- Research article
- Open Access
- Open Peer Review
ACE inhibition attenuates uremia-induced aortic valve thickening in a novel mouse model
© Simolin et al; licensee BioMed Central Ltd. 2009
- Received: 02 August 2008
- Accepted: 03 March 2009
- Published: 03 March 2009
We examined whether impaired renal function causes thickening of the aortic valve leaflets in hyperlipidemic apoE-knockout (apoE-/-) mice, and whether the putative effect on the aortic valves could be prevented by inhibiting the angiotensin-converting enzyme (ACE) with enalapril.
Thickening of the aortic valve leaflets in apoE-/- mice was induced by producing mild or moderate chronic renal failure resulting from unilateral nephrectomy (1/2 NX, n = 18) or subtotal nephrectomy (5/6 NX, n = 22), respectively. Additionally, the 5/6 NX mice were randomized to no treatment (n = 8) or enalapril treatment (n = 13). The maximal thickness of each leaflet was measured from histological sections of the aortic roots.
Leaflet thickness was significantly greater in the 5/6 NX mice than in the 1/2 NX mice (P = 0.030) or the unoperated mice (P = 0.003). The 5/6 NX mice treated with enalapril had significantly thinner leaflets than did the untreated 5/6 NX mice (P = 0.014).
Moderate uremia causes thickening of the aortic valves in apoE-/- mice, which can be attenuated by ACE inhibition. The nephrectomized apoE-/- mouse constitutes a new model for investigating the mechanisms of uremia-induced aortic valve disease, and also provides an opportunity to study its pharmacologic prevention.
- Aortic Valve
- Aortic Stenosis
The prevalence of cardiovascular disease (CVD) is far greater in patients with chronic renal failure (CRF) than in the general population . Similarly, the progression of aortic stenosis (AS) is accelerated in chronically uremic patients [2–4]. In addition to renal failure, epidemiological studies have identified that other atherosclerotic risk factors, including hypertension, smoking, hypercholesterolemia, diabetes mellitus, male gender, and age, predispose to AS development [5–7]. Stenotic aortic valves are characterized by an atherosclerosis-like lesion, consisting of inflammatory cells, cholesterol deposits, and calcified nodules . Furthermore, active bone formation and adverse extracellular matrix remodeling contribute to the thickening and stiffening of the valves [9–11]. Importantly, angiotensin-converting enzyme (ACE), angiotensin II (Ang II), and Ang II type 1 receptors (AT-1Rs) are expressed in the aortic valves and ACE activity is augmented in the stenotic valves [12, 13], suggesting that inappropriate activation of the renin-angiotensin system (RAS) participates in the pathogenesis of AS. To fully understand the pathogenic mechanisms of AS and eventually to be able to design potential drug therapies, animal models suitable for preclinical studies of AS are needed. To date, several rabbit models of AS have been introduced [14–17]. In addition, different mouse models of AS have been tested. These include old apoE-/- mice  and old LDLr-/- apoB100/100 mice , which are prone to develop functional valvular heart disease, and wild-type mice in which a high fat/high carbohydrate diet was shown to trigger thickening of the aortic valve leaflets .
In view of the higher prevalence of aortic valve calcification and stenosis among patients with renal failure, and the pathogenetic similarities between AS and atherosclerosis, we hypothesized that chronic uremia would cause aortic valve thickening, a condition known to ultimately lead to functional impairment and AS development. We chose the nephrectomized apoE-/- mouse, which develops extensive vascular disease and is already an established animal model in the study of uremic atherosclerosis [21, 22] and could thus serve as a suitable model of uremia-induced AS. Moreover, to learn whether Ang II-dependent pathways may contribute to uremia-associated aortic valve thickening, we tested the effect of enalapril, an ACE inhibitor, on valvular thickening in this particular mouse model.
