Review Article
Nebivolol: Does the Key Lie in β3 Agonism?
Hernán Cohen Arazi1* and Miguel Gonzalez2
1Department of Cardiology and Cardiovascular Surgery, Centro Médico Pilares, Buenos Aires Argentina CEMIC,
Buenos Aires Argentina
2Department of Cardiovascular Surgery, Sanatorio Finochietto, Buenos Aires, Argentina
*Corresponding author: Hernán Cohen Arazi, Department of Cardiology and Cardiovascular Surgery, Centro Médico Pilares, Buenos Aires Argentina CEMIC, Buenos Aires Argentina
Published: 10 Oct, 2017
Cite this article as: Arazi HC, Gonzalez M. Nebivolol: Does
the Key Lie in β3 Agonism?. Clin Surg.
2017; 2: 1660.
Abstract
Beta-blockers are drugs indicated in the treatment of multiple cardiovascular pathologies. The review highlights the mechanisms of action of Nebivolol and its particular potential effect on β3 receptors that increases nitric oxide that may mark very significant differences, which are traduced to benefits in clinical results. Nebivolol has an special place in the treatment of adrenergic hypertension associated with tachycardia and emotional stress, more frequently in young individuals, and may be considered adequate even in patients with glucose and lipid metabolism disorders due to its pleiotropic effect. In patients with heart failure, Nebivolol showed effectiveness and safety in patients over 75 years old. Nebivolol showed a reduction of cardiomyocyte apoptosis and improvement of contractile function through a mechanism related to β3 receptor agonism after an acute coronary syndrome. Because of all these actions Nebivolol should be considered not only a third-generation Beta-blocker.
Introduction
Beta-blockers are drugs indicated in the treatment of multiple cardiovascular pathologies, with different level of evidence. Despite the fact that they are divided into first-generation to thirdgeneration drugs and according to their selectivity by beta and alpha receptors, they are often mentioned as belonging to the same group [1]. The purpose of this review is to highlight that the mechanisms of action of the beta-blockers may mark very significant differences, which are seen in clinical results [2,3]. In this sense, Nebivolol seems to be a drug that due to its pharmacodynamics and its particular potential effect on β3 receptors and the increase of Nitric Oxide (NO) [4], may be considered in a different place in comparison to a conventional beta-blocker.
Most Frequently Used Beta-Blockers
Propranolol is the oldest beta-blocker, dating back to the 1960s. It has an equal affinity for β1 and β2 receptors and is a non-selective beta-adrenergic antagonist. It is highly lipophilic and has a half-life of 3 to 5 hours, even though the duration of action is higher. It is indicated in cases of high blood pressure [5], angina [6] and some arrhythmias [7,8], frequently with two or more daily doses taken orally. It was one of the first beta-blockers that showed benefits. Atenolol is a selective β1 receptor inhibitor, hydrophilic, highly used in spite of not having shown decrease of arrhythmias or mortality after myocardial infarction [9]. Compared with angiotensinconverting- enzyme inhibitors (ACE inhibitors), atenolol does not improve the arteriolar resistance in hypertensive patients [10] and has a short duration of action that does not allow for a homogeneous antihypertensive effect during 24 hours [11]. What is more, it was associated with an increase in diabetes and stroke risk and total mortality when compared with other agents [12], especially in elderly patients [13]. Bisoprolol, like atenolol, is also a second-generation beta-blocker, with greater selectivity for β1 receptors, is lipophilic and has a half-life of 11 to 17 hours. There are randomized clinical trials that have proven the benefits of bisoprolol in cases of heart failure [14]. However, despite the fact that the studies conducted on high blood pressure do not have the same methodological rigor, it is also approved for its use in cases of hypertension [15]. Carvedilol is a non-selective beta-blocker with additional blockades of ἀ receptors, which gives it a vasodilatory effect. At high doses, it blocks the entry of calcium. Milligram per milligram, it is two to four times more potent than propranolol as ß antagonist [17]. In the U.S. Carvedilol Heart Failure Program [18], it is used in the treatment of heart failure, and it is also indicated for high blood pressure and myocardial ischemia.
