously described [23]. In brief, a micromanometer-tipped catheter (1.4 F, SPR 835; Millar Instruments, Houston, TX) was inserted through the right carotid artery into the aorta of an anaesthetized mouse and carefully introduced into the left ventricle (LV). The transducer was connected to a Power Laboratory system (AD Instruments, Castle Hill, New South Wales, Australia) and variables derived from catheterization included maximal ascending and descending rates of left ventricular pressure (±dP/dt), left ventricular end-systolic pressure (LVSP), left ventricular end-diastolic pressure (LVEDP), and heart rate.

Echocardiographic measurements

At 20 weeks of age, mice were anaesthetized with 1.5% isoflurane, and two-dimensional echocardiographic views of the mid-ventricular short axis were obtained at the level of the papillary muscle tips below the mitral valve (Vevo 770, VisualSonic, Toronto, Canada). Variables measured on M-mode echocardiography including LV wall thickness, LV chamber dimensions, and systolic and diastolic function were analyzed as described previously [24].

Sirius red staining

LV myocardial sections were stained with 0.1% picric sirius red (Sigma-Aldrich, St Louis, MO) for fibrosis detection, as previously described [25]. The severity of cardiac fibrosis was evaluated after sirius red staining at 20 ×  μmagnification with the use of Image-pro plus 6.1 software (Media Cybernetics, Bethesda, MD). Collagen-positive area was normalized to the total cross-sectional area of left ventricle and was expressed as a percentage. Areas containing blood vessels and perivascular interstitial cells were excluded from fibrosis quantification [26].

Measurement of oxidative stress generation in heart tissue

Myocardial reactive oxygen species (ROS) generation was measured by confocal microscope via in situ DHE stain or lucigenin-enhanced chemiluminescence. For DHE stain, unfixed frozen cross-sections (5 μm) was incubated with DHE (5 μmol/L) at 37°C for 30 minutes in a humidified chamber protected from light, followed by 5 minutes of PBS washing to remove non-intercalated ethidium bromide molecules. Images were obtained and analyzed via Leica laser scanning confocal microscope (Leica TCS SP5 II). NADPH oxidase activity within the heart homogenates was measured by lucigenin-enhanced chemiluminescence via luminometer as previously described [11],[21],[22]. The lucigenin concentration in the final reaction mixture was 0.25 mmol/L, and NADPH-dependent superoxide production was expressed as relative light units (RLU) per mg per second (RLU • mg-1 • s-1).

Determination of nitrative stress generation in heart tissue

Myocardial reactive nitrative stress (RNS) was assessed by nitrotyrosine content, a footprint of in vivo peroxynitrite formation [11],[21],[22], by both immunostaining and enzyme-linked immunosorbent assay (ELISA). For immunostaining, paraffin-embedded slices were stained with primary antibody against nitrotyrosine (1:100), and then immunostained by Vectastain ABC kit (Vector Laboratories, Burlingame, CA; 1:200). For ELISA, cardiac tissue nitrotyrosine content was quantified by Nitrotyrosine ELISA Kit (Abnova, Taiwan). Results were expressed as nanomoles/g protein.

Assessment of inflammatory cytokines in cardiac tissue

Tumor necrosis factor alpha (TNF-α) and interleukin 1-beta (IL-1β) were quantified using an ELISA kit (Invitrogen, Camarillo, CA) per manufacturer’s instructions. The tissue supernatant fluids were added to each well, and treated with detection antibody, supplemented with substrate and stop solution. TNF-α and IL-1β levels were determined by microplate reader (450 nm).

Statistical analysis

All values in the text and figures are presented as the mean ± SEM of independent experiments from given n-sizes. Statistical significance of multiple treatments was determined by one-way analysis of variance (ANOVA) followed by Tukey’s post hoc analysis using GraphPad Prism 5 software (San Diego, California). Probabilities of 0.05 or less were considered to be statistically significant (2-tailed).

Results

Both LXRα and LXRβ are expressed in adult heart tissue, but LXRα is selectively upregulated by hyperglycemia in db/db mice

Both LXRα and LXRβ subtypes were detected in cardiac tissue, as demonstrated by both Western blot (Figure 1a) and real-time PCR (Figure 1b). Interestingly, endogenous LXRα protein level significantly increased in the db/db and db/db GW group, whereas LXRβ expression remained mostly unaffected.
Figure 1

LXRs expression in cardiac tissue. a-b. LXRα and LXRβ expression in cardiac tissue from db/+, db/+ GW, db/db and db/db GW mice were determined by Western blot and real-time PCR (n =5-6). **P < 0.01 vs db/+ group. Abbreviations: GW, GW3965.

