Mechanisms of the antihypertensive effects of Nigella sativa oil in L-NAME-induced hypertensive rats

Abstract

OBJECTIVES:

This study was conducted to determine whether the blood pressure-lowering effect of Nigella sativa might be mediated by its effects on nitric oxide, angiotensin-converting enzyme, heme oxygenase and oxidative stress markers.

METHODS:

Twenty-four adult male Sprague-Dawley rats were divided equally into 4 groups. One group served as the control (group 1), whereas the other three groups (groups 2-4) were administered L-NAME (25 mg/kg, intraperitoneally). Groups 3 and 4 were given oral nicardipine daily at a dose of 3 mg/kg and Nigella sativa oil at a dose of 2.5 mg/kg for 8 weeks, respectively, concomitantly with L-NAME administration.

RESULTS:

Nigella sativa oil prevented the increase in systolic blood pressure in the L-NAME-treated rats. The blood pressure reduction was associated with a reduction in cardiac lipid peroxidation product, NADPH oxidase, angiotensin-converting enzyme activity and plasma nitric oxide, as well as with an increase in heme oxygenase-1 activity in the heart. The effects of Nigella sativa on blood pressure, lipid peroxidation product, nicotinamide adenine dinucleotide phosphate oxidase and angiotensin-converting enzyme were similar to those of nicardipine. In contrast, L-NAME had opposite effects on lipid peroxidation, angiotensin-converting enzyme and NO.

CONCLUSION:

The antihypertensive effect of Nigella sativa oil appears to be mediated by a reduction in cardiac oxidative stress and angiotensin-converting enzyme activity, an increase in cardiac heme oxygenase-1 activity and a prevention of plasma nitric oxide loss. Thus, Nigella sativa oil might be beneficial for controlling hypertension.

Nigella sativa ; Antihypertensive; Angiotensin-converting Enzyme; Heme Oxygenase; NADPH Oxidase

INTRODUCTION

Hypertension is defined as a persistent elevation of systolic blood pressure of 140 mmHg or greater and/or diastolic blood pressure of 90 mmHg or greater. Hypertension is a major risk factor for cardiovascular, cerebrovascular and renal diseases (¹).

Oxidative stress is important in the pathogenesis of essential hypertension or in arterial damage related to essential hypertension (^{2 3}). This was shown by an elevation of lipid peroxidation in hypertensive patients (²). The increases in oxidative stress will reduce the bioavailability of nitric oxide (NO), a potent vasodilator (³) and this reduction contributes to the development of hypertension.

Many factors are involved in blood pressure control, including angiotensin-converting enzyme (ACE), heme oxygenase (HO-1) and the endothelial-derived relaxing factor (EDRF) NO. ACE promotes the production of angiotensin II (Ang II) from angiotensin I (Ang I), which has a direct vasoconstrictor effect on the vessels that increase blood pressure. Ang II has been reported to increase vascular superoxide anion production via membrane NADPH oxidase activation, which will then lead to an increase in lipid peroxidation, inflammation and vascular injury (⁴-⁵). HO-1 protects against cardiovascular diseases such as atherosclerosis and hypertension (⁶). The antihypertensive effect of HO-1 is likely to be mediated by carbon monoxide (CO). CO reduces peripheral resistance by directly dilating blood vessels via the activation of guanylate cyclase (⁷). CO exerts antihypertensive effects by stimulating the release of NO, reducing sympathetic outflow and promoting sodium excretion via the kidneys (⁶). Overexpression of the HO-1 gene reduces the Ang II-mediated pressure response in rats (⁶). However, HO-1 regulates blood pressure by reducing the activity of Ang II, which helps to reduce vascular inflammation and protects against vascular injuries (⁶). Cardiac-specific expression of HO-1 was shown to protect against inflammation and oxidative damage in healthy subjects (⁷). Treatment with heme-arginate, an HO-1 inducer, protects the heart by reducing subendocardial injury, interstitial fibrosis and cardiomyocyte hypertrophy, which is believed to occur via a reduction in several inflammatory and oxidative mediators (⁸).

The use of medicinal plants for the prevention of cardiovascular diseases has been increasing recently. Nigella sativa, which is also known as black cumin, has been shown to possess blood pressure-lowering effects in both animals and humans (⁹-¹³). It has been used for centuries for medicinal and culinary purposes throughout the Middle East, India and Northern Africa (¹¹). The seed oil of N. sativa was found to be rich in thymoquinone and polyphenols (¹³).

