Coronary angiogenic effect of long-term administration of Nigella sativa.

BACKGROUND: Coronary angiogenesis is one of the preferable adaptive responses of aerobic training. Previous studies found inotropic and hypertrophic cardiac effects for long-term administration of Nigella sativa (NS), but no studies have explored its coronary angiogenic effect. The present study compared the effect of long-term NS- administration and exercise training on the induction of coronary angiogenesis.
METHOD: Fifteen adult male Wistar rats were divided into three groups: control, NS-fed, and exercise-trained (Ex). The NS-fed rats were administered 800 mg/Kg NS orally for eight weeks. The (Ex) rats were trained on a five-lane treadmill at a speed of 18 m/min and a grade of 32° for two hour/day for eight weeks. After the experiment, the hearts were extracted and immunohistological slides were prepared using rat vascular endothelial growth factor (VEGF), platelet endothelial cell adhesion molecule-1 (PECAM-1), Von Willebrand factor (VWF) and nitric oxide synthase-2 (NOS-2) antibodies (Ab). Photomicrographs were analysed using ImageJ software, and the % of the immunostained-area of 10 fields per specimen was recorded. RESULT: VEGF was significantly higher in the NS- (2.59±1.37%) and Ex rats (2.51±1.86%) compared to the control group (1.58±0.78%) with P<0.01. The VWF was significantly lower in the two experimental groups (1.57±0.83%, 1.07±0.72%) for NS and Ex groups respectively, compared to the controls (2.38±1.72) with p<0.01. Only Ex group had a higher PECAM-1 (1.79±0.78%) and lower NOS-2 (0.83±0.57%) than the control group (1.19±1.17%, 1.25±1.19%) for PECAM-1 and NOS-2 with P<0.01 and P<0.05 respectively.
CONCLUSIONS: The present study demonstrated an increase in VEGF and a decrease of the VWF in the hearts of Nigella-fed and exercise-trained rats. This might indicate the potentiality for induction of coronary angiogenesis via long-term administration of NS and exercise training. NS effect on coronary angiogenesis needs to be explored further as it might lead to a new promising preventive and therapeutic agent of the ischemic heart disease.

Background

Coronary artery disease (CAD) is one of the leading causes of death worldwide. The World Health Organization (WHO) reports that 31% of deaths across the globe are due to cardiovascular diseases, and ischemic heart disease accounts for 46% of these deaths [1]. The current prevalence and consequences of CAD might also increase dramatically in the future due to the uncontrolled increment of multiple risk factors, including obesity, hypercholestrolemia, hypertension, diabetes and smoking [2].

Exercise training has long been recommended as a cardiovascular protective measure. Favourable cardiac and coronary adaptations to exercise training are well known, and they have been reported in the literature [3, 4]. Exercise training can culminate in the enhancement of myocardial blood flow through multiple structural and physiological alterations of the coronary vascular bed. This includes increments in the conduit of large arteries, increases in the number of arterioles and induction of capillary growth [5]. A wide range of stimuli have been suggested as explanations for the angiogenic effect of exercise training. During acute bouts of exercise, the increased myocardial blood flow leads to increased shear stress and the release of endothelial vasodilators and nitric oxide [6]. Growth factors such as fibroblast growth factors (FGFs), vascular endothelial growth factor (VEGF) and insulin like growth factor-I (IGF-I) have been found to be upregulated in the coronary circulation in exercise-trained animals [7].

Assessment of increases in the coronary circulation in exercise-trained human subjects and animals varies. In exercise-trained human subjects and athletes, coronary circulation capacity is assessed by evaluating coronary flow, using electromagnetic flowmeter or ultrasonic devices [8]. In animals, immunohistochemical studies are used to label the vascularity and measure the cross-sectional area [9].

Despite accumulating evidence of the prophylactic influence of exercise training on cardiac health and coronary circulation, the compliance toward training is low worldwide. Adjuvant therapeutics aimed to induce angiogenesis are of compelling need either as prophylaxis of ischemia or as an attempt to rescue ischemic tissue.

The black seed is a herbaceous plant used as a traditional remedy in the Arab countries, Iran and India. It received its name from the appearance of the seeds which are small (1–5 mg in weight) and have dark grey to black colour [10]. Generically, it is known as Nigella sativa Linn (NS). The main constituents of NS are crude fat (30–40%), crude protein (20–30%), crude fibre (5–10%) and multiple minerals including potassium, Magnesium, calcium, phosphorus and sodium. The crude fat is composed of fixed and volatile oil and it contains wide range of fatty acids such as linoleic, linolenic, oleic and palmitic acids. Thymoquinone was isolated and recognized as an important and active constituent of both the volatile and fixed oil [11].

