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  • Original investigation
  • Open Access

Apocynin influence on oxidative stress and cardiac remodeling of spontaneously hypertensive rats with diabetes mellitus

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  • 1Email author
Cardiovascular Diabetology201615:126

https://doi.org/10.1186/s12933-016-0442-1

©  The Author(s) 2016

  • Received: 21 June 2016
  • Accepted: 18 August 2016
  • Published:

Abstract

Purpose

Although increased oxidative stress is a major component of diabetic hypertensive cardiomyopathy, research into the effects of antioxidants on cardiac remodeling remains scarce. The actions of antioxidant apocynin include inhibiting reactive oxygen species (ROS) generation by nicotinamide adenine dinucleotide phosphate (NADPH) oxidases and ROS scavenging. We evaluated the effects of apocynin on cardiac remodeling in spontaneously hypertensive rats (SHR) with diabetes mellitus (DM).

Methods

Male SHR were divided into four groups: control (SHR, n = 16); SHR treated with apocynin (SHR-APO; 16 mg/kg/day, added to drinking water; n = 16); diabetic SHR (SHR-DM, n = 13); and SHR-DM treated with apocynin (SHR-DM-APO, n = 14), for eight weeks. DM was induced by streptozotocin (40 mg/kg, single dose). Statistical analyzes: ANOVA and Tukey or Mann–Whitney.

Results

Echocardiogram in diabetic groups showed higher left ventricular and left atrium diameters indexed for body weight, and higher isovolumetric relaxation time than normoglycemic rats; systolic function did not differ between groups. Isolated papillary muscle showed impaired contractile and relaxation function in diabetic groups. Developed tension was lower in SHR-APO than SHR. Myocardial hydroxyproline concentration was higher in SHR-DM than SHR, interstitial collagen fraction was higher in SHR-DM-APO than SHR-APO, and type III collagen protein expression was lower in SHR-DM and SHR-DM-APO than their controls. Type I collagen and lysyl oxidase expression did not differ between groups. Apocynin did not change collagen tissue. Myocardial lipid hydroperoxide concentration was higher in SHR-DM than SHR and SHR-DM-APO. Glutathione peroxidase activity was lower and catalase higher in SHR-DM than SHR. Apocynin attenuated antioxidant enzyme activity changes in SHR-DM-APO. Advanced glycation end-products and NADPH oxidase activity did not differ between groups.

Conclusion

Apocynin reduces oxidative stress independently of NADPH oxidase activity and does not change ventricular or myocardial function in spontaneously hypertensive rats with diabetes mellitus. The apocynin-induced myocardial functional impairment in SHR shows that apocynin actions need to be clarified during sustained chronic pressure overload.

Keywords

  • Systemic hypertension
  • Ventricular remodeling
  • Oxidative stress
  • NADPH oxidase
  • Myocardial fibrosis
  • Spontaneously hypertensive rat

Background

Systemic arterial hypertension and diabetes mellitus (DM) represent two important risk factors for cardiovascular disease, the leading cause of morbidity and mortality in the world [1, 2]. The coexistence of arterial hypertension and diabetes is commonly observed in adults and has been associated with a higher risk of cardiovascular events [1–3]. In the heart, the combination of DM and hypertension, also known as diabetic hypertensive cardiomyopathy leads to more extensive structural and functional cardiac changes than either condition alone [4–6]. However, the physiopathology of diabetes and hypertension-induced cardiac disease is not completely clear. Diabetes in hypertensive rodents impairs cardiac remodeling by exacerbating fibrosis, inflammation, microvascular changes, and oxidative stress resulting in intensified myocardial and cardiac dysfunction and increased mortality rate [5–11].

One of the major components of diabetic hypertensive cardiomyopathy is an increase in oxidative stress [5, 12, 13]. The term oxidative stress refers to disturbance in redox hemostasis occurring when reactive oxygen species (ROS) production exceeds their degradation by anti-oxidant defenses [14]. In diabetes, oxidative stress can be induced by hyperglycemia, hyperlipidemia, and inflammation. Antioxidants have been extensively evaluated for their potential to prevent or treat diabetic complications [15, 16]; however, research into the effects of anti-oxidants on cardiac remodeling remains scarce [17, 18].

Apocynin, a constituent of root extracts of the medicinal herb Picrorhiza kurroa [19], has been used in experimental studies as an antioxidant agent. Its actions include inhibiting ROS generation by the nicotinamide adenine dinucleotide phosphate (NADPH) oxidases and ROS scavenging [14, 20, 21]. NADPH oxidases produce ROS as their primary function and can be involved in the pathophysiology of cardiac diseases [14, 22–24]. As hyperglycemia increases NADPH oxidase activity [23–25], administration of its inhibitors has been tested in diabetic cardiomiopathy [26–29]. Studies performed in rodents with streptozotocin-induced DM have shown that NADPH oxidase activity is increased in DM [30]. Furthermore, inhibition of NADPH oxidase by apocynin alleviated myocardial contractile dysfunction in DM [28, 31, 32]. However, few studies have analyzed the effects of apocynin in diabetic and hypertensive animals [33], and none in cardiac remodeling. Despite the potential benefits of apocynin in oxidative stress, its effects are not completely understood and even pro-oxidant action has been reported in some experimental models [34, 35]. In this study, we evaluated the influence of apocynin on cardiac remodeling in spontaneously hypertensive rats with diabetes mellitus.

Methods

Experimental groups

Seven-month-old male spontaneously hypertensive rats (SHR) were purchased from the Multidisciplinary Center for Biological Investigation in Laboratory Animals Science, State University of Campinas, SP, Brazil. All animals were housed in a room under temperature control at 23 °C and kept on a 12-h light/dark cycle. Commercial chow and water were supplied ad libitum. The rats were assigned into four groups: control SHR (n = 16); SHR treated with apocynin (SHR-APO, n = 16); diabetic SHR (SHR-DM, n = 18); and diabetic SHR treated with apocynin (SHR-DM-APO, n = 19).

Diabetes was induced by intraperitoneal injection of streptozotocin (Sigma, St. Louis, MO, USA) at 40 mg/kg body weight diluted in 0.01 M citrate buffer pH 4.5 [36]. Control groups received an intraperitoneal injection of vehicle only. As the rats received only one moderate dose of streptozotocin, sucrose administration was not necessary to avoid hypoglycemia caused by sudden release of insulin due to massive islet β-cells necrosis [37]. Seven days after streptozotocin administration, blood glucose was measured by glucometer (Advantage®). Only rats with glycemia >220 mg/dL were considered diabetic and included in the study [5, 36]. Apocynin (Sigma, St. Louis, MO, USA) was added to drinking water at a dosage of 16 mg/kg/day for 8 weeks [38]. Water consumption was measured daily and body weight weekly. Systolic arterial pressure was measured before streptozotocin injection and at the end of experiment by tail-cuff method using a model 709-0610 electro-sphygmomanometer (Narco Bio-System ®, International Biomedical Inc., USA).

Echocardiographic study

Echocardiographic evaluation was performed before diabetes induction and at the end of the experimental period. We used a commercially available echocardiograph (General Electric Medical Systems, Vivid S6, Tirat Carmel, Israel) equipped with a 5–11.5 MHz multifrequency probe, as previously described [39–41]. Rats were anesthetized by intramuscular injection of a mixture of ketamine (50 mg/kg) and xylazine (0.5 mg/kg). Two-dimensionally guided M-mode images were obtained from short-axis views of the left ventricle (LV) just below the tip of the mitral-valve leaflets, and at the level of the aortic valve and left atrium. M-mode images were printed on a thermal printer (Sony UP-890MD) at a sweep speed of 100 mm/s. All LV structures were manually measured by the same observer (KO). Values obtained were the mean of at least five cardiac cycles on M-mode tracings. The following structural variables were measured: left atrium diameter (LA), LV diastolic diameter (LVDD), and LV diastolic and systolic posterior wall thickness (PWT and SWT, respectively). LV relative wall thickness (RWT) was calculated using the formula 2 × PWT/LVDD. LV mass was calculated using the formula [(LVDD + PWT + SWT)3 − (LVDD)3] × 1.04. LV function was assessed by the following parameters: midwall fractional shortening (MFS), tissue Doppler imaging (TDI) of mitral annulus systolic velocity (S’), myocardial performance index (Tei index), early and late diastolic mitral inflow velocities (E and A waves), E/A ratio, isovolumetric relaxation time (IVRT), TDI of early mitral annulus diastolic velocity (E’), and E/E’ ratio. Tissue Doppler variables (S’ and E’) were measured at the septal and lateral walls, and average values presented [42].

