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(Arteriosclerosis, Thrombosis, and Vascular Biology. 2005;25:39.)
© 2005 American Heart Association, Inc.

Brief Reviews

Vitamin D, Shedding Light on the Development of Disease in Peripheral Arteries

P.E. Norman; J.T. Powell

From the School of Surgery and Pathology (P.E.N.), The University of Western Australia, Fremantle Hospital, Fremantle, Western Australia; and the Division of Surgery (J.T.P.), Anaesthesia and Intensive Care, Imperial College, London, UK.

Correspondence to Jane Powell, Department of Vascular Surgery, Imperial College at Charing Cross, St Dunstan’s Road, London, W6 8RP, UK. E-mail j.powell{at}imperial.ac.uk

	Abstract

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Vitamin D is generally associated with calcium metabolism, especially in the context of uptake in the intestine and the formation and maintenance of bone. However, vitamin D influences a wide range of metabolic systems through both genomic and nongenomic pathways that have an impact on the properties of peripheral arteries. The genomic effects have wide importance for angiogenesis, elastogenesis, and immunomodulation; the nongenomic effects have mainly been observed in the presence of hypertension. Although some vitamin D is essential for cardiovascular health, excess may have detrimental effects, particularly on elastogenesis and inflammation of the arterial wall. Vitamin D is likely to have a role in the paradoxical association between arterial calcification and osteoporosis. This review explores the relationship between vitamin D and a range of physiological and pathological processes relevant to peripheral arteries.

Vitamin D influences a wide range of metabolic systems through both genomic and nongenomic pathways that have an impact on the properties of peripheral arteries. Although some vitamin D is essential for cardiovascular health, excess may have detrimental effects, including calcification, inflammation, and impaired elastogenesis in the arterial wall.

Key Words: vitamin D • peripheral artery disease • aortic aneurysm • vascular smooth muscle cell

	Introduction

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
The primary role of vitamin D and its active metabolites is maintaining calcium homeostasis by increasing intestinal calcium absorption and, depending on circulating calcium levels, influencing the balance between bone resorption and formation. The physiological role of vitamin D in skeletal and cellular health has been reviewed elsewhere.¹ Vitamin D also has effects on the microendocrine systems of the vasculature, some of which have only been appreciated recently. This review reflects on the possible influence of vitamin D on peripheral arterial disease, which includes diseases (both occlusive and dilating) of the abdominal aorta and the distal arteries supplying the lower limb. Atherosclerosis is a major contributor to peripheral arterial disease, but the risk factors are subtly different from those for coronary artery disease: smoking is the dominating risk factor for peripheral arterial disease. Does vitamin D have any influence on the disease process?

	Vitamin D Metabolites and Analogues

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Cholecalciferol is a prohormone that is synthesized in the skin by photochemical conversion of 7-dehydrocholesterol (Figure 1). It is subsequently hydroxylated to 25-hydroxycholecalciferol [25(OH)D₃] in the liver and finally to the active metabolite, 1,25 didydroxcholecalciferol [1,25(OH)₂D₃] in the kidney.² Some dietary sources provide a cholecalciferol derivative, with a double carbon-carbon at position 22,23 known as vitamin D₂ that also undergoes 1,25 hydroxylation. The active vitamin D metabolites are transported in the circulation by vitamin D-binding protein which has additional effects, including the binding of globular actin and fatty acids and immunomodulation. Because little vitamin D is available in most diets, photochemical synthesis of vitamin D is paramount for its homeostasis, and it is for this reason that rickets became a problem in industrialized cities. 1,25(OH)₂D₃ is conformationally flexible and is able to generate a large array of different ligand shapes with numerous effects.³ In addition, it is estimated that >1000 vitamin D analogues with variable biologic profiles have been synthesized.³

View larger version (28K): [in this window] [in a new window]   Figure 1. The biosynthetic pathway of vitamin D.

	Actions of Vitamin D in Target Cells and Tissues

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Genomic Effects
1,25(OH)₂D₃ is a steroid hormone shown to regulate >60 genes.^2,4 This is accomplished by the translocation of 1,25(OH)₂D₃ into cells where it binds with high affinity to the vitamin D receptor (VDR), which is a member of the nuclear receptor superfamily. This complex then interacts with the vitamin D response elements in the promoter region of target genes thereby altering rates of gene expression (Figure 2).⁵ By this pathway, 1,25(OH)₂D₃ influences a number of genes relevant to the arterial wall, including vascular endothelial growth factor, matrix metalloproteinase type 9, myosin, and structural proteins, such as elastin and type I collagen.^4–8 In addition, there is evidence of an alternative pathway for 1,25(OH)₂D₃ altering gene transactivation through intracellular vitamin D-binding proteins.⁹ The newly recognized use of 1,25(OH)₂D₃ analogues as immunomodulatory agents is based on the ability of these analogues to influence gene expression in cells of the immune system and cytokine expression by other cells (reviewed by Mathiew and Adorini¹⁰).

View larger version (28K): [in this window] [in a new window]   Figure 2. Genomic and nongenomic responses to1,25 dihydroxycholecalciferol (genomic responses based on Barsony et al and Brown et al5,13).

Nongenomic Effects
In common with other steroid hormones, 1,25(OH)₂D₃ induces a range of effects which occur too rapidly to involve gene expression. These include increases in intracellular calcium and cGMP levels, activation of protein kinase C and changes in phosphinositide metabolism¹¹ (Figure 2). The effects are known to be mediated by 1 or more plasma membrane receptors, but their role is unclear in most cell types.^2,11 An example relevant to the arterial wall includes the stimulation of vascular smooth muscle cell (VSMC) migration through activation of phosphatidylinositol 3-kinase.¹²

Target Cells and Tissues for 1,25(OH)₂D₃
Classically, the action of 1,25(OH)₂D₃ is to maintain calcium and phosphate homeostasis, with the intestine and bone being key targets. It also acts on a wide range of nonclassical target tissues, including the heart and arterial wall.¹³ The influence of 1,25(OH)₂D₃ on these tissues could have important implications for vascular function and disease. 1,25(OH)₂D₃ appears to cause cell cycle arrest and inhibit proliferation of most cell types, including lymphocytes.¹³ VDRs are present in VSMCs. There is controversy concerning the action of vitamin D on VSMCs, with some studies reporting stimulation of proliferation and others reporting inhibition of proliferation and a synthetic phenotype being induced by 1,25(OH)₂D₃.^14,15 The direction of the effect may depend on the culture conditions, with effects in vivo being uncertain.¹⁶ VDRs have been identified in dermal capillaries, and cultured endothelial cells appear to express a 1-hydroxylase enzyme, indicating the possibility of a vitamin D microendocrine system in endothelial cells.¹⁷ 1,25(OH)₂D₃ causes apoptosis in tumor endothelial cells, interferes with vascular endothelial growth factor signaling, and suppresses angiogenesis.¹⁸ Macrophages and lymphocytes are other important target cells for vitamin D in the diseased artery wall.¹⁹ The vitamin D microendocrine systems of the diseased arterial wall are shown in Figure 3.

