Introduction
High blood pressure (BP) has become a health issue, with a projected prevalence of about one third of the global population worldwide by 2025 [
1], and endothelial dysfunction is the hallmark of this condition [
2]. Among the different types of high BP, renovascular hypertension is an important cause of secondary hypertension, which is characterized by increased activation of the renin-angiotensin system (RAS) [
3]-[
5]. The prevalence of renovascular hypertension has been estimated to be 5% of all hypertensive individuals, but it can reach higher percentage depending on the population's characteristics, e.g., renal artery stenosis can reach approximately 5% of persons aged ≥ 65 years [
6],[
7]. We have focused this study on this secondary hypertension because these patients are highly susceptible to develop resistance to conventional antihypertensive drugs, increasing the morbidity and mortality [
4],[
8]. Thus, there is a need of studies to a better understanding and to develop new therapeutic approaches against the progression of this disease.
Experimental renovascular hypertension was introduced by Goldblatt in 1934 in dogs by performing unilateral clipping of the renal artery, referred to as the two-kidney, one-clip (2K1C) model. Three decades later, the rat became the main experimental model of 2K1C hypertension in our and other laboratories [
9]-[
11]. However, genetic discoveries and advances in molecular biotechnologies have provided the opportunity to develop mouse models of cardiovascular diseases, which has led to an increasing number of studies using this murine model of hypertension [
12]-[
15]. Physiologically, it is well known that unilateral renal artery stenosis reduces renal perfusion, which activates the RAS [
5]. Recently, this system has been extended by the addition of a novel axis consisting of the angiotensin-converting enzyme 2 (ACE2), the heptapeptide angiotensin (Ang) 1–7, and the G protein-coupled receptor Mas [
16]. ACE2 converts the vasoconstrictive and pro-oxidative peptide Ang II to Ang 1–7, which exerts vasodilatory and antioxidant effects via its receptor, Mas [
16]-[
19]. Although our laboratory analyzed some RAS peptides during the development phase of 2K1C hypertension in a murine model [
3],[
20],[
21], in the present study, we extended the analysis of the Ang I, II and 1–7 levels in both plasma and the stenotic kidney during the established phase of renovascular hypertension.
Endothelial dysfunction is commonly observed in chronic arterial hypertension and is characterized by impaired nitric oxide (NO) bioavailability and increased reactive oxygen species (ROS) levels. In recent years, our laboratory [
15],[
22],[
23] and others [
24],[
25] have investigated microvascular endothelial dysfunction in various models of cardiovascular disease, including the 2K1C mouse model of hypertension, which has greatly contributed to our understanding of the relationship between endogenous activation of the RAS and endothelial dysfunction in resistance arteries [
15]. This model provides suitable approach to evaluate the efficacy of new drugs for the treatment of renovascular hypertension.
The phosphodiesterase 5 (PDE5) inhibitor sildenafil, which increases the vascular signaling of the NO/cGMP pathway [
26],[
27], has successfully been used to treat erectile dysfunction and pulmonary hypertension [
28], emerging as a promising alternative therapy for systemic cardiovascular dysfunctions. Our laboratory has recently shown that sildenafil was able to restore the endothelial dysfunction and blood mononuclear and liver cell DNA damage, which accompany atherosclerosis [
27],[
29]. Moreover, Dias et al. [
21] recently reported that sildenafil ameliorates the oxidative damage to the stenotic kidney and reduces the intrarenal levels of Ang II in the 2K1C mouse.
Therefore, the present study was designed to evaluate the effect of chronic treatment with sildenafil on high BP, the levels of peptide components of the RAS and vascular function in the hypertensive 2K1C mouse. We hypothesized that sildenafil reduces the deleterious effects of Ang II, increases the levels of the counterbalancing peptide Ang 1–7 and restores the endothelial function of resistance vessels in hypertensive 2K1C mice. The confirmation of this hypothesis may provide a novel pharmacological approach to treat endothelial dysfunction and, especially, resistant hypertension.
