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Acta Pharmacologica Sinica logoLink to Acta Pharmacologica Sinica
. 2009 Jul 13;30(8):1081–1091. doi: 10.1038/aps.2009.95

Breviscapine ameliorates hypertrophy of cardiomyocytes induced by high glucose in diabetic rats via the PKC signaling pathway

Min Wang 1, Wen-bin Zhang 1, Jun-hui Zhu 1, Guo-sheng Fu 1, Bin-quan Zhou 1
PMCID: PMC4006682  PMID: 19597526

Abstract

Aim:

To investigate the influence of breviscapine on high glucose-induced hypertrophy of cardiomyocytes and the relevant mechanism in vitro and in vivo.

Methods:

Cultured neonatal cardiomyocytes were divided into i) control; ii) high glucose concentrations; iii) high glucose+PKC inhibitor Ro-31-8220; iv) high glucose+breviscapine; or v) high glucose+NF-κB inhibitor BAY11–7082. Cellular contraction frequency and volumes were measured; the expression of protein kinase C (PKC), NF-κB, TNF-α, and c-fos were assessed by Western blot or reverse transcription-polymerase chain reaction (RT-PCR). Diabetic rats were induced by a single intraperitoneal injection of streptozotocin, and randomly divided into i) control rats; ii) diabetic rats; or iii) diabetic rats administered with breviscapine (10 or 25 mg·kg−1·d−1). After treatment with breviscapine for six weeks, the echocardiographic parameters were measured. All rats were then sacrificed and heart tissue was obtained for microscopy. The expression patterns of PKC, NF-κB, TNF-α, and c-fos were measured by Western blot or RT-PCR.

Results:

Cardiomyocytes cultured in a high concentration of glucose showed an increased pulsatile frequency and cellular volume, as well as a higher expression of PKC, NF-κB, TNF-α, and c-fos compared with the control group. Breviscapine could partly prevent these changes. Diabetic rats showed relative cardiac hypertrophy and a higher expression of PKC, NF-κB, TNF-α, and c-fos; treatment with breviscapine could ameliorate these changes in diabetic cardiomyopathy.

Conclusion:

Breviscapine prevented cardiac hypertrophy in diabetic rats by inhibiting the expression of PKC, which may have a protective effect in the pathogenesis of diabetic cardiomyopathy via the PKC/NF-κB/c-fos signal transduction pathway.

Keywords: diabetic cardiomyopathy, protein kinase C, cardiomegaly, breviscapine

Introduction

The worldwide prevalence of diabetes mellitus was estimated to be 2.8% in 2000 and is projected to reach 4.4% by 20301. Diabetic cardiomyopathy that occurs independently of coronary artery disease and hypertension is one of the most prevalent cardiovascular complications of diabetes2, 3. Many epidemiological and clinical studies have shown that chronic hyperglycemia is a major initiator of diabetic cardiovascular complications. High glucose regulates structural and functional changes of cardiomyocytes via the activation of several signal transduction pathways, such as increased polyol pathway flux, altered cellular redox states, increased formation of diacylglycerol (DAG) and the subsequent activation of protein kinase C (PKC) isoforms, and accelerated non-enzymatic formation of advanced glycated end products4, 5. Increased expression and activity of PKC causes modifications in the extracellular matrix, induces hypertrophy of cardiomyocytes, microangiopathy of the heart, fibrosis of the interstitium, and eventually leads to heart failure6. Among the signal pathways listed above, the DAG-PKC signal pathway is considered to be one of the most important intracellular transduction pathways that functions as a core effector in the onset and progression of diabetic cardiomyopathy7.

The PKC family comprises more than ten different isozymes; with respect to the heart, PKC-α and PKC-β2 are the predominant Ca2+-dependent PKC isoforms. A number of reports have associated PKC with many structural and functional abnormalities in cardiovascular disease such as cardiac hypertrophy, dilated cardiomyopathy, ischemic injury and heart failure. Additionally, inhibition of PKC has been reported to have a protective effect on both structural abnormalities and cardiac dysfunction. Most studies have shown that hyperglycemia could induce over-expression of PKC-α and PKC-β2 in the early stages of the pathological development of diabetic cardiomyopathy, and is likely to be responsible for the pathologies in diabetic cardiomyopathy8, 9. However, the exact role that PKC plays in the alteration of cardiomyocytes and its underlying downstream signal transduction pathways is still unclear.

NF-κB is a transcription factor that directly regulates the expression of a number of genes that are involved in the stress and inflammatory response following a variety of physiological or pathological stimuli10. Recent studies have shown that activation of NF-κB may function as a causal event in the cardiac hypertrophic response as modeled in cultured cardiomyocytes11 and that NF-κB inhibition could attenuate or block the hypertrophy of cultured cardiomyocytes12. As NF-κB-induced oxidative stress generated by hyperglycemia is one of the major mediators of diabetic cardiomyopathy13, NF-κB is considered as a necessary regulator of the cardiac response in the pathogenesis of diabetic cardiomyopathy14.

Tumor necrosis factor alpha (TNF-α) is a significant contributor to myocardial dysfunction as cardiomyocytes have been identified as a principal target of the proinflammatory actions of TNF-α. Significantly increased expression of TNF-α is found in stretch-induced or hemodynamic overload-induced cardiac hypertrophy in cultured cardiomyocytes. In models of heart failure and cardiomyopathy, TNF-α transcription can be activated by NF-κB, and NF-κB itself is also dominantly regulated by TNF-α. Increased expression of TNF-α triggers NF-κB translocation to the nucleus, where it activates transcription of many inflammatory and immune response target genes.

c-fos is one of the immediate early genes and fetal contractile protein genes that regulates protein synthesis in cardiomyocytes. It is reported to be stimulated in ischemic injury, heart failure and cardiomyopathy15. Increased expression of c-fos has also been reported in both angiotensin II-induced or mechanical stress-induced hypertrophy of cardiomyocytes. The PKC/c-fos pathway has been shown to be involved in endothelin-1-induced proliferation and hypertrophy of rat cardiac myocytes16. As most of the studies above were carried out in models of heart failure and ischemic injury, little is known about the effect of c-fos on cardiac hypertrophy with respect to diabetic cardiomyopathy.