View larger version (43K): [in this window] [in a new window]   Figure 3. VDR-expressing cells of the diseased artery wall and their known responses to vitamin D. Cells with blue cytoplasm are known to express VDR, with the density of the blue corresponding approximately to the probable density of VDR expression; T lymphocytes have the highest density of VDR. Lymphocytes are shown as T or B. IEL indicates internal elastic lamina; EEL, external elastic lamina.

	Dietary Requirements and Human Consumption of Vitamin D

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
After the discovery that cod liver oil prevented rickets in 1919, overall consumption of vitamin D in Europe and North America was probably excessive during the first half of the 20th century.²⁰ It was not unusual for infants to consume 100 µg per day and an "epidemic" of infantile hypercalcemia and supravalvular aortic stenosis coincided with the increased vitamin D supplementation of milk in the 1940s. It was not until 1963 that infant food supplementation was reduced in the United States.²¹ Sensitivity to vitamin D appears to vary because not all infants developed hypercalcemia, and a reduced susceptibility to rickets may be associated with an increased susceptibility to vitamin D toxicity.²¹ Cod liver oil may have disappeared from infant food supplements, but a significant proportion of adults in Western countries continue to use fish oil supplements. A recent dietary study in southwest England indicated that 20% of healthy adults were using fish oil supplements.²²

Dietary recommendations for vitamin D consumption vary among advisory bodies, reflecting uncertainty about vitamin D status and health (particularly osteoporosis).²³ Recommended daily intake ranges from 0 in those at low risk of osteoporosis to 15 µg per day for those at high risk (>65years, dark skin, restricted exposure to sunlight).²³ Some authorities feel that fear of toxicity has tended to keep the recommended daily intake at "woefully inadequate" levels.²⁴

	Epidemiological Studies of Vitamin D and Arterial Disease

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Despite a number of articles over the last 50 years or more arguing that vitamin D is a risk factor in atherosclerosis,^25,26 the published data, at least with respect to ischemic heart disease, remain conflicting. Linden initially reported that patients with myocardial infarction appeared to have a higher intake of vitamin D than controls.²⁷ This has been followed by reports that serum levels of 25(OH)D₃ were not elevated in patients with myocardial infarction,^28,29 and the mortality from ischemic heart disease (in postmenopausal women) was not associated with intake of vitamin D.³⁰ Scragg et al even reported an inverse relationship between levels of 25(OH)D₃ and myocardial infarction.³¹ Ironically, vitamin D deficiency [serum levels of 25(OH)D₃ <9 ng/mL] because of immobility causing lack of sunlight exposure has been reported in patients with peripheral arterial disease.³²

Similar uncertainty surrounds the relevance of vitamin D in hypertension (an established risk factor for peripheral arterial disease³³). Despite evidence from various animal models that vitamin D may be important in blood pressure control and hypertension,³⁴ its clinical importance remains unclear. There is an inverse relationship between exposure to sunlight (needed to synthesize cholecalciferol) and both blood pressure and prevalence of hypertension.³⁵ Some studies have found a similar inverse relationship between levels of 1,25(OH)₂D₃ and blood pressure and plasma renin activity,^36,37 although others report a positive association.³⁸ Recent results from a large population-based study failed to find any convincing association between serum vitamin D concentrations and blood pressure.³⁹ Vitamin D supplementation appears to lower blood pressure in those with preexisting hypertension.⁴⁰ Li et al have recently shown this to be mediated through the direct actions of 1,25(OH)₂D₃ in suppressing renin expression.⁴¹ Critical assessment of the role of vitamin D in blood pressure control is beyond the scope of this review. However, in the context of blood pressure control, vitamin D may provide some protection against peripheral arterial disease.

	Vitamin D and Peripheral Arterial Calcification

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Arterial calcification is important because it has been shown to be a forerunner of cardiovascular events. The molecular biology of arterial calcification will not be described in detail as it has been the subject of recent reviews.^42,43 However, the possible role of vitamin D in arterial calcification will be discussed.

There are 2 distinct patterns of arterial calcification: calcification of the media (Monckeberg’s sclerosis, seen in aging, chronic renal failure, and diabetes) and calcification of the intima (seen in atherosclerosis). Intimal calcification has attracted considerable attention, particularly in the context of the prognostic significance of coronary artery and aortic arch calcification.^44,45 However, most of the increase in arterial calcium with age is concentrated in the medial layer.⁴⁶ This medial calcification is not usually occlusive or associated with atherosclerotic plaque but is nevertheless a predictor of lower limb amputation and cardiovascular mortality.^47,48 Medial calcification also results in incompressible arteries and difficulty in measuring true ankle pressures, which can complicate the noninvasive diagnosis of peripheral arterial disease. An inverse relationship between serum 1,25(OH)₂D₃ levels and total (intimal and medial) coronary artery calcification has been reported.^49,50 This association may depend on medial calcification, whereas another study failed to demonstrate an association between intimal calcification and serum 1,25(OH)₂D₃ levels.⁵¹ The significance of an inverse relationship between levels of 1,25(OH)₂D₃ and coronary calcification is uncertain, particularly as levels of 25(OH)D₃ are a better indicator of vitamin D status.²⁴

There is increasing evidence of a paradoxical association between osteoporosis and vascular calcification.^52–54 The mechanisms underlying this association are beginning to be unraveled^42,55–57 and may account for the inverse association between coronary artery calcification and serum levels of 1,25(OH)₂D₃.⁴⁹ Various inhibitors of bone resorption, including biphosphonates (alendronate and ibandronate), osteoprotegrin, and an inhibitor of osteoclastic V-H⁺-ATPase (SB 242784) have been shown to inhibit calcification of the arterial media in animal models.^55,56,58 Because none of these agents are known to act directly on the arterial smooth muscle cells, it has been proposed that arterial calcification is directly linked to bone resorption in this model.⁵⁶ 1,25(OH)₂D₃ may, however, act directly on smooth muscle cells or osteoclast-like cells within the arterial wall.^59,60

