Journal of Diabetes Research

Journal of Diabetes Research / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 263845 |

Qian Cai, Baoying Li, Fei Yu, Weida Lu, Zhen Zhang, Mei Yin, Haiqing Gao, "Investigation of the Protective Effects of Phlorizin on Diabetic Cardiomyopathy in db/db Mice by Quantitative Proteomics", Journal of Diabetes Research, vol. 2013, Article ID 263845, 9 pages, 2013.

Investigation of the Protective Effects of Phlorizin on Diabetic Cardiomyopathy in db/db Mice by Quantitative Proteomics

Academic Editor: Subrata Chakrabarti
Received06 Nov 2012
Revised07 Jan 2013
Accepted08 Jan 2013
Published25 Feb 2013


Patients with diabetes often develop hypertension and atherosclerosis leading to cardiovascular disease. However, some diabetic patients develop heart failure without hypertension and coronary artery disease, a process termed diabetic cardiomyopathy. Phlorizin has been reported to be effective as an antioxidant in treating diabetes mellitus, but little is known about its cardioprotective effects on diabetic cardiomyopathy. In this study, we investigated the role of phlorizin in preventing diabetic cardiomyopathy in db/db mice. We found that phlorizin significantly decreased body weight gain and the levels of serum fasting blood glucose (FBG), triglycerides (TG), total cholesterol (TC), and advanced glycation end products (AGEs). Morphologic observations showed that normal myocardial structure was better preserved after phlorizin treatment. Using isobaric tag for relative and absolute quantitation (iTRAQ) proteomics, we identified differentially expressed proteins involved in cardiac lipid metabolism, mitochondrial function, and cardiomyopathy, suggesting that phlorizin may prevent the development of diabetic cardiomyopathy by regulating the expression of key proteins in these processes. We used ingenuity pathway analysis (IPA) to generate an interaction network to map the pathways containing these proteins. Our findings provide important information about the mechanism of diabetic cardiomyopathy and also suggest that phlorizin may be a novel therapeutic approach for the treatment of diabetic cardiomyopathy.

1. Introduction

The prevalence of diabetes mellitus is rapidly increasing worldwide [1]. Patients with diabetes often develop hypertension and atherosclerosis leading to cardiovascular complications. However, some diabetic patients develop heart failure without hypertension and coronary artery disease [2]. This phenomenon was first described by Rubler et al. and was termed “diabetic cardiomyopathy” [3]. Diabetic cardiomyopathy is characterized by structural and functional changes in the heart, such as elevated left ventricular (LV) mass, myocardial fibrosis, and abnormal diastolic function [4, 5]. However, the mechanistic details of diabetic cardiomyopathy remain unclear, and this disease has not yet been sufficiently studied.

Phlorizin (phloretin-2′-O-glucoside), a dihydrochalcone derived from apple peels, is a known antioxidant [6]. The main pharmacological property of phlorizin is to produce renal glycosuria and block intestinal glucose absorption through inhibition of sodium/glucose cotransporters in the kidney and intestine [7]. Although cardioprotective benefits of phlorizin have been reported, little is known about the effect of phlorizin on cardiac damage in type 2 diabetes mellitus (T2DM).

In this study, we used phlorizin to treat T2DM in db/db mice. These mice exhibit symptoms such as hyperglycemia, obesity, insulin resistance, and renal damage, which occurs after 10–20 weeks of sustained hyperglycemia [8, 9]. Additionally, we used a quantitative proteomic assay, isobaric tag for relative and absolute quantitation (iTRAQ), combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS) to identify and characterize the protein profiles of phlorizin-treated and untreated db/db mice. The iTRAQ technique has been widely used to tag peptides for multiplexed protein quantification and provides increased experimental throughput and lower variability [10, 11].