Myocardial functional evaluation

At the end of the experimental period, myocardial contractile performance was evaluated in isolated LV papillary muscle preparation as previously described [43, 44]. Rats were anesthetized (pentobarbital sodium, 50 mg/kg, intraperitoneally) and decapitated. Hearts were quickly removed and placed in oxygenated Krebs–Henseleit solution at 28 °C. LV anterior or posterior papillary muscle was dissected free, mounted between two spring clips, and placed vertically in a chamber containing Krebs–Henseleit solution at 28 °C and oxygenated with a mixture of 95 % O2 and 5 % CO2 (pH 7.38). The composition of the Krebs–Henseleit solution in mM was as follows: 118.5 NaCl, 4.69 KCl, 1.25 CaCl2, 1.16 MgSO4, 1.18 KH2PO4, 5.50 glucose, and 25.88 NaHCO3. The spring clips were attached to a Kyowa model 120T-20B force transducer and a lever system, which allowed for muscle length adjustment. Preparations were stimulated 12 times/min at a voltage 10 % above threshold.

After a 60 min period, during which the preparations were permitted to shorten while carrying light loads, muscles were loaded to contract isometrically and stretched to the apices of their length-tension curves. After a 5 min period, during which preparations performed isotonic contractions, muscles were again placed under isometric conditions, and the apex of the length-tension curve (Lmax) was determined. A 15 min period of stable isometric contraction was imposed prior to the experimental period. One isometric contraction was then recorded for later analysis.

The following parameters were measured from the isometric contraction: peak developed tension (DT), resting tension (RT), time to peak tension (TPT), maximum tension development rate (+dT/dt), and maximum tension decline rate (−dT/dt). To evaluate myocardial contractile reserve, papillary muscle mechanical performance was evaluated after the following positive inotropic stimulation: 30 s post-rest contraction, extracellular Ca2+ concentration increase to 2.5 mM, and β-adrenergic agonist isoproterenol (10−6 M) addition to the nutrient solution [45]. Papillary muscle cross-sectional area (CSA) was calculated from muscle weight and length by assuming cylindrical uniformity and a specific gravity of 1.0. All force data were normalized for muscle CSA.

Histologic analysis

Transverse LV sections were fixed in 10 % buffered formalin and embedded in paraffin. Sections (5 µm thick) were stained with hematoxylin–eosin and collagen-specific stain picrosirius red (Sirius red F3BA in aqueous saturated picric acid) [46]. In at least 50 myocytes from each LV, where the nucleus could clearly be identified, the smallest transverse diameters were measured [47]. On average, 20 microscopic fields were used to quantify interstitial collagen fraction. Perivascular collagen was excluded from this analysis [48]. Measurements were performed using a Leica microscope (magnification 40×) attached to a video camera and connected to a computer equipped with image analysis software (Image-Pro Plus 3.0, Media Cybernetics, Silver Spring, MD, USA).

Myocardial hydroxyproline concentration

Hydroxyproline concentration was measured in LV to estimate myocardial collagen content [49]. Tissue was dried using a Speedvac Concentrator (SC 100) attached to a refrigerated condensation trap (TRL 100) and vacuum pump (VP 100, Savant Instruments, Inc., Farmingdale, NY, USA). Dry tissue weight was measured and samples were hydrolyzed overnight at 100 °C with 6 N HCl (1 mL/10 mg dry tissue). An aliquot of the hydrolysate (50 μL) was transferred to an eppendorf tube and dried in the speedvac concentrator. One milliliter of deionized water was added and the sample transferred to a tube with a teflon screw cap. One milliliter of potassium borate buffer (pH 8.7) was added to maintain constant pH and the sample was oxidized with 0.3 mL of chloramine T solution at room temperature for 20 min. The addition of 1 mL of 3.6 M/L sodium thiosulfate with thorough mixing for 10 s stopped the oxidative process. The solution was saturated with 1.5 g KCl. The tubes were heated in boiling water for 20 min. After cooling to room temperature, the aqueous layer was extracted with 2.5 mL of toluene. One and a half milliliters of toluene extract were transferred to a 12 × 75 mm test tube. Then 0.6 mL of Ehrlich’s reagent was added and color allowed to develop for 30 min. Absorbance was read at 565 nm against a reagent blank. Deionized water and 20 μg/mL hydroxyproline were used as the blank and standard, respectively.

Western blotting analysis

Protein expression of type I (Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA, col1a1, sc-8784-r) and type III collagen (Abcam, Cambridge, UK, col3a1, ab6310) and lysil oxidase (Abcam, LOX1, ab60178) was analyzed by Western blot as previously described [50, 51]. Samples were separated on polyacrylamide gel and then transferred to a nitrocellulose membrane. After blockage, the membrane was incubated with the primary antibodies overnight at 4 °C. The membrane was then washed with PBS and Tween 20 and incubated with secondary peroxidase-conjugated antibodies (Santa Cuz Biotechnology, anti-mouse, sc-2005, and anti-rabbit, sc-2004) for 90 min at room temperature. ECL western blotting substrate (Pierce Protein Research Products, Rockford, USA) was used to detect bound antibodies. The membrane was then stripped (Restore Western Blot Stripping Buffer, Pierce Protein Research Products, Rockford, USA) to remove antibodies. After blockage, membrane was incubated with anti-GAPDH antibody (Santa Cruz Biotechnology, GAPDH 6C5 sc-32233). Protein levels were normalized to GAPDH.

Myocardial oxidative stress evaluation

Frozen left ventricle myocardium (∼200 mg) was homogenized in phosphate buffer (0.1 M) pH 7.4 and centrifuged at 12,000g for 15 min at 4 °C. The supernatant was assayed for total protein, lipid hydroperoxide, and anti-oxidant enzyme activity [52]. Lipid hydroperoxide concentration was determined in a medium containing methanol 90 % (v/v), 250 μM ammonium ferrous sulfate, 100 μM xylenol orange, 25 mM sulfuric acid, and 4 mM butylated hydroxytoluene. The solution was incubated for 30 min at room temperature and measurement was performed at 560 nm. Glutathione peroxidase (GSH-Px, E.C.1.11.1.9) was assayed using 0.15 M phosphate buffer, pH 7.0, containing 5 mM EDTA, 0.1 mL of 0.0084 M NADPH, 4 μg of GSSG-reductase, 1.125 M sodium azide, and 0.15 M glutathione reduced form (GSH) in a total volume of 0.3 mL. Superoxide dismutase (SOD, E.C.1.15.1.1.) activity was determined based on its ability to inhibit reduction of nitroblue tetrazolium, in a medium containing 50 mM phosphate buffer pH 7.4, 0.1 mM EDTA, 50 μM nitroblue tetrazolium, 78 μM NADH, and 3.3 μM phenazine methosulfate. One unit of SOD was defined as the amount of protein needed to decrease the reference rate to 50 % of maximum inhibition. Catalase (E.C.1.11.1.6.) activity was evaluated in 50 mM phosphate buffer, pH 7.0, with 10 mM hydrogen peroxide. One unit of catalase was defined as the amount of enzyme needed to degrade 1 μmol H2O2 over 60 s, at 240 nm. Enzyme activity was analyzed at 25 °C using a microplate reader system (μQuant-MQX 200 with KC Junior software, Bio-TeK Instruments, Winooski, VT, USA). All reagents were purchased from Sigma (St. Louis, MO, USA).

Advanced glycation end-products (AGE) quantification

Paraffin-embedded myocardial tissue was cut, mounted on slides for immunohistochemical analysis, and deparaffinized with EDTA for antigen retrieval [53, 54]. Blockade was performed with hydrogen peroxide, goat serum, and avidin/biotin. Tissue sections were incubated with primary antibody (rabbit polyclonal antibody to AGE; Ab23722, Abcam) for 1 h, then with a secondary antibody (goat polyclonal secondary antibody to rabbit IgG HL—Biotin; Ab6720, Abcam) for 2 h, at room temperature, and for 15 min with streptavidin. Sections were then stained with 3,3′-diaminobenzidine and counterstained with hematoxylin [53]. Analysis was performed using a video camera coupled to a microscope connected to a computer with an image analyzes program (Image Pro Plus 6.0, Media Cybernetics, Silver Spring, Maryland, USA). Cardiac tissue components were identified according to color enhancement. AGEs yield a brown color while myocytes are seen in purple. Areas containing blood vessels were excluded from this analysis.