Breviscapine (C21H18O12) is a flavonoid extracted from Erigeron breviscapus and its essential active ingredient is flavones. Based on experimental study and clinical observation, the pharmacological actions of breviscapine include dilating micro-blood vessels, reducing blood viscosity, and improving microcirculation. Studies have shown that breviscapine could inhibit the activity of PKC17, 18, 19 and has a protective effect on diabetic nephropathy, but little is known about the influence of breviscapine on diabetic cardiomyopathy and its underlying mechanisms.

In this study, we aimed to investigate the role of PKC and its downstream PKC/NF-κB/c-fos signaling pathway in the hypertrophy associated with diabetic cardiomyopathy, and also to study the protective effect of the PKC inhibitor, breviscapine, in the pathogenesis of diabetic cardiomyopathy.

Materials and methods

Experimental animals

One-day-old Sprague-Dawley rats (provided by the experimental animal center of Zhejiang University) were used for in vitro cell cultures; male Sprague-Dawley rats [certificate number: SCXK (Zhe) 2007–0029; body weight: 166.72±10.26 g, total range 138–186 g] were used for the animal experiments. All procedures were approved by the Ethics Committee for the Use of Experimental Animals in Zhejiang University; all the experiments followed the instructions for animal care and usage provided by the institution.

Drugs and chemicals

Trypsin and DMEM were purchased from Gibco Chemical Co; glucose, streptozotocin, Ro-31-8220 and BAY11-7082 were obtained from Sigma Chemical Co. Breviscapine was obtained from Shanghai RongHe Bioengineering Co (C21H18O12, purity >98%; Shanghai, China). Primary antibodies included mouse anti-PKC-α, rabbit anti-PKC-β2, goat anti-p-PKC-α, goat anti-p-PKC-β2, mouse anti-NF-κB, rabbit anti-p-NF-κB, rabbit anti-c-fos antibody and rabbit anti-β-actin (Santa Cruz). Secondary antibodies included goat anti-rabbit, rabbit anti-goat, and goat anti-mouse antibody (Zhongshan Co, Beijing, China). The TNF-α primers were (387 bp): 5′-GAA CAA CCC TAC GAG CAC CT-3′, 5′-GGG TAG TTT GGC TGG GAT AA-3′ the GAPDH primer (350 bp): 5′-GGT CGG AGT CAA CGG ATT TG-3′, 5′-ATG AGC CCC AGC CTT CTC CAT-3′ (Shanghai Sangon Biological Engineering Technology and Services Co, Shanghai, China). dNTPs, Taq enzyme, M-MLV, MgCl2 and RNasin were purchased from Promega Co; Oligo(dT)15 was obtained from Shanghai Sangon Biological Engineering Technology and Services Co.

Culture of neonatal rat ventricular myocytes

Ventricular myocytes were cultured as described previously20, 21. Briefly, one-day-old Sprague-Dawley rats were sacrificed and their hearts were isolated, and the ventricles were dissected and digested with a buffer solution containing 0.125% trypsin and 1% collagenase for 10 min at 37 °C. The cell supernatant was collected and DMEM cell culture medium containing 15% fetal bovine serum was added to stop the digestive effect of trypsin and collagenase. The above steps were repeated three to five times until the ventricles were completely digested; the cell supernatant was then collected by centrifugation, after which the pellet was resuspended and collected by centrifugation again. After resuspension with DMEM and the cell culture medium containing 15% fetal bovine serum and penicillin-streptomycin, the cell suspension was diluted to (1–5)×l05/mL and placed in 6-well cell culture plates in a humidified 5%CO2/95% at 37 °C. In the first three days, 5-BrU (0.1 mmol/L) was added to inhibit the growth of fibroblasts. The cells were changed to a serum-free DMEM culture medium and cultured for 48 h before being divided into different groups.

Division of cultured cardiomyocytes

After the initial 48 h serum-free culture, cells were divided into different glucose levels according to previously described research22 as follows: the control glucose (5 mmol/L) group, high glucose (25.5 mmol/L) group, high glucose plus PKC inhibitor Ro-31-8220 (50 nmol/L) group, high glucose plus breviscapine (10, 20, and 60 mmol/L) group, and high glucose plus NF-κB inhibitor BAY11-7082 (5 μmol/L) group. After the addition of those drugs, the different groups of cardiomyocytes were cultured for an additional 12 h.

Determination of cellular pulsatile frequency and measurement of cellular size

An inverted microscope and dish were put into lucite couveuse, which was equipped with a homoiothermy air convection assembly. The dishes were fully covered by convection air at 37 °C. For the study of cellular pulsatile frequencies, five fields were randomly chosen from each group, and 20 individual cells were counted from each field using the high power (×400) ocular lens of the inverted microscope. The volume of ventricular myocytes was obtained by measuring cellular diameter under an inverted microscope; five fields were randomly chosen from each group and 20 individual cells were counted from each field for cellular size measurements.