2. Materials and Methods

2.1. Experimental Animal Treatment

Male C57BLKS/J db/db and db/m mice ( , 7 weeks old) were purchased from the Model Animal Research Center at Nanjing University (Jiangsu, China). All mice were housed in wire-bottomed cages and received laboratory pellet chow and tap water ad libitum in a constant environment (room temperature °C, room humidity %) with a 12 h-light, 12 h-dark cycle. All experimental protocols were verified and approved by the Animal Ethics Committee of Shandong University. C57BLKS/J db/m mice were used as a control group, which were administered normal saline solution ( ). The db/db mice were randomly divided into two groups: the vehicle-treated diabetic group (DM, ), which were administered normal saline solution, and the phlorizin-treated diabetic group (DMT, ), which were treated with 20 mg/kg phlorizin. Phlorizin (purity >98%, Jianfeng Inc., Tianjin, China) was dissolved in normal saline solution and administered intragastrically from week 8 to week 18 without hypoglycemic therapy. Animals were weighed each week. At the end of the study, all mice were fasted overnight. Fasting blood was collected before sacrifice to measure fasting blood glucose (FBG), blood triglycerides (TG), and blood total cholesterol (TC) using an Automatic Biochemistry and Analysis Instrument (DVI-1650, Bayer, Germany). Specific fluorescence determinations of serum advanced glycation end products (AGEs) were performed using a fluorescence spectrophotometer (Hitachi F-2500, Japan) by measuring 440 nm emissions after excitation at 370 nm. The hearts of the mice were immediately dissected. Tissue and sera were kept at −80°C until further analysis.

2.2. Histological Examination and Ultrastructure Observation

The LV myocardium was fixed in 4% paraformaldehyde and embedded in paraffin. Five-millimeter-thick sections were cut, stained with hematoxylin-eosin (H&E), and examined by light microscopy. Additionally, part of the LV free wall was fixed in 3% glutaraldehyde. Ultrathin sections cut from embedded blocks were stained with uranyl acetate and lead citrate and examined with an H-800 electron microscope (Hitachi, Japan).

2.3. iTRAQ Proteomic Analysis

Heart tissue (50 mg) from each of four mice per group was prepared and digested with trypsin, as previously described [12]. A total of 60 μg of peptides from each group were labeled with iTRAQ reagents following the manufacturer’s instructions (Applied Biosystems). The control group peptides were labeled with Reagent 114; the DMT group, Reagent 116; and the DM group, Reagent 117. The labeled samples were then separated into 10 fractions using PolySULFOETHYL A strong cation-exchange (SCX) columns (4.6 × 100 mm 5 μ, 200 Å, PolyLC). Mass spectrometric analysis was performed using a micro-liquid chromatography system (MDLC, GE Healthcare, Pittsburgh, PA, USA) and an LTQ Velos ion trap mass spectrometer (ThermoFinnigan, San Jose, CA, USA).

2.4. Protein Pathway Analysis

Differentially expressed genes were analyzed using Ingenuity Pathway Analysis (IPA, Ingenuity Systems, The data packet containing the differentially expressed proteins identified in the iTRAQ experiment was converted by IPA to “fold change” and uploaded into IPA. Each identifier was mapped to its corresponding gene object in the Ingenuity Pathways Knowledge Base.

2.5. Western Blotting Analysis

Proteins were separated by SDS-polyacrylamide gel electrophoresis and transferred onto polyvinylidene difluoride membranes as previously described [13]. Membranes were subsequently probed with antibodies against calnexin (1 : 500 dilution, Abcam), integrin-linked protein kinase (1 : 1000 dilution, Santa Cruz Biotechnology), or GAPDH (1 : 5000 dilution, Santa Cruz Biotechnology) overnight at 4°C, which was then followed by incubation with secondary antibody for 2 h. The band intensity was quantified using VisionWorks LS image acquisition and analysis software (UVP, Upland, CA, USA).

2.6. Statistical Analysis

The data are presented as the mean ± standard deviation. Statistical comparisons among the three experimental groups were made using the unpaired Student’s t-test and one-way ANOVA. A value of was considered statistically significant.

3. Results

3.1. General Metabolic Parameters and AGEs

During the observation period, the DM and DMT groups gained substantially more weight than the control group. Nevertheless, phlorizin treatment significantly reduced body weight gain in db/db mice at the second week after phlorizin administration (Figure 1(a)). After 10 weeks, serum FBG, TG, and TC levels in the DM group were significantly higher than those in the control group. However, phlorizin treatment dramatically reduced these values in the DMT group compared with the DM group (Figures 1(b), 1(c), and 1(d)). In addition, db/db mice had significantly elevated serum AGE levels. After phlorizin treatment, AGE levels in db/db mice were reduced (Figure 2).

3.2. Histological and Ultrastructural Observation

On H&E-stained sections, the DM group exhibited significant myocardial hypertrophy and myofiber disarray accompanied by damaged nuclei and increased degeneration. However, phlorizin treatment attenuated this cardiomyocyte hypertrophy to a level similar to the control group (Figures 3(a), 3(b), and 3(c)).

