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Trends Endocrinol Metab. Author manuscript; available in PMC Aug 1, 2010.
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PMCID: PMC2731551
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eNOS, metabolic syndrome and cardiovascular disease

Abstract

Large epidemiologic studies have established that diabetes, hyperlipidemia and obesity all increase the risk for cardiovascular disease. However, the precise mechanisms by which these metabolic disorders increase the propensity to develop atherosclerosis are not known. Recently, the concept of the metabolic syndrome – a constellation of conditions including obesity, hypertension, hyperlipidemia and insulin resistance – has received much attention. Studies on the metabolic syndrome might enable a better understanding of the underlying biological mechanisms that lead to cardiovascular disease. This review focuses on endothelial nitric oxide synthase and summarizes evidence that a reduction in the bioavailability of endothelium-derived nitric oxide serves as a key link between metabolic disorders and cardiovascular risk.

Why is metabolic syndrome important to cardiovascular disease?

The metabolic syndrome is a clustering of known cardiovascular risk factors, including obesity, hyperglycemia, dyslipidemia and hypertension. Although it had been known for many years that each of the component features of metabolic syndrome is also a cardiovascular risk factor, this concept received renewed interest with the description of ‘Syndrome X’ by Gerald Reaven at the 1988 Banting Lecture of the American Diabetes Association [1]. The concept of the metabolic syndrome has several important consequences. First, when applied to clinical settings, it identifies a group of patients at increased risk of developing type 2 diabetes (T2D) and cardiovascular disease (CVD). Depending on the definition used, people with metabolic syndrome have up to a fivefold higher risk of T2D and a two-to-threefold higher risk of atherosclerotic CVD than those without [2,3]. Second, the fact that the individual component features cluster together provides information about their interrelationships and shared pathophysiologic mechanisms. An active area of investigation is the molecular mechanisms by which cardiovascular disease risk is increased by metabolic syndrome and whether new treatment approaches can be developed to target these mechanisms. This review explores the relationships between metabolic syndrome, endothelial dysfunction and endothelial nitric oxide synthase (eNOS).

The concept of the metabolic syndrome

The National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATPIII)’s definition of metabolic syndrome was developed in 2001 [4] and revised in 2005 [3] (Table 1). This definition states that metabolic syndrome is present if any three of five criteria are met: obesity (waist circumference of more than 40 inches for men or 35 inches for women), hypertension (over 135 systolic or over 85 diastolic), fasting hypertriglyceridemia (over 150 mg/dl), low high-density lipoprotein (HDL) cholesterol (less than 40 in men or 50 in women) and fasting hyperglycemia (currently, glucose over 100 mg/dl). Being on medication for these conditions (for example, anti-hypertensives or fibrates) also meets these criteria. These criteria were selected because they are readily apparent from physical examination and/or commonly obtained laboratory tests. Thus, the NCEP ATPIII criteria are easily applied in patient care settings and large epidemiologic studies. Two additional features thought to play a part in the pathophysiology of the metabolic syndrome are hypercoagulability and systemic inflammation [5,6].

Table 1
Definitions of metabolic syndrome

The NCEP ATPIII criteria are similar to the other major definitions of metabolic syndrome (Table 1), including those from the World Health Organization (WHO) [7], the European Group for the Study of Insulin Resistance (EGIR) [8] and the International Diabetes Federation (IDF) [9]. Common features of all of these definitions include glucose intolerance or insulin resistance, obesity, hypertension and dyslipidemia. However, several important points deserve mention [10,11]. First, the specific absolute criteria are particular for each population; standards for waist circumference, for example, are different for diverse ethnic groups and nationalities. Second, the various definitions differ by how they are structured. The NCEP ATPIII definition requires any three of the five defining characteristics, but no single one is absolutely required. By contrast, the WHO and EGIR definitions require the presence of diabetes, impaired glucose tolerance or insulin resistance for the diagnosis of metabolic syndrome, and the IDF definition requires central obesity. These differences probably reflect the components each organization considers as the primary and central causes of the overall clustering of the component risks. Third, the more complicated definitions might involve tests and measurements not routinely used in patient care, such as euglycemic clamp measurements, limiting their widespread application. Finally, the utility of the syndrome depends on whether its purpose is to identify patients at increased risk of T2D or coronary disease.