Western blot analysis of cultured cardiomyocytes

The cells were washed twice with PBS and lysed at 4 °C with lysis buffer containing 25 mmol/L Tris (pH 7.4), 5 mmol/L EDTA, 10 mmol/L sodium pyrophosphate, 1 mmol/L Na3VO4, 1 mmol/L dithiothreitol, 1 mmol/L PMSF and 10 mg/L aprotinin. The protein expression of PKC, NF-κB, and c-fos were measured by Western blot and normalized to the protein level of β-actin. Equal amounts of total protein (40 μg) from each lysate were resolved by SDS/PAGE [10% (w/v) gel] and then transferred into PVDF membranes. After the membranes were blocked with 5% non-fat milk dissolved in TBS (20 mmol/L Tris HCl and 0.5 mol/L NaCl, pH 7.4) for 1 h at room temperature, the filters were incubated respectively with primary antibodies (mouse anti-PKC-α, rabbit anti-PKC-β2, goat anti-p-PKC-α, goat anti-p-PKC-β2, mouse anti-NF-κB, rabbit anti-p-NF-κB and rabbit anti-c-fos antibody, Santa Cruz, 1:1000 dilution) overnight at 4 °C. After being washed three times with TBST buffer (0.05% Tween 20 in TBS, pH 7.4) for 10 min each time, the filters were incubated with horseradish peroxidase-conjugated secondary antibodies for 1 h, followed by three washes with TBST buffer for 10 min each. At last, antibody-antigen complexes were detected in all the membranes by enhanced chemiluminescence (ECL)-detection reagents and exposed to an X-OMAT AR X-ray film (Kodak Inc). The intensity of these protein bands was quantified by densitometry and normalized to β-actin (Zhongshan Bio-tech, China).

Reverse transcription-polymerase chain reaction (RT-PCR) analysis of cultured cardiomyocytes

The cultured cardiomyocytes were washed twice with PBS and lysed in 1 ml of trizol reagent for 5 min. Total RNA was extracted with Trizol reagent according to the manufacturer's instructions. RNA content was assessed by light absorbance at 260 nm, and purity was determined according to A260/A280 ratios. A quantity of 5 μg of total RNA was reversely transcribed into cDNA in a 50-μL reaction mixture containing 0.1 μg random hexamers and 400 U of M-MLV transcriptase, and subsequently amplified by PCR using primers listed above. The 25 μL of reaction mixture for PCR contained 2 μL of the cDNA, 20 μmol/L of each dNTP, 400 pmol of each specific primer, 25 mmol/L MgCl2 1.5 μL, and 1U Taq DNA polymerase. The resulting products were separated on 1.2% agarose gel and stained with ethidium bromide. The intensity of the bands was quantified by an image analysis scanning system, and normalized by GAPDH as a control.

Animal experiment groups and measurement of cardiac hypertrophy

Diabetes in rats was induced by an intraperitoneal injection of 70 mg/kg streptozotozin, and the age and weight-matched control rats received saline only. All the rats were housed in groups of four per cage and given free access to food and water at a constant temperature of 22±2 °C, with a 12 h light/dark cycle. About 72 h after streptozotocin injection, blood samples were taken from the caudal vein to measure glucose levels using a glucometer (One Touch II glucometer) and were repeated every week for each rat. Rats in which glucose levels measured >16.7 mmol/L at least three times were categorized as diabetic rats. Four weeks after injection of strepozotozin or vehicle, all rats were randomly divided into the following groups: i) normal control rats (Control, n=10); ii) untreated diabetic rats (DM, n=10); iii) diabetic rats administered with low dose breviscapine (10 mg·kg−1·d−1, DM+LDB, n=10); or iv) diabetic rats administered with high-dose breviscapine (25 mg·kg−1·d−1, DM+HDB, n=10). Breviscapine was administered through an intragastric tube daily for six weeks and the control rats received saline only. In total, two rats in the DM group, and in the DM+LBD and the DM+HBD groups, we both found one rat dead during the experimental period. At the end of the experiment, all rats in different groups were weighed and anesthetized with 10% hydrated chloral (400 mg/kg); then, echocardiography was performed using a Hewlett-Packard 5500 instrument (Hewlett-Packard Co) with a 14-MHz compact linear-array probe. Echocardiographic measurements were taken on M-mode in triplicate for each rat. The following measurements were taken to evaluate the cardiac structure and function: interventricular septal dimensions, left ventricular posterior wall dimensions, and left ventricular internal dimensions at end diastole (IVSd, LVPWd, and LVIDd, respectively) and at end systole (IVSs, LVPWs, and LVIDs, respectively). Moreover, these dimensions were also used to calculate the cardiac function parameters such as ejection fraction (EF), IVS percentage and LVPW percentage. The rats were then killed by cervical dissociation, the hearts were isolated, and the whole heart weight (LW) and the left ventricular weight (LVW) of each rat were measured, respectively.

Transmission electron microscopy

Selected samples of cardiac tissue from rats of each group were minced into small pieces (≤1 mm3), and fixed in 2.5% glutaraldehyde in 0.1 mol/L sodium cacodylate buffer (pH 7.3) for 2 h. The specimens were then rinsed in buffer, post-fixed in cacodylate-buffered 2% OsO4, stained en bloc in uranyl acetate, dehydrated in an ethanol gradient, and embedded in epoxy resin by standard procedures. Finally, 50–70 mm super-thin slices were prepared. Thin sections were stained with uranyl acetate and lead citrate and examined with a Philips TECNA10 electron microscope.

Western blot analysis of animal heart tissues

After the hearts were removed rapidly from rats, the atria and aorta were cut off, then the ventricles were freeze-clamped at liquid N2 temperature and stored at -80 °C. Total proteins were extracted from the frozen LV tissues and the concentration was determined by the Lowry method. The myocardial expression of PKC, NF-κB, and c-fos was measured by Western blot and normalized to the protein level of β-actin as described above.