Myocardial ultrastructure could be visualized by electron microscopy (Figures 4(a), 4(b), and 4(c)). In the control group, the myofibrils were arranged in a striated pattern, and the mitochondria were positioned in rows along the myofibrils. Although the sarcomere was of the same length, some cardiomyocyte mitochondria in the DM group showed cristae loss. Large areas of the myocardium exhibited a complete disruption of myofibril and mitochondrial arrangements. The shape of the nuclei was altered, and the nuclear membrane was disrupted. However, due to the protective effect of phlorizin in the DMT group, the number of degenerated mitochondria was significantly decreased, and the myofibril disorder was markedly attenuated.

3.3. iTRAQ Proteomics Profiling

Using the iTRAQ approach, we analyzed the effect of phlorizin on the myocardial protein profile of db/db mice. A total of 1627 proteins were identified. Of the 113 differentially expressed proteins, 29 were elevated in the DM group compared with the control group but were still decreased by phlorizin treatment. An additional 84 proteins were decreased in the DM group compared with the control group, but these were restored by the phlorizin treatment (see Supplementary Material available online at

We used IPA software to conduct gene ontology analysis and to classify the molecular functions of significantly altered proteins. Figure 5 shows the top-ranked biological functions, including lipid metabolism and energy production, which are biological processes altered during diabetic cardiomyopathy. The top protein network was generated by pathway analysis of differentially expressed proteins (Figure 6). There was a cluster of 35 proteins in the network, of which 24 are included on our list. These proteins are likely to be involved in biological processes such as lipid metabolism, mitochondrial function, and cardiomyopathy.

3.4. Functional Classification of Proteins Involved in Metabolic Disorders in db/db Mice Detected by iTRAQ
3.4.1. Altered Proteins in Cardiac Lipid Metabolism

Lipotoxicity occurring with T2DM and obesity impairs cardiac lipid metabolism [14]. The identified proteins associated with cardiac lipid metabolism are listed in Table 1. Proteins upregulated after phlorizin treatment included microsomal triglyceride transfer protein (Mttp), nicotinamide phosphoribosyltransferase (Nampt), tyrosine-protein phosphatase nonreceptor type 11 (Ptpn11), low-density lipoprotein receptor (LDLr), protein-tyrosine phosphatase-like member B (Ptplb), and sorbin and SH3 domain-containing protein 1 (Sorbs1). However, glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (Gpihbp1), which was initially identified as an HDL-binding protein involved in reversing cholesterol transport, was downregulated in the DMT group compared with the DM group.

Accession no.SymbolProtein nameMolecular weight (Da)PIiTRAQ ratio (DM/C)iTRAQ ratio (DMT/DM)

Cardiac lipid metabolism

IPI00785217LDLrLow-density lipoprotein receptor94947.384.820.223.05
IPI00943405MttpMicrosomal triglyceride transfer protein large subunit100750.947.510.41.83
IPI00655029Sorbs1Sorbin and SH3 domain-containing protein 1103977.895.650.461.83
IPI00320188NamptNicotinamide phosphoribosyltransferase55446.826.690.531.78
IPI00133956Gpihbp1Glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 124566.224.815.710.19
IPI00124411PtplbProtein-tyrosine phosphatase-like member B28402.439.590.233.95
IPI00316479Ptpn11Tyrosine-protein phosphatase nonreceptor type 1168034.756.870.162.95

Mitochondrial components and function

IPI00882331LiasLipoyl synthase, mitochondrial32173.88.482.630.49
IPI00128345Ndufs6NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial13019.788.860.591.55
IPI00114840EndogEndonuclease G, mitochondrial32190.749.560.391.78
IPI00336348Atpaf2ATP synthase mitochondrial F1 complex assembly factor 234287.296.351.680.65
IPI00276157Aifm2Apoptosis-inducing factor 241355.638.162.580.45
IPI00929796Prkaa25′-AMP-activated protein kinase catalytic subunit alpha-262022.377.940.431.81


IPI00896736ApcAdenomatosis polyposis coli310880.67.442.390.45
IPI00116668IlkIntegrin-linked protein kinase51373.
IPI00555015Myl2Myosin regulatory light chain 2, ventricular/cardiac muscle isoform18864.354.860.381.73
IPI00117846Dapk3Death-associated protein kinase 351421.98.910.332.45
IPI00222188Col1a2Collagen alpha-2(I) chain129556.979.270.172.05
IPI00620256LmnaIsoform A of Lamin-A/C74237.826.540.182.05
IPI00874362Lama2Laminin subunit alpha-2342781.065.780.321.51
IPI00420996Cacnb2Voltage-dependent L-type calcium channel subunit beta-264714.539.170.591.69