Despite these differences in definition and controversy about the utility of the concept [1013], the clustering of defining characteristics in metabolic syndrome indicates that these individual characteristics – central obesity, insulin resistance, hypertension and dyslipidemia – are not independent of one another and are probably interrelated in many complex ways. One framework holds that obesity, particularly visceral or central obesity, is the primary abnormality [7,8]. Visceral obesity might lead to insulin resistance and T2D, and adipokines secreted by visceral fat can have vascular consequences that increase CVD risk [14]. Another framework holds that insulin resistance is the primary abnormality and results in metabolic derangements that lead to hypertension, dyslipidemia and an increased risk of CVD [9]. The connections between either obesity or insulin resistance and the actual mechanisms of increased atherogenesis involve effects on the vascular endothelium.

Endothelial dysfunction and eNOS

The endothelium comprises the inner lining of blood vessels. In contrast to the earlier viewpoint that the function of the endothelial lining of vessels is to serve as a mechanical barrier, we now know that the endothelium also senses and responds to physiologic and pathologic stimuli [15,16]. It produces vasoactive substances, including nitric oxide (NO), prostacyclin and endothelins. The expression of surface cell adhesion molecules governs interactions with circulating cells; these are leukocytes and monocytes, affecting inflammation, and platelets, ultimately affecting thrombosis. The endothelium also modulates the proliferation and injury response of the vascular smooth muscle layer, which contributes to neointima formation during the development of atherosclerotic plaques. These roles of the endothelium parallel current concepts about the pathogenesis of atherogenesis [17,18], which involve abnormalities in vascular signaling, oxidative stress, inflammatory cells and thrombosis. Normal endothelial function protects against these processes, and endothelial dysfunction is central to the pathogenesis of atherosclerotic lesion development.

NO is a gas produced by nitric oxide synthase (NOS) enzymes [19,20]. There are three major isoforms of NOS, encoded by separate genes on separate chromosomes (Table 2): neuronal NOS (nNOS), or type 1 NOS; inducible NOS (iNOS), or type 2 NOS; and eNOS, or type 3 NOS. The essential role of NO as the elusive endothelium-derived relaxing factor (EDRF) was the topic of the 1998 Nobel Prize in Physiology or Medicine [21,22]. eNOS-derived NO serves important functions, including regulation of vascular tone and regional blood flow, suppression of vascular smooth muscle cell proliferation, modulation of leukocyte–endothelial interactions and modulation of thrombosis. These functions are confirmed by the phenotypes of eNOS-knockout mice. eNOS gene deficiency results in hypertension [23], increased vascular smooth muscle cell proliferation in response to vessel injury [24], increased leukocyte–endothelial interactions [25], hypercoagulability [26] and increased diet-induced atherosclerosis [27,28].

Table 2
NOS isoforms

A common feature of many cardiovascular risk factors (including hypertension, diabetes, insulin resistance, obesity and hyperlipidemia) is endothelial dysfunction. Because the endothelium normally protects against the processes involved in atherogenesis – namely, smooth muscle cell proliferation, inflammation and thrombosis – endothelial dysfunction is an important final common pathway by which these risk factors increase atherosclerosis. Endothelial dysfunction, broadly defined, occurs when the endothelium fails to serve its normal physiologic and protective mechanisms [29,30]. This might occur because the endothelium is damaged or missing, as in the case of denuded endothelium in coronary arteries subjected to angioplasty or percutaneous intervention. It might also occur as a result of metabolic toxins, such as free fatty acids (FFAs) and inflammatory cytokines, including IL-6 and TNF-α. Hyperglycemia, advanced glycation products and other metabolic abnormalities might alter endothelial intracellular signaling pathways, such as the PI3K–Akt pathway. Finally, reactive oxygen species (ROS), particularly superoxide, might scavenge vascular NO and prevent it from inducing vascular smooth muscle relaxation [3133].