LXR agonist GW3965 attenuates the phenotype of type 2 diabetes in db/db mice

We first investigated whether the activation of LXR could suppress hyperglycemia and other metabolic abnormalities in diabetic mice. As illustrated in Table 1, the db/db group weighed more than the db/+ group, and demonstrated derangements of serum metabolic markers such as glucose, TC and TG. Chronic treatment of 8-week-old male diabetic db/db mice with LXR agonist GW3965 lowered body weight, blood glucose levels, and plasma TC levels. However, GW3965 showed no influence on the increased plasma TG level in diabetic mice. These findings indicate that LXR activation by GW3965 improved the metabolic disorders in this mouse model of T2DM.
Table 1

GW3965 attenuated diabetes-induced metabolism abnormalities

Group

Body weight

Blood glucose

TC

TG

(g)

(mmol/L)

(mmol/L)

(mmol/L)

db/+

27.84 ± 0.52

7.00 ± 0.53

2.08 ± 0.04

0.89 ± 0.02

db/+ GW

27.76 ± 0.60

5.30 ± 0.56

2.13 ± 0.13

0.97 ± 0.02

db/db

54.85 ± 0.70*

19.93 ± 1.56*

4.31 ± 0.15*

1.56 ± 0.04*

db/db GW

45.28 ± 0.66* #

7.00 ± 0.97 #

2.91 ± 0.13* #

1.71 ± 0.04*

Fasting blood glucose, TC, TG levels and body weight were all measured on the day of animal sacrifice. Data are means ± SEM; *P < 0.05 vs db/+ group; # P < 0.05 vs db/db group; n =8-10. Abbreviations: GW GW3965, TC total cholesterol, TG triglycerides.

LXR agonist GW3965 improves glucose tolerance and insulin sensitivity in db/db mice

We next tested the effect of LXR agonist on insulin resistance in db/db diabetic mice. At 20 weeks of age, there were no statistically significant differences in the GTT, the AUCg and HOMA-IR index between the db/+ and db/+ GW group (Figure 2). However, the levels of GTT, AUCg, and HOMA-IR index were markedly deteriorated in db/db diabetic mice, which were significantly reversed by the administration of GW3965 for 12 weeks (Figure 2).
Figure 2

GW3965 improved glucose tolerance and insulin sensitivity in db/db mice. a-b. GTT was performed at baseline and 12 weeks after treatment with GW3965 (n =7-9). c-d. Area under the curve of glucose levels during the GTT were also calculated (n =7-9 per group). e. HOMA-IR index was detected (n =7-9). **P < 0.01 vs db/+ group; ##P < 0.01 vs db/db group. Abbreviations: GTT, glucose tolerance test; GW, GW3965; HOMA-IR, homeostasis model assessment for insulin resistance.

LXR agonist GW3965 inhibits myocardial apoptosis and cardiac dysfunction in db/db mice

In an attempt to determine the cardioprotective role of LXR agonist, we investigated the effects of GW3965 on cellular apoptosis and cardiac function in type 2 diabetic db/db mice. Our results demonstrated that compared with the db/+ group, db/db mice clearly showed more TUNEL-positive particles (Figure 3, a and b), increased cleaved caspase-3 expression, enhanced caspase-3 activity (Figure 3, c and d) in cardiomyocytes, and deteriorated left ventricular dysfunction (Figure 4). GW3965 treatment significantly decreased cardiomyocyte apoptosis and improved cardiac function (Figures 3 and 4).
Figure 3

GW3965 inhibited diabetes-induced myocardial apoptosis. a. Representative image of TUNEL immunostaining. Left panel: 20 ×μmagnification, scale bar 100 μm. Right panel: TUNEL stain of box of left panel; 40 ×μmagnification, scale bar 25 μm. TUNEL positive cells were brown. b. The percentage of TUNEL positive cells was calculated. c-d. Myocardial apoptosis was determined by Western blot analysis of cleaved caspase-3 (n =5-6) and quantification of caspase-3 activation (n =6-10). *P < 0.05 or **P < 0.01 vs db/+ group; #P < 0.05 or ##P < 0.01 vs db/db group. Abbreviations: GW, GW3965; TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labeling; cas-3, caspase-3.

Figure 4

GW3965 limited diabetes-induced left ventricular dysfunction. a-f. Left ventricular function was assessed via echocardiography and cardiac catheterization in anesthetized mice (n =6-8). **P < 0.01 vs db/+ group; #P < 0.05 or ##P < 0.01 vs db/db group. Abbreviations: GW, GW3965; ±dP/dt, maximal ascending and descending rates of LV pressure; LVSP, left ventricular systolic pressure; LVEDP, left ventricular end-diastolic pressure; LVEF, left ventricular ejection fraction.

