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13 pages, 1525 KiB  
Review
Atrial Fibrillation in Elite Athletes: A Comprehensive Review of the Literature
by Christos Kourek, Alexandros Briasoulis, Elias Tsougos and Ioannis Paraskevaidis
J. Cardiovasc. Dev. Dis. 2024, 11(10), 315; https://doi.org/10.3390/jcdd11100315 - 9 Oct 2024
Viewed by 1491
Abstract
Although the benefits of exercise training have been shown repeatedly in many studies, its relationship with the occurrence of atrial fibrillation (AF) in competitive athletes still remains controversial. In the present review, we sought to demonstrate a comprehensive report of the incidence, pathophysiology, [...] Read more.
Although the benefits of exercise training have been shown repeatedly in many studies, its relationship with the occurrence of atrial fibrillation (AF) in competitive athletes still remains controversial. In the present review, we sought to demonstrate a comprehensive report of the incidence, pathophysiology, and therapeutic approaches to AF in elite athletes. A 2 to 10 times higher frequency of AF has been shown in many studies in high-intensity endurance athletes compared to individuals who do not exercise. Moreover, a U-shaped relationship between male elite athletes and AF is demonstrated through this finding, while the type and the years of physical activity seem to relate to AF development. A strong correlation seems to exist among the type of exercise (endurance sports), age (>55 years), gender (males), and the time of exercise training, all contributing to an increased risk of AF. The pathophysiology of AF still remains unclear; however, several theories suggest that complex mechanisms are involved, such as bi-atrial dilatation, pulmonary vein stretching, cardiac inflammation, fibrosis, and increased vagal tone. Elite athletes with AF require a comprehensive clinical evaluation and risk factor optimization, similar to the approach taken for nonathletes. Although anticoagulation and rate or rhythm control are cornerstones of AF management, there are still no specific guidelines for elite athletes. Full article
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Figure 1
<p>Atrial fibrillation (AF) risk varies across the spectrum of exercise training. Approaching the extreme borders of physical activities (minimum physical activity at the one border and endurance sports at the other), there is an increase in AF incidence.</p>
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<p>Presumed mechanisms of AF in elite athletes.</p>
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<p>A proposed algorithm of clinical assessment and therapeutic strategy of an elite athlete with AF.</p>
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20 pages, 2507 KiB  
Article
Cellular and Molecular Mechanisms Underlying Altered Excitability of Cardiac Efferent Neurons in Cirrhotic Rats
by Choong-Ku Lee, Huu Son Nguyen, Seong Jun Kang and Seong-Woo Jeong
Biomedicines 2024, 12(8), 1722; https://doi.org/10.3390/biomedicines12081722 - 1 Aug 2024
Viewed by 861
Abstract
Patients with cirrhosis often exhibit cardiac autonomic dysfunction (CAD), characterized by enhanced cardiac sympathetic activity and diminished cardiac vagal tone, leading to increased morbidity and mortality. This study delineates the cellular and molecular mechanisms associated with altered neuronal activities causing cirrhosis-induced CAD. Biliary [...] Read more.
Patients with cirrhosis often exhibit cardiac autonomic dysfunction (CAD), characterized by enhanced cardiac sympathetic activity and diminished cardiac vagal tone, leading to increased morbidity and mortality. This study delineates the cellular and molecular mechanisms associated with altered neuronal activities causing cirrhosis-induced CAD. Biliary and nonbiliary cirrhotic rats were produced by common bile duct ligation (CBDL) and intraperitoneal injections of thioacetamide (TAA), respectively. Three weeks after CBDL or TAA injection, the assessment of heart rate variability revealed autonomic imbalance in cirrhotic rats. We observed increased excitability in stellate ganglion (SG) neurons and decreased excitability in intracardiac ganglion (ICG) neurons in cirrhotic rats compared to sham-operated controls. Additionally, threshold, rheobase, and action potential duration exhibited opposite alterations in SG and ICG neurons, along with changes in afterhyperpolarization duration. A- and M-type K⁺ channels were significantly downregulated in SG neurons, while M-type K⁺ channels were upregulated, with downregulation of the N- and L-type Ca2⁺ channels in the ICG neurons of cirrhotic rats, both in transcript expression and functional activity. Collectively, these findings suggest that cirrhosis induces an imbalance between cardiac sympathetic and parasympathetic neuronal activities via the differential regulation of K+ and Ca2+ channels. Thus, cirrhosis-induced CAD may be associated with impaired autonomic efferent functions within the homeostatic reflex arc that regulates cardiac functions. Full article
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Figure 1
<p>Design of the experiments. Rats were allocated into three groups: sham-control (n = 20), CBDL (n = 20), and TAA (n = 20). Body weight and hemodynamic parameters were measured in the control and cirrhotic rats three weeks post-sham-operation or post-CBDL, and six weeks post-saline or TAA injections. Subsequent to hemodynamic assessment, liver histology and blood analysis were conducted. HRV was evaluated in six rats per group via ECG recordings to confirm the development of CAD. Following ECG recording, liver tissues were visually inspected, and SG and ICG were harvested for the dissociation of individual neurons for electrophysiological measurements and single-cell RT-PCR. This protocol was also followed for rats in each group not utilized for hemodynamics and HRV assessments.</p>