Materials and methods
Animals
Experiments were performed in male wild-type mice (C57BL/6) that weighed 23 g on average (10-week-old). Mice were bred and maintained in the Laboratory of Translational Physiology animal facility (Vitoria, ES, Brazil) and were fed with a standard chow diet and received water ad libitum. Animals were housed in individual plastic cages with automatic controlled temperature (22°C) and humidity (60%) and were exposed to a 12/12 h light–dark cycle. All of the experimental procedures were performed in accordance with the National Institutes of Health (NIH) guidelines, and the study protocols were approved by the Institutional Animal Care and Use Committee (CEUA-EMESCAM Protocol # 02/2013).
Induction of 2K1C renovascular hypertension and treatment
The 2K1C Ang-dependent hypertension was induced as previously described [
3],[
12],[
15],[
21],[
30]. Briefly, animals were anesthetized (91/9.1 mg/kg ketamine/xylazine, i.p.). The left renal artery was exposed through a retroperitoneal flank incision and carefully isolated from the renal vein, nerves, and connective tissues. Using an ophthalmic surgical microscope (Opto Eletronica SA, model SM 2002, Belo Horizonte, MG, Brazil), a U-shaped stainless steel clip with a 0.12 mm wide opening was placed around the renal artery near the abdominal aorta, which decreased renal perfusion [
31]. Two weeks after surgery, animals were divided into two groups (8 to 10 animals per group): renovascular hypertensive mice treated with vehicle (2K1C) and hypertensive mice treated with 40 mg/kg/day of the PDE5-inhibitor sildenafil (Viagra®, Pfizer) for 2 weeks by oral gavage (2K1C-sildenafil). Sham-operated mice were used as a normotensive control group. The effectiveness of this sildenafil dose [
32] was previously demonstrated in studies on endothelial dysfunction and DNA damage in our laboratory [
21],[
27],[
29]. The outcomes were examined 28 days after induction of hypertension.
Hemodynamic measurements
Twenty six days after 2K1C procedure or sham operation, mice were anesthetized with a combination of ketamine/xylazine (91/9.1 mg/kg, i.p.) and a catheter (0.040 mm outer × 0.025 mm inner diameters, MicroRenathane, Braintree Science, Massachusetts, USA) was inserted into the right carotid artery for the measurement of mean arterial pressure (MAP) and heart rate (HR) recordings. The free catheter end was tunneled under the skin of the back to the level of the shoulder blades. Hemodynamic measurements were performed in conscious, freely moving mice in their own cages, two days after catheter placement, as already validated as a sufficient period for complete recovery from surgery by others [
33] and standardized in our laboratory [
3],[
13]-[
15]. For the MAP and HR recordings, the arterial catheter was plugged into a disposable BP transducer (Cobe Laboratories, Colorado, USA) connected to a pressure processor amplifier and data-acquisition system (MP100, Biopac Systems, California, USA). At the beginning of the experimental session, a period of approximately 30 min was allowed for stabilization of cardiovascular parameters before the measurement of basal MAP and HR values in conscious mice (Acknowledge software, Biopac Systems).
Assessment of endothelial function
At the end of the treatment, animals were anesthetized using sodium pentobarbital (50 mg/kg, i.p.), and the mesenteric arterial bed (MAB) was isolated and prepared for vascular studies. The superior mesenteric artery was cannulated. Then, the MAB was transferred to a 37°C chamber and was perfused using a peristaltic pump (Peri-Star Pro 4-channel pump, WPI, Lu Jia Zui District, Shangai, China) at a constant flow rate (3 mL/min) with oxygenated (95% O2 - 5% CO2 mixture) physiological salt solution (in mmol/L: 130 NaCl, 4.7 KCl, 1.6 CaCl2♦2H2O, 1.18 KH2PO4, 4.7 MgSO4♦7H2O, 14.9 NaHCO3, 0.026 EDTA, 11.1 glucose, pH 7.4). The perfusion pressure was monitored using a T-tube inserted between the pump and the inflow cannula that was connected to a pressure transducer and a data acquisition system (Biopac Systems). Then, dose–response curves of acetylcholine (ACh, 3 × 10−7 to 3 × 10−2 M) and sodium nitroprusside (SNP, 3 × 10−7 to 3 × 10−2 M) were generated in the isolated MABs. The vascular responses were evaluated based on the changes in the perfusion pressure and the vasodilator responses to ACh and SNP, which were calculated as a percentage of the pre-contraction induced by norepinephrine (NE, 9.8 × 10−6 M). To assess the mechanisms underlying the vascular effect of ACh dose–response curves were generated in separate preparations containing an intact endothelium and using specific blocker agents: (a) the nonselective NO synthase (NOS) inhibitor N-nitro-L-arginine methyl ester (L-NAME, 10−4 M), (b) the nonselective inhibitor of cyclooxygenases 1 and 2 (Cox1 and Cox2) indomethacin (10−5 M) or (c) the NAD(P)H oxidase inhibitor apocynin (30 μM). The relaxation responses to ACh were expressed as the percentage of dilation relative to the maximal pre-contraction level. For each curve, the maximum effect (Rmax) and the log of the concentration of the agonist that produced half of Rmax (log EC50) were calculated via nonlinear regression analysis. The sensitivities of the agonists were expressed as pEC50 (−log EC50). The difference in the area under the curve (Δ AUC) for each of the responses of the MAB to ACh in the presence of each inhibitor were calculated, and these results were expressed in arbitrary units (a.u.).