In Study 1, the mice were assigned at the age of seven weeks to one of three groups: (1) unoperated (0 NX, n = 13), (2) unilateral nephrectomy (1/2 NX, n = 18) in which the left kidney was removed, or (3) subtotal nephrectomy (5/6 NX, n = 22) in which both the left kidney and the upper and lower poles of the right kidney were resected. The surgery was performed under anesthesia with postoperative analgetics as previously described . The mice were sacrificed 22 weeks after allocation to the different groups, and the portion of the heart containing the proximal ascending aorta was removed, fixed in formalin and embedded in paraffin .
In Study 2, the mice were allocated at the age of 10 weeks to either 5/6 NX or a sham operation (0 NX). In the 5/6 NX group, the upper and lower poles of the right kidney were resected, and two weeks later the entire left kidney was resected . The sham-operated mice underwent kidney exposure operations at the same time points. To study the effect of ACE inhibition on the development of aortic valve thickening, treatment with an ACE inhibitor (2 mg/kg/d enalapril) was started four weeks after nephrectomy. After 36 weeks of uremia, the mice were sacrificed and the tissues were snap frozen, thawed, and fixed in formalin, after which they were embedded in Tissue-Tek OCT (Sakura Finetek Europe B.V., Zoeterwoude, The Netherlands) and frozen again .
Measurements of body weight, blood pressure, blood hemoglobin, the plasma levels of urea, creatinine, phosphate, calcium, cholesterol, and triglycerides were performed as previously described [21, 22].
For Oil Red O staining, the sectioned samples were fixed with paraformaldehyde, washed, and dehydrated in propylene glycol. Thereafter the samples were incubated with O0625 stain (Sigma-Aldrich Corporation, Saint Louis, MO, USA) and differentiated in propylene glycol. Counterstaining was done with Harris's hematoxylin (Merck & Co. Inc., Whitehouse Station, NJ, USA). Masson's trichrome staining was done according to the standard method, modified by Lillie, using a Sigma-Aldrich HT15 kit.
Differences between groups were evaluated by Kruskal-Wallis test and two-group comparisons by Mann-Whitney U test unless specified otherwise. Spearman's (non-parametric data) and Pearson's (parametric data) correlation coefficients were used to assess relationships between continuous variables. Statistical analyses were performed using SPSS 15.0 for Windows (SPSS Inc., Chicago, IL, USA). P-values of < 0.05 were considered statistically significant. Data are expressed as mean ± standard deviation (SD).
Effects of uremia and enalapril treatment on plasma biochemistry, body weight, blood pressure, and aortic atherosclerosis
Effect of chronic renal failure on body weight, blood pressure, blood hemoglobin, plasma indices of uremia, plasma lipids, and aortic atherosclerosis in Study 1.
Unoperated (0 NX)
(n = 13)
(n = 18)
(n = 22)
26.4 ± 1.6
27.6 ± 1.5
23.0 ± 3.5a
Mean blood pressure
116.6 ± 6.5
113.0 ± 8.2
116.8 ± 14.3
8.38 ± 0.55
8.26 ± 0.26
6.85 ± 0.74a
10.6 ± 1.5
12.5 ± 2.1a
28.0 ± 9.7a
0.036 ± 0.005
0.038 ± 0.005
0.051 ± 0.007a
2.20 ± 0.16
1.89 ± 0.27a
2.61 ± 0.72a
2.22 ± 0.12
2.25 ± 0.06
2.52 ± 0.12a
P-Ca × P
4.89 ± 0.43
4.24 ± 0.64a
6.56 ± 1.82a
13.3 ± 1.9
15.0 ± 3.6
19.3 ± 3.6a
0.70 ± 0.37
0.58 ± 0.20
0.46 ± 0.14a
Aortic plaque area fraction
0.048 ± 0.025
0.085 ± 0.038a
0.258 ± 0.117a
Effects of chronic uremia and enalapril treatment on body weight, blood pressure, blood hemoglobin, plasma indices of uremia, plasma cholesterol, and aortic atherosclerosis in Study 2.