Medial calcification is common in diabetes and end-stage renal failure, both conditions being associated with peripheral arterial disease. In renal failure, 1,25(OH)₂D₃ analogues are used to prevent secondary and tertiary hyperparathyroidism, and treatment with vitamin D has been implicated in calcification of soft tissues, including the arterial wall.⁶¹ Recently a large observational study has indicated that a selective VDR antagonist (paricalcitol) improves survival for renal failure patients, by 16% to 25%, in comparison to traditional calcitriol therapy.⁶² In support of this finding, in vitro experiments show that VSMCs undergo calcification when treated with 1,25(OH)₂D₃ through a mechanism dependent on suppression of an endogenous inhibitor of calcification (PTH-related peptide) and PTH receptor signaling.^59,63 Hence, vitamin D exposure may downregulate the paracrine mechanisms that, under normal circumstances, protect the vasculature from calcification. This has led to recent speculation that inflammation of the vascular adventitia with local synthesis of 1,25(OH)₂D₃ by macrophages could lead to medial calcification.⁶⁴

1,25(OH)₂D₃, through its interaction with VDR, can induce the calcification of cultured arterial smooth muscle cells.⁵⁹ Apoptosis, which is well-documented in atherosclerosis and after arterial injury, may provide an initial stimulus for calcification within the arterial wall.^65,66 1,25(OH)₂D₃ can induce cell cycle arrest and apoptosis in some normal and malignant cell types.^18,67 Although 1,25(OH)₂D₃ has been shown to inhibit angiogenesis by induction of apoptosis, there is no direct evidence linking vitamin D to peripheral arterial calcification through this mechanism.

Although adequate vitamin D nutrition is essential for optimal vascular function,⁶⁸ both exogenous and endogenous 1,25(OH)₂D₃ are possible axes for the association. In contrast to endogenous vitamin D, which is carried by circulating vitamin D-binding protein, exogenous vitamin D may be carried by lipoproteins.⁶⁹ This may facilitate accumulation of vitamin D within atherosclerotic plaque and alter macrophage gene expression.^19,70,71

	Arterial Disease and the Genomic Effects of Vitamin D: Clinical Studies

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
The relationship between common polymorphisms of the VDR gene and osteoporosis has attracted considerable research (and controversy) over the last decade.^72,73 The link between osteoporosis and arterial calcification has led to the hypothesis that functional polymorphisms in the VDR gene are associated with the prevalence and severity of coronary artery disease. This has been tested in clinical populations, and although a possible association between the VDR BB genotype (resulting in decreased levels of vitamin D) and severity of coronary artery stenosis has been reported, the relationship was not statistically significant.⁷⁴ The importance of such studies depends on whether they are large enough to determine effects of the magnitude attributed to the polymorphism(s) or haplotypes in vitro. There are contradictory results reported as to whether the BsmI polymorphism in intron 8 or the FokI polymorphism in the 5' regulatory region of the VDR gene has functional effects in vitro. Therefore, even the results of large studies focusing on a single polymorphism must be treated with skepticism. Although Ortlepp et al⁷⁵ report that the BsmI polymorphism has no influence on the incidence of coronary artery disease in 3441 patients, such evidence does not refute the possibility that genetic variation in response to vitamin D has an impact on the development of arterial disease. There have been no studies of the role of the genomic effects of 1,25(OH)₂D₃ in the development of peripheral arterial disease. Genomic associations with the more relevant clinical phenotype of arterial calcification have not been evaluated.

	Nongenomic Effects of Vitamin D on Peripheral Vascular Resistance

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Although the evidence concerning vitamin D exposure and hypertension is controversial, it is possible that vitamin D influences vascular tone. The single study that has investigated the short-term effect of vitamin D on cardiovascular hemodynamics showed that vitamin D caused rapid changes in patients with essential hypertension but not in controls.⁷⁶ In patients with essential hypertension, the cardiac output decreased by 15% within 2 hours of intravenous administration of 1,25(OH)₂D₃ (0.2 µ/kg). This was associated with transient smaller increases in pulse rate and mean blood pressure, suggesting that 1,25(OH)₂D₃ had a nongenomic effect to increase peripheral resistance. This would be supported by an earlier report that indicated a correlation between calf vascular resistance, both before and during reactive hyperemia, with serum concentrations of 25(OH)D₃ in hypertensive patients.⁷⁷ The ability of 1,25(OH)₂D₃ to increase vascular resistance is supported by animal studies.⁷⁸ 1,25(OH)₂D₃ increases the sensitivity of resistance arteries to norepinephrine in hypertensive but not normotensive rats⁷⁹ and rapidly enhances arterial force generation by modulation of intracellular calcium concentration.^34,80 Taken together these studies suggest that hypertension induces or sensitizes putative plasma membrane VDRs which modulate intracellular calcium concentrations and hence resistance artery force generation. The identity of these plasma membrane receptors is obscure, as are the downstream kinase signaling cascades. In the absence of hypertension, these fast nongenomic responses have not been observed.

Even in the presence of hypertension, in the longer term, the fast nongenomic responses may be counteracted by the genomic effects of 1,25(OH)₂D₃ which may function to decrease vascular resistance. Likely mechanisms include altered expression of myosin isoforms in resistance vessels.⁸¹ This would be consistent with the reported decrease of systolic blood pressure after 8 weeks of oral calcium and vitamin D supplementation in the late winter.⁴⁰

	Vitamin D, Elastin, and Inflammatory Vascular Disease

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
Several years ago the hypothesis was elaborated that impaired synthesis of elastin in the walls of the aorta and other elastic or conduit arteries during fetal development was an initiating event in the pathogenesis of hypertension.⁸² Because tropoelastin synthesis is known to be downregulated by vitamin D, through a posttranscriptional mechanism,⁶ excess vitamin D during fetal development could cause the impaired synthesis of elastin discussed by Martyn and Greenwald. Loss of medial elastin is a pathological hallmark of abdominal aortic aneurysm (AAA). This led to Norman elaborating a further hypothesis, that excess vitamin D consumption in early life led to the development of AAA in later life.⁸³ The transportation of vitamin D across the placenta is specifically enhanced during the last one third of pregnancy (a period of maximal aortic elastin deposition).^84,85 The neonate is dependent on stored vitamin D, because mammalian milk contains minimal vitamin D.⁸⁶ This suggests that if maternal intake is excessive then fetal and neonatal exposure will also be excessive. Although there are no clinical studies to support an association between increased maternal vitamin D intake and impaired aortic elastogenesis, an experimental animal study demonstrated that exposure to increased vitamin D in early life was associated with a reduction in elastin content and elastic lamellae number in the abdominal aorta.⁸⁷ The studies were not extended to investigate the possibility of aneurysm formation in aging rats.