NSand its active component (thymoquinone) demonstrated multiple therapeutic effects in multiple studies. The therapeutic effect included anti-inflammatory [12], antioxidant [13], antibacterial [10], hypoglycemic and antilipidemic effects [14, 15]. Furthermore, available evidences showed multiple favourable cardiovascular responses of NS. Two previous studies reported antihypertensive effect of NS on humans and animals [16, 17]. Positive cardiac adaptation for long term administration of NS was also demonstrated. In a study performed by El Bahai et al. [18], long-term administration of NS for two months to adult Wistar rats, led to an increase in the peak force of cardiac contraction, myocardial flow rate and the rate of tension development [18]. Another study performed by the same group, showed structural remodelling of the myocardium, including myocardial hypertrophy manifested by increased heart weight/body weight (HW/BW), left ventricular weight/body weight (LVW/BW) and increased diameters of cardiomyocytes [19]. The histological and electrophysiological characteristics of hypertrophied hearts induced by NS were compared to exercise-induced cardiac hypertrophy, and multiple similarities were found [19, 20]. Furthermore, Ansam et al. reported a protective effect of NS against ischemia reperfusion insult in rat hearts when the animals were treated for three months with oral NS [21].

The previous reported studies of the cardiac adaptation to long term administration of NS drew the attention to a possible preferable coronary circulation response by the same dose of NS. Therefore, this present study aims to examine the effect of long-term administration of NS on the structural remodelling of coronary circulation, explore some of its underlying mechanisms and compare it to exercise-training induced coronary vascular remodelling.

Methods

Animals

Fifteen normal adult male Wistar rats (age: two months, weight: 200–300 g) were obtained from the animal house at the University of Dammam, in Dammam, Saudi Arabia. All the animals were housed individually in labelled cages with adequate ventilation and illumination, and in normal light cycle (12 light/12 dark). Normal laboratory chow and tap water were available ad libitum. The sample size was selected based on similar published work with the consideration of the minimum requirement [22].

Ethical approval was provided by the ethical committee of the Deanship of Scientific Research at Dammam University with reference number IRB-2014-01-165. This committee is a branch of the National Committee of Bioethics, Saudi Arabia. The rats were divided equally and randomly into three groups: the control group, the NS-treated group, and the exercise-trained (Ex) group. The NS-treated rats were given 800 mg/Kg NS daily for eight weeks. NS whole seeds were obtained from a local herb store in Dammam, Saudi Arabia. It is a product of the central region of Saudi Arabia. These seeds were previously analysed for its constituents by Al-Jassir [23]. The dose, duration and preparation of NS was similar to that used by El Bahai et al. and showed cardiac hypertrophy and positive inotropic effect [18]. Oral administration was done via a feeding needle. A suspension of NS was prepared by dissolving 10 g of freshly ground NS seeds in 100 ml of distilled water. The animals in the control group were given an equivalent volume of water.

The rats in Ex group were trained on a treadmill (IITC Life Science, five-lane rat treadmill), five days/week for eight weeks. The speed, grade and duration were progressively increased during the first week until the final protocol was achieved, with a speed of 18 m/min and an inclination of 32°, for a two-hour session [24]. An electric grid at the rear of the belt was used as the running stimulus. An equivalent volume of water was also administered to this group.

Extraction of the hearts

The rats were anaesthetized with a ketamine cocktail (60% ketamine, 40% xylasine). A dose of 0.2 ml/250 g body weight was injected intraperitoneally. Hearts were extracted through longitudinal abdominal incisions and soaked in cold Ringer’s solution. Excess connective tissue and great vessels were removed. Lumens were rinsed with Ringer’s solution to remove excess blood and clots. Finally, the hearts were blotted dry and weighed. The right ventricles and both atria were removed, and the remaining left ventricles were weighed. The free wall of the left ventricles was excised and stored in 4% formal-saline for histological preparation.

Preparation of the light microscope slides

The left ventricular free wall was initially fixed in 4% formal-saline. Later, the specimens were washed briefly in water, and then labelled and placed in a tissue processor (Tissue-Tek VIP) overnight. The specimens were dehydrated using ascending grades of alcohol: 70%, 90% and 100% two changes, and two changes of xylene for a period of two hours, respectively.

The process of embedding was initiated. The specimens were impregnated in two changes of molten paraffin wax for a period of two hours for each change, and they were subsequently embedded in molten paraffin wax at a temperature of 60 °C. Cassettes were used to control the position of the specimens. The blocked tissues were labelled and allowed to solidify; they were then sectioned using microtomy (LEICA RM 2235, Leica BioSystems Buffalo Grove, IL, USA) at a thickness of 3 um. The sectioned tissues were floated in warm water, and then placed on microscope slides, labelled and allowed to dry.