Figure 1
Figure 2
Beta-Blockers in High Blood Pressure (HBP)
Even though beta-blockers have been used for almost half a
century for the treatment of HBP, they are not drugs considered
as first-line treatment by national [19] and international [20,21]
treatment guidelines. The antihypertensive effect of secondgeneration
beta-blockers is achieved through the reduction of the
cardiac minute volume, the heart rate and the contractility, with no
effect on peripheral vascular resistance [22]. Third-generation betablockers
have vasodilatory properties through blockades of ἀ receptors
(carvedilol) or through the increase of nitric oxide (nebivolol), which
lowers the peripheral resistance maintaining the minute volume
[23]. The low effectiveness for the prevention of strokes with betablockers
has been attributed to a low ability to decrease the central
systolic pressure and the pulse pressure. However, they have proved
effective in the prevention of cardiovascular events in patients with a
recent myocardial infarction or with heart failure [24]. The national
and international treatment guidelines clearly state that beta-blockers
with a vasodilatory effect have advantages over other beta-blockers
since they reduce the central pressure of the pulse and the aortic
rigidity [25-27]. There is evidence that the central aortic pressure is
an independent predictor of cardiovascular structural damage and
clinical events [28-31].
Differences of nebivolol
Nebivolol has a greater selectivity of β1 receptor blockages
than other beta-blockers [32] Figure 1. Unlike carvedilol, Nebivolol
exercises its vasodilatory effect through the production of nitric
oxide derived from the endothelium by stimulating the Nitric Oxide
Synthase (NOS) mediated by β3 receptor agonism [33,34]Figure 2.
Endothelial dysfunction caused by oxidative stress is an essential
mechanism involved in high blood pressure [35]and is associated
with the prognosis in cardiovascular disease [36]. Nebivolol showed
reduction of oxidative stress, which may also be an explanation for
the better metabolic profile of Nebivolol in connection with glucose
and lipids [37-39]. The studies that assessed Nebivolol against placebo
in patients with high blood pressure showed a significant reduction of
systolic (SBP) and Diastolic Blood Pressure (DBP) [40], with a broad
safety margin, and few adverse effects (headache 7.1% versus 5.9 with
placebo, fatigue 3.6% vs. 1.5% with placebo and dizziness 2.9 vs. 2.0%
with placebo), without differences in the treatment discontinuation
rate (2.6% with Nebivolol versus 2.0% with placebo). These results
were concordant in the subgroup analysis [41] and especially
beneficial in the group of young patients [42], a special target for the
incidence of adrenergic hypertension. Compared with Angiotensin-
Converting-Enzyme inhibitors (ACE inhibitors), Nebivolol showed
a greater percentage of patients that reached the target values and
was comparable to the angiotensin 2 receptor antagonists (AT2) and
calcium channel blockers [43]. Maximum antihypertensive action is
observed between week 2 and 8 of treatment, which is intermediate
between the ACE inhibitors (slower) and amlodipine (faster) [44].
The action on nitric oxide may be of great benefit, preventing erectile
dysfunction [45] reported with other beta-blockers [46,47], which
is one of the main adverse effects feared by young patients. These
additional benefits reinforce the potential role of Nebivolol in the
treatment of adrenergic hypertension associated with tachycardia
and emotional stress, more frequently in young individuals, and
may be considered adequate even in patients with glucose and
lipid metabolism disorders [48] due to its pleiotropic effect [49].
In patients with hypertension and type 2 diabetes, Nebivolol has demonstrated reductions in mean glucose levels and HbA1c across
several age groups [50] and increases in HDL cholesterol (5 mg/dl)
were observed [51].
Figure3
Figure 4
Beta-Blockers in Cases of Heart Failure (HF)
There are no doubts about the benefit of beta-blockers in the
treatment of heart failure [52]. They reduce mortality and morbidity
by approximately 30% over 5 years [53]. They have a grade I
recommendation, with a level of evidence A in all international and
national treatment guidelines together with the ACE inhibitors. The
beneficial effect in this pathology would be associated with a reduction
of adrenergic stimulation modulating the sympathetic-vagal balance
and the variability of the heart rate, in addition to improving heart
performance. The deleterious effects of beta-blockers are related to
the reduction of inotropism and chronotropism, which is why they
must be administered in patients that are hemodynamically stable.