Another pathological hallmark of AAA is inflammation.⁸⁸ Interestingly, there are recent scientific observations to support an important role for vitamin D and its analogues on the immune system, particularly macrophages and T lymphocytes expressing VDR, which could have important implications for both AAA and other peripheral arterial disease. The highest expression of VDR is in CD8 lymphocytes, with less expression in CD4 lymphocytes and macrophages, whereas B cells do not express VDR. Moreover, VDR expression in CD8 cells increases in response to 1,25(OH)₂D₃.⁸⁹ Therefore, vitamin D can regulate cytokine expression in diseased arteries (Figure 3). Laboratory data suggest that 1,25(OH)₂D₃ influences cytokine production by both CD4+ and CD8+ subsets, preferentially inhibiting cytokine production (interleukin [IL]-2 and interferon-) from Th1 cells and hence favoring Th2 responses with the production of IL-4, IL-5, and IL-10, as well as IL-6.^90,91 It is these findings that might translate to a link between vitamin D and AAA, a condition where Th2 responses predominate.⁹²

Clinical studies of the effects of vitamin D supplementation are limited. In postmenopausal women, vitamin D supplementation (2 µg per day) increased CD3 and CD8+ subsets of lymphocytes.⁹³ Therefore, vitamin D may influence T cell activity and inflammation of the artery wall through several different pathways.

Wjst and Dold⁹⁴ have hypothesized that deficiency of vitamin D in early life leads to allergic diseases in later life. Allergy, autoimmune deficiency, and transplant rejection are all controlled by Th1 responses, inflammatory vascular disease being important in transplant rejection. Although there is abundant experimental evidence (eg, Raisanen-Sokolowski et al⁹⁵) to indicate that vitamin D supplementation reduces transplant rejection, there are no clinical studies or trials of this phenomenon. Instead vitamin D supplementation is used to target posttransplantation osteoporosis.

Activated macrophages express 1-hydroxylase and produce 1,25(OH)₂D₃.⁹⁶ This may have a role in limiting the extent of local inflammation^64,97 but also has the potential to alter smooth muscle cell migration and proliferation in the vessel wall. Moreover, 1,25(OH)₂D₃ influences the function of macrophages, with subsequent effects on the production of alkaline phosphatase by cultured smooth muscle cells, promoting calcification.¹⁹ These findings, together with the observation that vitamin D supplementation increases serum transforming growth factor type ß levels,⁹⁸ provide other mechanistic possibilities for a more widespread influence of vitamin D on peripheral arterial disease.

	Vitamin D and Animal Models of Atherosclerotic Arterial Disease

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
The harmful effect of excess vitamin D on arteries has been studied in many animal models over the last 40 years or more.^99,100 Numerous dosage regimens have been described although the majority have used short courses of potentially toxic doses of vitamin D resulting in acute hypercalcemia. Chronic less toxic treatment also results in metastatic calcification and deteriorating renal function.¹⁰¹ In general, vitamin D results in arterial wall calcification and a variety of other "arteriosclerotic" changes. Loss of collagen and disruption of elastic lamellae are additional features.¹⁰² These latter changes are usually associated with increased aortic stiffness,¹⁰² although one study reported a paradoxical reduction in stiffness.¹⁰³ Vitamin D also exacerbates the intimal hyperplasia seen in balloon-injured rat carotid arteries.¹⁰⁴ This is probably caused by the stimulation of migration¹² and proliferation of smooth muscle cells.^79,105,106 Recently, the combination of vitamin D₂ and cholesterol has been used to induce both peripheral atherosclerosis and aortic valve stenosis in a rabbit model.¹⁰⁷ In this model, the addition of vitamin D₂ to the high cholesterol diet resulted in significantly higher levels of circulating cholesterol.¹⁰⁷ A combination of vitamin D and nicotine, causing hypercalcemia, results in stiffer rat conductance arteries and exacerbates the atherosclerotic effects of cholesterol feeding.^102,107 The relevance of any of these models to the development of cardiovascular disease in humans is uncertain.

Another possible link between vitamin D and peripheral arterial disease has been found in a study of transgenic rats that constitutively express vitamin D-24-hydroxylase [which catalyzes the conversion of 25(OH)D₃ to 24,25(OH)₂D₃].¹⁰⁸ These rats had low levels of plasma 24,25(OH)₂D₃) and developed hyperlipidemia and aortic atherosclerosis.¹⁰⁸ This is an example of the complexity of the relationship between differing vitamin D metabolites and the arterial wall.

	Summary

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
In addition to its role in calcium and phosphate homeostasis, vitamin D is important in many physiological and pathological processes relevant to peripheral arterial disease. Vitamin D is essential for the development and maintenance of a healthy arterial tree. 1,25(OH)₂D₃ influences the migration, proliferation, gene expression of VSMCs, elastogenesis, and immunomodulation, all processes which are involved in the pathogenesis of atherosclerotic and aneurysmal arterial disease. 1,25(OH)₂D₃ has additional, poorly understood, nongenomic effects on vessel contractility in essential hypertension and is likely to have a pivotal role in the paradoxical association between osteoporosis and vascular calcification. New clinical studies are required to fully understand the contribution of vitamin D to the health of peripheral arteries.

Received July 12, 2004; accepted October 12, 2004.

	References

Top Abstract Introduction Vitamin D Metabolites and... Actions of Vitamin D... Dietary Requirements and Human... Epidemiological Studies of... Vitamin D and Peripheral... Arterial Disease and the... Nongenomic Effects of Vitamin... Vitamin D, Elastin, and... Vitamin D and Animal... Summary References

 
1. Holick M. Vitamin D: the underappreciated D-lightful hormone that is important for skeletal and cellular health. Curr Opin Endocrinol Diabetes. 2002; 9: 87–98.

2. Omdahl J, Morris H, May B. Hydroxylase enzymes of the vitamin D pathway: expression, function and regulation. Annu Rev Nutr. 2002; 22: 139–166.[CrossRef][Medline] [Order article via Infotrieve]

3. Norman A, Bishop J, Bula C, Olivera C, Mizwicki M, Zanello L, Ishida H, Okamura W. Molecular tools for study of genomic and rapid signal transduction responses initiated by 1 , 25(OH)₂-vitamin D₃. Steroids. 2002; 67: 457–466.[CrossRef][Medline] [Order article via Infotrieve]

4. Rachez C, Freedman L. Mechanisms of gene regulation by vitamin D₃ receptor: a network of coactivator interactions. Gene. 2000; 246: 9–21.[CrossRef][Medline] [Order article via Infotrieve]

5. Barsony J, Prufer K. Vitamin D receptor and retinoid X receptor interactions in motion. Vitam Horm. 2002; 65: 345–376.[Medline] [Order article via Infotrieve]

6. Pierce R, Kolodzie M, Parks W. 1,25-Dihydroxyvitamin D₃ represses tropoelastin expression by a post-transcriptional mechanism. J Biol Chem. 1992; 267: 11593–11599.[Abstract/Free Full Text]