NADPH oxidase activity

NADPH oxidase activity was evaluated in membrane-enriched cellular fraction by quantifying dihydroethidium (DHE) oxidation-derived fluorescent compounds, 2-hydroxyethidium (EOH) and ethidium, by HPLC according to a previously described method [55, 56]. Cardiac muscle was washed in PBS to remove blood. Muscle fragments (∼200 mg) were homogenized in 1 mL of ice-cold lysis buffer containing 50 mM Tris (pH 7.4), 100 mM DTPA, 0.1 % β-mercaptoethanol, and protease inhibitors. The samples were then sonicated (3 cycles of 10 s at 8 W) and centrifuged at 1000g for 3 min, at 4 °C. The supernatant was transferred to another microtube and centrifuged at 18,000g for 10 min at 4 °C. The supernatant was then centrifuged at 100,000g for 45 min, at 4 °C. The supernatant was discarded and the pellet resuspended in 100 µL of lysis buffer [56]. Total protein content was quantified by the Bradford method. Subsequently, 20 µg of membrane-enriched cellular fraction was incubated in phosphate buffer (50 mM, pH 7.4, with 0.1 mM DTPA) containing DHE (50 µM) and NADPH (300 µM), to a final volume of 100 µL, for 30 min at 37 °C in the dark. After adding 40 µL of 10 % trichloroacetic acid, the samples were ice-cooled for 10 min in the dark, and centrifuged at 12,000g for 10 min at 4 °C. The supernatant was analyzed by HPLC and the fluorescent DHE-derived products were quantified, as previously described [55, 56].

Statistical analysis

Results are expressed as mean and standard deviation or median and 25th and 75th percentiles according to normal or non-normal distribution, respectively. Variables were compared by two-factor ANOVA followed by the Tukey test for normal distribution data or the Dunn test for non-normal distribution data. All rats were subjected to functional studies as their parameters usually present an elevated variability. In papillary muscle preparations, some animals were discarded due to technical problems. For all morphological and molecular analyzes, samples were randomly chosen. Statistical significance was accepted at p < 0.05.

Results

Initial and final body weight, heart rate, systolic blood pressure, and blood glucose are shown in Table 1. Among streptozotocin injected rats, 27.5 % did not develop diabetes, and were excluded from the study. At the end of protocol both diabetic groups presented lower body weight and higher glycemia compared to the respective control groups; apocynin administration did not change body weight, heart rate or glycemia. Initial and final blood pressure did not differ between groups.
Table 1

Initial and final body weight, heart rate, systolic blood pressure, and blood glucose

 

SHR (n = 16)

SHR-APO (n = 16)

SHR-DM (n = 13)

SHR-DM-APO (n = 14)

Initial BW (g)

360 ± 27

361 ± 28

356 ± 16

359 ± 18

Final BW (g)

362 ± 25

364 ± 27

254 ± 36*

239 ± 37#

Initial heart rate (bpm)

294 ± 40.4

304 ± 46.7

308 ± 50.8

304 ± 46.7

Final heart rate (bpm)

269 ± 48.3

287 ± 45.0

255 ± 38.5

249 ± 35.9#

Initial BP (mm Hg)

189 ± 19

189 ± 18

191 ± 18

190 ± 17

Final BP (mm Hg)

184 ± 22

186 ± 21

187 ± 28

184 ± 25

Initial glucose mg/dL)

90 (83–101)

93 (83–100)

91 (90–100)

94 (90–99)

Final glucose (mg/dL)

93 (88–101)

94 (88–107)

600 (542–600)*

600 (538–600)#

Data are expressed as mean ± standard deviation or median and 25th and 75th percentiles

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; BW body weight; bpm beats per min; BP systolic blood pressure

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

At the beginning of the protocol, all echocardiographic variables were similar between groups (data not shown). Echocardiographic structural data assessed at the end of the protocol (Table 2) showed higher normalized LV diastolic diameter and left atrium diameter in both diabetic compared to normoglycemic groups. LV mass-to-body weight ratio was higher in SHR-DM than SHR, and LV posterior wall thickness was lower in SHR-DM-APO than SHR-APO. LV functional parameters are presented in Table 3. Systolic function did not differ between groups. Isovolumetric relaxation time was higher in diabetic groups, indicating diastolic dysfunction.
Table 2

Echocardiographic structural data

 

SHR (n = 16)

SHR-APO (n = 16)

SHR-DM (n = 13)

SHR-DM-APO (n = 14)

LVDD/BW (mm/kg)

19.5 ± 1.87

20.4 ± 2.27

26.2 ± 5.04*

26.6 ± 4.71#

LA/BW (mm/kg)

17.3 ± 2.06

17.3 ± 2.14

20.5 ± 3.97*

21.1 ± 3.23#

PWT (mm)

1.69 ± 0.17

1.71 ± 0.19

1.63 ± 0.17

1.55 ± 0.16#

RWT

0.46 ± 0.06

0.45 ± 0.07

0.47 ± 0.07

0.46 ± 0.07

LVM/BW (g/kg)

2.34 ± 0.37

2.54 ± 0.57

2.89 ± 0.64*

2.70 ± 0.59

Data are expressed as mean ± standard deviation

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; LVDD left ventricular (LV) diastolic diameter; BW body weight; LA left atrial diameter; PWT LV posterior wall thickness; RWT relative wall thickness; LVM LV mass

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

Table 3

Echocardiographic left ventricular functional data

 

SHR (n = 16)

SHR-APO (n = 16)

SHR-DM (n = 13)

SHR-DM-APO (n = 14)

MFS (%)

25.9 ± 3.02

25.1 ± 3.53

25.8 ± 2.36

26.3 ± 3.05

TDI S’ (average, cm/s)

3.25 (2.63–3.38)

2.75 (2.50–3.19)

3.00 (2.75–3.00)

2.75 (2.50–3.00)

Tei index

0.61 ± 0.09

0.61 ± 0.12

0.60 ± 0.09

0.61 ± 0.12

E/A

1.72 ± 0.56

1.64 ± 0.58

1.38 ± 0.45

1.70 ± 0.38

IVRT (ms)

31.9 ± 3.12

32.9 ± 5.05

37.2 ± 4.00*

38.9 ± 5.57#

E/E’

23.3 ± 4.65

24.3 ± 5.03

23.6 ± 4.19

24.1 ± 5.99

Data are expressed as mean ± standard deviation or median and 25th and 75th percentiles

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; MFS midwall fractional shortening; TDI S’ tissue Doppler imaging (TDI) of mitral annulus systolic velocity; E/A ratio between early (E)-to-late (A) diastolic mitral inflow; IVRT isovolumic relaxation time; E’ TDI of early mitral annulus diastolic velocity

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

Data from LV papillary muscle function at basal condition are shown in Table 4. Apocynin decreased developed tension only in non-diabetic rats. The +dT/dt and −dT/dt were lower and time to peak tension higher in both diabetic groups independently of apocynin treatment. Results from positive inotropic stimulation are shown in Table 5. In 30 s post-rest contraction, developed tension and +dT/dt were lower in SHR-APO than SHR. After all inotropic stimulation, −dT/dt was lower and time to peak tension higher in both diabetic groups than their respective controls, and +dT/dt was lower in SHR-DM than SHR. SHR-DM-APO did not differ from SHR-DM, except by −dT/dt which was lower in SHR-DM-APO during 30 s post-rest contraction.
Table 4

LV papillary muscle data

 

SHR (n = 13)

SHR-APO (n = 11)

SHR-DM (n = 11)

SHR-DM-APO (n = 10)

DT (g/mm2)

11.2 ± 2.37

9.22 ± 1.35*

10.5 ± 2.65

9.17 ± 2.52

RT (g/mm2)

1.06 ± 0.29

1.09 ± 0.30

1.10 ± 0.40

1.11 ± 0.63

+dT/dt (g/mm2/s)

112 ± 24.9

96.2 ± 18.2

92.4 ± 23.1*

85.0 ± 24.2#

TPT (ms)

203 ± 18.4

189 ± 14.5

235 ± 18.6*

227 ± 17.7#

−dT/dt (g/mm2/s)

40.6 ± 10.1

35.1 ± 5.05

33.3 ± 8.92*

27.5 ± 8.31#

CSA (mm2)

0.71 ± 0.13

0.78 ± 0,12

0.72 ± 0.11

0.75 ± 0.14

Data are expressed as mean ± standard deviation

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; DT peak of developed tension; RT resting tension; +dT/dt maximum rate of tension development; TPT time to peak tension; −dT/dt maximum rate of tension decline; CSA papillary muscle cross sectional area

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

Table 5

Isolated papillary muscle data after positive inotropic stimulation

  

SHR (n = 13)

SHR-APO (n = 11)

SHR-DM (n = 11)

SHR-DM-APO (n = 10)