LXR agonist GW3965 reduces cardiac fibrosis in db/db mice

By sirius red staining, we found that db/db mice exhibited more severe cardiac fibrosis than the control group (Figure 5, a and b). This induction of fibrosis was significantly ameliorated after GW3965 treatment for 12 weeks (Figure 5, a and b). Moreover, real-time PCR analysis revealed significant increases in the expression of profibrotic genes (TGF-β1 and collagen-1A1) in diabetic hearts, which were attenuated by GW3965 (Figure 5, c and d).
Figure 5

GW3965 reduced diabetes-induced cardiac fibrosis. a. Representative image of Sirius Red-stained LV sections, 20 ×μmagnification. b. Pooled data on quantification of collagen area per visual field (n =8-9). c-d. TGF-β1 and collagen 1A1 gene expression was determined by real-time PCR. Results were normalized against GAPDH and converted to fold induction relative to db/+ mice (n =6). *P < 0.05 or **P < 0.01 vs db/+ group; #P < 0.05 or ##P < 0.01 vs db/db group. Abbreviations: GW, GW3965; LV, left ventricle; TGF-α1, transforming growth factor beta1; collagen 1A1, collagen, type I, alpha 1.

LXR agonist GW3965 attenuates myocardial oxidative stress and nitrative stress in db/db mice

To further determine the underlying mechanisms of LXR agonist’s protective action, we investigated the effects of GW3965 on oxidative/nitrative stress in the diabetic myocardium. GW3965 significantly attenuated ROS production in db/db mice (Figure 6, a and b) and inhibited the expression of the NADPH oxidase subunit gp91phox (Figure 6c). Moreover, GW3965 significantly reduced tissue nitrotyrosine content (a well-accepted footprint of in vivo nitrative stress, Figure 6, d and e), and inhibited iNOS expression (Figure 6f). Collectively, these results demonstrate that GW3965 attenuated diabetes-induced oxidative/nitrative stress.
Figure 6

GW3965 attenuated diabetes-induced myocardial oxidative/nitrative stress. a-c. GW3965 attenuated oxidative stress in the myocardial tissues. a. Myocardial oxidative stress was measured by confocal microscopy with in situ dihydroethidium stain (n =5-6, scale bar 25 μm). b. NADPH oxidase activity was determined by lucigenin-enhanced chemiluminescence (n =6-11). c. NADPH oxidase gp91phox gene expression was determined by real-time PCR (n =6). Results were normalized against GAPDH and converted to fold induction relative to db/+ mice. d-f. GW3965 attenuated nitrative stress in the myocardial tissues. d. Myocardial nitrative stress was assessed via nitrotyrosine levels determined by immunohistochemistry (n =5-6, scale bar 25 μm). e. Myocardial nitrotyrosine content was determined by ELISA analysis (n =6-11). f. iNOS gene expression was determined by real-time PCR (n =6). Results were normalized against GAPDH and converted to fold induction relative to db/+ mice. *P < 0.05 or **P < 0.01 vs db/+ group; #P < 0.05 or ##P < 0.01 vs db/db group. Abbreviations: GW, GW3965; RLU, relative light units; iNOS, inducible nitric oxide synthase.

LXR agonist GW3965 suppresses diabetes-induced myocardial nuclear factor-κB activation and inflammation

To investigate whether LXR agonist provided cardioprotection by inhibiting the inflammatory response in the diabetic myocardium, we investigated the effect of GW3965 on inflammatory cytokine production. Protein levels of NF-κB p65 were markedly increased in the myocardium of db/db mice (Figure 7a). The expression of proinflammatory cytokines, including TNF- α and IL-1β, was significantly augmented in db/db mice (Figure 7, b and c). Furthermore, treatment with GW3965 significantly decreased nuclear NF-κB p65 expression and proinflammatory cytokine (TNF- α and IL-1β) levels in db/db mice (Figure 7). These results indicate that the anti-inflammatory effects of LXR agonist contribute to cardioprotection against DCM.
Figure 7

GW3965 suppressed diabetes-induced inflammatory response in the myocardial tissues. a. Expression of nuclear NF-κB p65 subunit in the myocardial tissue was determined by Western blot (n =5-6). Histone level served as loading control for nuclear protein expression. Results were normalized against histone and converted to fold induction relative to db/+ mice. b-c. TNF- α and IL-1β content in the myocardial tissue was determined by ELISA analysis (n =6-8). **P < 0.01 vs db/+ group; #P < 0.05 or ##P < 0.01 vs db/db group. Abbreviations: GW, GW3965; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B; TNF- α, tumor necrosis factor-α; IL-1β, interleukin-1β.