7. Kuroki Y, Shiozawa S, Kano J, Chihara K. Competition between c-fos and 1,25(OH)₂vitamin D₃ in the transcriptional control of type1 collagen synthesis in MC3T3–E1 osteoblastic cells. J Cell Physiol. 1995; 164: 459–464.[CrossRef][Medline] [Order article via Infotrieve]

8. Lin R, Amizuka N, Sasaki T, Aarts M, Ozawa H, Goltzman D, Henderson J, White J. 1 ,25-dihyrdoxy vitamin D3 promotes vascularization of the chondro-osseus junction by stimulating expression of vascular endothelial growth factor and matrix metalloproteinase 9. J Bone Min Res. 2002; 17: 1604–1612.[CrossRef][Medline] [Order article via Infotrieve]

9. Wu S, Ren S, Chen H, Chun R, Gacad M, Adams J. Intracellular vitamin D binding proteins: novel facilitators of vitamin D-directed transactivation. Mol Endocrinol. 2000; 14: 1387–1397.[Abstract/Free Full Text]

10. Mathiew C, Adorini L. The coming of age of 1,25-dihydroxyvitam D(3) analogs as immunomodulatory agents. Trends Mol Med. 2002; 8: 174–179.[CrossRef][Medline] [Order article via Infotrieve]

11. Falkenstein E, Tillmann H-C, Christ M, Feuring M, Wehling M. Multiple actions of steroid hormones - a focus on rapid, nongenomic effects. Pharmacol Rev. 2000; 52: 513–555.[Abstract/Free Full Text]

12. Rebsamen M, Sun J, Norman A, Liao J. 1,25-dihydroxyvitamin D₃ induces vascular smooth muscle cell migration via activation of phosphatidylinositol 3-kinase. Circ Res. 2002; 91: 17–24.[Abstract/Free Full Text]

13. Brown A, Dusso A, Slatopolsky E. Vitamin D. Am J Physiol. 1999; 277 (2 Pt 2): F157–F175.

14. MacCarthy E, Yamashita W, Hsu A, Ooi B. 1,25-Dihydroxyvitamin D₃ and rat vascular smooth muscle. Hypertension. 1989; 13: 954–959.[Abstract/Free Full Text]

15. Tukaj C, Wrzolkowa T. Effects of vitamin D on aortic smooth muscle cells in culture. Toxicology In Vitro. 1996; 10: 701–711.[CrossRef]

16. Mitsuhashi T, Morris R, Ives H. 1,25-dihydroxyvitamin D₃ modulated growth of vascular smooth muscle cells. J Clin Invest. 1991; 87: 1889–1895.

17. Merke J, Milde P, Lewicka S, Hugel U, Klaus G, Mangelsdorf D, Haussler M, Rauterberg E, Ritz E. Identification and regulation of 1,25-dihyroxy vitamin D₃ receptor activity and biosynthesis of 1,25-dihyroxyvitamin D₃. Studies in cultured bovine aortic endothelial cells and human dermal capillaries. J Clin Invest. 1989; 83: 1903–1915.

18. Mantell D, Owens P, Bundred N, Mawer E, Canfield A. 1,25-dihydroxyvitamin D₃ inhibits angiogenesis in vitro and in vivo. Circ Res. 2000; 87: 214–220.[Abstract/Free Full Text]

19. Shioi A, Katagi M, Okuno Y, Mori K, Juno S, Koyama H, Nishazawa Y. Induction of bone-type alkaline phosphatase in human vascular smooth muscle cells: roles of tumor necrosis factor- and oncostatin M derived from macrophages. Circ Res. 2002; 91: 9–16.[Abstract/Free Full Text]

20. Holmes R, Kummerow F. The relationship of adequate and excessive intake of vitamin D to health and disease. J Am Coll Nutr. 1983; 2: 173–199.[Abstract]

21. Seelig M. Vitamin D and cardiovascular, renal and brain damage in infancy and childhood. Ann N Y Acad Sci. 1969; 147: 537–582.

22. Darby S, Whitley E, Doll R, Key T, Silcocks P. Diet, smoking and lung cancer: a case-control study of 1000 cases and 1500 controls in South-West England. Br J Cancer. 2001; 84: 728–735.[CrossRef][Medline] [Order article via Infotrieve]

23. Prentice A. What are the dietary requirements for calcium and vitamin D? Calcif Tiss Int. 2002; 70: 83–88.[CrossRef][Medline] [Order article via Infotrieve]

24. Vieth R. Vitamin D supplementation, 25-hydroxyvitamin D concentrations, and safety. Am J Clin Nutr. 1999; 69: 842–856.[Abstract/Free Full Text]

25. de Langen C, Danoth W. Vitamin D sclerosis of the arteries and the danger of feeding extra vitamin D to older people, with a view on the development of different forms of arteriosclerosis. Acta Med Scand. 1956; 161: 317–323.

26. Moon J, Bandy B, Davison AJ. Hypothesis: etiology of atherosclerosis and osteoporosis: are imbalances in the calciferol endocrine system implicated? J Am Coll Nutr. 1992; 11: 567–583.[Abstract]

27. Linden V. Vitamin D and myocardial infarction. BMJ. 1974: 647–650.

28. Schmidt G, Gossen J, Lindle F, Seidel D. Serum 25-hydroxy cholecalciferol in myocardial infarction. Atherosclerosis. 1977; 26: 55–58.[CrossRef][Medline] [Order article via Infotrieve]

29. Rajasree S, Rajpal K, Kartha C, Sarma P, Kutty V, Iyer C, Girija G. Serum 25-hydroxyvitamin D levels are elevated in south Indian patients with ischaemic heart disease. Eur J Epidemiol. 2001; 17: 567–571.[CrossRef][Medline] [Order article via Infotrieve]

30. Bostick R, Kushi L, Wu Y, Meyer K, Sellars T, Folsom R. Relation of calcium, vitamin D and dietary food intake to ischemic heart disease mortality among post menopausal women. Am J Epidemiol. 1999; 149: 151–161.[Abstract/Free Full Text]

31. Scragg R, Jackson R, Holdaway I, Lim T, Beaglehole R. Myocardial infarction is inversely associated with plasma 25-hydroxyvitamin D₃ levels: a community-based study. Int J Epidemiol. 1990; 19: 559–563.[Abstract/Free Full Text]

32. Fahrleitner A, Dobnog H, Obernosterer A, Pilger E, Leb G, Weber K, Kudlacek S, Obermayer-Pietsch BM. Vitamin D deficiency and secondary hyperparathyroidism are common complications in patients with peripheral arterial disease. J Gen Intern Med. 2002; 17: 633–639.