PP30

DT

13.7 ± 3.09

11.1 ± 1.69*

11.9 ± 3.01

10.3 ± 2.87

RT

1.04 ± 0.30

1.06 ± 0.31

1.24 ± 0.52

1.25 ± 0.62

+dT/dt

140 ± 33.4

115 ± 23.1*

105 ± 25.0*

95.2 ± 27.8

TPT

215 ± 17.1

209 ± 13.0

255 ± 27.0*

250 ± 22.6#

−dT/dt

42.6 ± 9.67

35.8 ± 4.58

32.4 ± 8.73*

25.1 ± 8.45#§

2.5 mM [Ca+2]0

DT

12.5 ± 2.78

10.3 ± 1.49

11.0 ± 2.95

9.79 ± 2.85

RT

0.87 ± 0.30

0.90 ± 0.31

0.90 ± 0.34

0.92 ± 0.52

+dT/dt

140 ± 31.9

117 ± 21.4

108 ± 28.0*

97.9 ± 28.7

TPT

192 ± 16.9

186 ± 17.8

224 ± 23.2*

216 ± 15.1#

−dT/dt

48.3 ± 10.6

40.0 ± 6.27

38.4 ± 11.6*

30.7 ± 10.2#

Iso 10−6 M

DT

11.4 (8.33–13.5)

9.70 (8.77–10.1)

9.68 (8.60–10.1)

9.47 (6.08–10.8)

RT

0.85 ± 0.43

0.86 ± 0.34

0.84 ± 0.28

0.83 ± 0.52

+dT/dt

136 ± 34.0

118 ± 22.4

96.9 ± 26.6*

96.7 ± 31.7

TPT

163 ± 11.1

157 ± 9.49

184 ± 16.9*

190 ± 15.8#

−dT/dt

67.9 ± 16.6

58.3 ± 8.03

46.4 ± 13.4*

39.1 ± 13.7#

Data are expressed as mean ± standard deviation or median and 25th and 75th percentile

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; PP30 30 s post-rest contraction; 2.5 mM [Ca +2 ] 0 extracellular Ca2+ concentration increased to 2.5 mM; Iso 10 −6 M β-adrenergic agonist isoproterenol (10−6 M) added to the nutrient solution; DT peak of developed tension (g/mm2); RT resting tension (g/mm2); +dT/dt maximum rate of tension development (g/mm2/s); TPT time to peak tension (ms); −dT/dt maximum rate of tension decline (g/mm2/s)

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO; § p < 0.05 vs SHR-DM

Myocyte diameter did not differ between groups (Table 6). Regarding the extracellular matrix, left ventricular myocardial hydroxyproline concentration was higher in SHR-DM than SHR and interstitial collagen fraction was higher in SHR-DM-APO than SHR-APO. Specifically, type III collagen expression was lower in both diabetic groups (Table 7).
Table 6

Left ventricular morphometric parameters and hydroxyproline concentration

 

SHR (n = 10)

SHR-APO (n = 10)

SHR-DM (n = 10)

SHR-DM-APO (n = 10)

Diameter (μm)

11.1 (10.3–12.1)

10.3 (10.3–12.2)

10.2 (10.1–12.1)

10.6 (9.88–11.0)

ICF (%)

6.95 ± 2.57

5.47 ± 2.41

9.93 ± 3.59

9.47 ± 4.30#

HOP (mg/g)

2.66 ± 0.29

3.08 ± 0.58

3.27 ± 0.45*

3.29 ± 0.51

Data are expressed as mean ± standard deviation or median and 25th and 75th percentile

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; Diameter myocyte lower diameter; HOP myocardial hydroxyproline concentration; ICF myocardial interstitial collagen fraction

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

Table 7

Left ventricular myocardial protein expression

 

SHR (n = 7)

SHR-APO (n = 7)

SHR-DM (n = 7)

SHR-DM-APO (n = 7)

Type I collagen

1.00 ± 0.41

1.08 ± 0.33

0.99 ± 0.28

0.96 ± 0.14

Type III collagen

1.00 ± 0.10

0.97 ± 0.11

0.77 ± 0.17*

0.83 ± 0.10#

Type I/III collagen ratio

1.00 ± 0.37

1.16 ± 0.42

1.33 ± 0.33

1.15 ± 0.13

Lysyl oxidase

1.00 ± 0.19

0.91 ± 0.15

0.90 ± 0.20

0.89 ± 0.13

Data are expressed as mean ± standard deviation

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin

Two-factor ANOVA; * p < 0.05 vs SHR; # p < 0.05 vs SHR-APO

Oxidative stress parameters are shown in Fig. 1. Lipid hydroperoxide concentration was higher in SHR-DM than SHR and SHR-DM-APO. Glutathione peroxidase activity was lower in SHR-APO and SHR-DM than SHR and higher in SHR-DM-APO than SHR-DM. NADPH oxidase activity and advanced glycation end-products did not differ between groups Table 8.
Table 8

Left ventricular myocardial oxidative stress

 

SHR (n = 8)

SHR-APO (n = 8)

SHR-DM (n = 8)

SHR-DM-APO (n = 8)

AGEs

2.47 (2.35–4.16)

2.54 (1.90–3.86)

2.61 (1.83–4.16)

2.68 (2.09–4.97)

DHE

39.1 (38.2–39.7)

39.9 (39.0–40.2)

39.5 (37.4–40.6)

39.4 (38.2–40.2)

EOH

39.6 (31.9–47.6)

38.4 (31.7–40.2)

34.5 (22.4–38.0)

33.2 (29.1–40.1)

E

112 (86.6–165)

97.5 (85.9–222)

119 (112–163)

129 (106–164)

Data are expressed as mean ± standard deviation or median and 25th and 75th percentile

SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin; AGEs advanced glycation end-products (%); DHE dihydroethidium (µM); EOH 2-hydroxyethidium (µM); E ethidium (µM)

Two-factor ANOVA; p > 0.05

Fig. 1
Fig. 1

Left ventricular myocardial oxidative stress markers. Lipid hydroperoxide (a), superoxide dismutase (b), glutathione peroxidase (c) and catalase (d). Data are expressed as mean ± standard deviation. SHR spontaneously hypertensive rats; SHR-APO SHR treated with apocynin; SHR-DM diabetic SHR; SHR-DM-APO diabetic SHR treated with apocynin. Two-factor ANOVA; *p < 0.05 vs SHR; #p < 0.05 vs SHR-APO; §p < 0.05 vs SHR-DM-APO

Discussion

In this study we evaluated the influence of anti-oxidant apocynin on cardiac remodeling in spontaneously hypertensive rats with type 1 diabetes mellitus

SHR has extensively been used to evaluate long-term pressure overload-induced cardiac remodeling [48]. At 1 month old, arterial hypertension starts to increase stimulating left ventricular hypertrophy, which remains functionally stable until 18–22 months of age [57, 58]. Therefore, in this study we evaluated seven-month-old rats as they had already developed arterial hypertension and stable left ventricular hypertrophy.

Diabetes was caused by streptozotocin, which has been widely used to induce type 1 diabetes mellitus in rodents [59–61]. Rats with streptozotocin-induced DM can develop several diabetic complications, such as neuropathy, nephropathy, and atherosclerosis [37]. The models are used not only to study pathological consequences of DM, but also to evaluate experimental approaches for the treatment of this condition [37]. As previously reported [61–63], streptozotocin-induced diabetes mellitus is characterized by body weight loss and increased blood glucose. Despite the lower final body weight in diabetic rats, blood pressure did not differ between groups. This result is in accordance with previous studies on diabetic SHR [5, 8]. Therefore, we can discard blood pressure changes participating in the cardiac alterations observed in our diabetic SHR. In experimental studies, apocynin has been used in various dosages, ranging from 4 [32] to 100 mg/kg/day [64, 65]. However, moderate apocynin doses, as administered to our rats (16 mg/kg/day), have often been used in rodents [31, 66]. In this study, as in previous reports, apocynin did not modulate body weight, glycemia levels or systemic blood pressure [31, 32, 67, 68].

In this study, diabetic cardiomyopathy was characterized by left chambers dilation, LV mass increase, and diastolic dysfunction in SHR. Myocardial functional changes in SHR-DM included impaired systolic and diastolic function, characterized by a decreased maximum tension development rate and maximum tension decline rate and increased time to peak tension at basal contraction and after all positive inotropic stimulation. Similar structural and functional cardiac alterations have been described in normotensive and hypertensive diabetic rats [5, 18, 69–71]. Cardiac function in elderly SHR was more extensively jeopardized by diabetes than in this study with younger SHR [5].