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<p>Power spectral analysis of HRV in normal and cirrhotic rats. Representative traces show the power spectral densities (PSDs) of various frequency components calculated from the R-R interval variability using the fast Fourier transform algorithm in sham (<b>A</b>), CBDL (<b>B</b>), and TAA rats (<b>C</b>). (<b>D</b>) Summary of the LF/HF power ratio in normal and cirrhotic rats. Total power densities were calculated within the frequency range of 0 to 3 Hz. LF and HF powers were defined as the area under the curve in the frequency ranges of 0.04–1.0 Hz and 1.0–3.0 Hz for rats, respectively. Data are presented as the mean ± SEM. The number of experiments is indicated in parentheses. ** <span class="html-italic">p</span> &lt; 0.01 compared with normal rats.</p>
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<p>Cirrhosis-induced alterations in the excitability of SG and ICG neurons. Representative traces of AP discharges in response to depolarizing current steps to 1, 2, and 3 times-threshold (1×, 2×, and 3× Th) for 1 s in (<b>A</b>) SG, (<b>C</b>) ICG neurons from the sham, CBDL, and TAA rats. Each neuron was depolarized from a resting membrane potential between −51 and −56 mV. All recordings were performed under the gramicidin-perforated configuration of the whole-cell current-clamp technique. (<b>B</b>,<b>D</b>) Summary of the number of spikes per second measured respectively in SG and ICG neurons in the sham, CBDL, and TAA rats. Data are presented as the mean ± SEM. The number of neurons tested is indicated in parentheses. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 compared with the sham-operated rats.</p>
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<p>Downregulation of A-type K<sup>+</sup> currents in the SG neurons of cirrhotic rats. (<b>A</b>) Representative traces of the total, delayed rectifier (K<sub>DR</sub>), and A-type (K<sub>A</sub>) K<sup>+</sup> currents recorded in the SG neurons of the sham-operated, CBDL, and TAA rats. Total outward K<sup>+</sup> (K<sub>VTotal</sub>) and K<sub>DR</sub> currents were elicited by 1-s depolarizing pulses ranging from −50 mV to +20 mV, starting from holding potentials of −100 mV and −60 mV, respectively. K<sub>A</sub> current traces were derived by subtracting the K<sub>DR</sub> current from the K<sub>VTotal</sub> currents. (<b>B</b>) Summary of the K<sub>DR</sub> and K<sub>A</sub> current densities measured at −20 mV in the SG neurons of the sham, CBDL, and TAA rats. (<b>C</b>) Summary of the relative expression of the transcripts encoding Kv4.1, Kv4.2, and Kv4.3 in the SG neurons of the sham, CBDL, and TAA rats. Data are presented as the mean ± SEM. The number of neurons tested is indicated in parentheses. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 compared with the sham rats.</p>
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<p>Differential regulation of K<sub>M</sub> channels in cardiac efferent neurons of cirrhotic rats. (<b>A</b>) Representative K<sub>M</sub> current traces are recorded in the SG and ICG neurons of the sham-operated, CBDL, and TAA rats. K<sub>M</sub> currents were deactivated by a 500 ms test pulse to −60 mV from a holding potential of −30 mV (inset shows the pulse protocol). (<b>B</b>) Summary of the K<sub>M</sub> current densities in the SG and ICG neurons of the sham, CBDL, and TAA rats. (<b>C</b>) Summary of the relative expression of transcripts encoding KCNQ2 and KCNQ3 in the SG and ICG neurons of the sham, CBDL, and TAA rats. Data are presented as the mean ± SEM. The number of neurons tested is indicated in parentheses. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 compared with the sham rats.</p>
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<p>Regulation of AP firing by the inhibition of VDCCs in normal SG and ICG neurons and downregulation of the transcripts encoding N- and L-type Ca<sup>2+</sup> channel isoforms in the SG and ICG neurons of cirrhotic rats. (<b>A</b>) Effects of various VDCCs blockers on AP firing in SG and ICG neurons of normal rats. CdCl<sub>2</sub> (0.1 mM), a non-specific VDCC blocker, ω-conotoxin GVIA (1 µM), an N-type Ca<sup>2+</sup> channel blocker, and nimodipine (10 µM), an L-type Ca<sup>2+</sup> channel blocker were bath applied. Each neuron was depolarized from a resting membrane potential (SG neuron: −52 mV and ICG neuron: −54 mV). All recordings were performed under the gramicidin-perforated configuration of the whole-cell current-clamp technique. (<b>B</b>,<b>C</b>) Relative expression of the transcripts encoding N-type (α1B) and L-type (α1C and α1D) VDCCs, normalized to the β-actin transcript. Data are presented as the mean ± SEM. The number of neurons tested is indicated in parentheses. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 compared with the sham rats.</p>
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<p>Downregulation of L− and N−type Ca<sup>2+</sup> channels in the ICG neurons of cirrhotic rats. (<b>A</b>) Representative traces of Ca<sup>2+</sup> currents evoked by depolarizing voltage steps ranging from −60 mV to +50 mV from a holding potential of −80 mV (inset shows the pulse protocol). (<b>B</b>) Current–voltage relationships of Ca<sup>2+</sup> channel currents. (<b>C</b>) Summary of the peak Ca<sup>2+</sup> channel currents measured at +10 mV. (<b>D</b>) Summary of the relative contributions (% of total currents) of nifedipine-sensitive L-type and ω-conotoxin GVIA-sensitive N-type currents to the total Ca<sup>2+</sup> currents in the ICG neurons of the sham, CBDL, and TAA rats. Data are presented as the mean ± SEM. The number of neurons tested is indicated in parentheses. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 compared with the sham rats.</p>
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9 pages, 221 KiB  
Article
Impaired Modulation of the Autonomic Nervous System in Adult Patients with Major Depressive Disorder
by Elise Böttcher, Lisa Sofie Schreiber, David Wozniak, Erik Scheller, Frank M. Schmidt and Johann Otto Pelz
Biomedicines 2024, 12(6), 1268; https://doi.org/10.3390/biomedicines12061268 - 6 Jun 2024
Cited by 1 | Viewed by 1196
Abstract
Patients with major depressive disorder (MDD) have an increased risk for cardiac events. This is partly attributed to a disbalance of the autonomic nervous system (ANS) indicated by a reduced vagal tone and a (relative) sympathetic hyperactivity. However, in most studies, heart rate [...] Read more.