33. Fowkes G, Housley E, Riemersma R, Macintyre CA, Cawood EH, Prescott RJ, Ruckley CV. Smoking, lipids, glucose intolerance and blood pressure as risk factors for peripheral atherosclerosis compared with ischaemic heart disease in the Edinburgh Artery Study. Am J Epidemiol. 1992; 135: 331–340.[Abstract/Free Full Text]

34. Bian K, Ishibashi K, Bukoski R. 1,25 (OH)₂D₃ modulates intracellular Ca²⁺ and force generation in resistance arteries. Am J Physiol. 1996; 270: H230–H237.

35. Krause R, Buhring M, Hopfenmuller W, Holick M, Sharma A. Ultraviolet B and blood pressure. Lancet. 1998; 352: 709–710.

36. Burgess E, Hawkins R, Watanabe M. Interaction of 1,25-dihydroxyvitamin D and plasma renin activity in high renin essential hypertension. Am J Hypertens. 1990; 3: 903–905.[Medline] [Order article via Infotrieve]

37. Kristal-Boneh E, Froom P, Harari G, Ribak J. Association of calcitriol and blood pressure in normotensive men. Hypertension. 1997; 30: 1289–1294.[Abstract/Free Full Text]

38. Sowers M, Wallace R, Hollis B, Lemke J. Relationship between 1,25-dihydroxyvitamin D and blood pressure in a geographically defined population. Am J Clin Nutr. 1988; 48: 1053–1056.[Abstract/Free Full Text]

39. Jorde R, Bonaa K. Calcium from dairy products, vitamin D intake, and blood pressure: the Tromso study. Am J Clin Nutr. 2000; 71: 1530–1535.[Abstract/Free Full Text]

40. Pfeifer M, Begerow B, Minne H, Nachtigall D, Hansen C. Effects of short-term Vitamin D₃ and calcium supplementation on blood pressure and parathyroid hormone levels in elderly women. J Clin Endocrinol Metab. 2001; 86: 1633–1637.[Abstract/Free Full Text]

41. Li Y, Kong J, Wei M, Chen ZF, Liu S, Cao LP. 1,25-Dihydroxyvitamin D₃ is a negative endocrine regulator of the renin-angiotensin system. J Clin Invest. 2002; 110: 229–238.[CrossRef][Medline] [Order article via Infotrieve]

42. Abedin M, Tintut Y, Demer LL. Vascular calcification. Mechanisms and clinical ramifications. Arterioscler Thromb Vasc Biol. 2004; 24: 1161–1170.[Abstract/Free Full Text]

43. Doherty T, Fitzpatrick L, Inoue D, Qiao J-H, Fishbein M, Detrano R, Shah P, Rajavashisth T. Molecular, endocrine, and genetic mechanisms of arterial calcification. Endocrine Reviews. 2004; 25: 629–672.[Abstract/Free Full Text]

44. Arad Y, Spadaro L, Goodman K, Lledo-Perez A, Sherman S, Lerner G, Guerci AD. Predictive value of electron beam computed tomography of the coronary arteries. 19 month follow-up study of 1173 asymptomatic subjects. Circulation. 1996; 93: 1951–1953.[Abstract/Free Full Text]

45. Iribarren C, Sidney S, Sternfeld B, Browner W. Calcification of the aortic arch. Risk factors and the association with coronary heart disease, stroke, and peripheral vascular disease. JAMA. 2000; 283: 2810–2815.[Abstract/Free Full Text]

46. Elliott R, McGrath L. Calcification of the human thoracic aorta during aging. Calcif Tiss Int. 1994; 54: 268–273.[CrossRef][Medline] [Order article via Infotrieve]

47. Niskanen L, Siitonen O, Suhonen M, Uusitupa M. Medial artery calcification predicts cardiovascular mortality in patients with NIDDM. Diabetes Care. 1994; 17: 1252–1256.[Abstract]

48. Lehto S, Niskanen L, Suhonen M, Ronnemaa T, Laasko M. Medial artery calcification. A neglected harbinger of cardiovascular complications in non-insulin-dependent diabetes mellitus. Arterioscler Thromb Vasc Biol. 1996; 16: 978–985.[Abstract/Free Full Text]

49. Watson KE, Abrolat ML, Malone LL, Hoeg JM, Doherty T, Detrano R, Demer LL. Active serum vitamin D levels are inversely correlated with coronary calcification. Circulation. 1997; 96: 1755–1760.[Abstract/Free Full Text]

50. Doherty T, Tang W, Dascolas S, Watson KE, Demer L, Shavelle R, Detrano R. Ethnic origin and serum levels of 1,25-Dihydroxyvitamin D₃ are independent predictors of coronary calcium mass measured by electron-beam computed tomography. Circulation. 1997; 96: 1477–1481.[Abstract/Free Full Text]

51. Arad Y, Spadaro L, Roth M, Scordo J, Goodman K, Sherman S, Lerner G, Newstein D, Guerci AD. Serum concentration of calcium, 1,25 vitamin D and parathyroid hormone are not correlated with coronary calcifications. An electron beam computed tomography study. Coronary Artery Dis. 1998; 9: 513–518.[Medline] [Order article via Infotrieve]

52. Kiel D, Kauppila L, Cupples L, Hannan M, O’Donnell C. Bone loss and the progression of abdominal aortic calcification over a 25 year period: the Framingham Heart Study. Calcif Tiss Int. 2001; 68: 271–276.[CrossRef][Medline] [Order article via Infotrieve]

53. Tanko L, Bagger Y, Christiansen C. Low bone mineral density in the hip as a marker of advanced atherosclerosis in elderly women. Calcif Tiss Int. 2001; 73: 15–20.