Measurements of the angiotensin peptide levels
The plasma and intrarenal levels of Ang I, II and 1–7 were analyzed via high performance liquid chromatography (HPLC), as previously reported [
20],[
21],[
30]. For this analysis, blood was collected in the presence of EDTA and a protease inhibitor cocktail (Product # P2714, Sigma-Aldrich), and after centrifugation (9.5
g, for 20 min) using a refrigerated centrifuge (4°C), plasma was collected for further analysis. The Ang peptides were extracted using Oasis C18 columns previously activated with methanol (5 mL), tetrahydrofuran (5 mL), hexane (5 mL) and water (10 mL). After activation, the samples were eluted in ethanol/acetic acid/water at proportions 90% - 4% - 6%. The eluates were dried, re-dissolved in 500 μL of mobile phase A (5% acetonitrile in 0.1% phosphoric acid) and filtered for analysis by HPLC. The Ang peptides in each sample were separated using a reverse-phase ODS Aquapore 300 (250 × 4.6 mm) HPLC column with a particle size of 7 μm (Perkin-Elmer's Brownlee Columns, Norwalk, USA) using a 5–35% gradient of mobile phase B: 95% acetonitrile in 0.1% phosphoric acid at a flow of 1.5 mL/min for 40 min. The Ang peptides were identified by comparing them with the retention times and peak heights of standard peptides.
For renal analysis of the Ang peptides, they were extracted from kidney homogenates and purified as performed on plasma samples. The subsequent steps, from the activation step to the HPLC analysis step using the reverse-phase column, the procedures were the same as those for plasma sample analysis. The Ang peptides were identified based on the retention time (<6%) and peak height (<5%) of standard Ang peptides and were normalized according to the kidney weight.
Isolation and identification of endothelial cells from MAB
At the end of the treatment, animals were anesthetized with sodium pentobarbital (50 mg/kg, i.p.), the midline of the abdomen was incised and the MAB was isolated, minced and digested with type II collagenase (1000 U/mL) at 37°C for 60 min at constant agitation. The cellular digest was filtered through a sterile 70-μm nylon mesh to remove cell debris, centrifuged at 400 g for 10 min, and washed twice in PBS. The cell pellet was resuspended in freezing solution and stored at −80°C for further analysis. For flow cytometry analysis, the samples were thawed using a heated orbital shaker at 37°C and immediately transferred to a round-bottom tube, in which DMEM containing 20% FBS was added in a drop wise fashion during a gentle agitation. The presence of endothelial cells in MAB digest was confirmed using an APC-conjugated monoclonal antibody against APCCAM-1 (CD31-PE). After thawed, MAB digest cell samples were resuspended at a concentration of 1 × 105 cells/mL in PBS and incubated with 5 μL of CD31-APC for 20 min in the dark and at room temperature. In the flow cytometry analysis, a APC-conjugated rat IgG2a was used as an isotype-specific control to set the threshold values. From each sample, 100,000 events have been generated by a FACSCanto II flow cytometer (Becton Dickinson - BD, San Juan, CA, USA) using an appropriated filter for APC (660 nm).