However, the exact mechanism of the blood pressure-lowering effects of N. sativa remains uncertain. The antihypertensive effects of N. sativa may involve several mechanisms. El Tahir et al. (¹¹) suggested that N. sativa likely reduces blood pressure via a reduction in myocardial contractility and heart rate and that N. sativa might activate muscarinic receptors on blood vessels. However, Magyar et al. (¹⁴) suggested that N. sativa might have calcium channel-blocking properties. To the best of our knowledge, the effects of N. sativa on ACE, HO-1, NADPH oxidase and NO have not been thoroughly explored. Therefore, the present study was designed to determine the effects of N. sativa oil on ACE, HO-1 and cardiac redox status (NADPH oxidase and malondialdehyde) in N_ω-nitro-L-arginine methyl ester (L-NAME)-treated rats. Nicardipine was used in the study as a positive control because it has antioxidant effects and calcium channel-blocking properties.

MATERIALS AND METHODS

Experimental study design

After a week of adaptation, twenty-four male Sprague-Dawley rats (180-220 g) obtained from the Laboratory Animal Resource Unit, Faculty of Medicine, Universiti Kebangsaan Malaysia were divided into four experimental groups. One group served as a control whereas the other three groups were administered L-NAME intraperitoneally (25 mg/kg) (¹⁵). Groups 3 and 4 were given both oral N. sativa oil (2.5 mg/kg) (¹⁶) and oral nicardipine (3 mg/kg), respectively, (¹⁷) daily for 8 weeks concomitantly with L-NAME administration. After 8 weeks of treatment, the rats were sacrificed, and their hearts were harvested. Systolic blood pressure was measured weekly by a tail-cuff method (Powerlab, ADInstrument, NSW, Australia). Blood was obtained at weeks 0 and 8 for the determination of plasma nitric oxide. The rats were kept in polyethylene cages in a well-ventilated room at 27° C with a 12-hour light-dark cycle and had free access to water and food throughout the study. All animal management and handling procedures, in addition to the study design, were approved by the university ethical and research committee (Approval No.: 421-January-2012-December-2013).

Measurement of blood pressure

A non-invasive method was used to measure systolic blood pressure as described by Jaarin et al. (¹⁸) using PowerLab data acquisition systems (ADInstruments, Castle Hill, NSW, Australia). A monitoring cuff was placed on the proximal tail to detect changes in blood flow that occurred during occlusion or the release of the cuff. The rats were placed in an approximately body-sized plastic container prior to the blood pressure measurement. This step ensured acclimation and a faster blood pressure measurement. The animals were pre-warmed for 15 minutes to increase blood flow to the tails. A minimum of 5 measurements were recorded and the mean was used for analysis.

Heart malondialdehyde content measurement

Lipid peroxidation determined as malondialdehyde (MDA) was measured in the cardiac samples following a method by Ledwozyw et al. (¹⁹) with some modifications. The protein content in the heart was estimated using an established method (²⁰).

Heart NADPH oxidase assay

NADPH oxidase activity measured as superoxide production in the cardiac samples was based on a reduction of ferricytochrome c in ferrocytochrome at pH 7.8 as described by Mustapha et al. (²¹). The samples were homogenized in 0.25 M sucrose (pH 7.8). The reaction mixture containing 250 µg/l cytochrome c, 100 µM NADPH and 50 µg of protein samples was incubated at 37° C for 120 min, either in the presence or absence of diphenyleneiodonium (DPI, 100 µM). The absorbance of the reduction of cytochrome c was read at 550 nm. Superoxide production was calculated from the difference between the absorbance of the samples incubated with and without DPI using an extinction coefficient of 21 mM⁻¹cm⁻¹.

ACE and HO-1 assays

ACE (USCN Life, West Lake, Wuhan, China) and HO-1 (Enzo Life Sciences, MI, USA) activities were analyzed in cardiac samples using commercially available kits following the manufacturer's instructions. The colored end products of these enzymes were measured by a microplate reader (Molecular Devices, Sunnyvale, CA, USA) at 450 nm.