54. Pennisi P, Signorelli S, Riccobene S, Celotta G, Di Pino L, La Malfa T, Fiore C. Low bone density and abnormal bone turnover in patients with atherosclerosis of peripheral vessels. Osteoporosis Int. 2004; 15: 389–395.[CrossRef][Medline] [Order article via Infotrieve]

55. Price P, Faus S, Williamson M. Biphosphonates alendronate and ibamdronate inhibit artery calcification at doses comparable to those that inhibit bone resorption. Arterioscler Thromb Vasc Biol. 2001; 21: 817–824.[Abstract/Free Full Text]

56. Price P, June H, Buckley J, Williamson M. SB 242784, a selective inhibitor or the osteoclastic V-H⁺-ATPase, inhibits arterial calcification in the rat. Circ Res. 2002; 91: 547–552.[Abstract/Free Full Text]

57. Demer L. Vascular calcification and osteoporosis: inflammatory responses to oxidised lipids. Int J Epidemiol. 2002; 31: 737–741.[Free Full Text]

58. Price P, June H, Buckley J, Williamson M. Osteoprotegrin inhibits artery calcification induced by warfarin and by vitamin D. Arterioscler Thromb Vasc Biol. 2001; 21: 1610–1616.[Abstract/Free Full Text]

59. Jono S, Nishizawa Y, Shioi A, Morii H. 1,25-Dihydroxyvitamin D₃ increases in vitro vascular calcification by modulating secretion of endogenous parathyroid hormone-related peptide. Circulation. 1998; 98: 1302–1306.[Abstract/Free Full Text]

60. Doherty T, Uzui H, Fitzpatrick L, Tripathi P, Dunstan C, Astroke K, Rajavashisth T. Rationale for the role of osteoclast-like cells in arterial calcification. FASEB J. 2002; 16: 577–582.[Abstract/Free Full Text]

61. Milliner D, Zinsmeister A, Lieberman E, Landing B. Soft tissue calcification in pediatric patients with end-stage renal disease. Kidney Int. 1990; 38: 931–936.[Medline] [Order article via Infotrieve]

62. Teng M, Wolf M, Lowrie E, Ofsthun N, Lazarus J, Thadhani R. Survival of patients undergoing haemodialysis with paricalcitriol or calcitriol therapy. N Eng J Med. 2003; 349: 446–456.[Abstract/Free Full Text]

63. Inoue T, Kawasaki H. 1,25-Dihydroxyvitamin D₃ stimulates ⁴⁵Ca⁺-uptake by cultured vascular smooth muscle cells. Biochem Biophys Res Commun. 1988; 152: 1388–1394.[CrossRef][Medline] [Order article via Infotrieve]

64. Vattikuti R, Towler D. Osteogenic regulation of vascular calcification: an early perspective. Am J Physiol. 2004; 286: E686–E696.

65. Bennett M, Evan G, Schwartz S. Apoptosis of human vascular smooth muscle cells derived from normal vessels and coronary atherosclerotic plaques. J Clin Invest. 1995; 95: 2266–2274.

66. Gadeau A, Chaulet H, Daret D, Kockx M, Daniel-Lamaziere J-M, Desgranges C. Time course of osteopontin, osteocalcin and osteonectin accumulation and calcification after acute vessel wall injury. J Histochem Cytochem. 2001; 49: 79–86.[Abstract/Free Full Text]

67. Ylikomi T, Laaksi I, Lou Y-R, Martikainen P, Miettinen S, Pennanen P, Purmonen S, Syvala H, Vienonen A, Tuohimaa P. Antiproliferative actions of vitamin D. Vitam Horm. 2002; 64: 357–406.[Medline] [Order article via Infotrieve]

68. Holick M. Sunlight and vitamin D: both good for cardiovascular health. J Gen Intern Med. 2002; 17: 733–735.[CrossRef][Medline] [Order article via Infotrieve]

69. Haddad J, Matsuoka L, Hollis B, Hu Y, Wortsman J. Human plasma transport of vitamin D after its endogenous synthesis. J Clin Invest. 1993; 91: 2552–2555.

70. Hirsch D, Axzoury R, Sarig S, Kruth H. Colocalisation of cholesterol and hydroxyapatite in human atherosclerotic lesions. Calcif Tiss Int. 1993; 52: 94–98.[CrossRef][Medline] [Order article via Infotrieve]

71. Demer L. A skeleton in the atherosclerosis closet. Circulation. 1995; 92: 2029–2032.[Free Full Text]

72. Morrison N, Qi J, Tokita A, Kelly P, Crofts L, Nguyen T, Sambrook P, Eisman J. Prediction of bone density from vitamin D receptor alleles. Nature. 1994; 367: 284–287.[CrossRef][Medline] [Order article via Infotrieve]

73. Ralston S. Genetic control of susceptibility to osteoporosis. J Clin Endocrinol Metabol. 2002; 87: 2460–2466.[Abstract/Free Full Text]

74. van Schooten F, Hirvonen A, Maas L, de Mol B, Kleinjans J, Bell D, Durrer J. Putative susceptibility markers of coronary artery disease: association between VDR genotype, smoking, and aromatic DNA adduct levels in human right atrial tissue. FASEB J. 1998; 12: 1409–1417.[Abstract/Free Full Text]

75. Ortlepp J, von Korff A, Hanrath P, Zerres K, Hoffmann R. Vitamin D receptor gene polymorphism Bsml is not associated with the prevalence and severity of CAD in a large-scale angiographic cohort of 3441 patients. Eur J Clin Invest. 2003; 33: 106–109.[CrossRef][Medline] [Order article via Infotrieve]

76. Jespersen B, Randlov A, Abrahamsen J, Fogh-Andersen N, Olsen N, Kanstrup I. Acute cardiovascular effect of 1,25-dihydroxycholecalciferol in essential hypertension. Am J Hypertens. 1998; 11: 659–666.[CrossRef][Medline] [Order article via Infotrieve]

77. Duprez D, de Buyzere M, de Backer T, Clement D. Relationship between vitamin D₃ and the peripheral circulation in moderate arterial primary hypertension. Blood Pressure. 1994; 3: 389–393.[Medline] [Order article via Infotrieve]

78. Roca-Cusachs A, DiPette D, Carson J, Graham G, Holland O. Systemic and regional hemodynamic effects of 1,25-dihydroxyvitamin D₃ administration. J Hypertens. 1992; 10: 939–947.[Medline] [Order article via Infotrieve]

79. Bukoski R, DeWan P, McCarron D. 1,25 (OH)₂ Vitamin D₃ modifies growth and contractile function of vascular smooth muscle of spontaneously hypertensive rats. Am J Hypertens. 1989; 2: 553–556.[Medline] [Order article via Infotrieve]

80. Hatton D, Xue H, DeMerritt H, McCarron D. 1,25 (OH)₂ Vitamin D₃-induced alterations in vascular reactivity in the spontaneously hypertensive rat. Am J Med Sci. 1994; 307: S154–S158.

81. Ishibashi K, Evans A, Shigu T, Bian K, Bukoski R. Differential expression and effect of 1,25-dihydroxyvitamin D₃ on myosin in arterial tree of rats. Am J Physiol. 1995; 269: C443–C450.