Measurement of endothelium ROS
The ROS analysis was performed by flow cytometry using dihydroethidium (DHE), diaminofluorescein (DAF) and hydroxyphenyl fluorescein (HPF) to detect intracellular ♦O
2
−, NO and ♦ONOO
−, respectively, as previously described [
21],[
31]. Briefly, 160 mM of DHE or 10 μM of HPF or 2 μM of DAF was added to the cell suspension (10
6 cells) and incubated at 37°C for 30 min (DHE and HPF) or 180 min (DAF) in the dark. For positive control, samples were treated for 5 min with 50 mM H
2O
2 and/or 100 μM of SNP to create oxidative stress without being toxic to the cells, whereas for negative control, the cells were incubated with ethanol. Cells were then washed, resuspended in PBS and kept on ice for immediate detection by flow cytometry (BD). For quantification of DHE, DAF and HPF fluorescence, 100,000 events were acquired and data were analyzed using the FACSDiva software (BD).
Statistical analysis
The values are expressed as the means ± S.E.M. The Kolmogorov-Smirnov test indicated that the variables displayed a normal (Gaussian) distribution. Statistical comparisons between more than two means were performed using one-way or two-way analysis of variance (ANOVA) followed by Bonferroni's post hoc test. The statistical analyses were performed using Prism software (Prism 6, GraphPad Software, Inc., San Diego, CA, USA). A value of p < 0.05 was considered to be statistically significant.
Discussion
Previous results from our laboratory [
21] demonstrated by the first time that sildenafil repaired the hypoperfused kidney injury in 2K1C hypertensive mice by activation of the NO-mediated pathway. This pleiotropic protective role of sildenafil led us to investigate other additional beneficial effects of this drug on the systemic RAS and resistance vasculature in this model of hypertension. Our primary finding was that chronic treatment of these animals with this selective PDE5 inhibitor sildenafil restored the levels of BP and vascular relaxation to those of normotensive sham mice. Moreover, the present study is the first to reveal that the beneficial effects of sildenafil appear to be mediated by decreasing the levels of the vasoconstrictive and pro-oxidant peptide Ang II and increasing the levels of its physiological antagonist Ang 1–7.
A recent work from Navar's group and our collaborator Casarini's group [
34] revealed that the maintenance of high blood pressure in 2K1C is dependent of an imbalance between high levels of ACE/Ang II and low levels of ACE2/Ang 1–7, both being influenced by renin activity [
16],[
35]. In parallel, it has been reported that augmentation of chymase activity in the ischemic kidney of 2K1C rats [
36] may be a mechanism related with ACE-independent intrarenal Ang II production. Moreover, previous studies have demonstrated that Ang II downregulates ACE2 mRNA expression in some tissues, including the kidney [
37],[
38], which could be mediated by AT1 receptors [
39],[
40]. Based on the above findings and on our studies in 2K1C hypertensive mice, we speculate that the repair of the stenotic kidney by sildenafil (administered for 14 days) was mediated by attenuation of renal baroreceptor activity, with consequent deactivation of the intrarenal RAS, as confirmed in the present study by decrease in intrarenal Ang I (~33%) and II (~50%) and (contrasting) by increase in Ang 1–7 (~15%), as compared with 2K1C mice.
Regarding the plasma Ang I and II, our finding of normalized levels at the chronic phase was expected based on the fact that in the rat Ang-dependent renovascular hypertension has been separated in two phases [
5]. The initial phase is related to the development of hypertension, which occurs from the first day following the placement of the clip to the 14
th day, when the plasma levels of Ang II peak. The late (second) phase is related to the maintenance of hypertension, which has been evaluated at approximately 28 days after renal artery clipping, and that shows stabilized plasma levels of Ang II [
5]. In the mouse model, the few available studies have reported an increase in renin activity and the levels of Ang I (~50%) [
20],[
41], Ang II (~350%) [
20],[
30],[
42] and Ang 1–7 in plasma (~110%) [
20] during the first phase of renovascular hypertension (14 days following the clip placement). During the second phase of 2K1C hypertensive mice, neither increased plasma renin activity nor elevated levels of Ang I [
41] or Ang II [
42],[
43] has been detected, justifying the similar profile founded in this study. Altogether, the above data extend to the mice the time-course profile of Ang that has been demonstrated by Navar's research group in the rat [
5]. Surprisingly, we observed that sildenafil treatment increased plasma levels of Ang 1–7 (~45%), which is known to counterbalance the deleterious effects elicited by Ang II [
16],[
35]. Based on our findings, we speculate that the Ang 1–7 generated by the ACE2-mediated degradation of Ang II may also limit the intrarenal uptake of Ang II, as discussed above. It should be noted that, in a review of contemporary literature, it is notable a vast diversity in the methods that have been used for the analysis of the RAS in the few studies using the 2K1C mouse model, confounding the comparison of the plasma and tissue levels of RAS peptides. As a solution for this discrepancy, we considered that it would be most appropriate to compare our detected values in the hypertensive 2K1C mice and the 2K1C mice treated with sildenafil to the average values in the Sham mice, which were normalized to 100%; similarly, we will compare the data found by us and others using relative (%) values.