LXR agonist GW3965 ameliorates the impairment of insulin/Akt signaling pathway and mitigates diabetes-induced activation of MAP kinases

To further investigate the cellular mechanisms by which LXR activation may attenuate diabetes-induced insulin resistance and cardiac oxidative stress, we evaluated insulin/Akt signaling and MAPK pathways, which are the most important pathways involved in insulin resistance and oxidative/nitrative stress. Serine phosphorylation of Akt (serine 473) was impaired in the myocardium of db/db mice. However, 12-week treatment with GW3965 significantly restored Akt activation in db/db mice (Figure 8a). Likewise in diabetic myocardium, an increase in the activation of p38 MAPK (Figure 8b) and JNK (Figure 8c) could be observed. Treatment with GW3965 significantly inhibited diabetes-induced p38 MAPK and JNK phosphorylation without altering their protein levels (Figure 8, b and c). These data suggest that LXR activation alleviated DCM mainly by modulating Akt and MAP kinases pathways in type 2 diabetes.
Figure 8

GW3965 differentially regulated Akt and MAP kinases activation. a-c. Western blot analysis shows the phosphorylation and protein expression of Akt, p38 MAPK and JNK expression in the myocardial tissues (n =5-6). **P < 0.01 vs db/+ group; #P < 0.05 vs db/db group. Abbreviations: GW, GW3965; p38 MAPK, p38 mitogen-activated protein kinase; JNK, c-Jun N- terminal kinase.

Discussion

The major findings emanating from the current study are as follows: (1) Both LXRα and LXRβ subtypes were detected in adult cardiac tissue, but LXRα was selectively upregulated by hyperglycemia; (2) GW3965 ameliorated metabolism and improved glucose tolerance and insulin sensitivity; (3) GW3965 protected the heart in the db/db mouse model of type 2 diabetes from the development of diastolic dysfunction, cell death, and cardiac fibrosis; and (4) GW3965 also restored Akt phosphorylation and inhibited MAP kinases phosphorylation, and reduced oxidative/nitrative stress and inflammation response in the diabetic myocardium. Taken together, these results suggest that LXR agonist GW3965 may have great therapeutic potential in the treatment of DCM.

Originally cloned from a rat liver cDNA library and identified as an orphan nuclear hormone receptor [27], LXR is highly expressed in the enterohepatic tissue, playing a pivotal role in cholesterol and lipid metabolism, glucose homeostasis, and inflammatory response [5]. Recent evidence suggests the presence of LXR in the cardiovascular system and its significant role in cardiovascular physiology/pathology [8]-[11]. In the myocardium, the expression of LXRα was increased in streptozotocin-induced diabetic rats [28]. LXR agonist T0901317 attenuated high glucose-induced cardiomyocyte apoptosis in vitro[12]. However, the role of LXR in DCM in vivo remains unknown. To the best of our knowledge, the current study provides the first direct evidence demonstrating that GW3965 protects cardiomyocytes against hyperglycemia-induced chronic adverse changes in vivo. These data support the notion that LXR agonist may serve as a novel therapeutic modality in the management of DCM.

Hyperglycemia and insulin resistance have long been considered a central component in the pathogenesis of DCM [29],[30]. In insulin resistance states, impaired myocardial glucose uptake has been shown to provoke myocardial dysfunction [31]. In addition, insulin resistance independently predicts mortality in diabetic patients with heart failure [3]. Multiple lines of evidence have indicated that LXR is an important regulator of glucose metabolism in different animal models of T2DM. Previous studies showed that pharmacologic LXR activation by GW3965 improved glucose tolerance by limiting hepatic glucose output and improving peripheral glucose uptake in a murine model of diet-induced obesity and insulin resistance [32]. Moreover, LXR agonist GW3965 reduced blood glucose concentrations and improved insulin sensitivity in ob/ob mice [33]. The results of the present study further demonstrated that the LXR agonist GW3965 ameliorates systemic insulin resistance and myocardial dysfunction in a db/db murine model.

Hyperglycemia and insulin resistance contribute to the generation of excessive ROS/RNS which have damaging effects on myocardial function. Hyperglycemia enhances glucose oxidation and mitochondrial generation of ROS, which has been implicated as a key stimulator of these cardiac impairments [24],[34],[35]. Meanwhile, NO is overproduced by activated iNOS, reacts with ROS, and turns into the highly reactive ONOO- (RNS). ROS/RNS trigger myocardial apoptosis, and damage the mitochondrial membrane, leading to a “ROS-induced ROS release” vicious cycle, which further worsens myocardial damage and dysfunction [3],[36]. Because of these roles of ROS/RNS, reducing oxidative/nitrative stress should be favored in the management of DCM. In this report, we demonstrate that long-term administration of GW3965 significantly decreased the expression of myocardial NADPH oxidase, as well as superoxide production and tissue nitrotyrosine content (the footprint of in vivo nitrative stress). Furthermore, we showed that GW3965 treatment inhibited the downstream inflammatory response (i.e., activation of nuclear NF-κB and pro-inflammatory cytokines) in diabetic myocardium in vivo. Thus, inhibiting ROS/RNS and inflammatory pathways could be an important mechanism responsible for LXR agonist-mediated cardioprotection against DCM.