Although it is difficult to assess all of the functions of the endothelium, one commonly used surrogate endpoint for endothelial dysfunction is whether physiologic vasodilator responses are intact [29,30]. Vascular dilation to mediators such as acetylcholine or increased blood flow depends on NO produced by the endothelium [15,3436]. In the catheterization laboratory, this can be measured by monitoring the effect of intracoronary acetylcholine infusion. In the clinical setting, it is reflected by flow-mediated dilation (FMD), measured by ultrasound detection of the response of the brachial artery diameter to reflow after a period of vascular occlusion by a blood pressure cuff [37]. Although each method measures responses in different vascular beds, FMD correlates with the catheterization laboratory measurements of coronary circulation responses [38]. Furthermore, FMD predicts future cardiovascular events [39]. Thus, FMD is a commonly used method to assess endothelial function, and impaired FMD is taken to reflect endothelial dysfunction. Overall, endothelial dysfunction is an important pathophysiologic link between atherogenesis and many known cardiovascular risk factors such as hypertension, obesity, diabetes and dyslipidemia.

There are multiple mechanisms for endothelial dysfunction [20,40], as shown in Figure 1. A common feature of endothelial dysfunction is reduced bioavailability of NO in the vasculature. Possible mechanisms for impaired NO availability include a reduction in eNOS mRNA or protein expression levels [41]. However, studies in animal models and humans suggest that diabetes and atherosclerosis are not necessarily associated with a decrease in the amount of total eNOS [42,43]. L-arginine, the substrate for eNOS, can also be a limiting factor in tissues [44]. An endogenous competitive inhibitor, asymmetric dimethylarginine (ADMA), might reduce endothelial NO production even in the presence of adequate L-arginine levels [44]. This is the basis for recommendations for arginine supplementation to enhance eNOS-derived NO production. However, under certain conditions, increased eNOS enzymatic activity in the setting of cofactor deficiency might be more harmful than beneficial [45]. eNOS requires enzymatic cofactors, including flavin adenine dinucleotide, flavin mononucleotide, nicotine adenine dinucleotide hydrogen phosphate (NADPH), and tetrahydrobiopterin (BH4). BH4, the synthesis of which is rate limited by guanosine 5′ triphosphate cyclohydrolase, is particularly important because in its absence, electron transport through eNOS can become ‘uncoupled’, resulting in superoxide anion generation [46]. For full enzymatic activity, eNOS requires proper dimerization and intracellular localization to caveolae, mediated in part by protein-protein interactions with caveolin and heat shock protein 90 (hsp90) [15,47]. eNOS is phosphorylated at serine 1177 (S1177) by Akt kinase and other kinases [4851], discussed in detail below. Finally, NO produced by eNOS might be rapidly inactivated by reaction with superoxide (O2) to form peroxynitrite anion (OONO−) [52]. Superoxide can be formed by NAD(P)H oxidase [53] or by uncoupled eNOS [46]. Thus, there are multiple mechanisms that can lead to endothelial dysfunction. They are not mutually exclusive, and multiple mechanisms can operate simultaneously. However, the common feature is a reduction in the amount of bioavailable NO, which normally serves to protect the vessel from the molecular events that lead to atherosclerosis.

Figure 1
Regulation of eNOS activity and mechanisms of endothelial dysfunction. The bioavailability of NO produced by eNOS might be affected at multiple levels, including (i) eNOS mRNA or protein expression; (ii) availability of L-arginine, its substrate, which ...