Nitric oxide

The production of NO was indirectly detected by measuring the nitrite (NO₂-) metabolite content in the samples. Plasma and cardiac NO content were estimated based on a previously described method (²²) using Griess reagent (Sigma-Aldrich, St. Louis, MO, USA). Briefly, 50 µg of tissue samples were incubated with the same volume of Griess reagent in a microplate for 5 min in the dark at room temperature. The colored end product was measured using a microplate reader at 540 nm. Plasma NO was expressed as the percentage difference between weeks 0 and 8.

Statistical analysis

The data are presented as the mean±SEM. The statistical analyses were conducted using Statistical Product for Social Science 16.0 software (SPSS, Inc., Chicago, IL). The normality of the data was evaluated using a Kolmogorov-Smirnov test. Differences between the groups for each parameter were compared using a one-way analysis of variance (ANOVA) with Tukey’s Honestly Significant Differences post-hoc test. Statistical significance was defined as p<0.05.

RESULTS

Effects on systolic blood pressure

There was a significant increase in systolic blood pressure in the L-NAME-treated rats from week 2 to week 8 of the study. Conversely, the treatment of the L-NAME-treated hypertensive rats with N. sativa and nicardipine resulted in a significantly lower blood pressure (Figure 1). The blood pressures of the control, N. sativa- and nicardipine-treated groups were similar.

Figure 1
Systolic blood pressure in rats given N. sativa oil (NS) and concurrent administration of L-NAME. The data represent the mean±SEM (n=6). *p<0.01 versus control, #p<0.05 versus L-NAME.

Effect on cardiac MDA

The L-NAME-treated group displayed a significant increase in cardiac MDA content compared to the control. L-NAME+nicardipine and L-NAME+Nigella sativa significantly lowered the MDA content compared to the L-NAME alone (p<0.05) (Figure 2). There was no significant difference in cardiac MDA content in the control, L-NAME+nicardipine and L-NAME+Nigella sativa groups.

Figure 2
Effect of N. sativa oil on heart lipid peroxidation product in rats administered L-NAME for 8 weeks. The bars represent the mean±SEM (n=6). *p<0.01 versus control, # p<0.05 versus L-NAME.

Effect on cardiac NADPH oxidase activity

A significant elevation of cardiac NADPH oxidase activity was observed in the L-NAME group. The nicardipine- and N. sativa-treated groups displayed lower enzyme activity. No significant difference was noted among the control, nicardipine- and N. sativa-treated groups (Figure 3).

Figure 3
Effects of N. sativa oil on NADPH oxidase enzyme activity in L-NAME administered rats. The bars represent the mean±SEM (n=6). *p<0.005 versus control, #p<0.05 versus L-NAME.

Effect on cardiac ACE, HO-1 activities and NO content

L-NAME administration increased cardiac ACE activity compared to control, nicardipine and N. sativa treatments. In contrast, enzyme activity was significantly reduced in the nicardipine- and N. sativa-treated groups (p<0.05) (Table 1). No significant difference was observed in ACE activity between these two groups. The HO-1 activity in cardiac tissues was unaffected by L-NAME. However, the activity of HO-1 was significantly higher in the N. sativa-treated group than in the control (p<0.005) and nicardipine (p<0.05) groups (Table 1). The NO content in the heart was unaffected by either the treatment of L-NAME or the treatment of N. sativa (Table 1).

Table 1
Cardiac angiotensin-converting enzyme, heme oxygenase activities and nitric oxide level.

	ACE (pg/g)	HO (ng/g)	Nitric oxide (µmol/g)
Control	520.27 ± 42.59	8.66 ± 0.45	0.129 ± 0.004
L-NAME	637.40 ± 14.95*	11.69 ± 0.94	0.106 ± 0.011
L-NAME+Nicardipine	483.07 ± 31.29#	9.79 ± 0.84	0.132 ± 0.010
L-NAME+Nigella	464.07 ± 31.29#	15.48 ± 2.02* §	0.098 ± 0.008

• *versus control (p<0.05), #versus L-NAME (p<0.05)
• §versus L-NAME+Nicardipine (p<0.05).

Effect on plasma NO

There was a significant reduction in plasma NO levels in the L-NAME and nicardipine-treated groups compared to the control (p<0.001). The NO level was significantly higher in the N. sativa-treated group compared to the L-NAME and nicardipine-treated groups (p<0.001) (Figure 4).