As potential mechanisms involved in cardiac dilation and dysfunction, we observed that SHR-DM had increased oxidative stress, characterized by higher myocardial lipid hydroperoxide concentration, with altered activity of anti-oxidant enzymes glutathione peroxidase and catalase. SHR-DM also present higher myocardial fibrosis, as shown by the increased myocardial hydroxyproline concentration. Hydroxyproline is the main component of the collagen molecule and can only be found at small concentrations in a limited number of other proteins. Evaluation of myocardial fibrosis through hydroxyproline is considered more precise than histological analyses [49]. Mechanical properties of myocardium are influenced by both the content and type of collagen. Fibrillar collagen types I and III are the main components of the cardiac extracellular matrix [72]. Type I collagen is associated with higher stiffness in different tissues than type III collagen [73, 74]. Alterations in collagen fiber quantities and type have often been observed in diabetic cardiomyopathy [69, 75]. Therefore, in this study, the increased collagen concentration, reduced type III collagen expression, and augmented oxidative stress may be involved in the cardiac and myocardial dysfunction observed in SHR-DM.

Apocynin administration did not change cardiac structures or function in control SHR. However, in papillary muscles, apocynin reduced developed tension at basal conditions and in post-rest contraction in SHR-APO compared to SHR. Despite lower glutathione peroxidase activity in SHR-APO, oxidative stress did not differ between SHR-APO and SHR. We can therefore conclude that apocynin impaired myocardial function independently of changes in oxidative stress. This result was unexpected as apocynin displayed beneficial effects in different experimental models of cardiac injury. In rodents with pressure overload induced by abdominal aorta banding [76] or angiotensin II infusion [77], apocynin attenuated cardiac hypertrophy, oxidative stress, cardiac fibrosis, and diastolic dysfunction. These effects were mediated at least in part through a pathway involving NADPH oxidase [77]. Also in type 4 cardiorenal syndrome [78] and chronic renal failure [79], apocynin attenuated cardiac injury. On the other hand, apocynin can exert cytotoxic effects in cell cultures [80]. One study recently showed that apocynin downregulates Akt activity in mouse embryonic stem cells [35]. Also in vascular smooth muscle cells, apocynin prevented the activation of Akt by hydrogen peroxide and by intracellular radical generator menadione [20]. The Akt signaling pathway is involved in myocyte cell surviving [81]; it is therefore possible that its inhibition contributed to the myocardial impairment seen in SHR-APO. As, to the best of our knowledge, this is the first study to evaluate the effects of apocynin on cardiac remodeling in adult SHR, we cannot compare our results with literature data.

In diabetic SHR, apocynin reduced oxidative stress, evaluated by the myocardial lipid hydroperoxide concentration, and preserved anti-oxidant enzyme activity in SHR-DM-APO compared to SHR-DM. Despite the lower oxidative stress, LV and myocardial function was not changed by apocynin, except for a lower post-rest contraction −dT/dt in SHR-DM-APO than SHR-DM. Myocardial fibrosis did not differ from SHR-DM.

Apocynin can be isolated and purified from several plant species such as Picrorhiza kurroa, and has been evaluated in experimental studies as an anti-oxidant agent [82–84]. It has mostly been used as an inhibitor of NADPH oxidase activity [20, 21, 82, 85]. In this study, NADPH oxidase activity and AGEs did not differ between groups. It is possible that adult SHR already have increased basal levels of NADPH oxidase activity and AGEs [86, 87] which could not be modulated by diabetes or apocynin. In fact, 3-month old diabetic SHR presented higher cardiac NADPH oxidase activity than control SHR [88]. Thus, apocynin reduced myocardial oxidative stress in SHR-DM-APO through mechanisms not involving NADPH oxidase activity. In cultured cells, apocynin acted as a ROS scavenger and not an NADPH oxidase inhibitor [20]. Apocynin can also modulate nitric oxide-dependent pathways. Apocynin has been shown to increase nitric oxide bioavailability through, at least partly, induction of nitric oxide synthase [89]. In vivo studies showed that apocynin restored normal flow mediated nitric oxide signaling in young SHR arteries [90] and increased nitric oxide synthase activity in persistent pulmonary hypertension of the newborn [91]. Additional studies are needed to clarify the effects of apocynin on cardiac remodeling in SHR with and without diabetes.

In conclusion, apocynin reduces oxidative stress through unrelated NADPH oxidase activity mechanisms and does not change ventricular or myocardial function in spontaneously hypertensive rats with type 1 diabetes. The apocynin-induced myocardial functional impairment in spontaneously hypertensive rats without diabetes shows that apocynin action during sustained chronic pressure overload needs to be clarified.

Abbreviations

A wave: 

late diastolic mitral inflow velocity

AGE: 

advanced glycation end-products

APO: 

apocynin

BP: 

systolic blood pressure

BW: 

body weight

CSA: 

cross-sectional area

DHE: 

dihydroethidium

DM: 

diabetes mellitus

DT: 

peak developed tension

−dT/dt: 

maximum tension decline rate

+dT/dt: 

maximum tension development rate

E: 

ethidium

E’: 

tissue Doppler imaging of early mitral annulus diastolic velocity

E wave: 

early diastolic mitral inflow velocity

E/A: 

ratio between early (E)-to-late (A) diastolic mitral inflow

EOH: 

2-hydroxyethidium

GSH: 

glutathione reduced

GSH-Px: 

glutathione peroxidase

HOP: 

myocardial hydroxyproline concentration

ICF: 

myocardial interstitial collagen fraction

Iso: 

isoproterenol

IVRT: 

isovolumetric relaxation time

LA: 

left atrium diameter

LH: 

lipid hydroperoxide

Lmax: 

apex of the length-tension curve

LV: 

left ventricle

LVDD: 

left ventricle diastolic diameter

LVM: 

left ventricle mass

MFS: 

midwall fractional shortening

NADPH: 

nicotinamide adenine dinucleotide phosphate

PP30: 

30 s post-rest contraction

PWT: 

left ventricle diastolic posterior wall thickness

ROS: 

reactive oxygen species

RT: 

resting tension

RWT: 

left ventricle relative wall thickness

S’: 

mitral annulus systolic velocity

SHR: 

spontaneously hypertensive rats

SOD: 

superoxide dismutase

SWT: 

left ventricle systolic posterior wall thickness

TDI: 

tissue Doppler imaging

TPT: 

time to peak tension

[Ca+2]0 : 

extracellular Ca2+ concentration

Declarations

Authors’ contributions

CMR and KO contributed to conception and design of study, acquisition of data, analysis and interpretation of data, and manuscript writing; RG, DHSC, GNG, CG, RMQ, DMS and PR contributed to data collection; AAHF, ACC, IFP, FRL, DCF and CRC contributed to data collection and analysis; MPO contributed to manuscript writing. All authors have given final approval of the version to be published. All authors read and approved the final manuscript.

Acknowledgements

We are grateful to Jose C Georgette for technical assistance and Colin Edward Knaggs for English editing.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

All authors have read and approved the publication of this manuscript.

Availability of data and materials

All data supporting the conclusions of the manuscript are presented in the main paper.

Ethics approval

All experiments and procedures were approved by the Ethics Committee of Botucatu Medical School, Sao Paulo State University, UNESP, Botucatu, SP, Brazil (protocol CEUA 1124-2015).

Grants

Financial support was provided by CAPES, CNPq (306770/2015-6 and 308674/2015-4), FAPESP (2015/17539-5 and 2015/02324-3), and PROPe, UNESP.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Internal Medicine, Botucatu Medical School, Sao Paulo State University-UNESP, Botucatu, Sao Paulo, Brazil
(2)
Sagrado Coração University-USC, Bauru, Sao Paulo, Brazil
(3)
Department of Chemistry and Biochemistry, Institute of Biosciences, Sao Paulo State University-UNESP, Botucatu, Sao Paulo, Brazil
(4)
Department of Physiology and Cardiothoracic Surgery, Faculty of Medicine, University of Porto, Porto, Portugal
(5)
Department of Cardiopneumology, Medical School, Sao Paulo University-USP, Sao Paulo, Brazil
(6)
Department of Pathology, Medical School, Sao Paulo State University-UNESP, Botucatu, Sao Paulo, Brazil