Differential aspects of nebivolol
The distinctive pharmacologic profile of Nebivolol is explained
by some relevant hemodynamic effects: 1- The highly selective β1
blockade reduces heart rate at rest and on exertion as well as SBP
and DBP, without causing adverse effects related to the β2 receptor
blockade [54] and maintaining the balance with the alpha receptors
at vascular level. 2- Vasodilation mediated by NO results in the
reduction of peripheral vascular resistance, the improvement of
remodeling and of arterial stiffness [55,56] and in the increase of
systolic volume and ejection fraction maintaining the minute volume
[57]. When compared to other beta-blockers, Nebivolol did not
cause negative hemodynamic effects such as increase of pulmonary
artery pressure and Pulmonary Capillary Pressure (PCP) and
decrease of cardiac minute volume [58], unlike Metoprolol tartrate.
The hemodynamic profile and tolerance to exertion was also better
in comparison to Atenolol [59], and when compared to Carvedilol
(CARNEBI (Multiparametric comparison of CARvedilol, vs.
NEbivolol, vs. BIsoprolol in moderate heart failure cardiopulmonary
trial), patients with moderate HF had better physical capacity [60].
Nebivolol is a 1:1 racemic combination of a D- and an L-isomer. The
D-isomer grants it a blocking effect for β1 receptors and the L-isomer
is mainly responsible for the stimulating action of NOSe Figure 3.
When studying the Randomized Clinical Trials (RCT) conducted on
patients with heart failure, it is observed that they included younger
populations than the average age of patients that are hospitalized in
real life due to this pathology. The average age of RCT patients is
around 60 years old and only 25% are >75 years old. In our country,
according to the last census [61], there are more than 4 million people
older than 70, and in accordance with the prevalence of the disease, it
is estimated that there are more than 300,000 people with heart failure
in that age group [62]. Although some of the studies that have assessed
the treatment with beta-blockers in HF have analyzed the results in
elderly patients, these studies were not designed to reach statistically
significant conclusions [63,64]. The SENIORS study (Study of Effects
of Nebivolol Intervention on Outcomes and Rehospitalization in
Seniors With Heart Failure) [65] enrolled patients with heart failure,
and established as inclusion criteria that the patients were 70 years
old or older and incorporated a high percentage of women and
patients with preserved systolic function. It showed a reduction of
14% in the mortality from all causes, and there were no more adverse
effects than with placebo. This last datum is also relevant considering
that, in the treatment with other beta-blockers, advanced age was
a determining factor of intolerance risk [66]. The SENIORS study
reported an improvement in cardiac function and diameter, but the
hospitalization rate had not decreased. In patients under 75 years
old (median age of the population) and with ejection fraction < 35%,
a decrease of the primary final event of 38% (hazard ratio of 0.62)
was observed, in concordance with other beta-blockers in previous
studies.
Nebivolol in cases of coronary disease
Treatment with beta-blockers is indicated in patients with
acute and chronic coronary artery disease (67-69). Although in
some countries Nebivolol is not indicated in this pathology, there
is evidence that, in comparison to Atenolol, it improves exercise
tolerance and the time until the onset of angina in the exercise test
in patients with stable coronary artery disease [70] and also improves
coronary flow reserve [72]. Even in patients with cardiac syndrome
X and endothelial dysfunction, Nebivolol was associated with an
improvement of the exercise time, less exercise-induced ischemia
and less angina attacks than Metoprolol [72]. In acute coronary
syndromes, a small-scale study showed that patients that had an
infraction with ventricular dysfunction had fewer events (infarction/
death/hospitalization due to coronary syndrome/stroke or need of
revascularization) over 12 months than those patients treated with
Metoprolol and similar to those treated with Carvedilol [73]. The
additional benefit may be related to an antiplatelet effect showed with
Nebivolol [74,75]. However, there is a new paradigm related to the
agonist effect of β3 receptor.