3.4.2. Altered Proteins Related to Myocardial Mitochondria

Diabetic cardiomyopathy is usually associated with abnormal energy production due to impaired mitochondrial function. We detected several proteins related to myocardial mitochondria (Table 1). Proteins that were significantly upregulated in the DMT group compared with the DM group include the following: 5′-AMP-activated protein kinase catalytic subunit alpha-2 (Prkaa2), endonuclease G (EndoG), and NADH dehydrogenase (ubiquinone) iron-sulfur protein 6 (Ndufs6). Other proteins such as apoptosis-inducing factor 2 (Atpaf2), ATP synthase mitochondrial F1 complex assembly factor 2 (Aifm2), and lipoic acid synthase (Lias) were significantly downregulated in the DMT group compared with the DM group.

3.4.3. Altered Proteins Involved in Cardiomyopathy

Several factors contribute to diabetic cardiomyopathy, including myocardial hypertrophy, elevated wall-thickness-to-chamber ratios, and increased stiffness of the LV wall [15]. We found that several proteins associated with cardiac contraction and diastolic function were decreased in the DM group and reversed after phlorizin treatment (Table 1). For example, the cytoskeletal protein titin (Ttn) and death-associated protein kinase 3 (DAPK3 or ZIPK) were upregulated in the DMT group compared with the DM group.

There were also some differentially expressed proteins on this list. Missense mutations or small deletions in some genes, for example, desmin (Des), integrin-linked protein kinase (Ilk), myosin regulatory light chain 2 (My12), dystrophin (Dmd), gelsolin (Gsn), lamin A/C (Lmna), and laminin subunit α-2 (Lama2), have been linked to cardiomyopathy. These proteins were upregulated in the DMT group compared with the DM group, indicating that diabetic cardiomyopathy improved after phlorizin treatment. We also listed the differentially expressed proteins involved in cardiac hypertrophy, including glutaredoxin-3 (Glrx3) and collagen alpha-2(I) chain (Col1a2). These proteins were upregulated in the DMT group compared with the DM group. Other important proteins involved in heart development and disease that were altered in db/db mice and reversed after phlorizin treatment include adenomatous polyposis coli (Apc), calnexin (Canx), myomesin-1 (Myom1), and voltage-dependent L-type calcium channel subunit beta-2 (Cacnb2).

3.5. Validation of iTRAQ Data for Selected Candidate Proteins

We selected two proteins for Western blot analysis to validate the iTRAQ data. As shown in Figure 7(a), calnexin was found to be decreased, whereas integrin-linked protein kinase was increased in the DMT group compared with the DM group. Quantification of band intensity showed that the results from density of bands are almost consistent with the iTRAQ data (Figure 7(b)). This indicates that the iTRAQ data are reliable.

4. Discussion

Diabetic cardiomyopathy accompanying T2DM is a complicated disorder caused by multifactorial pathology including altered cardiac energy metabolism and increased oxidative stress [16]. Obesity is associated with high levels of circulating fatty acids, which result in increased fatty acid uptake and TG accumulation in the myocardium. Furthermore, increased oxygen damage and generation of reactive oxygen species (ROS) augment cardiac damage [17]. Thus, the normalization of cardiac energy metabolism and reduction in oxidative stress may be important factors in the treatment of diabetic cardiomyopathy.

Phlorizin has been reported to have an antidiabetic effect due to its antioxidant properties [18]. In this study, we observed that the levels of serum FBG, TG, and TC in the DM group were dramatically elevated compared with the control group and that the oral administration of phlorizin significantly reduced these levels. These results suggest that phlorizin may be able to prevent diabetes and its complications by lowering blood FBG, TG, and TC levels.