In the present study, 2K1C mice exhibited a high BP, approximately 20% higher than that of the Sham mice, in agreement with other studies reporting similar increases (20-25%) [
12],[
15],[
30],[
31],[
41]-[
45]. The high BP was accompanied by tachycardia, which is consistent with other reports [
20],[
21],[
41]. As expected, and based on previous studies using the rat model [
21],[
46]-[
48], we found that sildenafil normalized the BP and HR. Moreover, the novelty of the present study is that according to the profile of intrarenal and plasma Ang that we observed, it could be speculated that these beneficial effects of sildenafil are partially mediated by the reciprocal changes in Ang, i.e., a decrease of Ang II and increase of Ang 1–7. This hypothesis may be reinforced by the finding that chronic treatment of spontaneously hypertensive rats (SHR) with Mas receptor agonists or with Ang 1–7 led to vasorelaxation, anti-hypertensive and cardioprotective effects [
49],[
50]. Additionally, the plasma levels of Ang 1-7 were increased during treatment with ACE inhibitors or AT1 receptor blockers, indicating a potential dependence of the anti-hypertensive effects of those compounds on Ang 1–7 [
18],[
39]. Despite of our results demonstrate a drop in Ang II, we cannot rule out the possibility the participation of AT2 receptor in this model of hypertension, since this protein can stimulates NO signaling [
51], potentiating the effects of sildenafil. This hypothesis is corroborated by other recent studies that demonstrated the importance of AT2 receptor in renovascular hypertension [
52],[
53]. Thus, targeting the ACE2-Ang (1–7)-Mas and AT2 receptor axis using new pharmacological tools, such as sildenafil, which we used in the current study, may represent a novel therapeutic strategy for renovascular hypertension.
It has been demonstrated that the interruption of the ACE2-Ang (1–7)-Mas axis is an underlying mechanism responsible for the worsening of the developmental and maintenance phases in 2K1C Mas knockout mice [
39], as well as impairing the baroreflex control, endothelial function and the balance of NO/ROS in normotensive mice [
40],[
41]. In parallel, recent data have demonstrated specific and beneficial effects of AT2 receptor via central areas in hypertensive rats [
54]. Considering the evidence that sildenafil crosses the blood–brain barrier [
55],[
56] and that it affects the angiotensin profile, one cannot rule out the possibility of also a central action on the sympathetic/parasympathetic drive. In this context, although recent studies have shown an increased sympathetic drive imposed on the cardiovascular system by sildenafil in both rats [
56] and humans [
57],[
58], we speculate that in our study (in which sildenafil was chronically administered) its systemic antioxidant effects overtook the possible undesirable sympathetic-mediated effects.
Endothelial dysfunction is an important abnormal function commonly observed in cardiovascular diseases, including atherosclerosis [
22] and various models of arterial hypertension [
15]. Previous studies by our group revealed that the MAB exhibits an increased response to vasoconstrictors and a decreased response to vasodilators in RAS-dependent hypertensive rats [
24],[
59] and mice [
15]. Thus, in the current study, we designed an experiment to evaluate the effects of sildenafil treatment on endothelial dysfunction in hypertensive 2K1C mice. We selected the 2K1C model that was developed by Goldblatt decades ago because endothelial dysfunction is an early characteristic of RAS-dependent 2K1C-mediated hypertension [
15],[
60]. As expected, ACh evoked endothelium-dependent relaxation, which was greatly diminished in the 2K1C mice. However, no significant difference was detected in the dose–response curve to the NO donor SNP, indicating that vascular dysfunction may be due to dysfunctional molecular pathways in endothelial cells but not in vascular smooth muscle cells. This result is in agreement with studies showing that impaired endothelium-dependent vasorelaxation is associated with the second phase of chronic 2K1C hypertension in the rat model [
5],[
61]. Because we hypothesized that 2K1C-induced endothelial dysfunction may be improved by chronic treatment with sildenafil, standard experiments using pharmacological inhibitors were designed to assess the relative contribution of each molecular pathway to the relaxation responses to ACh in the MAB and the effectiveness of sildenafil in restoring or improving endothelial function in the 2K1C mice.