(n = 7)
(n = 8)
(n = 13)
32.1 ± 2.0
27.3 ± 2.1a
27.4 ± 2.0
Systolic blood pressure
112.9 ± 6.1
116.8 ± 4.6
105.2 ± 7.2b
9.60 ± 0.83
7.31 ± 0.97a
6.99 ± 0.66
11.9 ± 1.1
28.6 ± 5.4a
26.3 ± 6.2
0.016 ± 0.002
0.030 ± 0.007a
0.025 ± 0.006
2.47 ± 0.47
2.78 ± 0.65
2.54 ± 0.39
2.70 ± 0.21
2.95 ± 0.41
2.61 ± 0.07
P-Ca × P
6.65 ± 1.45
8.40 ± 3.19
6.63 ± 0.99
16.3 ± 2.4
16.6 ± 3.3
13.5 ± 2.9b
Aortic plaque area fraction
0.10 ± 0.07
0.23 ± 0.08a
0.11 ± 0.04b
Effect of uremia on aortic valve leaflet thickening in unoperated, 1/2 NX, and 5/6 NX apoE-/-mice (Study 1 and Study 2)
Effect of enalapril on aortic valve leaflet thickening in 5/6 NX apoE-/-mice (Study 2)
After 36 weeks of uremia, we examined the effect of ACE inhibition on maximal valve thickness in the 5/6 NX apoE-/- mice. The 5/6 NX mice that had been treated with 2 mg/kg/d enalapril for 32 weeks had significantly thinner aortic valve leaflets when compared with the 5/6 NX mice that had not been treated with enalapril (159 ± 67 μm vs. 261 ± 88 μm, P = 0.014) (see Figure 5B).
Histopathologic findings (Study 2)
To examine for the presence of fibrous and neutral lipid components in the valves, the sections were stained with Massons's trichrome and Oil Red O, respectively. As shown in Figure 4G–I, the valvular leaflets in all three groups contained collagen. In the thickened leaflets, there was not only more collagen, but the collagen bundles formed dense deposits, reflecting fibrous thickening of the valves. The leaflets of the 5/6 NX mice treated with enalapril appeared to contain less collagen than the leaflets of their untreated littermates, and the collagen bundles were arranged in a looser fashion.
Since all the animals in this animal model of aortic valvular thickening were hyperlipidemic apoE-/- mice, their aortas contained atherosclerotic plaques (see Tables 1 and 2). As expected, also the aortic wall in the aortic root region contained Oil Red O-positive intimal thickenings (see Figure 4J–L). In sharp contrast, Oil Red O staining was negative in the leaflets, demonstrating that, despite the presence of marked hyperlipidemia and uremia, the valvular pathology did not involve deposition of neutral lipids, i.e. cholesteryl esters or triglycerides, in the leaflets.
The present study demonstrates that uremia accelerates aortic valve thickening in genetically hyperlipidemic mice. Importantly, aortic valve thickening in the nephrectomized mice was inhibited by enalapril, suggesting that uremia induces aortic valve sclerosis or stenosis via Ang II-mediated mechanisms. These findings emphasize the significance of local RAS in the pathobiology of aortic valve disease and raise pharmacological prevention of RAS actions as a potential treatment option in this disease.
Indeed, recent investigations have portrayed the possibility that activation of RAS promotes AS progression and, thus, inhibition of its actions may be beneficial in this disease . ACE is locally produced in aortic valves and its enzymatic activity is augmented in stenotic leaflets . Furthermore, Ang II and profibrotic Ang II type 1 receptors (AT-1Rs) are present in diseased valves and colocalize with ACE in valvular lesions [12, 13]. In addition to ACE, two alternative Ang II-forming enzymes, namely chymase and cathepsin G, are upregulated in stenotic valves, further enhancing the Ang II-forming potential of the affected valves [10, 13]. Accordingly, Ang II, as a powerful proinflammatory and profibrotic mediator , may participate in the pathogenesis of AS both in subjects with preserved renal function and, as suggested by the present results, also in uremic patients. Preliminary support for the benefit of ACE inhibitors in AS patients originates from small clinical studies in which ACE inhibitors have been shown to be well tolerated in AS patients and to even improve their hemodynamic status and exercise tolerance [25–27]. Moreover, in a recent retrospective study by O'Brien and co-workers, the use of ACE inhibitors was associated with slower progression of aortic valve calcification . In contrast, Rosenhek and co-workers were not able to demonstrate any beneficial effects of ACE inhibitors on the hemodynamic progression of AS . Considering the retrospective nature and small sample sizes of these trials, additional research in this area is indispensable.