References

  1. Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, et al. Heart disease and stroke statistics—2016 update: a report from the American Heart Association. Circulation. 2016;133:e38–360.View ArticlePubMedGoogle Scholar
  2. Association American Diabetes. Classification and diagnosis of diabetes. Diabetes Care. 2016;39:S13–22.Google Scholar
  3. Matheus AS, Tannus LR, Cobas RA, Palma CC, Negrato CA, Gomes MB. Impact of diabetes on cardiovascular disease: an update. Int J Hypertens. 2013;2013:653789.View ArticlePubMedPubMed CentralGoogle Scholar
  4. Falcão-Pires I, Palladini G, Gonçalves N, van der Velden J, Moreira-Gonçalves D, Miranda-Silva D, et al. Distinct mechanisms for diastolic dysfunction in diabetes mellitus and chronic pressure-overload. Basic Res Cardiol. 2011;106:801–14.View ArticlePubMedGoogle Scholar
  5. Rosa CM, Xavier NP, Campos DHS, Fernandes AAH, Cezar MDM, Martinez PF, et al. Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats. Cardiovasc Diabetol. 2013;12:152.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Gonçalves N, Gomes-Ferreira C, Moura C, Roncon-Albuquerque R Jr, Leite-Moreira AF, Falcão-Pires I. Worse cardiac remodeling in response to pressure overload in type 2 diabetes mellitus. Int J Cardiol. 2016;217:195–204.View ArticlePubMedGoogle Scholar
  7. Pijl AJ, van der Wal AC, Mathy MJ, Kam KL, Hendriks MG, Pfaffendorf M, et al. Streptozotocin-induced diabetes mellitus in spontaneously hypertensive rats: a pathophysiological model for the combined effects of hypertension and diabetes. J Pharmacol Toxicol Methods. 1994;32:225–33.View ArticlePubMedGoogle Scholar
  8. Wienen W, Richard S, Champeroux P, Audeval-Gerard C. Comparative antihypertensive and renoprotective effects of telmisartan and lisinopril after long-term treatment in hypertensive diabetic rats. J Renin Angiotensin Aldosterone Syst. 2001;2:31–6.View ArticlePubMedGoogle Scholar
  9. Wold LE, Relling DP, Colligan PB, Scott GI, Hintz KK, Ren BH, et al. Characterization of contractile function in diabetic hypertensive cardiomyopathy in adult rat ventricular myocytes. J Mol Cell Cardiol. 2001;33:1719–26.View ArticlePubMedGoogle Scholar
  10. Black MJ, D’Amore A, Auden A, Stamp L, Osicka T, Panagiotopoulos S, et al. Chronic type 1 diabetes in spontaneously hypertensive rats leads to exacerbated cardiac fibrosis. Cardiovasc Pathol. 2010;19:361–70.View ArticlePubMedGoogle Scholar
  11. Russo I, Frangogiannis NG. Diabetes-associated cardiac fibrosis: cellular effectors, molecular mechanisms and therapeutic opportunities. J Mol Cell Cardiol. 2016;90:84–93.View ArticlePubMedGoogle Scholar
  12. Paravicini TM, Touyz RM. NADPH oxidases, reactive oxygen species, and hypertension: clinical implications and therapeutic possibilities. Diabetes Care. 2008;31(Suppl 2):170–80.View ArticleGoogle Scholar
  13. Biswas SK. Does the interdependence between oxidative stress and inflammation explain the antioxidant paradox? Oxid Med Cell Longev. 2016;2016:5698931.View ArticlePubMedPubMed CentralGoogle Scholar
  14. Altenhofer S, Radermacher KA, Kleikers PWM, Wingler K, Schmidt HH. Evolution of NADPH oxidase inhibitors: selectivity and mechanisms for target engagement. Antioxid Redox Signal. 2014;23:406–27.View ArticlePubMedGoogle Scholar
  15. Freidja ML, Vessières E, Toutain B, Guihot AL, Custaud MA, Loufrani L, et al. AGEs breaking and antioxidant treatment improves endothelium-dependent dilation without effect on flow-mediated remodeling of resistance arteries in old Zucker diabetic rats. Cardiovasc Diabetol. 2014;13:55.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Oyenihi AB, Ayeleso AO, Mukwevho E, Masola B. Antioxidant strategies in the management of diabetic neuropathy. Biomed Res Int. 2015;2015:515042.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Liu Q, Wang S, Cai L. Diabetic cardiomyopathy and its mechanisms: role of oxidative stress and damage. J Diabetes Invest. 2014;5:623–34.View ArticleGoogle Scholar
  18. Guimarães JF, Muzio BP, Rosa CM, Nascimento AF, Sugizaki MM, Fernandes AAH, et al. Rutin administration attenuates myocardial dysfunction in diabetic rats. Cardiovasc Diabetol. 2015;14:90.View ArticlePubMedPubMed CentralGoogle Scholar
  19. Van den Worm E, Beukelman CJ, Van den Berg AJ, Kroes BH, Labadie RP, Van Dijk H. Effects of methoxylation of apocynin and analogs on the inhibition of reactive oxygen species production by stimulated human neutrophils. Eur J Pharmacol. 2001;433:225–30.View ArticlePubMedGoogle Scholar
  20. Heumüller S, Wind S, Barbosa-Sicard E, Schmidt HH, Busse R, Schröder K, et al. Apocynin is not an inhibitor of vascular NADPH oxidases but an antioxidant. Hypertension. 2008;51:211–7.View ArticlePubMedGoogle Scholar
  21. Touyz RM. Apocynin, NADPH oxidase, and vascular cells: a complex matter. Hypertension. 2008;51:172–4.View ArticlePubMedGoogle Scholar
  22. Heymes C, Bendall JK, Ratajczak P, Cave AC, Samuel JL, Hasenfuss G, et al. Increased myocardial NADPH oxidase activity in human heart failure. J Am Coll Cardiol. 2003;41:2164–71.View ArticlePubMedGoogle Scholar
  23. Teshima Y, Takahashi N, Nishio S, Saito S, Kondo H, Fukui A, et al. Production of reactive oxygen species in the diabetic heart. Roles of mitochondria and NADPH oxidase. Circ J. 2014;78:300–6.View ArticlePubMedGoogle Scholar
  24. Kayama Y, Raaz U, Jagger A, Adam M, Schellinger IN, Sakamoto M, et al. Diabetic cardiovascular disease induced by oxidative stress. Int J Mol Sci. 2015;16:25234–63.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Ding H, Hashem M, Triggle C. Increased oxidative stress in the streptozotocin-induced diabetic apoE-deficient mouse: changes in expression of NADPH oxidase subunits and eNOS. Eur J Pharmacol. 2007;567:121–8.View ArticleGoogle Scholar
  26. Privratsky JR, Wold LE, Sowers JR, Quinn MT, Ren J. AT1 blockade prevents glucose-induced cardiac dysfunction in ventricular myocytes: role of the AT1 receptor and NADPH oxidase. Hypertension. 2003;42:206–12.View ArticlePubMedGoogle Scholar
  27. Zhou G, Li X, Hein DW, Xiang X, Marshall JP, Prabhu SD, et al. Metallothionein suppresses angiotensin II-induced nicotinamide adenine dinucleotide phosphate oxidade activation, nitrosative stress, apoptosis, and pathological remodeling in the diabetic heart. J Am Coll Cardiol. 2008;52:655–66.View ArticlePubMedGoogle Scholar
  28. Li J, Zhu H, Shen E, Wan L, Arnold JM, Peng T. Deficiency of Rac1 blocks NADPH oxidase activation, inhibits endoplasmic reticulum stress and reduces myocardial remodeling in type-I diabetic mice. Diabetes. 2010;59:2033–42.View ArticlePubMedPubMed CentralGoogle Scholar
  29. Cairong L, Shouyi G, Fei C. NADPH oxidase-dependent NLRP3 inflammasome activation and its important role in diabetic cardiomyopathy. J Am Coll Cardiol. 2015. doi:10.1016/j.jacc.2015.06.070.Google Scholar
  30. Maalouf RM, Eid AA, Gorin YC, Block K, Escobar GP, Bailey S, et al. Nox4-derived reactive oxygen species mediate cardiomyocyte injury in early type 1 diabetes. Am J Physiol Cell Physiol. 2012;302:C597–604.View ArticlePubMedGoogle Scholar
  31. Olukman M, Orhan CE, Celenk FG, Ulker S. Apocynin restores endothelial dysfunction in streptozotocin diabetic rats through regulation of nitric oxide synthase and NADPH oxidase expressions. J Diabetes Complications. 2010;24:415–23.View ArticlePubMedGoogle Scholar