Based on the iTRAQ data and the IPA results, protein expression involved in cardiac lipid metabolism seems to be markedly stimulated by phlorizin. In diabetic patients, elevated circulating fatty acids and TG, together with hyperinsulinemia, augment cardiac uptake of fatty acids and storage of TG [19, 20]. However, when fatty acid delivery overtakes the metabolic capacity of cardiomyocytes, impaired cardiac lipid homeostasis ultimately leads to lipotoxic cardiomyopathy [21]. Among the proteins related to cardiac lipid metabolism that we identified here, Mttp and Namtp deserve additional attention. Studies have shown that Mttp expression is increased in obese mouse hearts compared with healthy ones. Upregulation of cardiac Mttp expression prevents myocardial lipid accumulation when the supply of fatty acids exceeds the need for energy generation [22]. Namtp, also known as visfatin, is elevated in patients with T2DM, obesity, and cardiovascular disease. The elevated level of circulating visfatin may be associated with insulin resistance and metabolic syndrome [23]. Mttp and Namtp were both upregulated in the DMT group compared with the DM group, suggesting that phlorizin may modulate cardiac lipid metabolism by lowering the level of circulating fatty acids and attenuating cardiac lipid accumulation.

In a diabetic heart, glucose utilization is diminished. Instead, the heart relies almost exclusively on fatty acids for ATP generation. Increased fatty acid uptake by the heart reduces energy efficiency by inducing mitochondrial damage [16]. In this study, we identified several important proteins connected to mitochondrial structure and function. The altered expression of these proteins may cause deleterious effects on cells, resulting in cardiac energy deficit and cardiomyopathy. Here, we found that the phlorizin treatment reversed the expression of these proteins, suggesting a correlation between the cardioprotective effect of phlorizin and proteins involved in mitochondrial energy production.

Oxidative stress has been implicated in the pathogenesis of diabetes. A high rate of fatty acid oxidation also causes a pathological ROS accumulation, which leads to mitochondrial damage in cardiomyocytes [17]. Several factors contribute to ROS production in T2DM, such as AGEs [24]. In this study, we found that phlorizin treatment can significantly lower plasma AGE levels in db/db mice, which is consistent with its antioxidative ability to decrease ROS generation.

The development of diabetic cardiomyopathy has been divided into two phases: early metabolic alterations and later myocardial degenerative changes [25]. These irreversible pathological alterations include an increased stiffness of the LV wall, the accumulation of connective tissue and insoluble collagen, and abnormalities of various proteins [26]. Among the identified proteins that are involved in cardiac remodeling, titin was upregulated in the DMT group compared with the DM group. Recent observations have shown that the intrasarcomeric protein titin can alter myocardial diastolic stiffness through a number of different mechanisms such as isoform shifts, phosphorylation by protein kinase G or protein kinase A and titin-actin interactions at the Z-disc [27]. Another upregulated protein was Dapk3, also called ZIPK. Recent studies have identified smooth muscle myosin regulatory light chain and the regulatory subunit of the smooth muscle myosin light chain phosphatase as substrates for ZIPK [28]. This evidence suggests a key role for ZIPK in the regulation of cardiac contractility [29]. Here, our results demonstrate a cardioprotective role for phlorizin through the regulation of genes modulating cardiac contraction and diastolic function.

In conclusion, for the first time, the present study has established the quantitative iTRAQ profile of global cardiac proteins using a db/db diabetic mouse model treated with or without phlorizin. We found that phlorizin treatment may protect against diabetic cardiomyopathy by modulating cardiac lipid and energy metabolism and altering the expression of a set of proteins involved in cardiac damage. We also observed that phlorizin treatment significantly decreased body weight, blood glucose, blood TG, and blood TC. These findings suggest that, in the future, phlorizin may be utilized as a novel effective therapeutic approach for the treatment of diabetic cardiomyopathy.


The authors wish to thank the personnel at the Medical Science Academy of Shandong and the personnel at the Research Center for Proteome Analysis, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences. They thank Dr. Qing-song Liu in the Department of Pharmacology and Toxicology, Medical College of Wisconsin, for his invaluable assistance. They also thank Professor Jun-hui Zhen for her assistance. This work was supported by the National Natural Science Foundation of China (30873145, 81000340, and 81100595), a Shandong Province Outstanding Young Scientist Research Award Fund (BS2009YY046), the China Postdoctoral Science Foundation (20100471520, 2011M500748), and the Shandong Province Natural Science Foundation (Y2008C100, ZR2010HQ067).

Supplementary Materials

The description along with the Supplementary Material is as following: An accession no. is a unique identifier given to protein sequence when it is submitted to a sequence database. Theoretical molecular weight (Da) or PI are based on the amino acid sequence of the identified proteins.