There is accumulating evidence that in the setting of type 2 diabetes, insulin resistance and ROS/RNS may be coconspirators in cardiac dysfunction, each capable of triggering or worsening the other [37]. The insulin-Akt signaling and MAPK are the most important pathways involved in insulin resistance and oxidative stress [38]. It has been demonstrated the synthetic LXR agonists ameliorated insulin resistance by restoring the insulin-Akt signalling cascade and preventing JNK activation in adipocytes [39],[40]. In the current study, the insulin-Akt pathway was blunted, compared with the activated MAPK pathway in the myocardium of db/db mice. Treatment with GW3965 restored Akt activation and inhibited MAP kinases phosphorylation in the diabetic myocardium, suggesting that differential regulation of Akt and MAP kinases activation are likely responsible for the aforementioned cardioprotective effects of the LXR agonist against DCM; further studies are warranted to define in more detail the complex mechanisms involved in regulation of oxidative stress, inflammatory response, and the cardioprotective effect of GW3965.

Conclusion

Our data demonstrate that the LXR agonist GW3965 exerts a protective effect on DCM by (at least in part) attenuating insulin resistance, modulating Akt and MAP kinases pathways, and reducing oxidative/nitrative stress and inflammatory response (Figure 9). LXR, therefore, is a potentially attractive molecular target for the treatment of DCM.
Figure 9

Proposed scheme for the cardioprotective effect of LXR agonist GW3965 against DCM. Abbreviations: MAPK, mitogen-activated protein kinase; ROS, reactive oxygen species; RNS, reactive nitrative stress; DCM, diabetic cardiomyopathy.

Authors’ contributions

All authors fulfill the criteria for authorship. JP, BH and QH conceived and designed the study. QH and ACY carried out the experiments and interpreted the results. TBY, YXY, YCZ, LWX and HT assisted in conducting the experiments and analyzed the data. QH and JP wrote the manuscript. JP and QH edited the text and Figures during assembly and finalization of the manuscript. All authors read and approved the final version of the manuscript.

Abbreviations

AUCg: 

Area under the curve of the glucose concentrations

DCM: 

Diabetic cardiomyopathy

DHE: 

Dihydroethidium

±dP/dt: 

Ascending and descending rates of left ventricular pressure

ELISA: 

Enzyme-linked immunosorbent assay

GLUT4: 

Glucose transporter 4

HOMA-IR: 

Homeostasis model assessment- insulin resistance

GAPDH: 

Glyceraldehyde-3-phosphate dehydrogenase

GTT: 

Glucose tolerance test

IL-1β: 

Interleukin 1-beta

iNOS: 

Inducible nitric oxide synthase

JNK: 

c-Jun N-terminal kinase

LV: 

Left ventricle

LVEF: 

Left ventricular ejection fraction

LVEDP: 

Left ventricular end-diastolic pressure

LVSP: 

Left ventricular end-systolic pressure

LXR: 

Liver X receptor

MAP: 

Kinase (MAPK) mitogen-activated protein kinase

NADPH: 

Oxidase nicotinamide adenine dinucleotide phosphate oxidase

NF- κB: 

Nuclear factor kappa-light-chain-enhancer of activated B

p38 MAPK: 

p38 mitogen-activated protein kinase

RLU: 

Relative light units

RNS: 

Reactive nitrogen species

ROS: 

Reactive oxygen species

T2DM: 

Type 2 diabetes mellitus

TC: 

Total cholesterol

TG: 

Triglyceride

TGF-β1: 

Transforming growth factor beta1

TNF-α: 

Tumor necrosis factor alpha

TUNEL: 

Terminal transferase dUTP nick end labeling

Declarations

Acknowledgements

This work was supported by grants from the National Natural Science Foundation of China (81330006, 81170192, 81470389, 81270282, 81070176, and 81200163 to B.H., J.P., and Q.H.), Key Basic Research Program of Shanghai Committee of Science and Technology (14JC1404500 to J.P.), Program for New Century Excellent Talents from Ministry of Education of China (NCET-12-0352 to J.P.), Shanghai Shuguang Program (12SG22 to J.P.), International Cooperation Program of Shanghai Committee of Science and Technology (12410708300 to J.P.), and Foundation of Shanghai Jiao Tong University (YG2013MS42 and YG2012MS07 to J.P. and A.Y.).

Authors’ Affiliations

(1)
Department of Cardiology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University