Patients with major depressive disorder (MDD) have an increased risk for cardiac events. This is partly attributed to a disbalance of the autonomic nervous system (ANS) indicated by a reduced vagal tone and a (relative) sympathetic hyperactivity. However, in most studies, heart rate variability (HRV) was only examined while resting. So far, it remains unclear whether the dysbalance of the ANS in patients with MDD is restricted to resting or whether it is also evident during sympathetic and parasympathetic activation. The aim of this study was to compare the responses of the ANS to challenges that stimulated the sympathetic and, respectively, the parasympathetic nervous systems in patients with MDD. Forty-six patients with MDD (female 27 (58.7%), mean age 44 ± 17 years) and 46 healthy controls (female 26 (56.5%), mean age 44 ± 20 years) underwent measurement of time- and frequency-dependent domains of HRV at rest, while standing (sympathetic challenge), and during slow-paced breathing (SPB, vagal, i.e., parasympathetic challenge). Patients with MDD showed a higher heart rate, a reduced HRV, and a diminished vagal tone during resting, standing, and SPB compared to controls. Patients with MDD and controls responded similarly to sympathetic and vagal activation. However, the extent of modulation of the ANS was impaired in patients with MDD, who showed a reduced decrease in the vagal tone but also a reduced increase in sympathetic activity when switching from resting to standing. Assessing changes in the ANS during sympathetic and vagal activation via respective challenges might serve as a future biomarker and help to allocate patients with MDD to therapies like HRV biofeedback and psychotherapy that were recently found to modulate the vagal tone. Full article
22 pages, 3436 KiB  
Article
The Action Potential Clamp Technique as a Tool for Risk Stratification of Sinus Bradycardia Due to Loss-of-Function Mutations in HCN4: An In Silico Exploration Based on In Vitro and In Vivo Data
by Arie O. Verkerk and Ronald Wilders
Biomedicines 2023, 11(9), 2447; https://doi.org/10.3390/biomedicines11092447 - 2 Sep 2023
Cited by 3 | Viewed by 2076
Abstract
These days, in vitro functional analysis of gene variants is becoming increasingly important for risk stratification of cardiac ion channelopathies. So far, such risk stratification has been applied to SCN5A, KCNQ1, and KCNH2 gene variants associated with Brugada syndrome and long [...] Read more.
These days, in vitro functional analysis of gene variants is becoming increasingly important for risk stratification of cardiac ion channelopathies. So far, such risk stratification has been applied to SCN5A, KCNQ1, and KCNH2 gene variants associated with Brugada syndrome and long QT syndrome types 1 and 2, respectively, but risk stratification of HCN4 gene variants related to sick sinus syndrome has not yet been performed. HCN4 is the gene responsible for the hyperpolarization-activated ‘funny’ current If, which is an important modulator of the spontaneous diastolic depolarization underlying the sinus node pacemaker activity. In the present study, we carried out a risk classification assay on those loss-of-function mutations in HCN4 for which in vivo as well as in vitro data have been published. We used the in vitro data to compute the charge carried by If (Qf) during the diastolic depolarization phase of a prerecorded human sinus node action potential waveform and assessed the extent to which this Qf predicts (1) the beating rate of the comprehensive Fabbri–Severi model of a human sinus node cell with mutation-induced changes in If and (2) the heart rate observed in patients carrying the associated mutation in HCN4. The beating rate of the model cell showed a very strong correlation with Qf from the simulated action potential clamp experiments (R2 = 0.95 under vagal tone). The clinically observed minimum or resting heart rates showed a strong correlation with Qf (R2 = 0.73 and R2 = 0.71, respectively). While a translational perspective remains to be seen, we conclude that action potential clamp on transfected cells, without the need for further voltage clamp experiments and data analysis to determine individual biophysical parameters of If, is a promising tool for risk stratification of sinus bradycardia due to loss-of-function mutations in HCN4. In combination with an If blocker, this tool may also prove useful when applied to human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) obtained from mutation carriers and non-carriers. Full article
(This article belongs to the Special Issue Mechanisms and Novel Therapeutic Approaches for Cardiac Arrhythmia)
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Graphical abstract

Graphical abstract
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<p>Schematic topology of the <span class="html-italic">HCN4</span> protein and the set of loss-of-function mutations in <span class="html-italic">HCN4</span> associated with familial sinus bradycardia for which both clinical and in vitro data were available, requiring that these clinical data include quantitative heart rate data from at least two mutation carriers. Tetramers of <span class="html-italic">HCN4</span> α-subunits form the cardiac ion channels that conduct the hyperpolarization-activated ‘funny’ current (I<sub>f</sub>). The <span class="html-italic">HCN4</span> protein has six transmembrane segments (S1–S6), a pore-forming loop (P), and intracellular N- and C-termini. The voltage sensor of the channel is formed by the positively charged S4 helix. The C-terminus contains the C-linker (dotted line) and the cyclic nucleotide-binding domain (CNBD), which is known to mediate cyclic AMP (cAMP)-dependent changes in HCN channel gating. Colored dots indicate the location of the loss-of-function mutations in the <span class="html-italic">HCN4</span> protein of the present study. This set of mutations includes eleven substitutions (R375C, R378C, A414G, G480R, Y481H, G482R, A485V, K530N, R550C, R666Q, and S672R) and one truncation (695X).</p>
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<p>Voltage dependence of wild type (WT; solid blue lines) and heteromeric R375C mutant (WT + R375C; orange dotted lines) <span class="html-italic">HCN4</span> current (de)activation. (<b>A</b>) Steady-state activation (y<sub>∞</sub>). Horizontal arrow: the mutation-induced hyperpolarizing shift in half-maximum activation voltage. Vertical arrow: the mutation-induced decrease in maximally available <span class="html-italic">HCN4</span> current. (<b>B</b>) Time constant of (de)activation (τ<sub>y</sub>). Horizontal arrow: the mutation-induced hyperpolarizing shift in the bell-shaped curve. Upward vertical arrow: the mutation-induced decrease in the rate of (de)activation at highly negative membrane potentials. Downward vertical arrow: the mutation-induced increase in the rate of (de)activation at less negative membrane potentials.</p>