  32. Roe ND, Thomas DP, Ren J. Inhibition of NADPH oxidase alleviates experimental diabetes-induced myocardial contractile dysfunction. Diabetes Obes Metab. 2011;13:465–73.View ArticlePubMedGoogle Scholar
  33. Dhaunsi GS, Yousif MH, Akhtar S, Chappell MC, Diz DI, Benter IF. Angiotensin-(1-7) prevents diabetes-induced attenuation in PPAR-gamma and catalase activities. Eur J Pharmacol. 2010;638:108–14.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Castor LRG, Locatelli KA, Ximenes VF. Pro-oxidant activity of apocynin radical. Free Radic Biol Med. 2010;48:1636–43.View ArticlePubMedGoogle Scholar
  35. Kučera J, Binó L, Štefková K, Jaroš J, Vašíček O, Večeřa J, et al. Apocynin and diphenyleneiodonium induce oxidative stress and modulate PI3K/Akt and MAPK/Erk activity in mouse embryonic stem cells. Oxid Med Cell Longev. 2016;2016:7409196.PubMedGoogle Scholar
  36. Gimenes C, Gimenes R, Rosa CM, Xavier NP, Campos DH, Fernandes AA, et al. Low intensity physical exercise attenuates cardiac remodeling and myocardial oxidative stress and dysfunction in diabetic rats. J Diabetes Res. 2015;2015:457848.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Furman BL. Streptozotocin-induced diabetic models in mice and rats. Curr Protoc Pharmacol. 2015;1:5–47.Google Scholar
  38. Lu J, Pontré B, Pickup S, Choong S, Li M, Xu H, et al. Treatment with a copper-selective chelator causes substantive improvement in cardiac function of diabetic rats with left-ventricular impairment. Cardiovasc Diabetol. 2013;12:28.View ArticlePubMedPubMed CentralGoogle Scholar
  39. Okoshi K, Fioretto JR, Okoshi MP, Cicogna AC, Aragon FF, Matsubara LS, et al. Food restriction induces in vivo ventricular dysfunction in spontaneously hypertensive rats without impairment of in vitro myocardial contractility. Braz J Med Biol Res. 2004;37:607–13.View ArticlePubMedGoogle Scholar
  40. Okoshi K, Ribeiro HB, Okoshi MP, Matsubara BB, Gonçalves G, Barros R, et al. Improved systolic ventricular function with normal myocardial mechanics in compensated cardiac hypertrophy. Jpn Heart J. 2004;45:647–56.View ArticlePubMedGoogle Scholar
  41. Martinez PF, Okoshi K, Zornoff LAM, Carvalho RF, Oliveira Junior SA, Lima AR, et al. Chronic heart failure-induced skeletal muscle atrophy, necrosis, and myogenic regulatory factors changes. Med Sci Monit. 2010;16:374–83.Google Scholar
  42. Gomes MJ, Martinez PF, Campos DH, Pagan LU, Bonomo C, Lima AR, et al. Beneficial effects of physical exercise on functional capacity and skeletal muscle oxidative stress in rats with aortic stenosis-induced heart failure. Oxid Med Cell Longev. 2016;2016:8695716.View ArticlePubMedPubMed CentralGoogle Scholar
  43. Cicogna AC, Padovani CR, Okoshi K, Matsubara LS, Aragon FF, Okoshi MP. The influence of temporal food restriction on the performance of isolated cardiac muscle. Nutr Res. 2001;21:639–48.View ArticleGoogle Scholar
  44. Okoshi MP, Okoshi K, Dal Pai V, Dal Pai-Silva M, Matsubara LS, Cicogna AC. Mechanical, biochemical, and morphological changes in the heart from chronic food-restricted rats. Can J Physiol Pharmacol. 2001;79:754–60.View ArticlePubMedGoogle Scholar
  45. Sugizaki MM, Carvalho RF, Aragon FF, Padovani CR, Okoshi K, Okoshi MP, et al. Myocardial dysfunction induced by food restriction is related to morphological damage in normotensive middle-aged rats. J Biomed Sci. 2005;12:641–9.View ArticlePubMedGoogle Scholar
  46. Okoshi MP, Matsubara LS, Franco M, Cicogna AC, Matsubara BB. Myocyte necrosis is the basis for fibrosis in renovascular hypertensive rats. Braz J Med Biol Res. 1997;30:1135–44.View ArticlePubMedGoogle Scholar
  47. Pagan LU, Damatto RL, Cezar MD, Lima AR, Bonomo C, Campos DH, et al. Long-term low intensity physical exercise attenuates heart failure development in aging spontaneously hypertensive rats. Cell Physiol Biochem. 2015;36:61–74.View ArticlePubMedGoogle Scholar
  48. Damatto RL, Lima ARR, Martinez PF, Cezar MDM, Okoshi K, Okoshi MP. Myocardial myostatin in spontaneously hypertensive rats with heart failure. Int J Cardiol. 2016;215:384–7.View ArticlePubMedGoogle Scholar
  49. Matsubara LS, Matsubara BB, Okoshi MP, Franco M, Cicogna AC. Myocardial fibrosis rather than hypertrophy induces diastolic dysfunction in renovascular hypertensive rats. Can J Physiol Pharmacol. 1997;75:1328–34.View ArticlePubMedGoogle Scholar
  50. Yan X, Schuldt AJ, Price RL, Amende I, Liu FF, Okoshi K, et al. Pressure overload-induced hypertrophy in transgenic mice selectively overexpressing AT2 receptors in ventricular myocytes. Am J Physiol Heart Circ Physiol. 2008;294:H1274–81.View ArticlePubMedGoogle Scholar
  51. Damatto RL, Martinez PF, Lima AR, Cezar MD, Campos DH, Oliveira Junior SA, et al. Heart failure-induced skeletal myopathy in spontaneously hypertensive rats. Int J Cardiol. 2013;167:698–703.View ArticlePubMedGoogle Scholar
  52. Martinez PF, Bonomo C, Guizoni DM, Oliveira Junior SA, Damatto RL, Cezar MDM, et al. Influence of N-acetylcysteine on oxidative stress in slow-twitch soleus muscle of heart failure rats. Cell Physiol Biochem. 2015;35:148–59.View ArticlePubMedGoogle Scholar
  53. van Heerebeek L, Hamdani N, Falcão-Pires I, Leite-Moreira AF, Begieneman MP, Bronzwaer JG, et al. Low myocardial protein kinase G activity in heart failure with preserved ejection fraction. Circulation. 2012;126:830–9.View ArticlePubMedGoogle Scholar
  54. Chen PM, Gregersen H, Zhao JB. Advanced glycation end-product expression is upregulated in the gastrointestinal tract of type 2 diabetic rats. World J Diabetes. 2015;6:662–72.PubMedPubMed CentralGoogle Scholar
  55. Fernandes DC, Wosniak JJ, Pescatore LA, Bertoline MA, Liberman M, Laurindo FR, et al. Analysis of DHE-derived oxidation products by HPLC in the assessment of superoxide production and NADPH oxidase activity in vascular systems. Am J Phyiol Cell Physiol. 2007;292:C413–22.View ArticleGoogle Scholar
  56. Laurindo FRM, Fernandes DC, Santos CXC. Assessment of superoxide production and NADPH oxidase activity by HPLC analysis of dihydroethidium oxidation products. Methods Enzymol. 2008;441:237–60.View ArticlePubMedGoogle Scholar
  57. Okoshi MP, Okoshi K, Matsubara LS, Dal Pai-Silva M, Gut AL, Padovani CR, et al. Myocardial remodeling and dysfunction are induced by chronic food restriction in spontaneously hypertensive rats. Nutr Res. 2006;26:567–72.View ArticleGoogle Scholar
  58. Cezar MD, Damatto RL, Martinez PF, Lima ARR, Campos DH, Rosa CM, et al. Aldosterone blockade reduces mortality without changing cardiac remodeling in spontaneously hypertensive rats. Cell Physiol Biochem. 2013;32:1275–87.View ArticlePubMedGoogle Scholar
  59. Yamamoto H, Uchigata Y, Okamoto H. Streptozotocin and alloxan induce DNA strand breaks and poly(ADP-ribose) synthetase in pancreatic islets. Nature. 1981;294:284–6.View ArticlePubMedGoogle Scholar
  60. Bedoya FJ, Solano F, Lucas M. N-monomethyl-arginine and nicotinamide prevent streptozotocin-induced double strand DNA break formation in pancreatic rat islets. Experientia. 1996;52:344–7.View ArticlePubMedGoogle Scholar
  61. Sarkhail P, Rahmaipour S, Fadyevatan S, Mohammadirad A, Dehghan G, Amin G. Antidiabetic effect of Phlomis anisodonta: effects on hepatic cells lipid peroxidation and antioxidant enzymes in experimental diabetes. Pharmacol Res. 2007;51:261–6.View ArticleGoogle Scholar