  1. Supplementary Tables


  1. J. Stamler, O. Vaccaro, J. D. Neaton, and D. Wentworth, “Diabetes, other risk factors, and 12-yr cardiovascular mortality for men screened in the multiple risk factor intervention trial,” Diabetes Care, vol. 16, no. 2, pp. 434–444, 1993. View at: Google Scholar
  2. N. Sarwar, P. Gao, S. R. Seshasai et al., “Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies,” The Lancet, vol. 375, no. 9733, pp. 2215–2222, 2010. View at: Google Scholar
  3. S. Rubler, J. Dlugash, Y. Z. Yuceoglu, T. Kumral, A. W. Branwood, and A. Grishman, “New type of cardiomyopathy associated with diabetic glomerulosclerosis,” The American Journal of Cardiology, vol. 30, no. 6, pp. 595–602, 1972. View at: Google Scholar
  4. J. K. Boyer, S. Thanigaraj, K. B. Schechtman, and J. E. Pérez, “Prevalence of ventricular diastolic dysfunction in asymptomatic, normotensive patients with diabetes mellitus,” The American Journal of Cardiology, vol. 93, no. 7, pp. 870–875, 2004. View at: Publisher Site | Google Scholar
  5. F. S. Fein and E. H. Sonnenblick, “Diabetic cardiomyopathy,” Progress in Cardiovascular Diseases, vol. 27, no. 4, pp. 255–270, 1985. View at: Google Scholar
  6. A. Wojdyło, J. Oszmiański, and P. Laskowski, “Polyphenolic compounds and antioxidant activity of new and old apple varieties,” Journal of Agricultural and Food Chemistry, vol. 56, no. 15, pp. 6520–6530, 2008. View at: Publisher Site | Google Scholar
  7. J. R. Ehrenkranz, N. G. Lewis, C. R. Kahn, and J. Roth, “Phlorizin: a review,” Diabetes/Metabolism Research and Reviews, vol. 21, no. 1, pp. 31–38, 2005. View at: Publisher Site | Google Scholar
  8. K. P. Hummel, M. M. Dickie, and D. L. Coleman, “Diabetes, a new mutation in the mouse,” Science, vol. 153, no. 3740, pp. 1127–1128, 1966. View at: Google Scholar
  9. L. Herberg and D. L. Coleman, “Laboratory animals exhibiting obesity and diabetes syndromes,” Metabolism, vol. 26, no. 1, pp. 59–99, 1977. View at: Google Scholar
  10. J. Hu, J. Qian, O. Borisov et al., “Optimized proteomic analysis of a mouse model of cerebellar dysfunction using amine-specific isobaric tags,” Proteomics, vol. 6, no. 15, pp. 4321–4334, 2006. View at: Publisher Site | Google Scholar
  11. P. L. Ross, Y. N. Huang, J. N. Marchese et al., “Multiplexed protein quantitation in Saccharomyces cerevisiae using amine-reactive isobaric tagging reagents,” Molecular and Cellular Proteomics, vol. 3, no. 12, pp. 1154–1169, 2004. View at: Publisher Site | Google Scholar
  12. G. Zhao, H. Gao, J. Qiu, W. Lu, and X. Wei, “The molecular mechanism of protective effects of grape seed proanthocyanidin extract on reperfusion arrhythmias in rats in vivo,” Biological and Pharmaceutical Bulletin, vol. 33, no. 5, pp. 759–767, 2010. View at: Publisher Site | Google Scholar
  13. X. L. Li, B. Y. Li, H. Q. Gao et al., “Proteomics approach to study the mechanism of action of grape seed proanthocyanidin extracts on arterial remodeling in diabetic rats,” International Journal of Molecular Medicine, vol. 25, no. 2, pp. 237–248, 2010. View at: Publisher Site | Google Scholar
  14. T. van de Weijer, V. B. Schrauwen-Hinderling, and P. Schrauwen, “Lipotoxicity in type 2 diabetic cardiomyopathy,” Cardiovascular Research, vol. 92, no. 1, pp. 10–18, 2011. View at: Publisher Site | Google Scholar
  15. P. K. Battiprolu, T. G. Gillette, Z. V. Wang, S. Lavandero, and J. A. Hill, “Diabetic cardiomyopathy: mechanisms and therapeutic targets,” Drug Discovery Today, vol. 7, no. 2, pp. e135–e143, 2010. View at: Publisher Site | Google Scholar
