- Original investigation
- Open Access
Effect of vitamin D on aortic remodeling in streptozotocin-induced diabetes
© Salum et al.; licensee BioMed Central Ltd. 2012
- Received: 12 March 2012
- Accepted: 25 May 2012
- Published: 25 May 2012
Diabetes mellitus is associated with micro- and macrovascular complications and increased cardiovascular risk. Elevated levels of serum asymmetric dimethylarginine (ADMA) may be responsible for endothelial dysfunction associated with diabetes-induced vascular impairment. Vitamin D may have potential protective effects against arterial stiffening. This study aimed to examine both the effects of diabetes on the functional/structural properties of the aorta and the endothelial function and the effects of vitamin D supplementation.
Male Wistar rats (n = 30) were randomly assigned to control untreated, diabetic untreated, and diabetic + cholecalciferol groups. Diabetes was induced by intraperitoneal injection of streptozotocin, followed by oral administration of cholecalciferol (500 IU/kg) for 10 weeks in the treatment group. Aortic pulse wave velocity (PWV) was recorded over a mean arterial pressure (MAP) range of 50 to 200 mmHg using a dual pressure sensor catheter. Intravenous infusion of phenylephrine and nitroglycerine was used to increase and decrease MAP, respectively. Serum 25-hydroxyvitamin D [25(OH)D] levels were measured using a radioimmune assay. ADMA levels in serum were measured by enzyme-linked immunoassay. Aortic samples were collected for histomorphometrical analysis.
PWV up to MAP 170 mmHg did not reveal any significant differences between all groups, but in diabetic rats, PWV was significantly elevated across MAP range between 170 and 200 mmHg. Isobaric PWV was similar between the treated and untreated diabetic groups, despite significant differences in the levels of serum 25(OH)D (493 ± 125 nmol/L vs 108 ± 38 nmol/L, respectively). Serum levels of ADMA were similarly increased in the treated and untreated diabetic groups, compared to the control group. The concentration and integrity of the elastic lamellae in the medial layer of the aorta was impaired in untreated diabetic rats and improved by vitamin D supplementation.
PWV profile determined under isobaric conditions demonstrated differential effects of uncontrolled diabetes on aortic stiffness. Diabetes was also associated with elevated serum levels of ADMA. Vitamin D supplementation did not improve the functional indices of aortic stiffness or endothelial function, but prevented the fragmentation of elastic fibers in the aortic media.
- Aortic stiffness
- Pulse wave velocity
- Asymmetric dimethylarginine
- Vitamin D
Cardiovascular (CV) events are considered to be a principal cause of mortality in patients with diabetes mellitus (DM) . Macrovascular complications of DM are associated with stiffening of the aorta, which is a major contributing factor to the target organ damage, such as impaired coronary perfusion  and cardiac hypertrophy . Aortic stiffness can be assessed with measurement of aortic pulse wave velocity (PWV) that is largely determined by the structural properties of the vessel wall and blood pressure (BP) level. PWV is regarded as a strong and independent predictor of CV complications in patients with DM .
Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxide synthase  which is produced by vascular endothelial cells . Elevated levels of ADMA in plasma have been found associated with impaired endothelial function  and decreased arterial elasticity , characterised by decreased bioavailability of nitric oxide (NO). There is substantial evidence that endothelial dysfunction in diabetes is directly associated with increased aortic stiffness .
It is now widely recognised that vitamin D not only plays a major role in bone and calcium metabolism, but may also improve CV health and reduce the risk of CV morbidity and mortality [10, 11]. There is evidence that hypovitaminosis D may adversely affect endothelial function , leading to increased aortic stiffness . The association between vitamin D deficiency and increased aortic stiffness has been demonstrated in healthy subjects [14, 15] and in different chronic inflammatory diseases, including systemic lupus erythematosus  and DM [17, 18]. Furthermore, the administration of vitamin D to subjects with DM been shown to improve insulin secretion and insulin resistance . However, the potential role of vitamin D in diabetic macrovascular complications remains unclear. We designed the current study to investigate the effects of streptozotocin-induced diabetes on the functional/structural properties of the aorta and endothelial function and the potential protective effects of vitamin D supplementation.
The experiments were performed in 30 male Wistar rats (RccHan:WIST, age 4 months) obtained from Harlan Laboratories (Harlan Laboratories, Inc., The Netherlands). The animals were kept in a room with controlled temperature (21 ± 2°C) and lighting (12:12-h light–dark cycle) with free access to food pellets and tap water. All experimental procedures were approved by the Estonian National Board of Animal Experiments and were conducted in accordance with the European Communities Directive (86/609/EEC).