The sections were dewaxed, washed in water and stained using the following antibodies:

Rat VEGF 164 affinity purified polyclonal antibody (Ab), Goat IgG (R&D Systems, Minneapolis, MN, USA) [25].

Anti CD31 (PECAM-1) for endothelial cells to determine the density of the capillaries, purified polyclonal Ab, Goat IgG (R&D Systems, Minneapolis, MN, USA) [26].

Anti Von Willebrand factor (VWF) antibody purified polyclonal Ab, Goat IgG (R&D Systems, Minneapolis, MN, USA) [9].

Anti NOS-2 antibody staining, using a commercially available kit (Novostain Super) ABC Kit (universal), NCL-ABCu (Novocastra Laboratories, Ltd., Newcastle upon Tyne, UK).

Estimation of the antibody labelling in the light microscopic slides

Each rat specimen was stained using all the antibodies listed above. Estimation of the immunostained area of each antibody was performed using photomicrographs obtained via a digital microscope (Coolscope, Nikon Instruments Europe BV, Amsterdam Netherlands). Ten fields were selected randomly from each section. All the selected fields were clear from freezing defects, gaps or folds. The overlap of fields was clearly avoided. The slide selection and analysis was conducted by a blind operator. The sections were labelled with numbers that were unknown to the operator.

Image J software was used to analyse the sections. The total immunostained area in each field was measured in pixels and expressed as percentage of the total field area (%). The mean value of the immunostained area for all fields of a specific antibody in each group was obtained [22]. (see Fig. 1 for the photomicrographs of all antibodies).

Fig. 1

Photomicrographs illustrated immunohistochemistry study of left ventricular tissue labeled by I. VEGF, II. Von Willebrand III. PECAM-1, IV. NOS-II Antibodies obtained from: a. control, . nigella sativa fed rats, c. exercise trained rats

Statistical analysis

IBM - Statistical analysis software package - SPSS version 20 was used to analyse the data. All data were expressed as mean ± SD. Analysis of variance (ANOVA) and LSD post-hoc test were used to compare data among the groups. The level of significance was set at p < 0.05.

Results

All rat groups were matched in regard the initial and the final body weight.

There was no significant difference in HW, LVW, and LVW/HW between the groups. No difference were also found between the heart weight and left ventricular weight when normalized to body weight and tibial length. (Data are not shown).

VEGF was significantly higher in the Nigella-fed (2.59 ± 1.37%) and the exercise-trained (2.51 ± 1.86%) groups compared to the control (1.58 ± 0.78%), P < 0.01. VWF was significantly lower in the Nigella-fed (1.57 ± 0.83%) and the exercise-trained (1.07 ± 0.72%) groups compared to the control (2.38 ± 1.72%), P < 0.01. Only the exercise-trained group was found to have a higher PECAM-1 (1.79 ± 0.78%) and a lower NOS-2 (0.83 ± 0.57%) than the control (PECAM-1: 1.19 ± 1.17%, NOS-2:1.25 ± 1.19%), P < 0.01, P < 0.05 respectively (Fig. 2).

Fig. 2

Comparison of the angiogenic growth factors and antigens (VEGF, VWF, PECAM-1, and NOS-2) between the experimental groups: Control, NS (Nigella sativa fed), Exercise (Exercise trained), *P < 0.05, **P < 0.01

Discussion

The present study aimed to explore the effect of long-term administration of NS on coronary circulation in Wister rats using immunohistochemical methods. The immunohistological slides were prepared using PECAM-1, to target endothelial cell antigens, VEGF, known to induce capillary growth, VWF that regulates and limits vascular growth, and NOS-2 which is responsible for the production of nitric oxide (NO). Analysis of the data revealed a significant increase in VEGF in both the NS-fed and the Ex-trained groups, and a significant decrease in the VWF in the NS-fed and the Ex-trained groups. In addition, only the exercise-trained group showed significant increase in PECAM-1 and a significant decrease in NOS-2.

VEGF is a growth factor that induces the sprouting of the capillaries. It does so by dissolving the basement membrane of the existing capillaries, and then stimulating the proliferation and migration of endothelial cells [27]. VEGF interacts with the endothelial cell adhesion molecules during the process of endothelial growth and proliferation [28]. In a previous study reported by Marini et al., exercise-trained rats for four weeks showed upregulation of VEGF, accompanied simultaneously with capillary sprouting and capillary angiogenesis [9]. Induction of VEGF production in an endothelial cell culture has been found to promote cell division and cell proliferation [29]. Administration of VEGF genes into porcine myocardium induced angiogenesis and increase the microvascular bed about 1.8 folds as demonstrated by Nurro et al. [30].