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<p>Charge carried by I<sub>f</sub> during diastolic depolarization. (<b>A</b>) Prerecorded AP waveform of an isolated human sinus node pacemaker cell. During the diastolic depolarization from the maximum diastolic potential (MDP) to the take-off potential (TOP), which takes 538 ms, the membrane potential (V<sub>m</sub>) depolarizes by 23 mV. (<b>B</b>) Associated reconstructed WT I<sub>f</sub>, which carries a charge of 1.00 pC (filled area) as an inward current during diastolic depolarization. (<b>C</b>) Associated reconstructed WT + R375C I<sub>f</sub>, which carries a charge of 0.20 pC during diastolic depolarization. The AP waveform of panel A is a typical waveform obtained from a set of single isolated human SAN pacemaker cells [<a href="#B61-biomedicines-11-02447" class="html-bibr">61</a>], and the I<sub>f</sub> curve of panel B is reconstructed from this typical AP waveform and the I<sub>f</sub> equations of the Fabbri–Severi model [<a href="#B62-biomedicines-11-02447" class="html-bibr">62</a>], which are based on the I<sub>f</sub> data obtained in voltage clamp experiments on the same set of single-isolated human SAN pacemaker cells [<a href="#B61-biomedicines-11-02447" class="html-bibr">61</a>,<a href="#B63-biomedicines-11-02447" class="html-bibr">63</a>].</p>
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<p>Electrical activity of the Fabbri–Severi model of a human SAN pacemaker cell with its default ‘wild-type’ I<sub>f</sub> (WT; solid blue lines) and heteromeric R375C mutant I<sub>f</sub> (WT + R375C; orange dotted lines) at different levels of autonomic tone. (<b>A</b>) Vagal tone (simulated ACh concentration of 20 nmol/L). (<b>B</b>) No rate modulation (default model). (<b>C</b>) β-Adrenergic tone (‘High Iso’ settings of the model).</p>
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<p>The beating rate of the Fabbri–Severi model of a human SAN pacemaker cell with its default ‘wild-type’ I<sub>f</sub> (WT) and heteromeric mutant I<sub>f</sub>, simulated with the settings presented in <a href="#sec3dot2-biomedicines-11-02447" class="html-sec">Section 3.2</a> as a function of Q<sub>f</sub> (<a href="#sec3dot3-biomedicines-11-02447" class="html-sec">Section 3.3</a>) at different levels of autonomic tone. <sup>a</sup> I<sub>f</sub> parameters are based on Milano et al. [<a href="#B71-biomedicines-11-02447" class="html-bibr">71</a>]. <sup>b</sup> I<sub>f</sub> parameters are based on Schweizer et al. [<a href="#B74-biomedicines-11-02447" class="html-bibr">74</a>]. Dashed lines are linear fits.</p>
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<p>Minimum, average, and maximum heart rates obtained during 24 h Holter recordings from heterozygous carriers of the mutations in <span class="html-italic">HCN4</span> as indicated or from non-carriers of the same family (<a href="#biomedicines-11-02447-t001" class="html-table">Table 1</a>) as a function of Q<sub>f</sub> (<a href="#sec3dot3-biomedicines-11-02447" class="html-sec">Section 3.3</a>). <sup>a</sup> I<sub>f</sub> parameters are based on Milano et al. [<a href="#B71-biomedicines-11-02447" class="html-bibr">71</a>]. <sup>b</sup> I<sub>f</sub> parameters are based on Schweizer et al. [<a href="#B74-biomedicines-11-02447" class="html-bibr">74</a>]. Dashed lines are linear fits.</p>
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<p>(<b>A</b>) Resting heart rates and (<b>B</b>) maximum heart rates during exercise testing from heterozygous carriers of the mutations in <span class="html-italic">HCN4</span> as indicated or from non-carriers of the same family (<a href="#biomedicines-11-02447-t002" class="html-table">Table 2</a>) as a function of Q<sub>f</sub> (<a href="#sec3dot3-biomedicines-11-02447" class="html-sec">Section 3.3</a>). Dashed lines are linear fits.</p>
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18 pages, 343 KiB  
Review
Sympathetic Modulation in Cardiac Arrhythmias: Where We Stand and Where We Go
by Wei-Hsin Chung, Yen-Nien Lin, Mei-Yao Wu and Kuan-Cheng Chang
J. Pers. Med. 2023, 13(5), 786; https://doi.org/10.3390/jpm13050786 - 1 May 2023
Cited by 2 | Viewed by 2546
Abstract
The nuance of autonomic cardiac control has been studied for more than 400 years, yet little is understood. This review aimed to provide a comprehensive overview of the current understanding, clinical implications, and ongoing studies of cardiac sympathetic modulation and its anti-ventricular arrhythmias’ [...] Read more.
The nuance of autonomic cardiac control has been studied for more than 400 years, yet little is understood. This review aimed to provide a comprehensive overview of the current understanding, clinical implications, and ongoing studies of cardiac sympathetic modulation and its anti-ventricular arrhythmias’ therapeutic potential. Molecular-level studies and clinical studies were reviewed to elucidate the gaps in knowledge and the possible future directions for these strategies to be translated into the clinical setting. Imbalanced sympathoexcitation and parasympathetic withdrawal destabilize cardiac electrophysiology and confer the development of ventricular arrhythmias. Therefore, the current strategy for rebalancing the autonomic system includes attenuating sympathoexcitation and increasing vagal tone. Multilevel targets of the cardiac neuraxis exist, and some have emerged as promising antiarrhythmic strategies. These interventions include pharmacological blockade, permanent cardiac sympathetic denervation, temporal cardiac sympathetic denervation, etc. The gold standard approach, however, has not been known. Although neuromodulatory strategies have been shown to be highly effective in several acute animal studies with very promising results, the individual and interspecies variation between human autonomic systems limits the progress in this young field. There is, however, still much room to refine the current neuromodulation therapy to meet the unmet need for life-threatening ventricular arrhythmias. Full article
(This article belongs to the Special Issue The Challenges and Prospects in Cardiology)
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11 pages, 3854 KiB  
Case Report
Cartilaginous Intrusion of the Atrioventricular Node in a Quarter Horse with a High Burden of Second-Degree AV Block and Collapse: A Case Report
by Sarah Dalgas Nissen, Arnela Saljic, Sofie Troest Kjeldsen, Thomas Jespersen, Charlotte Hopster-Iversen and Rikke Buhl
Animals 2022, 12(21), 2915; https://doi.org/10.3390/ani12212915 - 24 Oct 2022
Cited by 4 | Viewed by 2351
Abstract
Second-degree atrioventricular (AV) block is the most common cardiac arrhythmia in horses, affecting 40–90% depending on breed. Usually, the AV blocks occur while the horses are resting and disappear upon exercise and are, therefore, considered to be uneventful for horses. However, if the [...] Read more.