Rats were randomly assigned to three groups of equal size: control group, diabetic group, and cholecalciferol-treated diabetic group. Diabetes was induced by a single intraperitoneal injection of streptozotocin (STZ) 50 mg/kg (Sigma-Aldrich, St. Louis, MO, USA) freshly dissolved in 0.9% NaCl solution. Blood samples were taken 48 h later from the tail vein and glucose levels were measured with a glucometer (Glucocard X-meter, Arkray Inc., Japan). Rats with glucose levels >15 mmol/L were considered diabetic. One animal died 2 days following STZ injection and another animal did not develop hyperglycemia. Immediately after confirmation of diabetes, one diabetic group of animals was submitted to supplementation with cholecalciferol (Sigma-Aldrich, St. Louis, MO, USA) 12.5 μg (500 IU) kg-1 body weight, dissolved in 0.3 ml olive oil administered orally. This dose was expected to be below that which causes hypercalcemia and soft tissue calcification since animal models of arterial wall calcification require the administration of much higher doses of vitamin D . Cholecalciferol was chosen over calcitriol, the hormonal form of vitamin D, to further reduce the risk of soft tissue calcification. Cholecalciferol was administered every other day by gavage for a period of 10 weeks. Weekly, body weight was monitored and glycosuria was assessed with reagent strips (Combur Test, Roche, Germany) to exclude ketosis.
After 10 weeks, the animals were anesthetised with a mixture of fentanyl (0.07 mg/kg, Gedeon-Richter Plc., Hungary), midazolam (5 mg/kg, Roche Pharma AG, Germany), and ketamine (75 mg/kg Vetoquinol Biowet Sp. z.o.o., Poland) administered subcutaneously. The optimal concentrations of the anesthetic substances were determined in pilot experiments. After induction of anesthesia, animals were placed on a heating pad and body temperature was maintained at 37°C. A 2.5 F high-fidelity, dual pressure sensor catheter with 50 mm separation between sensors (SPC-721, Millar Instruments Inc., TX, USA) was introduced via the femoral artery into the descending aortic trunk so that the distal sensor was positioned at the beginning of the descending aorta and the resulting position of the proximal sensor was just proximal to the aortic bifurcation. Mean arterial pressure (MAP) was determined from measurements made by the proximal pressure transducer. Arterial pressure was increased and decreased by infusion of phenylephrine (50 μg/min) and nitroglycerine (30 μg/min), respectively, via a catheter inserted into the femoral vein. Measurements of PWV were performed similarly to what has been described by other investigators [21, 22]. Briefly, pulse pressure waves were recorded simultaneously at the two aortic sites and PWV was calculated by dividing the propagation distance by propagation time using an automated foot-to-foot method. The foot of the pressure wave was defined by the peak of the second time derivative of pressure during each pulse. As the distance between the sensors is fixed at 50 mm, this calculation provides a highly accurate measurement of PWV. Data were acquired at a sampling rate of 2 kHz (PowerLab, ADInstruments, Australia) and feature extraction and calculations made with custom scripts in Spike2 v.6. software (Cambridge Electronic Design, UK). PWV was plotted against MAP at 5 mmHg increments to characterise PWV over a wide range of MAP from 50 to 200 mmHg.
After the haemodynamic measurements were completed, blood samples were taken from the tail vein for assessment of glucose levels. The rats were euthanised by drawing blood by cardiac puncture; part was used to measure glycated haemoglobin (HbA1c) level and the remaining portion was centrifuged at 3000 rpm for 15 minutes to obtain serum. Serum 25-hydroxyvitamin D [25(OH)D] level was measured using a radioimmune assay (25-Hydroxyvitamin D, 125I Ria Kit, Diasorin Corporation, USA). ADMA was determined from serum samples by an enzyme-linked immunoassay using a commercial kit (DLD Diagnostika, Germany). Calcium concentration in serum was determined by a colorimetric test (Calcium liquicolor, HUMAN Gesellschaft für Biochemica und Diagnostica mbH, Germany).
Histological analysis and morphometric parameters
The aortic samples for histological analysis were fixed in 10% formalin for 12 hours and embedded in paraffin with vacuum infiltration processor (Tissue-Tek® VIPTM 5 Jr, Sakura, USA). Specimens were cut with microtome Ergostar HM 200 (Microm, Germany) at four-μm thickness sections and stained using the hematoxylin-eosin, resorcin-fuchsin, and van Gieson methods for examination by light microscopy (Olympus BX50, Japan).