RT-PCR analysis of animal heart tissues

Ventricular tissues were pulverized to a powder and lysed in 1 mL of Trizol reagent for 5 min. Total RNA was extracted with Trizol reagent according to the manufacturer's instructions and assessed by light absorbance at 260 nm; purity was determined according to A260/A280 ratios. A quantity of 5 μg of total RNA was reversely transcribed and subsequently amplified by PCR as described above. The resulting products were separated on 1.2% agarose gel and stained with ethidium bromide. The intensity of the bands was quantified by an image analysis scanning system, and normalized by GAPDH as the control.

Statistics

All data were presented as mean±SEM, and were analyzed using SPSS 15.0 software. Comparisons among groups were made by an unpaired Student's t test. A value of P<0.05 was considered statistically significant.

Results

Breviscapine decreased the pulsatile frequency and cellular size of cardiomyocytes cultured in high glucose levels

The cardiomyocytes cultured in a high glucose concentration showed an increased pulsatile frequency and higher cellular volumes compared with those cultured in normal glucose levels (P<0.05). After adding PKC inhibitor Ro-31-8220 (50 nmol/L), breviscapine (10, 20, and 60 mmol/L), and NF-κB inhibitor BAY11-7082 (5 μmol/L), the pulsatile frequency and cellular size of cardiomyocytes decreased significantly (P<0.05). The result is shown in Table 1.

Table 1. Effect of Ro-31-8220, BAY11-7082, breviscapine on pulsatile frequency and cellular size of cultured cardiomyocytes.

  Diameter (μm) Pulsatile frequency (bpm/min)
Normal glucose (5 mmol/L) 18.64±0.83 63.35±2.830
High glucose (25.5 mmol/L) 24.29±1.04b 86.04±4.299b
High glucose+Ro-31-8220 19.68±1.01e 78.55±4.024e
High glucose+BAY11-7082 20.03±0.88e 78.51±3.669e
High glucose+breviscapine (10 mmol/L) 21.49±1.22e 81.33±4.652e
High glucose+breviscapine (20 mmol/L) 20.74±1.14eh 76.57±3.441eh
High glucose+breviscapine (60 mmol/L) 19.71±0.97ek 73.00±3.551ek
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Compared with normal glucose (5 mmol/L) group, the pulsatile frequency and diameters of cardiomyocytes cultured in high glucose (25.5 mmol/L) increased significantly, after adding Ro-31-8220, BAY11-7082, and breviscapine, the pulsatile frequency and size of the cells all decreased significantly, the reverse effect was more obvious as the concentration of breviscapine increased. The results were expressed as means±SEM (n=100).

bP<0.05 vs control group (glucose: 5 mmol/L).

eP<0.05 vs high glucose group (glucose: 25.5 mmol/L),

hP<0.05 vs high glucose+breviscapine (10 mmol/L) group.

kP<0.05 vs high glucose+breviscapine (20 mmol/L) group.

Breviscapine decreased the expression and activity of PKC-α and PKC-β2 in cardiomyocytes cultured in high glucose levels

Cardiomyocytes cultured in high glucose levels showed higher expression of PKC-α and PKC-β2 and increased activity of PKC-α and PKC-β2 at the same time, as reflected by higher expression of p-PKC-α and p-PKC-β2 than seen in the control group (P<0.05). After adding PKC inhibitor Ro-31-8220 and breviscapine (10 mmol/L, 20 mmol/L, 60 mmol/L), the expression and activity of PKC-α and PKC-β2 decreased significantly (P<0.05; Figures 1, 2).

Figure 1.

Figure 1

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Breviscapine decreased the expression of PKC-α in high glucose cultured cardiomyocytes. Cardiomyocytes cultured in high glucose levels showed higher expression and activity of PKC-α compared with control group. After adding PKC inhibitor Ro-31-8220 (50 nmol/L) and breviscapine (10, 20, and 60 mmol/L), the expression and activity of PKC-α decreased. n=4 or 5. Mean±SEM. bP<0.05 vs control group. eP<0.05 vs high glucose group. (L: control glucose group; H: high glucose group; Ro: high glucose+PKC inhibitor Ro-31-8220 group; B-10: high glucose+10 mmol/L breviscapine; B-20: high glucose+20 mmol/L breviscapine; B-60: high glucose+60 mmol/L breviscapine group).

Figure 2.

Figure 2

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Breviscapine decreased the expression of PKC-β2 in high glucose cultured cardiomyocytes. Cardiomyocytes cultured in high glucose levels showed higher expression and activity of PKC-β2 compared with control group. After adding PKC inhibitor Ro-31-8220 (50 nmol/L) and breviscapine (10, 20, and 60 mmol/L), the expression and activity of PKC-β2 decreased. The results were shown in Figure 2 expressed as means±SEM (n=4 or 5). bP<0.05 vs control group. eP<0.05 vs high glucose group. (L: control glucose group; H: high glucose group; Ro: high glucose+PKC inhibitor Ro-31-8220 group; B-10: high glucose+10 mmol/L breviscapine; B-20: high glucose+20 mmol/L breviscapine; B-60: high glucose+60 mmol/L breviscapine group).

Breviscapine decreased the expression of NF-κB, TNF-α, and c-fos in cardiomyocytes cultured in high glucose levels

The expression of NF-κB, TNF-α, and c-fos was higher in cardiomyocytes cultured in high glucose levels than in those cultured in normal glucose levels, as the protein level of NF-κB, p-NF-κB, c-fos, and mRNA level of TNF-α all significantly increased (P<0.05). After adding PKC inhibitor, Ro-31-8220, breviscapine (10, 20, and 60 mmol/L) and NF-κB inhibitor BAY11-7082, the expression of NF-κB, TNF-α and c-fos all decreased significantly (P<0.05), as shown in Figures 3, 4, and 5.

Figure 3.