Insulin signaling

Normal insulin signaling results in glucose uptake by skeletal muscle and fat, suppression of hepatic gluconeogenesis, and vasodilation from increased eNOS enzymatic activity [32,33]. These effects are mediated by insulin binding to the insulin receptor, a ligand-activated tyrosine kinase receptor. Binding and activation of the insulin receptor results in tyrosine phosphorylation of insulin receptor substrates (IRS) and Shc, resulting in the activation of two parallel pathways: the PI3 Kinase (PI3K)–Akt pathway and the Ras/Raf/MAP kinase pathway (Figure 2). Phosphorylation of IRS-1 leads to activation of the PI3K–Akt pathway. Akt kinase phosphorylates eNOS at S1177 and activates it, as discussed below. In skeletal muscles and adipose tissue, Akt stimulates the expression of the glucose transporter GLUT4, resulting in glucose uptake. Phosphorylation of Shc leads to activation of the Ras/Raf/MAP kinase pathways, resulting in mitogenic effects, as well as increased endothelin 1 (ET-1) expression [54,55].

Figure 2
Insulin signaling. Insulin signaling in endothelial cells occurs after insulin binding to the insulin receptor. This causes activation of two separate and parallel pathways: (i) PI3K–Akt and (ii) Ras/Raf/MAP kinase. (i) Akt kinase phosphorylates ...

Insulin resistance is defined as decreased sensitivity of peripheral tissues to insulin effects [32,33]. Insulin resistance alters the balance between the two pathways to downstream insulin signaling. Specifically, the PI3K–Akt pathway is altered in insulin resistance [56,57]. This results in diminished eNOS activity, less NO generation and diminished insulin-mediated vasodilation [32]. In the peripheral tissues, insulin resistance leads to decreased glucose uptake in skeletal muscle and adipose tissues because of downregulation of GLUT4 translocation [54,55]. By contrast, the Ras/Raf/MAP kinase pathway is generally preserved in insulin resistance [32]. Thus, unopposed ET-1 production and mitogenic effects persist and contribute to the vascular effects of insulin resistance.

The relationship between endothelial dysfunction and insulin resistance is complex, as shown in Figure 3. Metabolic abnormalities seen in obesity, diabetes and metabolic syndrome include insulin resistance and visceral adiposity. Both might cause endothelial dysfunction and, as a result, lead to development of atherosclerosis [33,58,59]. Conversely, endothelial dysfunction, specifically deficiency of endothelial NO, might lead to metabolic abnormalities, including insulin resistance [31,60]. In addition, insulin resistance can cause atherogenic dyslipidemia and contribute to visceral adiposity [32].

Figure 3
Relationships between insulin resistance, visceral adiposity, and endothelial dysfunction. Insulin 3 resistance can cause endothelial dysfunction through altered PI3K–Akt signaling. Endothelial dysfunction, in turn, can cause insulin resistance ...

Oxidative stress and eNOS

Under conditions of oxidative stress, O2 production increases. O2 reacts with NO to form OONO− in an extremely rapid reaction that is essentially diffusion limited [52]. Thus, O2 scavenges NO and renders it unavailable to mediate its physiologic functions, including binding to soluble guanylate cyclase to stimulate vasodilation. In addition, OONO- can cause direct oxidative damage, as well as tyrosine phosphorylation of endogenous proteins, affecting their function [61].

Because uncoupled eNOS not only generates NO but also generates O2, increasing eNOS transcription, translation or activity does not guarantee improved endothelial function [47]. In fact, as a potential source of O2, uncoupled eNOS might actually worsen the situation as compared with enzymatically inactive or absent eNOS. This is an important limitation to transgenic or gene therapy approaches to increase vascular eNOS expression.

Effects on eNOS S1177 phosphorylation

eNOS is phosphorylated at various serine and threonine residues [20,62]. Of these potential phosphorylation sites, S1177 seems to be a crucial regulator of its enzymatic activity. S1177 phosphorylation results in increased electron flux through the reductase domain and reduced calmodulin dissociation. As a result, eNOS becomes more active and produces more NO, even at resting levels of intracellular calcium [63].