Second-degree atrioventricular (AV) block is the most common cardiac arrhythmia in horses, affecting 40–90% depending on breed. Usually, the AV blocks occur while the horses are resting and disappear upon exercise and are, therefore, considered to be uneventful for horses. However, if the AV blocks occur frequently, this may result in syncope and collapse. Identifying the cause of second-degree AV block is difficult and often subscribed to high vagal tone. In this report, we present an eight-year-old Quarter horse with a high burden of second-degree AV blocks and multiple collapses. The clinical examination, including neurological examination, blood analysis, 24-h ECG recording and cardiac echocardiography, did not reveal any signs of general or cardiovascular disease besides a high burden of second-degree AV blocks (~300 blocks per hour) and a hyperechoic area in the AV nodal region. An implantable loop recorder (ILR) was inserted to monitor the cardiac rhythm. The ILR detected several consecutive second-degree AV blocks and pauses above 5 s. However, unfortunately, no recordings were available during the collapses. Eventually, the horse was euthanized and the heart inspected. The aortic root was severely cartilaginous and appeared to penetrate the AV node, especially in the His bundle region, possibly explaining the hampered AV conduction. Nevertheless, it is still uncertain if the AV nodal disruption caused the collapses and more knowledge on AV nodal diseases in horses is warranted. Full article
(This article belongs to the Special Issue Latest Advancements in Equine Cardiology)
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Figure 1
<p>Resting electrocardiogram. Top: Representative electrocardiographic (ECG) strip of four minutes’ continuous recording from the 24-h resting ECG recording. Several second-degree AV blocks were present throughout most of the ECG recording often in patterns of 4:3 in P to QRS ratio. Red lines indicate post AV block beats. Bottom: The PR interval (black clamps) varied in duration prior to AV block most often showing progressive prolongation of the PR interval corresponding to the Mobitz type I block seen in humans. AV: Atrioventricular.</p>
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<p>Echocardiogram. Right parasternal, long-axis, four-chamber view of the heart with focus on left atrium. Arrow highlights hyperechogenic zone in the proximal interventricular region (AV nodal area). AV: Atrioventricular, LA: Left atrium, LV: Left ventricle, RA: Right atrium, RV: Right ventricle.</p>
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<p>ECG from the implantable loop recorder. Several episodes were detected as pauses by the implantable loop recorder. All stored ECGs from the loop revealed several second-degree AV blocks. Often, two consecutive P waves were blocked. The amplitude of the P waves was very low and is, therefore, pointed out by arrows. The P waves are more readily visible directly in the programmer used to investigate with the loop recorder in order to extract data. Unfortunately, data were only printed on pdf files and no data were stored on the programmer; therefore, quality and amplitude are low. The above representative is a continuous recording sampled by the loop one afternoon in October 2019. VS: ventricular sensing.</p>
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<p>Tissue sample of the atrioventricular node and His bundle. (<b>Left</b>): Representative images of transvers sectioning of the AV nodal region from the case and a healthy horse. The very prominent cartilaginous aortic root was already visible macroscopically. (<b>Middle</b>): Sirius red histology of the AV node when it transits through the CFB corresponding to the His bundle. Red is collagen whereas yellow is cardiomyocytes. The black encircled area is the His bundle. White areas within the tissue are artifacts induced by freezing of the tissue. (<b>Right</b>): Magnified view of the His bundle. Note the very compact bundle and the large cartilaginous part of the AoR in the case horse. AM: Atrial myocardium, AoR: Aortic root, CFB: Central fibrous body, VM: Ventricular myocardium.</p>
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10 pages, 1062 KiB  
Article
Effect of Algorithmic Music Listening on Cardiac Autonomic Nervous System Activity: An Exploratory, Randomized Crossover Study
by Alfredo Raglio, Roberto Maestri, Elena Robbi, Antonia Pierobon, Maria Teresa La Rovere and Gian Domenico Pinna
J. Clin. Med. 2022, 11(19), 5738; https://doi.org/10.3390/jcm11195738 - 28 Sep 2022
Cited by 3 | Viewed by 1780
Abstract
It is proven that music listening can have a therapeutic impact in many clinical fields. However, to assume a curative value, musical stimuli should have a therapeutic logic. This study aimed at assessing short-term effects of algorithmic music on cardiac autonomic nervous system [...] Read more.