The relative importance of vasoactive substances, such as NO, PGI
2, EDHF and ROS, depends on the size of the blood vessels and the experimental animal. Studies have shown that in the rat, NO is the primary contributor to ACh-induced vasodilation in the aorta, whereas EDHF plays a predominant role in resistance vessels [
62]. Our data show that in both the wild type and hypertensive 2K1C mice, the EDHF pathway was the primary contributor and was scarcely altered in the endothelium-dependent relaxation response to ACh in the MAB. This finding corroborates a previous study showing that EDHF-mediated dilatory responses were unaffected in mesenteric resistance vessels in RAS-dependent hypertensive mice [
63]. Moreover, our data show that in the vasodilator pathway, the impairment of NO/cGMP was the primary contributor to endothelial dysfunction, followed by PGI
2, as determined using hypertensive 2K1C mice. Indeed, the contribution of NO and PGI
2 to endothelial function in the 2K1C mice was reduced to approximately 35% and 50%, respectively, of that in the Sham mice. By blocking NAD(P)H using apocynin, we also found that the levels of ROS, which have opposing effects to those of NO and PGI
2, were increased approximately 6-fold in the 2K1C mice, in agreement with the rat model of renovascular hypertension [
48],[
64]. This finding may be because high BP (enhanced shear stress) and activation of the RAS have been shown to increase ROS production by NAD(P)H oxidase via the AT
1 receptor axis, decreasing NO bioavailability in the 2K1C mice [
27],[
30],[
45],[
65]. The hypothesis that it occurs an imbalance between NO and O
2 levels in the endothelial cells isolated from MAB, but not only systemically [
21],[
30],[
31], was confirmed in a separated set of experiments by flow cytometry in the present study. Additionally, by using the HPF staining, we found in renovascular hypertensive mice an increase of endothelial production of peroxynitrite, which is derived from the reaction of NO with the superoxide anion. Taken together, these results suggest a relevant role of impairments of the NOS/cGMP and prostanoid/cAMP pathways and the activation of the ROS/cGMP pathway in the endothelial dysfunction observed in RAS-dependent hypertension [
66].
The second novel finding based on endothelial function analysis is that sildenafil recovered endothelial function to normal levels, as indicated by the parameters of the dose–response curve to ACh (R
max and AUC) and flow cytometry analysis of ROS. The recovery of endothelial function by sildenafil treatment primarily occurred due to a marked increase in the vasodilatory contribution of NO and a marked decrease in the levels of superoxide and (consequently) peroxynitrite anions. Recent data have shown that this vasodilator effect of sildenafil may involve indirect mechanisms, such as upregulation of BH
4 and soluble guanylate cyclase (sGC) enzyme, besides the inhibition of NADPH oxidase activity, leading to the increase of NO bioavailability [
67]. These findings corroborate the notion that the inhibition of PDE5 in the vessels in smooth muscle directly enhances the NO/cGMP signaling pathway by inhibiting cGMP degradation and subsequently facilitating vessel relaxation [
68].
Competing interests
The authors declare that they have no competing interest.
Authors' contributions
ATD, ALG, ASC and JCF carried out experimental analysis and acquisition of data, analysis and interpretation of the data and drafted the manuscript. ZP and DEC carried out the protocol of analysis of Angiotensin II at the Federal University of Sao Paulo. CMB participated in the study's design and in the critical revision of the manuscript. IBSG co-supervised the graduated students and revised the manuscript. BPC and TMCP participated in the supervision and in the critical revision of the manuscript. SSM and ECV contributed to the conception, design and supervision of the study and interpretation of data. All authors read and approved the final version of the manuscript.