Figure 4
Percentage change of plasma NO (weeks 0 and 8) in rats administered L-NAME and N. sativa oil for 8 weeks. The bars represent the mean±SEM (n=6). *p<0.001 versus control, #p<0.001 versus L-NAME, §p<0.001 versus nicardipine-treated group.

DISCUSSION

In this study, we demonstrated that the intraperitoneal administration of an NO synthase inhibitor (L-NAME) at a dose of 25 mg/kg increased blood pressure in rats. This finding was similar to previous studies, which reported that L-NAME at a dose of 40-55 mg/kg per day increased blood pressure (^{23 24}). The blood pressure raising effect of L-NAME in this study was not only associated with a significant decrease in serum NO but also with an increase in stress oxidative biomarkers, including MDA and NADPH oxidase. These findings suggest that the blood pressure-raising effects of L-NAME might not be purely attributed to the inhibition of NO synthase but may involve oxidative stress via the activation of NADPH oxidase expression. Our results were consistent with those of another study, which reported that L-NAME administration at a dose of 0.7 mg/ml in drinking water for 2 weeks enhanced NADPH oxidase expression in aortic tissue (²⁵). Toba et al. (²⁶) reported that L-NAME administration increased oxidative stress, vascular inflammation and ACE activity and expression. Our result suggests that L-NAME may increase blood pressure via the activation of the renin-angiotensin system. This finding was in line with Zanchi et al. (²³), who reported that L-NAME might increase blood pressure via activation of the renin-angiotensin system. In this study, L-NAME reduced NO levels in the plasma but not in the cardiac tissues. This finding was contrasted with Bernatova et al. (²⁴), who reported that L-NAME reduced the activity of NO synthase in the left ventricle. Moreover, Ndisang et al. (⁸) reported that L-NAME-treated rats had increased cyclic guanosine and pro-inflammatory chemokines and cytokines in the heart. The reason for this finding was not clear. We postulated that the negative effect of L-NAME on cardiac NO levels may be a result of the lower dose of L-NAME used in this study, which was 25 mg/kg/day, whereas Bernatova et al. (²⁴) used a higher dose of L-NAME (40 mg/kg/day).

The administration of N. sativa oil a dose of 2.5 mg/kg for 8 weeks attenuated the systolic blood pressure increase in the rats that were co-treated with L-NAME. The effect of the oil on blood pressure in this study was in agreement with other studies (⁹-¹³). The reduction in systolic blood pressure with N. sativa in this study was accompanied by significant reductions in MDA, ACE and NADPH oxidase activities and by an increase in HO-1 activity in cardiac tissue, in addition to an increase in plasma NO. Khattab and Nagi (¹²) also reported that thymoquinone at a dose of 0.5 mg/kg/day and 1 mg/kg/day orally prevented L-NAME-induced hypertension and renal damage, most likely via an antioxidant effect.

Reductions in L-NAME-induced MDA content and NADPH oxidase activity by the N. sativa oil in this study indicate that the oil has an antioxidant effect and may contribute to blood pressure reduction. The antioxidant effects of N. sativa have been reported previously (¹¹-¹³). This finding concurs with Sayed et al. (¹³) and the Khatab and Nagi (¹²) studies, which suggested that the antioxidant effect of N. sativa contributed towards its antihypertensive effect. The seed oil that contains thymoquinone, dithymoquinone and thymol might contribute to this effect (¹⁰,¹³). Thymol acts as a singlet oxygen quencher whereas thymoquinone and dithymoquinone have superoxide dismutase (SOD)-like activity and also act as free radical scavengers (²⁷-²⁹). Oxidative stress causes endothelial dysfunction, leading to a reduction in the release or production of NO (^{30 31 32}), the proliferation of vascular smooth muscle cells and collagen deposition, which causes a thickening of the tunica media, and a narrowing of the vascular lumen (²⁸), which in turn impairs vasodilation (³⁰-³²). Apart from its antioxidant properties, the blood pressure-lowering effect of N. sativa may be attributed to its diuretic properties (³³), its anti-inflammatory effect (³⁴) or its reno-protective effect (³⁵).

The activation of HO-1 plays an important role in reducing blood pressure by reducing Ang II-induced inflammation and NADPH oxidase-mediated oxidative stress via the production of anion superoxide (⁴-⁶). The antihypertensive effect of HO-1 is attributable to its production of CO, which also has a vasodilator effect (⁶). In our study, cardiac HO-1 activity was significantly increased in rats that were treated with L-NAME and N. sativa. The effect of thymoquinone on the overexpression of HO-1 expression was also reported by Kundu et al. (³⁶).