  16. J. G. Duncan, “Mitochondrial dysfunction in diabetic cardiomyopathy,” Biochimica et Biophysica Acta, vol. 1813, no. 7, pp. 1351–1359, 2011. View at: Publisher Site | Google Scholar
  17. D. An and B. Rodrigues, “Role of changes in cardiac metabolism in development of diabetic cardiomyopathy,” The American Journal of Physiology, Heart and Circulatory Physiology, vol. 291, no. 4, pp. H1489–H1506, 2006. View at: Publisher Site | Google Scholar
  18. B. M. Rezk, G. R Haenen, W. J. F. van der Vijgh, and A. Bast, “The antioxidant activity of phloretin: the disclosure of a new antioxidant pharmacophore in flavonoids,” Biochemical and Biophysical Research Communications, vol. 295, no. 1, pp. 9–13, 2002. View at: Publisher Site | Google Scholar
  19. K. Cusi, “The role of adipose tissue and lipotoxicity in the pathogenesis of type 2 diabetes,” Current Diabetes Reports, vol. 10, no. 4, pp. 306–315, 2010. View at: Publisher Site | Google Scholar
  20. M. Kankaanpää, H. R. Lehto, J. P. Pärkkä et al., “Myocardial triglyceride content and epicardial fat mass in human obesity: relationship to left ventricular function and serum free fatty acid levels,” Journal of Clinical Endocrinology and Metabolism, vol. 91, no. 11, pp. 4689–4695, 2006. View at: Publisher Site | Google Scholar
  21. A. R. Wende and E. D. Abel, “Lipotoxicity in the heart,” Biochimica et Biophysica Acta, vol. 1801, no. 3, pp. 311–319, 2010. View at: Publisher Site | Google Scholar
  22. E. D. Bartels, J. M. Nielsen, L. I. Hellgren, T. Ploug, and L. B. Nielsen, “Cardiac expression of microsomal triglyceride transfer protein is increased in obesity and serves to attenuate cardiac triglyceride accumulation,” PLoS ONE, vol. 4, no. 4, Article ID e5300, 2009. View at: Publisher Site | Google Scholar
  23. Y.-H. Chang, D.-M. Chang, K.-C. Lin, S.-J. Shin, and Y.-J. Lee, “Visfatin in overweight/obesity, type 2 diabetes mellitus, insulin resistance, metabolic syndrome and cardiovascular diseases: a meta-analysis and systemic review,” Diabetes/Metabolism Research and Reviews, vol. 27, no. 6, pp. 515–527, 2011. View at: Publisher Site | Google Scholar
  24. M. T. Coughlan, D. R. Thorburn, S. A. Penfold et al., “Rage-induced cytosolic ROS promote mitochondrial superoxide generation in diabetes,” Journal of the American Society of Nephrology, vol. 20, no. 4, pp. 742–752, 2009. View at: Publisher Site | Google Scholar
  25. Y. F. Zhi, J. B. Prins, and T. H. Marwick, “Diabetic cardiomyopathy: evidence, mechanisms, and therapeutic implications,” Endocrine Reviews, vol. 25, no. 4, pp. 543–567, 2004. View at: Publisher Site | Google Scholar
  26. F. Saito, M. Kawaguchi, J. Izumida, T. Asakura, K. Maehara, and Y. Maruyama, “Alteration in haemodynamics and pathological changes in the cardiovascular system during the development of type 2 diabetes mellitus in OLETF rats,” Diabetologia, vol. 46, no. 8, pp. 1161–1169, 2003. View at: Publisher Site | Google Scholar
  27. A. Borbély, L. van Heerebeek, and W. J. Paulus, “Editorial: transcriptional and posttranslational modifications of titin: implications for diastole,” Circulation Research, vol. 104, no. 1, pp. 12–14, 2009. View at: Publisher Site | Google Scholar
  28. E. Ihara and J. A. MacDonald, “The regulation of smooth muscle contractility by zipper-interacting protein kinase,” Canadian Journal of Physiology and Pharmacology, vol. 85, no. 1, pp. 79–87, 2007. View at: Publisher Site | Google Scholar
  29. K. E. Kamm and J. T. Stull, “Signaling to myosin regulatory light chain in sarcomeres,” Journal of Biological Chemistry, vol. 286, no. 12, pp. 9941–9947, 2011. View at: Publisher Site | Google Scholar

Copyright © 2013 Qian Cai et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.