There are several lines of evidence that indicate that eNOS S1177 phosphorylation is crucial to the link between metabolism and vascular dysfunction. First, animal models of diabetes, hypercholesterolemia and atherosclerosis, such as db/db mice and apoE-knockout mice, show diminished eNOS phosphorylation [64,65]. Second, estrogens [66], statins [67], and peroxisome proliferator activated receptors PPARα and PPARγ agonists [68,69] increase eNOS S1177 phosphorylation. Third, vasculoprotective signaling molecules such as insulin, IGF-1, vascular endothelial growth factor (VEGF), adiponectin and leptin [49,51,7072] all increase eNOS S1177 phosphorylation. Fourth, laminar shear stress and flow increase S1177 phosphorylation [48,50,73]. Thus, eNOS S1177 phosphorylation seems to be a crucial step in regulating eNOS activity and an important target for intervention to treat endothelial dysfunction [40].

In addition to Akt kinase [4851], eNOS S1177 is known to be phosphorylated by several other kinases, including AMP kinase [70], protein kinase A (PKA) and protein kinase G (PKG) [74], and calmodulin-dependent kinase II (CaMKII) [75]. Shear stress, VEGF, insulin, estrogens, statins and leptin stimulate eNOS S1177 phosphorylation by Akt kinase activation [66,67,72,76]. By contrast, adiponectin and resistin modulate S1177 phosphorylation through AMP kinase [70,77]. That diverse signaling pathways affect multiple kinases that converge to modulate eNOS activity by S1177 phosphorylation suggests that this might be a common integration point that underlies endothelial dysfunction from various causes (Figure 4).

Figure 4
Role of eNOS S1177 phosphorylation in integrating effects of multiple mediators. eNOS S1177 is phosphorylated by multiple kinases, including (i) Akt kinase and (ii) AMP kinase. Shear stress, VEGF, insulin, estrogen, statins and leptin all act through ...

Insulin resistance causes endothelial dysfunction by decreasing Akt kinase activity, resulting in diminished eNOS phosphorylation and activity. Because eNOS S1177 phosphorylation is required for the hemodynamic actions of insulin, its lack of phosphorylation results in diminished blood flow to skeletal muscle, creating a vicious cycle [32]. In addition, insulin-mediated ET-1 expression and mitogenic effects are not affected by insulin resistance [32], further contributing to endothelial dysfunction.

Effects of adipokines and FFA from visceral fat

The primary metabolic abnormalities seen in metabolic syndrome lead to the accumulation of visceral fat. White adipose tissue is known to play a part not only in energy storage but also in the production of factors that affect other tissues, including the vasculature [14,78]. These factors include resistin, IL-6 and TNF-α, which decrease eNOS S1177 phosphorylation, resulting in diminished eNOS activity and less NO generation. In addition to blocking IRS-1 activation, TNF-α directly activates NADPH oxidase, increasing O2 generation, and stimulates lipolysis, resulting in more FFA release [79]. In visceral fat, leptin resistance also increases the generation of ROS [80]. In contrast to these other adipokines, adiponectin is protective against CVD [14,77], in that it stimulates eNOS S1177 phosphorylation by AMP kinase to enhance physiologic endothelial function and NO production. Interestingly, adiponectin levels are decreased in T2D, obesity and IR [58,59]. FFA production from visceral fat is increased under conditions of insulin resistance. FFA contributes to endothelial dysfunction by a combination of diminished PI3K–Akt signaling, increased ROS and increased ET-1 production [32,58,59].