It is proven that music listening can have a therapeutic impact in many clinical fields. However, to assume a curative value, musical stimuli should have a therapeutic logic. This study aimed at assessing short-term effects of algorithmic music on cardiac autonomic nervous system activity. Twenty-two healthy subjects underwent a crossover study including random listening to relaxing and activating algorithmic music. Electrocardiogram (ECG) and non-invasive arterial blood pressure were continuously recorded and were later analyzed to measure Heart Rate (HR) mean, HR variability and baroreflex sensitivity (BRS). Statistical analysis was performed using a general linear model, testing for carryover, period and treatment effects. Relaxing tracks decreased HR and increased root mean square of successive squared differences of normal-to-normal (NN) intervals, proportion of interval differences of successive NN intervals greater than 50 ms, low-frequency (LF) and high-frequency (HF) power and BRS. Activating tracks caused almost no change or an opposite effect in the same variables. The difference between the effects of the two stimuli was statistically significant in all these variables. No difference was found in the standard deviation of normal-to-normal RR intervals, LFpower in normalized units and LFpower/HFpower variables. The study suggests that algorithmic relaxing music increases cardiac vagal modulation and tone. These results open interesting perspectives in various clinical areas. Full article
(This article belongs to the Section Mental Health)
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<p>Algorithmic Music (creation process).</p>
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<p>Schematic diagram of the experimental design of the study. Each recording subsection (baseline, stimulation, recovery) lasted 5 min. Act = activating; Rel = relaxing.</p>
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15 pages, 1948 KiB  
Article
Association of Cardiac Autonomic Responses with Clinical Outcomes of Myasthenia Gravis: Short-Term Analysis of the Heart-Rate and Blood Pressure Variability
by Monika Zawadka-Kunikowska, Łukasz Rzepiński, Małgorzata Tafil-Klawe, Jacek J. Klawe, Paweł Zalewski and Joanna Słomko
J. Clin. Med. 2022, 11(13), 3697; https://doi.org/10.3390/jcm11133697 - 27 Jun 2022
Cited by 7 | Viewed by 2361
Abstract
Introduction: The aim of the study was to assess cardiac and autonomic function in patients with myasthenia gravis (MG) and to explore its relationship with disease outcomes. Methods: Thirty-eight patients with an MG were enrolled (median age 40.5 years; median disease duration 5.5 [...] Read more.
Introduction: The aim of the study was to assess cardiac and autonomic function in patients with myasthenia gravis (MG) and to explore its relationship with disease outcomes. Methods: Thirty-eight patients with an MG were enrolled (median age 40.5 years; median disease duration 5.5 years). Cardiovascular parameters, baroreflex sensitivity (BRS), spectral indices of short-term heart rate (HRV), and systolic blood pressure variability (SBPV) were compared with age- and gender-matched controls (n = 30). Cardiac autonomic function was assessed during the response to standing (tilt) and deep breathing tests (expiration/inspiration ratio-E/I). Results: HR and BP responses to the tilt test were similar in both groups. MG patients, as compared to controls, were characterized by altered SBPV at rest, significantly reduced HR response to the deep breathing test (p < 0.001), increased sympathovagal balance after tilt (delta LF/HF-RRI, p = 0.037), and lower values of BRS (p = 0.007) and hemodynamic parameters, i.e., cardiac index, index contractility, left ventricular work index, at rest and during tilt. There was no association between disease duration and autonomic parameters. Disease severity, as determined by MGFA (Myasthenia Gravis Foundation of America) corrected for age and sex, was an independent predictor of diminished vagal tone (E/I ratio) and increased sympathetic response to tilt (delta LF/HF-RRI) as measured with HRV. Lower BRS was associated with greater disease severity and older age. Hemodynamic parameters were predominantly predicted by age and sex. Conclusion: Our results confirm cardiac autonomic dysfunction among MG patients with predominant parasympathetic impairment. Clinicians should consider evaluation of autonomic balance in MG patients with, or at risk for, cardiovascular disease. Full article
(This article belongs to the Special Issue Update in the Management of Myasthenia Gravis)
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<p>Scatter box plot showing the median, minimum and maximum values of CI, cardiac index (<b>A</b>); EDI, end-diastolic index (<b>B</b>); IC, index of contractility (<b>C</b>); LVWI, left ventricular work index (<b>D</b>); TFC, thoracic fluid content (<b>E</b>); TPRI, total peripheral resistance index (<b>F</b>); BRS, baroreflex sensitivity (<b>G</b>); E/I-ratio, expiration/inspiration ratio (<b>H</b>); (<b>I</b>) HF-sBP, high frequency of systolic blood pressure variability; LF/HF-sBP, the ratio between low and high band for systolic blood pressure variability (<b>J</b>) in MG group; respectively for compared to HCs.</p>
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<p>Scatter box plot showing the median, minimum and maximum values of CI, cardiac index (<b>A</b>); LVWI, left ventricular work index (<b>B</b>); LF-RRI, low frequency of heart rate variability (<b>C</b>); HF-RRI, high frequency of heart rate variability (<b>D</b>); TFC, thoracic fluid content (<b>E</b>); LF/HF-RRI, ratio between low and high band for heart rate variability (<b>F</b>) in MG group; respectively for compared to HCs.</p>
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18 pages, 979 KiB  
Article
Psychophysiological Regulation and Classroom Climate Influence First and Second Graders’ Well-Being: The Role of Body Mass Index
by Sara Scrimin, Marta Peruzza, Libera Ylenia Mastromatteo and Elisabetta Patron
Eur. J. Investig. Health Psychol. Educ. 2021, 11(4), 1581-1598; https://doi.org/10.3390/ejihpe11040112 - 3 Dec 2021
Cited by 1 | Viewed by 3057
Abstract
This study examines the associations between physical and emotional well-being and classroom climate, cardiac vagal response, and body mass index (BMI) in a sample of 6- to-8-year-olds. Specifically, we expected a direct link between classroom climate, vagal withdrawal, BMI and children’s physical and [...] Read more.