Estimation of the internal diameter of the aorta was performed by measuring two inner diameters at right angle for each cross-section of the thoracic aorta. At least eight different cross-sections of the aorta were analysed for each rat.
Thickness of the medial layer of the aorta was determined in thoracic aorta cross-sections by ten consecutive measurements in a systematic manner to evaluate all segments of the circumference of the aorta. At least six different cross-sections of aorta were analysed for each rat.
The staining intensities of the elastic fibers in the media and collagen fibers in the media and adventitia were evaluated on a subjective scale ranging from 0 to 3 (0 – no staining of fibers, 1 – poor staining of fibers, 2 – moderate staining of fibers, 3 – intensive staining of fibers). The evaluations were performed by two independent observers in a blinded fashion; the scores were summed and used for statistical analysis.
Results are expressed as means ± standard deviation (SD). Differences between the groups were evaluated using the one-way analysis of variance (ANOVA) followed by Tukey’s post-hoc analysis for multiple comparisons of group means. Semi-quantitative data were compared by the Kruskal-Wallis one-way ANOVA followed by Mann–Whitney U test. Differences were considered to be statistically significant when p was <0.05. All statistical comparisons were performed with Statistica software (version 8; StatSoft, USA).
Basic and biochemical parameters
Basic and laboratory parameters
Body weight (g)
Blood glucose (mmol/L)
Control (n = 10)
405 ± 26
450 ± 30
6.3 ± 1.6
4.0 ± 0.1
140 ± 21#
0.68 ± 0.18
2.7 ± 0.3
Diabetes (n = 9)
406 ± 56
370 ± 50*
28.3 ± 3.9*
10.3 ± 0.7*
108 ± 38#¶
0.87 ± 0.14¶
2.6 ± 0.3
Diabetes + vitamin D (n = 10)
406 ± 51
352 ± 43*
28.5 ± 5.9*
9.5 ± 1.3*
494 ± 125
0.85 ± 0.16¶
2.7 ± 0.2
Resting anesthetic haemodynamic parameters obtained before the administration of vasoactive substances
Control (n = 10)
140 ± 30
106 ± 27
118 ± 28
34 ± 6
364 ± 96
5.0 ± 0.6
Diabetes (n = 9)
135 ± 15
103 ± 18
114 ± 17
31 ± 4
343 ± 53
5.2 ± 0.3
Diabetes + vitamin D (n = 9)
136 ± 14
104 ± 12
115 ± 12
32 ± 3
348 ± 107
4.9 ± 0.3
Histological analysis and morphometric parameters
Morphometric parameters and estimations of staining intensity of connective tissue fibers in the medial and adventitial layers of the thoracic aorta
Control (n = 10)
Diabetes (n = 9)
Diabetes + vitamin D (n = 9)
Internal diameter of aorta (mm)
1.40 ± 0.27
1.65 ± 0.18*
1.55 ± 0.21
Thickness of media (μm)
86.41 ± 8.15
79.09 ± 14.61
82.93 ± 11.29
Elastic fibers in media (arbitrary units)
2.44 ± 0.33
1.84 ± 0.33¶;#
2.29 ± 0.26
Collagen fibers in media (arbitrary units)
1.20 ± 0.38
1.38 ± 0.46
1.24 ± 0.41
Collagen fibers in adventitia (arbitrary units)
2.90 ± 0.41
2.56 ± 0.40
2.52 ± 0.43
Elastin/collagen ratio in media (%)
1.72 ± 0.55
1.33 ± 0.43*;#
1.88 ± 0.47
In the current study, we have investigated the effects of experimental diabetes on the functional/structural properties of the aorta and the endothelial function and the possible protective effects of vitamin D supplementation. The principal finding of this study was that diabetes was associated with differential effects on the aortic stiffness, demonstrated by higher isobaric PWV at a supraphysiological range of MAP (170–200 mmHg), but not at a lower MAP range. Untreated diabetic rats also exhibited lower levels of serum 25(OH)D and elevated levels of serum ADMA, a marker of endothelial dysfunction. Administration of vitamin D for 10 weeks significantly increased the levels of serum 25(OH)D, but did not protect from aortic stiffening as evidenced by isobaric PWV. Serum ADMA levels were also not affected by vitamin D supplementation. However, vitamin D effectively preserved the structure of elastic fibers and the ratio of elastic fibers to collagen fibers in the aortic media.