Figure 3

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Breviscapine decreased the expression of NF-κB in high glucose cultured cardiomyocytes. Cardiomyocytes cultured in high glucose levels showed higher expression and increased activity of NF-κB compared with control group. After adding PKC inhibitor Ro-31-8220 (50 nmol/L), NF-κB inhibitor BAY11-7082 (5 μmol/L) and breviscapine (10, 20, and 60 mmol/L), the expression and activity of NF-κB decreased as shown in Figure 3. The results were expressed as means±SEM. n=4 or 5. bP<0.05 vs control group. eP<0.05 vs high glucose group. (L: control glucose group; H: high glucose group; Ro: high glucose+PKC inhibitor Ro-31-8220 group; B-10: high glucose+10 mmol/L breviscapine; B-20: high glucose+20 mmol/L breviscapine; B-60: high glucose+60 mmol/L breviscapine group; BAY: high glucose+NF-κB inhibitor BAY11-7082 group).

Figure 4.

Figure 4

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Breviscapine decreased the expression of TNF-α in high glucose cultured cardiomyocytes. Cardiomyocytes cultured in high glucose levels showed higher expression of TNF-α compared with control group. After adding PKC inhibitor Ro-31-8220 (50 nmol/L), NF-κB inhibitor BAY11-7082 (5 μmol/L) and breviscapine (10, 20, and 60 mmol/L), the expression of TNF-α decreased compared with the cardiomyocytes cultured in high glucose levels as shown in Figure 4. The results were expressed as means±SEM. n=4 or 5. bP<0.05 vs control group. eP<0.05 vs high glucose group. (L: control glucose group; H: high glucose group; Ro: high glucose+PKC inhibitor Ro-31-8220 group; B-10: high glucose+10 mmol/L breviscapine; B-20: high glucose+20 mmol/L breviscapine; B-60: high glucose+60 mmol/L breviscapine group; BAY: high glucose+NF-κB inhibitor BAY11-7082 group).

Figure 5.

Figure 5

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Breviscapine decreased the expression of c-fos in high glucose cultured cardiomyocytes. Cardiomyocytes cultured in high glucose levels showed higher expression of c-fos compared with control group. After adding PKC inhibitor Ro-31-8220 (50 nmol/L), NF-κB inhibitor BAY11-7082 (5 μmol/L) and breviscapine (10, 20, and 60 mmol/L), the expression of c-fos decreased as shown in Figure 5. The results were expressed as means±SEM. n=4 or 5. bP<0.05 vs control group. eP<0.05 vs high glucose group. (L: control glucose group; H: high glucose group; Ro: high glucose+PKC inhibitor Ro-31-8220 group; B-10: high glucose+10 mmol/L breviscapine; B-20: high glucose+20 mmol/L breviscapine; B-60: high glucose+60 mmol/L breviscapine group; BAY: high glucose+NF-κB inhibitor BAY11-7082 group).

Breviscapine ameliorated cardiac hypertrophy and dysfunction in diabetic rats

The body weight (BW), blood glucose (BG) level, LVW-to-HW (left ventricular weight to heart weight ratio), LVW-to-BW (left ventricular weight to body weight ratio) and HW-to-BW (heart weight to body weight ratio) of all the rats in different groups are presented in Table 2. The STZ-induced diabetic rats had significantly lower mean body weights than those of the age-matched control rats (P<0.05). Breviscapine treatment significantly alleviated the weight loss in diabetic rats (P<0.05). The average blood glucose levels were more than 16.7 mmol/L in the diabetic group and remained at this level during the experimental period of ten weeks; treatment with low (10 mg·kg−1·d−1) or high (25 mg·kg−1·d−1) doses of breviscapine did not affect the blood glucose levels in diabetic rats. The HW and LVW of the diabetic rats were lower than those of the control rats (P<0.05), but the LVW-to-BW and LVW-to-HW ratios in diabetic rats were significantly higher than those of the control rats (P<0.05). After treatment with breviscapine, the HW and LVW of diabetic rats increased while the LVW-to-BW and LVW-to-HW ratios decreased significantly compared to diabetic rats (P<0.05). The lower EF, IVS% and LVPW% showed that diabetic rats displayed impaired cardiac function (P<0.05). At the same time, diabetic rats showed rela tive cardiac hypertrophy, as presented by the increased ratio of IVS-to-LVPW (P<0.05). After treatment with breviscapine, the diabetic rats showed improved cardiac function as the parameters of EF, IVS percentage, and LVPW percentage all increased significantly (P<0.05). Also, cardiac hypertrophy was prevented as the IVS-to-LVPW ratio decreased significantly (P<0.05), as shown in Table 3. The protective effects of breviscapine on cardiac function and hypertrophy were more obvious in the high (25 mg·kg−1·d−1) dose group than in the low dose (10 mg·kg−1·d−1) group.

Table 2. General characteristics of experimental rats.

Groups BW BG LVW/HW (%) LVW/BW (%) HW/BW (%)
Control 554.00±26.05 8.973±4.403 74.08±0.259 0.185±0.012 0.233±0.017
DM 250.00±31.43b 20.625±1.371b 80.11±2.302b 0.235±0.015b 0.303±0.007b
DM+LDB 313.00±18.19e 18.511±1.406b 76.88±0.827e 0.204±0.000e 0.275±0.001e
DM+HDB 357.33±12.66eh 19.050±3.803b 74.25±1.211eh 0.198±0.002e 0.267±0.006e
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The body weight (BW), blood glucose level (BG), LVW-to-HW, LVW-to-BW, HW-to-BW ratio of all rats in different groups are presented in Table 1 (mean±SEM. n = 8–10 for each group).

bP<0.05 vs control.

eP<0.05 vs DM.

hP<0.05 vs DM+LDB.