This study examines the associations between physical and emotional well-being and classroom climate, cardiac vagal response, and body mass index (BMI) in a sample of 6- to-8-year-olds. Specifically, we expected a direct link between classroom climate, vagal withdrawal, BMI and children’s physical and emotional comfort. Furthermore, we explored whether these individual and environmental characteristics influenced well-being in an interactive fashion. Participants were 142 (63 boys, 44%) first and second graders living in the North of Italy who were interviewed on their emotional and physical comfort. Heart rate and a measure of vagal influence on the heart (cardiac vagal tone) were recorded at rest and during an oral academic test. Height and weight were collected. Classroom climate was positively linked with physical well-being, whereas emotional well-being was negatively related with BMI. In addition, an inverted U-shaped effect of cardiac vagal withdrawal (i.e., cardiac vagal tone during stress minus resting vagal tone) on emotional well-being was found. Two regression models highlighted the role played by BMI when interacting with vagal withdrawal in predicting children’s physical and emotional well-being. The interplay between BMI and cardiac vagal withdrawal played an important role in primary school children’s well-being. From a clinical perspective, preventive training to improve autonomic regulation in concert with interventions promoting healthy eating attitudes might be critical for supporting primary school children’s emotional and physical health. Full article
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<p>Interaction effect of rMSSD change and BMI on physical comfort (N = 130). <span class="html-italic">Note.</span> The Johnson–Neyman technique identified that rMSSD change had a significant effect on physical well-being only when zBMI was lower than −2.51, that is, when children were in the underweight range, and higher than 3.82 (not applicable to our sample), that is, when children were in the obese range.</p>
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<p>Interaction effects of rMSSD change with BMI Panel (<b>A</b>) and of satisfaction with classroom climate with BMI Panel (<b>B</b>) on emotional comfort (N = 130). <span class="html-italic">Note.</span> Panel (<b>A</b>). The Johnson–Neyman technique identified that rMSSD change had a significant effect on emotional well-being for values of zBMI lower than −3.65 (not applicable to our sample) and higher than −2.15, hence being within a normal range. Panel (<b>B</b>). The Johnson–Neyman technique identified that satisfaction with classroom climate had a significant effect on emotional well-being for values of zBMI lower than −2.57, that is, between thinness and underweightness, and higher than 5.84 (the latter is not applicable to our sample).</p>
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<p>Interaction effects of rMSSD change with BMI Panel (<b>A</b>) and of satisfaction with classroom climate with BMI Panel (<b>B</b>) on emotional comfort (N = 130). <span class="html-italic">Note.</span> Panel (<b>A</b>). The Johnson–Neyman technique identified that rMSSD change had a significant effect on emotional well-being for values of zBMI lower than −3.65 (not applicable to our sample) and higher than −2.15, hence being within a normal range. Panel (<b>B</b>). The Johnson–Neyman technique identified that satisfaction with classroom climate had a significant effect on emotional well-being for values of zBMI lower than −2.57, that is, between thinness and underweightness, and higher than 5.84 (the latter is not applicable to our sample).</p>
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9 pages, 601 KiB  
Article
The Effect of Transcutaneous Vagus Nerve Stimulation in Patients with Polymyalgia Rheumatica
by Jacob Venborg, Anne-Marie Wegeberg, Salome Kristensen, Birgitte Brock, Christina Brock and Mogens Pfeiffer-Jensen
Pharmaceuticals 2021, 14(11), 1166; https://doi.org/10.3390/ph14111166 - 16 Nov 2021
Cited by 7 | Viewed by 2826
Abstract
(1) Polymyalgia rheumatica (PMR) is an inflammatory disease characterised by pain, morning stiffness, and reduced quality of life. Recently, vagus nerve stimulation (VNS) was shown to have anti-inflammatory effects. We aimed to examine the effect of transcutaneous VNS (t-VNS) on PMR. (2) Fifteen [...] Read more.
(1) Polymyalgia rheumatica (PMR) is an inflammatory disease characterised by pain, morning stiffness, and reduced quality of life. Recently, vagus nerve stimulation (VNS) was shown to have anti-inflammatory effects. We aimed to examine the effect of transcutaneous VNS (t-VNS) on PMR. (2) Fifteen treatment-naïve PMR patients completed the study. Patients underwent a 5-day protocol, receiving 2 min of t-VNS stimulation bilaterally on the neck, three times daily. Cardiac vagal tone (CVT) measured on a linear vagal scale (LVS), blood pressure, heart rate, patient-reported outcome, and biochemical changes were assessed. (3) t-VNS induced a 22% increase in CVT at 20 min after initial stimulations compared with baseline (3.4 ± 2.2 LVS vs. 4.1 ± 2.9 LVS, p = 0.02) and was accompanied by a 4 BPM reduction in heart rate (73 ± 11 BPM vs. 69 ± 9, p < 0.01). No long-term effects were observed. Furthermore, t-VNS induced a 14% reduction in the VAS score for the hips at day 5 compared with the baseline (5.1 ± 2.8 vs. 4.4 ± 2.8, p = 0.04). No changes in CRP or proinflammatory analytes were observed. (4) t-VNS modulates the autonomic nervous system in patients with PMR, but further investigation of t-VNS in PMR patients is warranted. Full article
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<p>Raw data points, mean, and 95% CI of selected outcomes.</p>
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16 pages, 1433 KiB  
Review
Angiotensin II and the Cardiac Parasympathetic Nervous System in Hypertension
by Julia Shanks and Rohit Ramchandra
Int. J. Mol. Sci. 2021, 22(22), 12305; https://doi.org/10.3390/ijms222212305 - 14 Nov 2021
Cited by 27 | Viewed by 9287
Abstract
The renin–angiotensin–aldosterone system (RAAS) impacts cardiovascular homeostasis via direct actions on peripheral blood vessels and via modulation of the autonomic nervous system. To date, research has primarily focused on the actions of the RAAS on the sympathetic nervous system. Here, we review the [...] Read more.