In epidemiological studies, the prevalence of aortic valve abnormalities, including valve sclerosis, calcification, and stenosis, is increased in patients with renal failure [30–32]. Moreover, in patients with renal insufficiency, the rate of AS progression is higher than in those with normal renal function [3, 33]. In view of these observations, chronic uremia and its consequences seem to exert detrimental effects on the aortic valve leaflets. Several uremia-related mechanisms may contribute to the thickening of the aortic valve leaflets. Renal failure is associated with abnormal calcium-phosphate homeostasis, including hyperphosphatemia, a high serum calcium phosphate product, and secondary hyperpharathyroidism, which may lead to metastatic calcification of tissues, including the aortic valve leaflets [3, 34]. Furthermore, chronic renal insufficiency leads to activation of RAS , which constitutes a risk factor of cardiovascular calcification in humans. Bilateral total nephrectomy (6/6 NX) in rats has been shown to cause plasma renin to fall below the limits of detection within 24–48 hours, thus effectively eliminating circulating RAS . Because of the massive reduction in kidney tissue, it is also likely that the levels of circulating renin were decreased in the 5/6 nephrectomized mice in the present study, as well. However, ACE is produced mainly in the vascular bed of the lungs . According to our previously published results, 5/6 nephrectomy increases plasma ACE activity by 36 percent . Thus, inhibition of ACE should be an effective and appropriate treatment strategy in the present animal model.
In addition to the mouse models described above, several rabbit models of AS have been introduced [14–17]. Rajamannan and co-workers described a hypercholesterolemic rabbit model in which hypercholesterolemia resulted in aortic valve thickening, atherosclerotic changes, and bone matrix production in the valves, and these adverse processes were prevented by atorvastatin [15, 38, 39]. In contrast, in the rabbit model described by Drolet and co-workers, hypercholesterolemia alone did not cause any significant functional aortic valve abnormality when assessed by echocardiography . Instead, hypercholesterolemia combined with toxic doses of vitamin D resulted in decreased aortic valve area (AVA) and increased transvalvular gradients in these animals . In a recent rabbit model of AS, hypercholesterolemia induced fatty deposition, macrophage accumulation, and osteopontin expression in the aortic valves, and these atherosclerotic changes and expression of osteoblastic factors were attenuated by the AT-1R antagonist olmesartan . Furthermore, dietary hypercholesterolemia disrupted endothelial integrity in lesion-prone areas of the valves, whereas preservation of the endothelium was attained with olmesartan . These observations indicate that aortic valve lesion development caused by hypercholesterolemia is not only related to cholesterol accumulation. Instead, activation of RAS appears as a key element in lesion development, including both induction of inflammation and osteoblastic transdifferentiation of valvular cells.
The exact molecular mechanism by which enalapril prevents aortic valve leaflet thickening remains unknown. Besides being capable of inhibiting ACE enzyme locally, enalapril is also able to exert multiple systemic effects. The only statistically significant changes in metabolic indices due to the enalapril treatment were lowering of systolic blood pressure and plasma total cholesterol. Interestingly, a recent study in humans has shown that ACE inhibitors may have a beneficial effect on the lipid profile . However, the very recently published SEAS study has clearly shown that even a long-lasting lowering of the plasma cholesterol level by 60 percent fails to affect the progression of aortic stenosis . Importantly, enalapril may contribute to the inhibition of valvular thickening also by lowering systolic blood pressure. Excluding this possibility remains a challenge for future studies.