Table 3. Breviscapine ameliorate cardiac dysfunction in diabetic cardiomyopathy.

Groups Control DM DM+LDB DM+HDB
EF% 0.92±0.01 0.80±0.0b 0.85±0.02e 0.89±0.01eh
LVIDd 0.63±0.02 0.44±0.02b 0.50±0.01e 0.54±0.02eh
IVSs/LVPW 0.64±0.02 0.75±0.02b 0.72±0.02e 0.68±0.01eh
IVSd/LVPW 1.05±0.07 1.66±0.10b 1.55±0.03e 1.30±0.05eh
IVS% 54.86±4.47 45.22±1.24b 52.47±2.50e 57.03±2.63e
LVPW% 34.30±1.69 13.08±1.38b 35.33±1.54e 35.37±1.25e
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The heart EF, LVIDd, IVSs-to-LVPW ratio, IVSd-to-LVPW ratio, IVS%, LVPW% of all rats in different groups are presented as the mean±SEM in Table 2. n = 8–10 for each group.

bP<0.05 vs control.

eP<0.05 vs DM.

hP<0.05 vs DM+LDB.

The effects of breviscapine on ultrastructural changes of the diabetic rats' heart tissues by transmission electron microscopy analysis

Electron microscopic analysis of the myocardium revealed a spectrum of abnormalities in the diabetic rats compared with age-matched normal rats. Cardiac muscle cells in diabetic hearts showed loss and derangement of myofibrils compared with controls. Swollen, clumped, fragmented and distended mitochondria were evident in diabetic rat hearts, and the cristae in the mitochondria appeared distorted and in some cases were completely lysed. In addition, diabetic rat cardiomyocytes had a dilated and swollen sarcoplasmic reticulum, and the space between the intercalated disks was also widened. Some disks were distorted and ruptured. After treatment with breviscapine, the diabetic rats showed improved cardiac structure with a reversal of the loss and derangement of myofibrils. At the same time, the changes in the mitochondria were reversed, and the dilated and swollen sarcoplasmic reticulum was not as severe as in diabetic rats. The improvement of cardiac structure was more obvious in diabetic rats administered with 25 mg·kg−1·d−1 breviscapine than in those who received 10 mg·kg−1·d−1 breviscapine, so the beneficial effect of breviscapine on the structural changes of diabetic cardiomyopathy may be dose-related, as shown in Figures 6 and 7.

Figure 6.

Figure 6

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Ultrastructure of myocardium in rats. Control rat (×20 000); diabetic rat (DM, ×20 000); diabetic rat treated with low dose of breviscapine (DM+LDB, ×20 000); diabetic rat treated with high dose of breviscapine (DM+HDB, ×20 000); 1: the loss and derangement of myofibrils; 2: swollen and distended of mitochondria; 3: dilated and fragmented sarcoplasmic reticulum.

Figure 7.

Figure 7

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Ultrastructure of myocardium in rats. Control rat (×50 000); diabetic rat (DM, ×50 000); diabetic rat treated with low dose of breviscapine (DM+LDB, ×50 000); diabetic rat treated with high dose of breviscapine (DM+HDB, ×50 000). 1: the loss and derangement of myofibrils; 2: swollen and distended of mitochondria; 3: dilated and fragmented sarcoplasmic reticulum.

Breviscapine decreased the expression and activity of PKC-α and PKC-β2 in diabetic rat hearts

Protein expression of PKC-α and PKC-β2 and their activity, p-PKC-α and p-PKC-β2, increased significantly in diabetic rats compared with normal control rats (P<0.05). After treatment with breviscapine, the increased expression of PKC-α and PKC-β2 and their activity p-PKC-α and p-PKC-β2 in the diabetic rats hearts decreased significantly (P<0.05) as shown in Figures 8 and 9. The reduced expression of PKC-α, PKC-β2, p-PKC-α, and p-PKC-β2 was more obvious in diabetic rats treated with 25 mg·kg−1·d−1 breviscapine than in those which received 10 mg·kg−1·d−1 breviscapine, so the protective effect of breviscapine on diabetic cardiomyopathy may be dose-related.

Figure 8.

Figure 8

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Breviscapine decreased the expression of PKC-α in diabetic rats hearts. Diabetic rats (DM) showed higher expression of PKC-α in heart tissues compared with normal control ones (Control) analyzed by Western blot. Treatment with breviscapine reduced the expression of PKC-α in diabetic cardiomyopathy, the reduced expression of PKC-α was more obvious in diabetic rats treated with breviscapine 25 mg·kg−1·d−1 (DM+HDB) than those received 10 mg·kg−1·d−1 breviscapine (DM+LDB), β-actin was an endogenous control. Each bar represents the mean±SEM. n=8−10 rats for each group. bP<0.05 vs control group. eP<0.05 vs high glucose group.

Figure 9.

Figure 9

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Breviscapine decreased the expression of PKC-β2 in diabetic rats hearts. Diabetic rats (DM) showed higher expression of PKC-β2 in heart tissues compared with normal control rats (Control). Treatment with breviscapine could reduced the expression of PKC-β2 in diabetic cardiomyopathy, the reduced expression of PKC-β2 was more obvious in diabetic rats treated with 25 mg·kg−1·d−1 (DM+HDB) breviscapine than those received 10 mg·kg−1·d−1 breviscapine (DM+LDB), β-actin was an endogenous control. Each bar represents the mean±SEM. n=8−10 rats for each group. bP<0.05 vs control. eP<0.05 vs DM.