Endothelial dysfunction causes insulin resistance

In addition to the effects of obesity, insulin resistance and metabolic abnormalities on eNOS and endothelial function, eNOS itself is required for intact insulin signaling [54,71,81]. Insulin-mediated increases in eNOS activity and NO production lead to increased blood flow and functional capillary recruitment to peripheral tissues [32]. This results in increased delivery of insulin and glucose to skeletal muscle and fat, which contributes to insulin-mediated glucose uptake. Thus, when endothelial dysfunction occurs and vascular redistribution effects of insulin are blunted, there is a vicious cycle that results in further reduction in the metabolic effects of insulin in peripheral tissues owing to decreased delivery of glucose and insulin to the tissues.

eNOS and mitochondrial function

An additional important link between eNOS and insulin resistance is the essential role of eNOS-derived NO in mitochondrial biogenesis [8285]. In many different cell types, including white and brown adipocytes, NO donors or the exogenous expression of eNOS stimulates mitochondrial biogenesis through a cyclic GMP-dependent mechanism [86]. A reduction in bioavailability of eNOS-derived NO might result in abnormalities in energy homeostasis, resulting in insufficient generation of energy from stored fat in white adipose tissue and insufficient generation of heat (thermogenesis) from brown adipose tissue. Both of these effects would lead to increased fat storage. Systemic treatment of mice with pharmacologic inhibitors of eNOS results in defective adaptive thermogenesis. Furthermore, eNOS-knockout mice fail to respond to cold exposure by thermogenesis, and their brown adipose tissue development and function are defective [86]. eNOS-knockout mice also fail to show mitochondrial biogenesis in response to exercise or caloric restriction [87]. Taken together, these results show that reduction in bioavailable eNOS-derived NO might lead to abnormalities in energy homeostasis and adipocyte differentiation that increase the risk for metabolic syndrome. In fact, eNOS-knockout mice have been considered to be an important mouse model for the metabolic syndrome [83] because they combine many of its defining features, including hypertension, endothelial dysfunction, insulin resistance and obesity.

Directions for future research

Insulin resistance and visceral adiposity, two key features of the metabolic syndrome, contribute to endothelial dysfunction by reducing endothelial NO bioavailability. The mechanisms for these effects include alterations in PI3K–Akt signaling, resulting in diminished eNOS phosphorylation at S1177, direct effects of adipokines and FFA on endothelial cell function, and generation of ROS and scavenging of NO (Figure 3). In addition, endothelial dysfunction itself affects insulin signaling and perpetuates a vicious cycle whereby reduction in tissue perfusion and delivery of glucose and insulin causes further insulin resistance, leading to continued effects on endothelial function. Endothelial dysfunction also leads to defects in mitochondrial biogenesis, which contribute to insulin resistance and abnormal energy homeostasis.

An important unanswered question is whether intervention at any of these interrelated points – insulin resistance, visceral adiposity or endothelial dysfunction – can effectively break this cycle. For example, can interventions designed to increase insulin sensitivity at the peripheral tissue level translate into decreased adiposity or improved endothelial function? Can interventions designed specifically to improve endothelial function improve insulin sensitivity? Can small molecules that increase eNOS S1177 phosphorylation reverse endothelial dysfunction associated with diabetes, obesity or metabolic syndrome? Such small molecules might act on the kinases that phosphorylate S1177 (Akt, AMPK, PKA, PKG and CaMKII) or the phosphatases that mediate its dephosphorylation, which have not yet been well characterized. In this regard, genetically altered mice carrying phosphomimetic or unphosphorylatable mutations at eNOS S1177 might serve as useful tools to establish proof of principle of eNOS phosphorylation as an effective drug target [88].

With pharmacologic or transgenic interventions designed to increase eNOS activity, it will be important to assess possible effects on eNOS uncoupling because eNOS can serve not only as a source for NO but also as a source for O2. For future studies, it will be crucial to use experimental models of human disease in intact animals that reflect these complexities of NO signaling. Better yet, to the extent possible, examination of responses in patients will yield the most clinically relevant and dependable information. Now that we understand the complex relationships between insulin resistance, visceral adiposity and endothelial dysfunction, the task before us is to translate this knowledge into effective treatments to reduce CVD, which is the leading cause of morbidity and mortality from diabetes and related metabolic diseases.

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