In the present study, VEGF was significantly high and comparable in the NS-fed and the Ex-trained groups, indicating that both NS administration and exercise training are potential factors for the induction of capillary growth.

The process of angiogenesis is also governed by antiangiogenic factors. VWF is a glycoprotein that is synthesised in the endothelial cells, and it is known for its essential haemostatic effect. It stimulates the adhesion and aggregation of platelets in injured tissue, and it acts as a carrier of coagulation factor VIII [31]. VWF plays a role in the regulation of angiogenesis, limits the release of angiogenic factors, such as VEGF, and stabilises the capillary bed [32]. In VWF deficiency, abnormal growth of vessels has been found in a condition known as angiodysplasia [33]. Inhibition of the release and synthesis of VWF by interfering with its genetic expression in mice leads to enhanced angiogenesis, increased VEGF receptor-2 dependent proliferation and migration of endothelial cells [32]. In this study, all the experimental groups (the NS, and Ex groups) demonstrated a significantly lower VWF expression level than the control. This finding might support the angiogenic effect of both long-term administration of NS and exercise training on coronary circulation. It also supports the similarities in the actions of these two interventions.

NO is a multifunctional cellular signalling molecule, known for its vasodilation action. Recently, evidence has shown that NO plays a role as a mediator of angiogenesis. NO is released from the endothelial cells under the influence of VEGF. VEGF upregulates and activates NOS in endothelial cells [34]. Increased expression of NOS was demonstrated in the hind-limbs of mice after three weeks of wheel running [35]. The effect of exercise training on the different isoforms of NOS i.e. endothelial NOS (eNOS), and inducible NOS (NOS-2), might differ. [34]. In a recent study, exercise training stimulated eNOS and reduced iNOS in control rats and normalized iNOS and showed no effect on eNOS in high fat fructose diet rats after ischemia reperfusion injury [36]. In the current experiment, exercise training demonstrated a significant reduction in the expression of NOS-2 in the cross-section of the left ventricles of the exercise-trained rats. A reduction of iNOS might be an indication of cardioprotective effect of exercise training through the mitigation of oxidative stress [37]. eNOS was not assessed in this study due to technical difficulties in providing antibodies with rat species reactivity. NS administration showed no effect on NOS-2. Although, NS is known to be an anti-inflammatory and antioxidant mediator [15], but it did not show similar effect to exercise training on NOS-2. Other isoforms of NOS might need to be studied under the effect of these two intervention i.e. exercise training and long term administration of NS for better comparison of their effects on NOS and NO production.

PECAM-1 is the platelet-endothelial adhesion molecule known as CD31 [38]. The interaction of PECAM-1 with growth factors is essential for angiogenesis. Some studies have used PECAM-1 to estimate capillary density [39, 40]. In a recent study, diabetic rats were exposed to testosterone treatment and exercise training to investigate the effect on these two interventions on neoangiogenesis [30]. That study demonstrated higher PECAM-1 antibody staining after both treatment modalities were administered [41]. Similarly, our study found a significantly higher PECAM-1 density in the Ex-trained group. Our NS-fed groups failed to demonstrate a significant increase in PECAM-1. However, the possibility of the presence of ongoing capillary angiogenesis is still valid, as supported by the significant increase in VEGF and the decrease in VWF. A longer duration of NS administration might be required to achieve a higher capillary bed density. This finding might be related to the delayed onset of cardiac hypertrophy induced by NS due to the lack of continuity of administration of the NS treatment during the weekends. Different stages of cardiac and coronary adaptation to exercise training have also been reported [42].

Conclusion

In conclusion, the present study demonstrated evidence of active coronary angiogenesis induced by eight weeks’ administration of NS and aerobic exercise training in adult Wistar rats. This evidence includes a significant increase in VEGF and a reduction of VWF. This finding might be promising for the emergence of a new therapeutic and preventive strategy for CAD in specific and other peripheral artery diseases in general. Further studies are required to explore the potential effect of NS on coronary angiogenesis and confirm the present findings.

Limitations

The present study might be limited by the number of growth factors and antigens tested. Other growth factors known to be involved in the process of angiogenesis whether stimulatory or inhibitory need to be investigated. In addition, all isoforms of NOS need to be assessed and compared. This limitation arises due to the difficulty in recruiting antibodies with good reactivity to rat species.