Breviscapine decreased the expression of NF-κB, TNF-α, and c-fos in diabetic rat hearts

Protein expression of NF-κB and c-fos as well as the mRNA level of TNF-α significantly increased in diabetic rats compared with normal control rats (P<0.05). After treatment with breviscapine, the increased protein expression of NF-κB, TNF-α and c-fos in diabetic rats heart decreased (P<0.05) as shown in Figures 10, 11, and 12. The regulatory effect of breviscapine on the expression of NF-κB, TNF-α, and c-fos was more obvious in diabetic rats treated with 25 mg·kg−1·d−1 breviscapine than in those who received 10 mg·kg−1·d−1 breviscapine.

Figure 10.

Figure 10

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Breviscapine decreased the expression of NF-κB in diabetic rats hearts. Diabetic rats (DM) showed higher expression of NF-κB in heart tissues compared with normal control rats (Control). Treatment with breviscapine reduced the expression of NF-κB in diabetic cardiomyopathy, the reduced expression of NF-κB was more obvious in diabetic rats treated with breviscapine 25 mg·kg−1·d−1 (DM+HDB) than those received 10 mg·kg−1·d−1 breviscapine (DM+LDB), β-actin was an endogenous control. Each bar represents the mean±SEM. n=8−10 rats for each group. bP<0.05 vs control. eP<0.05 vs DM.

Figure 11.

Figure 11

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Breviscapine decreased the expression of TNF-α in diabetic rats hearts. Diabetic rats (DM) showed higher expression of TNF-α in heart tissues compared with normal control rats (Control) analyzed by RT-PCR. Treatment with breviscapine reduced the expression of TNF-α in diabetic cardiomyopathy, the reduced expression of TNF-α was more obvious in diabetic rats treated with breviscapine 25 mg·kg−1·d−1 (DM+HDB) than those received 10 mg·kg−1·d−1 breviscapine (DM+LDB), GAPDH was an endogenous control. Each bar represents the mean±SEM. n=8−10 rats for each group. bP<0.05 vs control. eP<0.05 vs DM.

Figure 12.

Figure 12

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Breviscapine decreased the expression of c-fos in diabetic rats hearts. Diabetic rats (DM) showed higher expression of c-fos in heart tissues compared with normal control rats (Control). Treatment with breviscapine reduced the expression of c-fos in diabetic cardiomyopathy, the reduced expression of c-fos was more obvious in diabetic rats treated with breviscapine 25 mg·kg−1·d−1 (DM+HDB) than those received 10 mg·kg−1·d−1 breviscapine (DM+LDB), β-actin was an endogenous control. Each bar represents the mean±SEM. n=8−10 rats for each group. bP<0.05 vs control. eP<0.05 vs DM.

Discussion

Diabetic cardiomyopathy is one of the most prevalent cardiovascular complications of diabetes mellitus, occurring independently of coronary artery disease and hypertension2. The associated typical pathological changes include hypertrophy of cardiomyocytes, microangiopathy of the heart and fibrosis of the interstitial substance23. Cardiomyopathy in diabetic patients is characterized by early diastolic dysfunction, followed by late systolic dysfunction24, 25, 26. However, the mechanism underlying the development of structural and functional impairment in cardiomyopathy remains unknown; in particular, the intracellular signal transduction pathway that leads to the pathological change of cardiomyocyte hypertrophy is still unclear.

Previous studies have indicate that high glucose levels could induce structural and functional changes in cardiac myocytes. In this study, we discovered that cardiomyocytes cultured in high levels of glucose showed increased pulsatile frequency and obvious hypertrophy compared with cells cultured in normal glucose levels, which correlates with previous studies. High glucose could increase the pulsatile frequency of cardiomyocytes by regulating the opening of voltage-dependent channels that exist in the cytoplasmic membrane due to activation of tyrosine kinase27. Accelerated pulsatile frequency causes increased energy expenditure, leading to energy insufficiency and a series of negative manifestations, which aggravate the impairment of cardiomyocytes induced by high glucose levels.

We found that diabetic rats had a lower body weight, higher blood glucose level, relative cardiac hypertrophy and impaired cardiac function compared with those of the age-matched control rats. Breviscapine treatment did not influence the average blood glucose levels, but the body weight increased, and the cardiac hypertrophy and the impaired cardiac dysfunction were also reversed in diabetic rats. The improvement of cardiac hypertrophy and cardiac dysfunction was more obvious in diabetic rats administrated with 25 mg·kg−1·d−1 breviscapine than in those that received 10 mg·kg−1·d−1 breviscapine. Therefore, breviscapine has a protective effect on both the structural changes and cardiac dysfunction found in diabetic cardiomyopathy.

To investigate whether the protective effect of breviscapine is related to PKC, we examined the expression of PKC in cardiomyocytes. We found that both the cardiomyocytes cultured in high glucose levels and the myocardium of diabetic rats showed increased expression and activity of PKC-α and PKC-β2, as reflected by the higher protein expression of PKC-α, PKC-β2, p-PKC-α, and p-PKC-β2 when examined by Western blot. This is in agreement with similar studies on diabetic and heart failure animal models28, 29. After treatment with breviscapine, both the cardiomyocytes cultured in high levels of glucose and the diabetic rat hearts showed decreased expression of PKC-α and PKC-β2, and the activity of PKC-α and PKC-β2 also decreased significantly, which indicated that increased levels of PKC-α and PKC-β2 are involved in the pathogenesis of diabetic cardiomyopathy, and breviscapine has a protective effect on the diabetic cardiomyopathy.

Thus, pharmacological inhibition of PKC activity could reverse the hypertrophic changes in the myocardium in diabetic cardiomyopathy. There have been some studies on the therapeutic action of PKC inhibitors on heart failure and ischemic injury. Studies that were done on ischemic and heart failure animal models have also shown that NF-κB activation as well as TNF-α were closely related to cardiac hypertrophy, and over-expression of PKC could induce the expression of proto-oncogenes such as c-fos and c-jun, leading to increased activator protein one (AP-1) expression. AP-1 potentially stimulates the transcription of type IV collagen, fibronectin, TGF-β and so on, leading to decreased contractility and permeability of cardiomyocytes. This causes changes in the extracellular matrix and induces hypertrophy of cardiomyocytes, microangiopathy of the heart and fibrosis of the interstitial substance, which ultimately leads to heart failure.