  62. Parvizi MR, Parviz M, Tavangar SM, Soltani N, Kadkhodaee M, Seifi B, et al. Protective effect of magnesium on renal function in STZ-induced diabetic rats. Diabetes Metab Disord. 2014;13:84.View ArticleGoogle Scholar
  63. Malfitano C, de Souza Junior AL, Carbonaro M, Bolsoni-Lopes A, Figueroa D, de Souza LE, et al. Glucose and fatty acid metabolism in infarcted heart from streptozotocin-induced diabetic rats after 2 weeks of tissue remodeling. Cardiovasc Diabetol. 2015;14:149.View ArticlePubMedPubMed CentralGoogle Scholar
  64. Cotter MA, Cameron NE. Effect of the NAD(P)H oxidase inhibitor, apocynin, on peripheral nerve perfusion and function in diabetic rats. Life Sci. 2003;73:1813–24.View ArticlePubMedGoogle Scholar
  65. Shi XY, Hou FF, Niu HX, Wang GB, Xie D, Guo ZJ, et al. Advanced oxidation protein products promote inflammation in diabetic kidney through activation of renal nicotinamide adenine dinucleotide phosphate oxidase. Endocrinology. 2008;149:1829–39.View ArticlePubMedGoogle Scholar
  66. Asaba K, Tojo A, Onozato ML, Goto A, Quinn MT, Fujita T, et al. Effects of NADPH oxidase inhibitor in diabetic nephropathy. Kidney Int. 2005;67:1890–8.View ArticlePubMedGoogle Scholar
  67. Schlüter T, Steinbach AC, Steffen A, Rettig R, Grisk O. Apocynin-induced vasodilation involves Rho kinase inhibition but not NADPH oxidase inhibition. Cardiovasc Res. 2008;80:271–9.View ArticlePubMedGoogle Scholar
  68. Rehman A, Dugic E, Benham C, Lione I, Mackenzie LS. Selective inhibition of NADPH oxidase reverses the over contraction of diabetic rat aorta. Redox Biology. 2014;2:61–4.View ArticlePubMedGoogle Scholar
  69. Miki T, Yuda S, Kouzu H, Miura T. Diabetic cardiomyopathy: pathophysiology and clinical features. Heart Fail Rev. 2013;18:149–66.View ArticlePubMedGoogle Scholar
  70. Yong QC, Thomas CM, Seqqat R, Chandel N, Baker KM, Kumar R. Angiotensin type 1a receptor-deficient mice develop diabetes-induced cardiac dysfunction, which is prevented by renin-angiotensin system inhibitors. Cardiovasc Diabetol. 2013;12:169.View ArticlePubMedPubMed CentralGoogle Scholar
  71. Marangoni MN, Brady ST, Chowdhury SA, Piano MR. The co-occurrence of myocardial dysfunction and peripheral insensate neuropathy in a streptozotocin-induced rat model of diabetes. Cardiovasc Diabetol. 2014;13:11.View ArticlePubMedPubMed CentralGoogle Scholar
  72. Fan D, Takawale A, Lee J, Kassiri Z. Cardiac fibroblasts, fibrosis and extracellular matrix remodeling in heart disease. Fibrogenesis Tissue Repair. 2012;5:15.View ArticlePubMedPubMed CentralGoogle Scholar
  73. Brower GL, Gardner JD, Forman MF, Murray DB, Voloshenyuk T, Levick SP, et al. The relationship between myocardial extracellular matrix remodeling and ventricular function. Eur J Cardiothorac Surg. 2006;30:604–10.View ArticlePubMedGoogle Scholar
  74. López B, González A, Hermida N, Valencia F, de Teresa E, Díez J. Role of lysyl oxidase in myocardial fibrosis: from basic science to clinical aspects. Am J Physiol Heart Circ Physiol. 2010;299:H1–9.View ArticlePubMedGoogle Scholar
  75. Fuentes-Antrás J, Picatoste B, Ramírez E, Egido J, Tuñón J, Lorenzo O. Targeting metabolic disturbance in the diabetic heart. Cardiovasc Diabetol. 2015;14:17.View ArticlePubMedPubMed CentralGoogle Scholar
  76. Liu J, Zhou J, An W, Lin Y, Yang Y, Zang W. Apocynin attenuates pressure overload-induced cardiac hypertrophy in rats by reducing levels of reactive oxygen species. Can J Physiol Pharmacol. 2010;88:745–52.View ArticlePubMedGoogle Scholar
  77. Li YQ, Li XB, Guo SJ, Chu SL, Gao PJ, Zhu DL, et al. Apocynin attenuates oxidative stress and cardiac fibrosis in angiotensin II-induced cardiac diastolic dysfunction in mice. Acta Pharmacol Sin. 2013;34:352–9.View ArticlePubMedPubMed CentralGoogle Scholar
  78. Liu Y, Liu Y, Liu X, Chen J, Zhang K, Huang F, et al. Apocynin attenuates cardiac injury in type 4 cardiorenal syndrome via suppressing cardiac fibroblast growth factor-2 with oxidative stress inhibition. J Am Heart Assoc. 2015;4:e001598.PubMedPubMed CentralGoogle Scholar
  79. Zhang K, Liu Y, Liu X, Chen J, Cai Q, Wang J, et al. Apocynin improving cardiac remodeling in chronic renal failure disease is associated with up-regulation of epoxyeicosatrienoic acids. Oncotarget. 2015;6:24699–708.View ArticlePubMedPubMed CentralGoogle Scholar
  80. Riganti C, Costamagna C, Bosia A, Ghigo D. The NADPH oxidase inhibitor apocynin (acetovanillone) induces oxidative stress. Toxicol Appl Pharmacol. 2006;212:179–87.View ArticlePubMedGoogle Scholar
  81. Fujio Y, Nguyen T, Wencker D, Kitsis RN, Walsh K. Akt promotes survival of cardiomyocytes in vitro and protects against ischemia-reperfusion injury in mouse heart. Circulation. 2000;101:660–7.View ArticlePubMedPubMed CentralGoogle Scholar
  82. Abrigo J, Morales MG, Simon F, Cabrera D, Di Capua G, Cabello-Verrugio C. Apocynin inhibits the upregulation of TGF-β1 expression and ROS production induced by TGF-β in skeletal muscle cells. Phytomedicine. 2015;22:885–93.View ArticlePubMedGoogle Scholar
  83. Cagin YF, Erdogan MA, Sahin N, Parlakpinar H, Atayan Y, Polat A, et al. Protective effects of apocynin on cisplatin-induced hepatotoxicity in rats. Arch Med Res. 2015;46:517–26.View ArticlePubMedGoogle Scholar
  84. Cagin YF, Parlakpinar H, Polat A, Vardi N, Atayan Y, Erdogan MA, et al. The protective effects of apocynin on ionizing radiation-induced intestinal damage in rats. Drug Dev Ind Pharm. 2016;42:317–24.View ArticlePubMedGoogle Scholar
  85. Choi BY, Kim JH, Kho AR, Kim IY, Lee SH, Lee BE, et al. Inhibition of NADPH oxidase activation reduces EAE-induced white matter damage in mice. J Neuroinflammation. 2015;12:104.View ArticlePubMedPubMed CentralGoogle Scholar
  86. Vasdev S, Gill V, Singal P. Role of advanced glycation end products in hypertension and atherosclerosis: therapeutic implications. Cell Biochem Biophys. 2007;49:48–63.View ArticlePubMedGoogle Scholar
  87. Miguel-Carrasco JL, Baltanás A, Cebrián C, Moreno MU, López B, Hermida N, et al. Blockade of TGF-β 1 signalling inhibits cardiac NADPH oxidase overactivity in hypertensive rats. Oxid Med Cell Longev. 2012;2012:726940.View ArticlePubMedPubMed CentralGoogle Scholar
  88. Lee TI, Kao YH, Chen YC, Pan NH, Lin YK, Chen YJ. Cardiac peroxisome-proliferator-activated receptor expression in hypertension co-existing with diabetes. Clin Sci. 2011;121:305–12.View ArticlePubMedGoogle Scholar
  89. Riganti C, Costamagna C, Doublier S, Miraglia E, Polimeni M, Bosia A, et al. The NADPH oxidase inhibitor apocynin induces nitric oxide synthesis via oxidative stress. Toxicol Appl Pharmacol. 2008;228:277–85.View ArticlePubMedGoogle Scholar
  90. Zhou X, Bohlen GH, Miller SJ, Unthank JL. NAD(P)H oxidase-derived peroxide mediates elevated basal and impaired flow-induced NO production in SHR mesenteric arteries in vivo. Am J Physiol Heart Circ Physiol. 2008;295:H1008–16.View ArticlePubMedPubMed CentralGoogle Scholar
  91. Wedgwood S, Lakshminrusimha S, Farrow KN, Czech L, Gugino SF, Soares F, et al. Apocynin improves oxygenation and increases eNOS in persistent pulmonary hypertension of the newborn. Am J Physiol Lung Cell Mol Physiol. 2012;302:L616–26.View ArticlePubMedGoogle Scholar

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Cardiovascular Diabetology

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