STZ-induced diabetes is a well-accepted experimental model of uncontrolled type 1 DM and studies have reported STZ-induced impairment of aortic elastic properties in rats [23, 24]. Increased arterial stiffness has also been demonstrated in Zucker diabetic fatty rats, an animal model of type 2 DM. [25, 26]. These findings have been supported by clinical observations, which have shown associations between increased aortic PWV and type 1 or type 2 DM [5, 27, 28]. In accordance with previous studies, we demonstrate increased aortic stiffness in STZ-diabetic rats compared to nondiabetic rats.
It is important to note that as PWV is strongly dependent on BP , measurements of PWV can be accurately and independently compared only if obtained over a range of BP that is often not feasible to induce in patients. We assessed PWV over a wide range of MAP using phenylephrine and nitroglycerine to raise and lower MAP, respectively. As a result, we found that differences in isobaric PWV only became evident at high levels of MAP which demonstrates that intrinsic aortic stiffness was not increased in diabetic animals at the physiological BP levels. These results indicate that, during the course of diabetes, early changes in the arterial integrity are reflected in the increased central artery stiffness that can remain undetected since blood pressure may not be elevated in that stage. Increased aortic stiffness can be established when diabetic patients develop hypertension, which highlights the importance of adequate and early blood pressure control for prevention of diabetic macrovascular complications.
The possible mechanisms implicated in the differential effects of diabetes on aortic stiffness may include alterations in the proportions and structural integrity of elastic fibers, collagen fibers, or the extracellular matrix in the vessel wall . Biomechanically, collagen fibers mediate stiffness at higher pressure, while elastin provides support at a lower pressure range [31, 32]. In our experiment, a decrease in the elastic lamellae in the aortic media was noted in the untreated diabetic group whilst no clear changes in collagen fibers were detected. Nevertheless, a decrease in elastic fibers and a relative increase of collagen in relation to elastin can result in increased stiffness that may become evident at a high-pressure range as was observed in our experiments. The absence of differences in aortic stiffness at a lower BP range may also be attributed to a compensatory mechanism of preserved smooth muscle activity.
Endothelial dysfunction, characterised by impaired production of nitric oxide (NO), plays an important role in the development of diabetic vascular complications . Several studies have indicated that the impairment of endothelium-dependent vasodilation is an important factor contributing to aortic stiffening [9, 34]. Our experiment shows that the serum level of ADMA, a marker of endothelial dysfunction, is significantly elevated in STZ-induced diabetes in parallel with impaired structural and functional properties of the aorta. These findings are consistent with studies showing that endothelial dysfunction occurs early in the course of diabetic vascular complications, as evidenced by functional assessment of the endothelium [35, 36] and elevated levels of circulating ADMA .
Previous studies have reported that treatment with vitamin D may lower arterial blood pressure , improve endothelial function , and decrease aortic stiffness . In our study, the isobaric PWV in diabetic animals receiving vitamin D was similar to that of diabetic untreated animals. Furthermore, there were no differences in the serum ADMA concentrations between the diabetic groups. These findings may be attributed to the fact that the levels of blood glucose and HbA1c were unaffected by vitamin D supplementation, suggesting that the possible protective effects of vitamin D against diabetes-induced increase in aortic stiffness and endothelial dysfunction may have been abolished by the persistent high-grade hyperglycemia.
Although vitamin D supplementation could not protect from the early impairment of large artery function, it still had a positive effect on relative preservation of elastic fiber organisation in the medial layer of the aorta. The mechanisms involved in this process remain unknown, but may include the down-regulation of the renin-angiotensin system , since angiotensin II is known to stimulate tissue remodeling in the arteries  and agents that inhibit this system have been shown to have beneficial effects on the structural properties of the arterial wall [41, 42]. Nevertheless, the effects of vitamin D supplementation on the diabetic complications at a molecular level remain to be established. Indeed, our preliminary experiments have shown that vitamin D may affect several oxidative stress parameters in STZ-induced diabetes, including serum total antioxidant capacity and advanced glycation end-products (manuscript in preparation), which requires further investigation.
In summary, the present study demonstrated that in rats, STZ-induced diabetes impairs endothelial function and exerts differential effects on aortic stiffness, characterised by the increased PWV at supraphysiological MAP levels, whereas aortic elasticity was preserved at a lower pressure range. Chronic administration of vitamin D did not have an effect on the diabetes-induced aortic stiffness and endothelial dysfunction, but preserved the proportions and integrity of elastic fibers in the aortic media. Further investigations will provide more information on the effects and role of vitamin D in the macrovascular complications of type 1 diabetes.
This study was supported by the Estonian Science Foundation grants Nos. 9094 and 8273 and by target financing (Nos. 0180001 s07 and 0180012 s11) by the European Union through the European Regional Development Fund.
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