In this study, we have found that the expression of NF-κB, TNF-α and c-fos of the cardiomyocytes cultured in the high glucose levels as well as diabetic rat hearts increased compared with those of control groups. To investigate the mechanism of action of PKC on the structural and functional changes of diabetic cardiomyopathy, we used a PKCα/β2 inhibitor (Ro-31-8220) and an NF-κB inhibitor (BAY11-7082) to study the signal transduction pathway of PKC and its downstream effects. We discovered that the increased beating frequency and hypertrophy of cardiomyocytes induced by high glucose level were obviously reversed after using the selective PKCα/β2 inhibitor Ro-31-8220, with depressed expression and activity of PKC-α and PKC-β2 and a remarkably decreased expression pattern of NF-κB, TNF-α, and c-fos. Similarly, after using the NF-κB inhibitor, BAY11-7082, the increased beating frequency and cardiac hypertrophy were also reversed, and the expression of NF-κB, TNF-α, and c-fos were also remarkably reduced. Due to this phenomenon, we hypothesize that hyperglycemia could result in a higher content of intracellular DAG in the cardiomyocytes cultured in high levels of glucose, leading to increased expression and activity of PKC-α and PKC-β2, which induce over-expression of NF-κB via the PKC-IKK-NF-κB signal transduction pathway. NF-κB is a transcription factor that can directly regulate the expression of immediate-early genes and other genes that are involved in the stress response following a variety of physiological or pathological stimuli30, 31. Activation of NF-κB is necessary and sufficient for the hypertrophic response in heart failure, as modeled in cultured cardiomyocytes. Recent studies have shown that oxidative stress generated by hyperglycemia is one of the major mediators of diabetic cardiomyopathy, and that the activation of NF-κB is one possible mechanism for the oxidative stress-induced vascular complications in diabetes. Therefore, NF-κB may function as a causal event in the cardiac hypertrophic response of diabetic cardiomyopathy. It is clear that after entering the cellular nucleus, NF-κB could increase the transcription of TNF-α and NF-κB itself is dominantly regulated by the cytokine TNF-α32, 33. TNF-α is one of the relevant mediators of cardiomyopathic disease and is considered to be a parameter of hypertrophy that could be induced by angiotension II, endothelin-1, phenylephrine, myotrophin and so on. Increased expression of TNF-α could obviously have been inhibited through over-expression of the degradation-resistant mutant of IκBα34, 35, 36, 37, which supports the hypothesis that NF-κB inhibition could attenuate or block the hypertrophic response of cultured cardiomyocytes. There have been studies that show that the increased expression of TNF-α could further lead to the expression of proto-oncogenes such as c-fos, which cause increased cell size and protein content of cardiomyocytes. This results in an accelerated rate of general protein synthesis, as well as an increase in ventricular mass, including the accumulation of collagen fibers, deposition of collagen protein and fibrosis of the interstitial substance in the interstitial tissue of the heart. Increased expression of c-fos was viewed as an adaptive response for maintaining cardiac output after stimulation with TNF-α or angiotensin II, as in isolated adult cardiac myocytes or heart failure, ischemic injury and stress-induced hypertrophy models. Those pathological changes ultimately result in remodeling of the cardiac muscle, leading to the development of diabetic cardiomyopathy. PKC may lead to diabetic cardiomyopathy via the PKC/NF-κB/TNF-α/c-fos signal transduction pathway.

Breviscapine is isolated from the Asteraceae plant E breviscapus and can be prepared as a Chinese patent medicine, where the essential active ingredients are flavones38, 39. It possesses an anti-platelet and anti-thrombus action and can lower plasma fibrin content and promote fibrinolytic activity. Studies have found that breviscapine could inhibit the activity of PKC, promote apoptosis of cardiomyocytes via regulation of the expression of the apoptosis-inhibiting gene bcl-240, 41 and have a protective effect against ischemia/reperfusion injury. It has been used in cardiovascular disease with satisfactory tolerance and safety. It has also been proved that breviscapine can significantly inhibit increased PKC-β expression and activity seen in diabetic nephropathy in the same manner as LY-33353142. Our research has found that breviscapine inhibits PKC expression both in cardiomyocytes cultured in high concentrations of glucose and in diabetic hearts, and can reverse the hypertrophic changes and cardiac dysfunction found in diabetic cardiomyopathy. We also found that cardiomyocytes cultured in high concentrations of glucose and diabetic rats treated with breviscapine showed decreased expression of NF-κB, TNF-α, and c-fos, which was consistent with the change in PKC expression. In summary, breviscapine may have a protective effect against diabetic cardiomyopathy via the PKC-induced NF-κB/TNF-α/c-fos signal transduction pathway.

In conclusion, PKC is involved in the pathogenesis of diabetic cardiomyopathy, and the PKC/NF-κB/TNF-α/c-fos signal transduction pathway plays an important role in regulating cardiac hypertrophy. Treatment with breviscapine can significantly reverse the cardiac structure disorganization and ameliorate cardiac dysfunction in diabetic cardiomyopathy.

Author contribution

Bin-quan ZHOU designed research; Min WANG performed research; Jun-hui ZHU contributed new analytical tools and reagents; Guo-sheng FU analyzed data; Min WANG and Wen-bin ZHANG wrote the paper.

Acknowledgments

We thank the Department of Cardiovascular Diseases, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University for the use of test instruments and equipment.

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