References

  1. Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Franco S, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Huffman MD, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Magid D, Marcus GM, Marelli A, Matchar DB, McGuire DK, Mohler ER, Moy CS, Mussolino ME: American Heart Association Statistics Committee and Stroke Statistics Subcommittee: Executive summary: heart disease and stroke statistics-2013 update: a report from the American Heart Association. Circulation. 2013, 127: 143-152. 10.1161/CIR.0b013e318282ab8f.View ArticlePubMedGoogle Scholar
  2. Bugger H, Abel ED: Molecular mechanisms of diabetic cardiomyopathy. Diabetologia. 2014, 57: 660-671. 10.1007/s00125-014-3171-6.PubMed CentralView ArticlePubMedGoogle Scholar
  3. Huynh K, Bernardo BC, McMullen JR, Ritchie RH: Diabetic cardiomyopathy: mechanisms and new treatment strategies targeting antioxidant signaling pathways. Pharmacol Ther. 2014, 142: 375-415. 10.1016/j.pharmthera.2014.01.003.View ArticlePubMedGoogle Scholar
  4. Battiprolu PK, Lopez-Crisosto C, Wang ZV, Nemchenko A, Lavandero S, Hill JA: Diabetic cardiomyopathy and metabolic remodeling of the heart. Life Sci. 2013, 92: 609-615. 10.1016/j.lfs.2012.10.011.PubMed CentralView ArticlePubMedGoogle Scholar
  5. Calkin AC, Tontonoz P: Transcriptional integration of metabolism by the nuclear sterol-activated receptors LXR and FXR. Nat Rev Mol Cell Biol. 2012, 13: 213-224.PubMed CentralPubMedGoogle Scholar
  6. Im SS, Osborne TF: Liver x receptors in atherosclerosis and inflammation. Circ Res. 2011, 108: 996-1001. 10.1161/CIRCRESAHA.110.226878.PubMed CentralView ArticlePubMedGoogle Scholar
  7. Giannarelli C, Cimmino G, Connolly TM, Ibanez B, Ruiz JM, Alique M, Zafar MU, Fuster V, Feuerstein G, Badimon JJ: Synergistic effect of liver X receptor activation and simvastatin on plaque regression and stabilization: an magnetic resonance imaging study in a model of advanced atherosclerosis. Eur Heart J. 2012, 33: 264-273. 10.1093/eurheartj/ehr136.View ArticlePubMedGoogle Scholar
  8. Wu S, Yin R, Ernest R, Li Y, Zhelyabovska O, Luo J, Yang Y, Yang Q: Liver X receptors are negative regulators of cardiac hypertrophy via suppressing NF-kappaB signalling. Cardiovasc Res. 2009, 84: 119-126. 10.1093/cvr/cvp180.PubMed CentralView ArticlePubMedGoogle Scholar
  9. Kuipers I, Li J, Vreeswijk-Baudoin I, Koster J, der Harst PV, Sillje HH, Kuipers F, van Veldhuisen DJ, van Gilst WH, de Boer RA: Activation of liver X receptors with T0901317 attenuates cardiac hypertrophy in vivo. Eur J Heart Fail. 2010, 12: 1042-1050. 10.1093/eurjhf/hfq109.View ArticlePubMedGoogle Scholar
  10. Lei P, Baysa A, Nebb HI, Valen G, Skomedal T, Osnes JB, Yang Z, Haugen F: Activation of Liver X receptors in the heart leads to accumulation of intracellular lipids and attenuation of ischemia-reperfusion injury. Basic Res Cardiol. 2013, 108: 323-10.1007/s00395-012-0323-z.View ArticlePubMedGoogle Scholar
  11. He Q, Pu J, Yuan A, Lau WB, Gao E, Koch W, Ma XL, He B: Activation of LXRα but not LXRβ protects against myocardial ischemia/reperfusion injury.Circ Heart Fail in press.Google Scholar
  12. Cheng Y, Feng Y, Zhu M, Yan B, Fu S, Guo J, Hu J, Song X, Guo S, Liu G: Synthetic liver X receptor agonist T0901317 attenuates high glucose-induced oxidative stress, mitochondrial damage and apoptosis in cardiomyocytes. Acta Histochem. 2014, 116: 214-221. 10.1016/j.acthis.2013.07.007.View ArticlePubMedGoogle Scholar
  13. Morales JR, Ballesteros I, Deniz JM, Hurtado O, Vivancos J, Nombela F, Lizasoain I, Castrillo A, Moro MA: Activation of liver X receptors promotes neuroprotection and reduces brain inflammation in experimental stroke. Circulation. 2008, 118: 1450-1459. 10.1161/CIRCULATIONAHA.108.782300.View ArticlePubMedGoogle Scholar
  14. Leik CE, Carson NL, Hennan JK, Basso MD, Liu QY, Crandall DL, Nambi P: GW3965, a synthetic liver X receptor (LXR) agonist, reduces angiotensin II-mediated pressor responses in Sprague-Dawley rats. Br J Pharmacol. 2007, 151: 450-456. 10.1038/sj.bjp.0707241.PubMed CentralView ArticlePubMedGoogle Scholar