82. Martyn C, Greenwald S. Impaired synthesis of elastin in walls of aorta and large conduit arteries during development as an initiating event in pathogenesis of hypertension. Lancet. 1997; 350: 953–955.[CrossRef][Medline] [Order article via Infotrieve]

83. Norman P, Wysocki S, Lamawansa M. The role of vitamin D₃ in the aetiology of abdominal aortic aneurysms. Medical Hypotheses. 1995; 45: 17–20.[CrossRef][Medline] [Order article via Infotrieve]

84. Toda T, Toda Y, Kummerow F. Coronary arterial lesions in piglets from sows fed moderate excesses of vitamin D. Tohoku J Exp Med. 1985; 145: 303–310.[Medline] [Order article via Infotrieve]

85. Clements MR, Fraser DR. Vitamin D supply to the rat fetus and neonate. J Clin Invest. 1988; 81: 1768–1773.

86. Hollis BW, Roos BA, Draper HH, Lambert PW. Vitamin D and its metabolites in human and bovine milk. J Nutr. 1981; 111: 1240–1248.

87. Norman P, Moss I, Sian M, Gosling M, Powell J. Maternal and postnatal vitamin D ingestion influences rat aortic structure, function and elastin content. Cardiovasc Res. 2002; 55: 169–174.

88. Shah P. Inflammation, metalloproteinases, and increased proteolysis. An emerging pathophysiological paradigm in aortic aneurysm. Circulation. 1997; 96: 2115–2117.[Free Full Text]

89. Veldman C, Cantorna M, DeLuca H. Expression of 1,25-dihydroxyvitamin D₃ receptor in the immune system. Arch Biochem Biophys. 2000; 374: 334–338.[CrossRef][Medline] [Order article via Infotrieve]

90. Boonstra A, Barrat F, Crain C, Heath V, Savelkoul H, O’Garra A. 1,25-dihydroxyvitamin D₃ has a direct effect on naive CD4+T cells to enhance the development of Th2 cells. J Immunol. 2001; 167: 4974–4980.[Abstract/Free Full Text]

91. Willheim M, Thien R, Schrattbauer K, Bajna E, Holub M, Gruber R, Baier K, Pietschmann P, Reinisch W, Scheiner O, Peterlik M. Regulatory effects of 1,25-dihydroxyvitamin D₃ on the cytokine production of human peripheral blood lymphocytes. J Clin Endocrinol Metab. 1999; 84–89.

92. Schonbeck U, Sukhova GK, Gerdes N, Libby P. T(H)2 predominant immune responses prevail in human abdominal aortic aneurysm. Am J Pathol. 2002; 161: 499–506.[Abstract/Free Full Text]

93. Zofkova I, Kancheva R. The effect of 1,25(OH)₂ vitamin D₃ on CD4+/CD8+ subsets of T lymphocytes in post menopausal women. Life Sciences. 1997; 61: 147–152.[CrossRef][Medline] [Order article via Infotrieve]

94. Wjst M, Dold S. Genes, factor X and allergens: what causes allergic diseases? Allergy. 1999; 54: 757–759.[CrossRef][Medline] [Order article via Infotrieve]

95. Raisanen-Sokolowski A, Pakkala I, Samila S, Binderup L, Hayry P, Pakkala S. A vitamin D analog, MC1288, inhibits adventitial inflammation and suppresses intimal lesions in rat aortic allografts. Transplantation. 1997; 63: 936–941.[CrossRef][Medline] [Order article via Infotrieve]

96. Gyetko M, Hsu C, Wilkinson C, Patel S, Young E. Monocyte -hydroxylase regulation: induction by inflammatory cytokines and suppression by dexamethasone and uremia toxin. J Leukoc Biol. 1993; 54: 17–22.[Abstract]

97. Parhami F, Morrow A, Balucan J, Leitinger N, Watson AD, Tintut Y, Berliner JA, Demer LL. Lipid oxidation products have opposite effects on calcifying vascular cell and bone cell differentiation. A possible explanation for the paradox of arterial calcification in osteoporotic patients. Arterioscler Thromb Vasc Biol. 1997; 17: 680–687.[Abstract/Free Full Text]

98. Mahon B, Gordon S, Cruz J, Cosman F, Cantorna M. Cytokine profile in patients with multiple sclerosis following vitamin D supplementation. J Neuroimmunol. 2003; 134: 128–132.[CrossRef][Medline] [Order article via Infotrieve]

99. Hass G, Trueheart R, Hemmens A. Experimental arteriosclerosis due to hypervitaminosis D. Am J Pathol. 1960; 37: 521–549.

100. Hong M, Vossoughi J, Haudenschild C, Wong S, Zuckenman B, Leon M. Vascular effects of diet-induced hypercalcemia after balloon artery injury in giant Flemish rabbits. Am Heart J. 1995; 130: 758–764.[CrossRef][Medline] [Order article via Infotrieve]

101. Mortensen JT, Brinck P, Binderup L. Toxicity of vitamin D analogues in rats fed diets with standard or low calcium contents. Pharmacol Toxicol. 1993; 72: 124–127.[Medline] [Order article via Infotrieve]

102. Niederhoffer N, Bobryshev Y, Larttaud-Idjouadiene I, Guimmelly P, Atkinson J. Aortic calcification produced by vitamin D₃ plus nicotine. J Vasc Res. 1997; 34: 386–398.[Medline] [Order article via Infotrieve]

103. Fischer E, Armentano R, Levenson J, Barra J, Morales M, Breitbart G, Pichel R, Simon A. Paradoxically decreased aortic wall stiffness in response to vitamin D3-induced calcinosis. Circ Res. 1991; 68: 1549–1559.[Abstract/Free Full Text]

104. Lamawansa M, Wysocki S, House A, Norman P. Vitamin D₃ exacerbates intimal hyperplasia in balloon-injured arteries. Br J Surg. 1996; 83: 1101–1103.[Medline] [Order article via Infotrieve]

105. Mohtai M, Yamamoto T. Smooth muscle cell proliferation in the rat coronary artery induced by vitamin D. Atherosclerosis. 1987; 63: 193–202.[CrossRef][Medline] [Order article via Infotrieve]

106. Koh E, Morimoto S, Fukuo K, Itoh K, Hironaka T, Shirashi T, Onishi T, Kumahara Y. 1,25 dihydroxyvitamin D3 binds specifically to rat vascular smooth muscle cells and stimulates their proliferation in vitro. Life Sci. 1988; 42: 215–223.[CrossRef][Medline] [Order article via Infotrieve]

107. Drolet M-C, Arsenault M, Couet J. Experimental aortic valve stenosis in rabbits. J Am Coll Cardiol. 2003; 41: 1211–1217.[Abstract/Free Full Text]

108. Kasuga H, Hosogane N, Matsuoka K, Mori I, Sakura Y, Shimakawa K, Shinki T, Suda T, Taketomi S. Characterization of transgenic rats constitutively expressing vitamin D-24-hydroxylase gene. Biochem Biophys Res Commun. 2002; 297: 1332–1338.[CrossRef][Medline] [Order article via Infotrieve]

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