ACE converts Ang I to Ang II. The reduction of ACE activity leads to a reduction in blood pressure because of the reduction in Ang II synthesis. Ang II acts as a potent vasoconstrictor. Ang II exacerbates oxidative stress by increasing the production of superoxide (⁴-⁵). Increased ACE activity and oxidative stress was observed in hypertensive animals (²³-²⁵). Increased plasma Ang II availability was reported in L-NAME-treated rats because of endothelial NO synthase (eNOS) inhibition (²⁵). In the current study, N. sativa oil reduced cardiac ACE activity in rats receiving L-NAME. This result suggests that the antioxidant properties of N. sativa oil contributed to the reduction of the enzyme activity. We are unsure of how the reduction in cardiac ACE reduced blood pressure because our study did not measure serum ACE and aldosterone levels. Further study of serum ACE and aldosterone must be performed in the future. However, a previous study by Zeggwagh et al. (³⁷) demonstrated that N. sativa aqueous extract had no effect on plasma ACE activity in spontaneously hypertensive rats.

EDRF, better known as NO, causes vasodilation, which subsequently reduces total peripheral resistance and hence reduces blood pressure. The inhibition of eNOS reduces NO production, whereas eNOS stimulation increases NO production. Our study showed that treatment with N. sativa prevented the loss of plasma NO caused by L-NAME. The mechanism on how N. sativa reversed the reduction in NO levels in spite of L-NAME was unclear. We postulated that the effect is most likely attributable to the high antioxidant content of N. sativa, which helps prevent oxidative stress, vascular inflammation and dysfunction induced by L-NAME. A similar antioxidant effect on NO was reported by Nurul-Iman et al. (³⁸).

The effect of N. sativa in this study was comparable to that of nicardipine, which is a short-acting calcium antagonist. We chose nicardipine for this study because it has antioxidant effects and N. sativa was reported to possess calcium channel-blocking properties (¹⁴). The nicardipine-induced reduction of blood pressure in this study was associated with a reduction in MDA and NADPH oxidase, which indicated that nicardipine has antioxidant properties. The antioxidant effect of a calcium antagonist has been previously reported (³⁹). In this study, similar to N. sativa, nicardipine reduced cardiac ACE. The effect of nicardipine on ACE in this study was in accordance with Kataoka et al. (⁴⁰), who reported that a calcium channel blocker had an effect on the renin-angiotensin system and hypothesized that the anti-inflammatory and antioxidant effects of calcium channel blockers might be a result of the inhibition of the local renin-angiotensin system. The effect of a calcium antagonist on ACE was further supported by Toba et al. (²⁵); they reported that amlodipine prevented the increase in ACE in L-NAME treated rats. However, in this study, nicardipine was not able to inhibit the loss of NO induced by L-NAME treatment. The effect of nicardipine in this study differed from the results of a few other studies that demonstrated that the long-acting calcium antagonists amlodipine and felodipine increased endothelial NO synthase (eNOS) activity and gene expression, respectively and hence increased NO (²⁵). The reason for the discrepancy between our results and those of the other two studies was unclear. We postulated that short- and long-acting calcium channel blockers might have different effects on NO. In this study, we used nicardipine, which belongs to a short-acting dihydropyridine group of calcium antagonists, whereas the other study (²⁵) used a long-acting drug. Further study will be necessary to clarify this discrepancy. Unlike N. sativa, nicardipine had no effect on HO-1. In conclusion, N. sativa oil at a dose of 2.5 mg/kg attenuates the L-NAME-induced increase in blood pressure and was associated with a reduction in cardiac redox status and angiotensin-converting enzyme activity and an increase in HO-1 activity. N. sativa oil also prevented plasma NO loss. Notably, the blood pressure-lowering effect was comparable to that of nicardipine.

ACKNOWLEDGMENTS

This study was supported by grants from the Universiti Kebangsaan Malaysia (UKM-GUP-SK-08-21-299 and FF-2013-476). The authors would like to acknowledge the Center of Research and Innovation Management of UKM for the use of the ELISA reader.

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Publication Dates

• Publication in this collection
  Nov 2015

History

• Received
  16 Feb 2015
• Reviewed
  1 July 2015
• Accepted
  9 Sept 2015