No animal model for uremia-induced aortic valve thickening has been published previously. In the present study, the increased prevalence of aortic valve leaflet thickening among the hyperlipidemic mice with unilateral nephrectomy, and consequently mild renal impairment, suggests that even mild renal insufficiency promotes aortic valve leaflet thickening and eventually may increase the risk of aortic stenosis in hyperlipidemic mice. Importantly, in the 5/6 nephrectomized uremic mice, we noted that 22 weeks of uremia (Study 1) induced less thickening of the leaflets than did 36 weeks of uremia (Study 2), providing additional support for the idea that uremia induces gradual valve thickening in this hyperlipidemic mouse model. Furthermore, a strong correlation appeared between aortic atherosclerotic lesional area and aortic valve thickness (see Figure 6A). This is of interest, since epidemiological studies have shown that AS and arterial atherosclerosis share common risk factors, including uremia, hypercholesterolemia, hypertension, smoking, diabetes, age, and male gender [5–7]. Furthermore, coronary artery disease coexists in approximately 50% of patients with AS , and even patients with aortic valve sclerosis, an early stage of AS, possess an elevated risk of myocardial infarction and cardiovascular death . Also, there was a significant correlation between plasma creatinine level and aortic valve thickness (see Figure 6B). Creatinine, being the marker of renal dysfunction, suggests that uremia is an important etiological factor of aortic valve thickening in this particular model.
The following facts could be considered as limitations of this study. The blood pressure-lowering effect of enalapril may have contributed to the decreased thickening of the valve leaflets. Although we demonstrate here that enalapril prevents aortic valve thickening in nephrectomized apoE-/- mice, we do not provide evidence concerning the efficacy of enalapril in other mouse models of AS. Appropriate animal models of AS that closely mimic the disease etiology and manifestations in humans are difficult to establish, and the utilized models have several limitations. In this sense, the present model of uremic apoE-/- mice has the advantage of sharing the same etiology with human AS in patients whose aortic valve disease is associated with chronic renal failure and hypercholesterolemia. Previously, several mouse models of AS have been tested, i.e. senile apoE-/- mice , LDLr-/- apoB100/100 mice , nephrectomized fetuin-A-knockout mice with a high phosphate diet , and wild-type mice fed a high fat/high carbohydrate diet . The general problem in mouse models is the difficulty in assessing functional impairment in the valve, i.e. challenging echocardiography. In the present study, aortic valve echocardiography was not part of the study design, as the focus was placed on early histopathological changes in the valves, i.e. at a stage in which no significant functional impairment of the valves was to be expected (22 weeks in Study 1 and 36 weeks in Study 2). Indeed, previous models have described functional changes only in older animals, and echocardiac abnormalities were not evident in the apoE-/- mice studied by Tanaka and co-workers until 80–120 weeks of age . Finally, the duration of uremia was different in the two studies (22 weeks in Study 1 vs. 36 weeks in Study 2). However, aortic valve thickening was observed in both studies.
The present study demonstrates a novel mouse model of aortic valve thickening, the uremic apoE-/- mouse, and reveals a potential treatment of uremia-induced valvular pathology by an ACE inhibitor. Although the mice were severely hyperlipidemic and atherosclerotic, aortic valve thickening presented itself as a fibrotic disease, not a lipid disease. As aortic valve thickening represents an early stage of AS, this animal constitutes a model for exploring the development and pathogenesis of AS and its treatment by pharmacological therapy, particularly with drugs that inhibit the production and pathological effects of Ang II.
Suvi Sokolnicki and Tina Axen are thanked for their excellent technical assistance with the sectioning and stainings. Wihuri Research Institute is maintained by the Jenny and Antti Wihuri Foundation in Helsinki, Finland. This study was also funded by the Finnish Foundation for Cardiovascular Research (M.I.M. and S.H.), the Danish National Research Council (L.B.N. and S.B.) and the Danish Kidney Foundation (S.B.).
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