New paradigm: the importance of β3 receptor
For many years we understood the hemodynamic and myocardial
functioning based on two beta receptors at myocardial level: β1 and β2
and the ἀ receptors at a vascular level, together with the neurohumoral
behavior of the Renin-Angiotensin-Aldosterone System (RAAS).
The endogenous catecholamines act at a myocardial level through
the union to these β myocardial receptors regulating heart rate
and contractility. Special situations may cause an increase of the
catecholamine levels and an increase of the cardiac activity, as occurs,
for instance, in adrenergic hypertension or in heart failure. In this last
case, a mechanism that is initially compensatory becomes harmful due
to cellular toxicity and apoptosis, consequence of the activation and
“overstimulation” of β1 receptors at myocardial level. The discovery
of β3 receptors in atria and in ventricles [76] forces us to redefine the
model. These receptors, encoded in chromosome 8 [77], were known
in the adipose tissue, where they regulate thermogenesis, and were
also described at the muscular level of bladder and gallbladder. In
the myocardium, it was observed that in situations where there are
high levels of catecholamines, the upregulation of β3 receptors occurs
[78,79]. The union to these receptors causes attenuation of inotropism,
favoring a counterbalance of β1 receptors against "deleterious
overexposure" of catecholamines that may derive in hypertrophy,
fibrosis and apoptosis. Thus, the β3 receptor agonism may exercise
a protective effect at myocardial level [80,81]. The activation of
one or another β receptor depends on the clinical situation and the
circulating catecholamine levels. The β3 effect is connected with the
activation through NO. There are 3 isoforms of NO synthase (NOS).
In patients with heart failure, the NOSe (endothelial) and ONSn
(neural) are the ones responsible for the protective effect through
the increase of NO at myocardial level [82,83]. Several studies have
shown that Nebivolol causes its effect through the combined action
of β1 receptors blockade and β3 receptors agonism. At a vascular
level, the increase of NO causes vasodilation, and at a myocardial level, it favors the necessary balance to achieve a balanced inotropic
effect, preventing the increase of catecholamines from becoming
deleterious Figure 4. β3 receptor agonism at a coronary vascular level
causes vasorelaxation mediated by Nitric Oxide (NO), especially
in microvasculature. Considering that an important component of
cardiac remodeling is the adaptation of the capillary density under
hemodynamic stress and neoangiogenesis [84], the action at the
vascular level of β3 agonists may be part of the improvement of postinfarction
remodeling [85] observed with Nebivolol, jointly with a
paracrine effect at fibroblast level that improves the formation of scar
tissue and peripheral vasodilation contributing to the improvement of
ventricular relaxation. In experimental studies in animals with recent
myocardial infarction, treatment with Nebivolol showed a reduction
of cardiomyocyte apoptosis and improvement of contractile function
through a mechanism related to β3 receptor agonism. These same
mechanisms could explain part of the benefit observed in the SENIOR
study in patients with chronic heart failure.
Conclusion
Beta-blockers proved beneficial in different clinical scenarios. A big part of the benefit was explained by the antiarrhythmic and antihypertensive effect of these drugs, added to a decrease of the deleterious action of catecholamines against excessively high levels. The initial approach was to differentiate beta-blockers according to their affinity to β1 and β2 receptors. Then, focusing on the neurohumoral hypothesis and reassessing the hemodynamic control of ventricular dysfunction, an action on peripheral resistance was considered essential, and carvedilol differed due to its vasodilatory effect through blockade of ἀ receptors at vascular level. However, NO is a more potent vasodilator and is physiologically present in situations of ischemia. The discovery of the β3 agonist action with the consequent action of NO at myocardial and vascular level could change the paradigm. Nebivolol acting as agonist would have additional beneficial effects, at the level of ventricular remodeling, in patients with different degrees of ventricular dysfunction and in subpopulations specifically assessed as elderly patients.
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