  15. Pu J, Yuan A, Shan P, Gao E, Wang X, Wang Y, Lau WB, Koch W, Ma XL, He B: Cardiomyocyte-expressed farnesoid-X-receptor is a novel apoptosis mediator and contributes to myocardial ischaemia/reperfusion injury. Eur Heart J. 2013, 34: 1834-1845. 10.1093/eurheartj/ehs011.PubMed CentralView ArticlePubMedGoogle Scholar
  16. Bindom SM, Hans CP, Xia H, Boulares AH, Lazartigues E: Angiotensin I-converting enzyme type 2 (ACE2) gene therapy improves glycemic control in diabetic mice. Diabetes. 2010, 59: 2540-2548. 10.2337/db09-0782.PubMed CentralView ArticlePubMedGoogle Scholar
  17. Hsu FL, Huang CF, Chen YW, Yen YP, Wu CT, Uang BJ, Yang RS, Liu SH: Antidiabetic effects of pterosin A, a small-molecular-weight natural product, on diabetic mouse models. Diabetes. 2013, 62: 628-638. 10.2337/db12-0585.PubMed CentralView ArticlePubMedGoogle Scholar
  18. Xiong WT, Gu L, Wang C, Sun HX, Liu X: Anti-hyperglycemic and hypolipidemic effects of Cistanche tubulosa in type 2 diabetic db/db mice. J Ethnopharmacol. 2013, 150: 935-945. 10.1016/j.jep.2013.09.027.View ArticlePubMedGoogle Scholar
  19. Lu D, Lian H, Zhang X, Shao H, Huang L, Qin C, Zhang L: LMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic mice. PLoS One. 2010, 5: e15167-10.1371/journal.pone.0015167.PubMed CentralView ArticlePubMedGoogle Scholar
  20. Pu J, Mintz GS, Biro S, Lee JB, Sum ST, Madden SP, Burke AP, Zhang P, He B, Goldstein JA, Stone GW, Muller JE, Virmani R, Maehara A: Insights into echo-attenuated plaques, echolucent plaques, and plaques with spotty calcification: novel findings from comparisons among intravascular ultrasound, near-infrared spectroscopy, and pathological histology in 2,294 human coronary artery segments. J Am Coll Cardiol. 2014, 63: 2220-2233. 10.1016/j.jacc.2014.02.576.View ArticlePubMedGoogle Scholar
  21. Wang Y, Gao E, Tao L, Lau WB, Yuan Y, Goldstein BJ, Lopez BL, Christopher TA, Tian R, Koch W, Ma XL: AMP-activated protein kinase deficiency enhances myocardial ischemia/reperfusion injury but has minimal effect on the antioxidant/antinitrative protection of adiponectin. Circulation. 2009, 119: 835-844. 10.1161/CIRCULATIONAHA.108.815043.PubMed CentralView ArticlePubMedGoogle Scholar
  22. Tao L, Gao E, Jiao X, Yuan Y, Li S, Christopher TA, Lopez BL, Koch W, Chan L, Goldstein BJ, Ma XL: Adiponectin cardioprotection after myocardial ischemia/reperfusion involves the reduction of oxidative/nitrative stress. Circulation. 2007, 115: 1408-1416. 10.1161/CIRCULATIONAHA.106.666941.View ArticlePubMedGoogle Scholar
  23. Choudhary R, Palm-Leis A, Scott RC, Guleria RS, Rachut E, Baker KM, Pan J: All-trans retinoic acid prevents development of cardiac remodeling in aortic banded rats by inhibiting the rennin-angiotensin system. Am J Physiol Heart Circ Physiol. 2008, 294: H633-H644. 10.1152/ajpheart.01301.2007.View ArticlePubMedGoogle Scholar
  24. Rajesh M, Mukhopadhyay P, Bátkai S, Patel V, Saito K, Matsumoto S, Kashiwaya Y, Horváth B, Mukhopadhyay B, Becker L, Haskó G, Liaudet L, Wink DA, Veves A, Mechoulam R, Pacher P: Cannabidiol attenuates cardiac dysfunction, oxidative stress, fibrosis, and inflammatory and cell death signaling pathways in diabetic cardiomyopathy. J Am Coll Cardiol. 2010, 56: 2115-2125. 10.1016/j.jacc.2010.07.033.PubMed CentralView ArticlePubMedGoogle Scholar
  25. Junqueira LC, Bignolas G, Brentani RR: Picrosirius staining plus polarization microscopy, a specific method for collagen detection in tissue sections. Histo chem J. 1979, 11: 447-455. 10.1007/BF01002772.View ArticleGoogle Scholar
  26. Schunke KJ, Coyle L, Merrill GF, Denhardt DT: Acetaminophen attenuates doxorubicin-induced cardiac fibrosis via osteopontin and GATA4 regulation: reduction of oxidant levels. J Cell Physiol. 2013, 228: 2006-2014. 10.1002/jcp.24367.PubMed CentralView ArticlePubMedGoogle Scholar
  27. Apfel R, Benbrook D, Lernhardt E, Ortiz MA, Salbert G, Pfahl M: A novel orphan receptor specific for a subset of thyroid hormone-responsive elements and its interaction with the retinoid/thyroid hormone receptor subfamily. Mol Cell Biol. 1994, 14: 7025-7035.PubMed CentralView ArticlePubMedGoogle Scholar
  28. Cheng Y, Liu G, Pan Q, Guo S, Yang X: Elevated expression of liver X receptor alpha (LXRα) in myocardium of streptozotocin-induced diabetic rats. Inflammation. 2011, 34: 698-706. 10.1007/s10753-010-9281-5.View ArticlePubMedGoogle Scholar
  29. Mencarelli A, Cipriani S, Renga B, D'Amore C, Palladino G, Distrutti E, Baldelli F, Fiorucci S: FXR activation improves myocardial fatty acid metabolism n a rodent model of obesity-driven cardiotoxicity. Nutr Metab Cardiovasc Dis. 2013, 23: 94-101. 10.1016/j.numecd.2011.06.008.View ArticlePubMedGoogle Scholar
  30. Lee JE, Yi CO, Jeon BT, Shin HJ, Kim SK, Jung TS, Choi JY, Roh GS: α-Lipoic acid attenuates cardiac fibrosis in Otsuka Long-Evans Tokushima Fatty rats. Cardiovasc Diabetol. 2012, 11: 111-10.1186/1475-2840-11-111.PubMed CentralView ArticlePubMedGoogle Scholar
  31. Mellor KM, Ritchie RH, Delbridge LM: Reactive oxygen species and insulin-resistant cardiomyopathy. Clin Exp Pharmacol Physiol. 2010, 37: 222-228. 10.1111/j.1440-1681.2009.05274.x.View ArticlePubMedGoogle Scholar
  32. Laffitte BA, Chao LC, Li J, Walczak R, Hummasti S, Joseph SB, Castrillo A, Wilpitz DC, Mangelsdorf DJ, Collins JL, Saez E, Tontonoz P: Activation of liver X receptor improves glucose tolerance through coordinate regulation of glucose metabolism in liver and adipose tissue. Proc Natl Acad Sci U S A. 2003, 100: 5419-5424. 10.1073/pnas.0830671100.PubMed CentralView ArticlePubMedGoogle Scholar
  33. Grefhorst A, van Dijk TH, Hammer A, van der Sluijs FH, Havinga R, Havekes LM, Romijn JA, Groot PH, Reijngoud DJ, Kuipers F: Differential effects of pharmacological liver X receptor activation on hepatic and peripheral insulin sensitivity in lean and ob/ob mice. Am J Physiol Endocrinol Metab. 2005, 289: E829-E838. 10.1152/ajpendo.00165.2005.View ArticlePubMedGoogle Scholar
  34. Dalen KT, Ulven SM, Bamberg K, Gustafsson JA, Nebb HI: Expression of the insulin-responsive glucose transporter GLUT4 in adipocytes is dependent on liver X receptor alpha. J Biol Chem. 2003, 278: 48283-48291. 10.1074/jbc.M302287200.View ArticlePubMedGoogle Scholar
  35. Devereux RB, Roman MJ, Paranicas M, O'Grady MJ, Lee ET, Welty TK, Fabsitz RR, Robbins D, Rhoades ER, Howard BV: Impact of diabetes on cardiac structure and function: the strong heart study. Circulation. 2000, 101: 2271-2276. 10.1161/01.CIR.101.19.2271.View ArticlePubMedGoogle Scholar
  36. Shan P, Pu J, Yuan A, Shen L, Shen L, Chai D, He B: RXR agonists inhibit oxidative stress-induced apoptosis in H9c2 rat ventricular cells. Biochem Biophys Res Commun. 2008, 375: 628-633. 10.1016/j.bbrc.2008.08.074.View ArticlePubMedGoogle Scholar
  37. Khullar M, Al-Shudiefat AA, Ludke A, Binepal G, Singal PK: Oxidative stress: a key contributor to diabetic cardiomyopathy. Can J Physiol Pharmacol. 2010, 88: 233-240. 10.1139/Y10-016.View ArticlePubMedGoogle Scholar
  38. Ti Y, Xie GL, Wang ZH, Bi XL, Ding WY, Wang J, Jiang GH, Bu PL, Zhang Y, Zhong M, Zhang W: TRB3 gene silencing alleviates diabetic cardiomyopathy in a type 2 diabetic rat model. Diabetes. 2011, 60: 2963-2974. 10.2337/db11-0549.PubMed CentralView ArticlePubMedGoogle Scholar
  39. Fernández-Veledo S, Nieto-Vazquez I, Rondinone CM, Lorenzo M: Liver X receptor agonists ameliorate TNFalpha-induced insulin resistance in murine brown adipocytes by downregulating protein tyrosine phosphatase-1B gene expression. Diabetologia. 2006, 49: 3038-3048. 10.1007/s00125-006-0472-4.View ArticlePubMedGoogle Scholar
  40. Fernández-Veledo S, Vila-Bedmar R, Nieto-Vazquez I, Lorenzo M: c-Jun N-terminal kinase 1/2 activation by tumor necrosis factor-alpha induces insulin resistance in human visceral but not subcutaneous adipocytes: reversal by liver X receptor agonists. J Clin Endocrinol Metab. 2009, 94: 3583-3593. 10.1210/jc.2009-0558.View ArticlePubMedGoogle Scholar

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