The renin–angiotensin–aldosterone system (RAAS) impacts cardiovascular homeostasis via direct actions on peripheral blood vessels and via modulation of the autonomic nervous system. To date, research has primarily focused on the actions of the RAAS on the sympathetic nervous system. Here, we review the critical role of the RAAS on parasympathetic nerve function during normal physiology and its role in cardiovascular disease, focusing on hypertension. Angiotensin (Ang) II receptors are present throughout the parasympathetic nerves and can modulate vagal activity via actions at the level of the nerve endings as well as via the circumventricular organs and as a neuromodulator acting within brain regions. There is tonic inhibition of cardiac vagal tone by endogenous Ang II. We review the actions of Ang II via peripheral nerve endings as well as via central actions on brain regions. We review the evidence that Ang II modulates arterial baroreflex function and examine the pathways via which Ang II can modulate baroreflex control of cardiac vagal drive. Although there is evidence that Ang II can modulate parasympathetic activity and has the potential to contribute to impaired baseline levels and impaired baroreflex control during hypertension, the exact central regions where Ang II acts need further investigation. The beneficial actions of angiotensin receptor blockers in hypertension may be mediated in part via actions on the parasympathetic nervous system. We highlight important unknown questions about the interaction between the RAAS and the parasympathetic nervous system and conclude that this remains an important area where future research is needed. Full article
(This article belongs to the Special Issue Renin-Angiotensin-Aldosterone System in Pathologies)
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<p>Sites of Ang II modulation of the cardiac baroreflex. AT1 receptor is marked with yellow circles. Baroreceptors are marked with dark grey circles.</p>
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<p>Baroreflex signally is altered in hypertension. Altered integration of the afferent baroreflex signal in the brain regions of the NTS and NA, affect heart rate response to baroreflex activation. NTS, nucleus tractus solitarii. DMV, dorsal motor nucleus of the vagus. NA, nucleus ambiguous. RVLM, rostral ventrolateral medulla. CVLM, caudal ventrolateral medulla.</p>
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<p>Ang II contributes to the generation of hypertension through actions on vasculature and the autonomic nervous system. Targeting these pathways may be therapeutically beneficial in the treatment of hypertension.</p>
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8 pages, 251 KiB  
Article
Autonomic Imbalance in Lymphoma Survivors
by Keyla Vargas-Román, Jonathan Cortés-Martín, Juan Carlos Sánchez-García, Raquel Rodríguez-Blanque, Emilia Inmaculada De La Fuente-Solana and Lourdes Díaz-Rodríguez
J. Clin. Med. 2021, 10(19), 4391; https://doi.org/10.3390/jcm10194391 - 26 Sep 2021
Cited by 1 | Viewed by 1803
Abstract
Among the types of blood cancers, non-Hodgkin lymphoma is the most common. The usual treatments for this type of cancer can cause heart failure. A descriptive observational study was conducted that included 16 non-Hodgkin lymphoma survivors and 16 healthy controls matched by age [...] Read more.
Among the types of blood cancers, non-Hodgkin lymphoma is the most common. The usual treatments for this type of cancer can cause heart failure. A descriptive observational study was conducted that included 16 non-Hodgkin lymphoma survivors and 16 healthy controls matched by age and sex. Vagal tone was evaluated in the short term with a three-channel Holter device, and the time and frequency domains were analyzed following a previously accepted methodology to evaluate cardiac autonomic balance. The results of the analysis revealed that the standard deviation of the NN interval (F = 6.25, p = 0.021) and the square root of the mean of the sum of the differences between NN intervals (F = 9.74, p = 0.004) were significantly higher in healthy subjects than in lymphoma survivors. In the heart rate variability (HRV) index, there were no significant differences between the groups (F = 0.03, p = 0.85), nor in the parameters of the frequency domains LF (F = 1.94, p = 0.17), HF (F = 0.35, p = 0.55), and the ratio LF/HF (F = 3.07, p = 0.09). HRV values were lower in non-Hodgkin lymphoma survivors in the first year after treatment, resulting in autonomic imbalance compared to healthy paired subjects. Full article
(This article belongs to the Section Hematology)
17 pages, 2677 KiB  
Article
Postoperative Stroke after Spinal Anesthesia and Responses of Carotid or Cerebral Blood Flow and Baroreflex Functionality to Spinal Bupivacaine in Rats
by Yan-Yuen Poon, Yueh-Wei Liu, Ya-Hui Huang, Samuel H. H. Chan and Ching-Yi Tsai
Biology 2021, 10(7), 617; https://doi.org/10.3390/biology10070617 - 2 Jul 2021
Cited by 1 | Viewed by 2798
Abstract
Spinal anesthesia is generally accepted as an effective and safe practice. Three rare incidents of postoperative cerebral infarction after surgery under spinal anesthesia prompted us to assess whether spinal bupivacaine may compromise carotid or cerebral blood flow. Postoperative examination after the stroke incident [...] Read more.
Spinal anesthesia is generally accepted as an effective and safe practice. Three rare incidents of postoperative cerebral infarction after surgery under spinal anesthesia prompted us to assess whether spinal bupivacaine may compromise carotid or cerebral blood flow. Postoperative examination after the stroke incident revealed that all three patients shared a common pathology of stenosis or atheromatosis in the carotid or middle cerebral artery. In a companion study using 69 Sprague-Dawley rats, subarachnoid application of bupivacaine elicited an initial (Phase I) reduction in the mean arterial pressure, carotid blood flow (CBF) and baroreflex-mediated sympathetic vasomotor tone, all of which subsequently returned to baseline (Phase II). Whereas heart rate (HR) exhibited sustained reduction, cardiac vagal baroreflex, baroreflex efficiency index (BEI) and tissue perfusion and oxygen in the cerebral cortex remained unaltered. However, in one-third of the rats studied, Phase II gave way to Phase III characterized by secondary hypotension and depressed baroreflex-mediated sympathetic vasomotor tone, along with declined HR, sustained cardiac vagal baroreflex, decreased BEI, reduced CBF and waning tissue perfusion or oxygen in the cerebral cortex. We concluded that carotid and cerebral blood flow can indeed be compromised after spinal anesthesia, and an impaired baroreflex-mediated sympathetic vasomotor tone, which leads to hypotension, plays a contributory role. Full article
(This article belongs to the Section Physiology)
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<p>Experimental setup and animals used in each group in this study.</p>
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<p>(<b>a</b>) Demonstration of lodging of the tip of the catheter (orange arrow) in the subarachnoid space below the middle portion of L6 vertebra. (<b>b</b>) Representative examples of myelographic examination before (1) and after intrathecal administration of four successive doses of contrast medium, given at 40 (2), 60 (3), 80 (4) or 100 (5) μL. Note that all demarcations denote levels of the spinal cord: the lower yellow arrows mark the location of the tip of the catheter, and the upper yellow arrows indicate the highest points reached by the enhanced roentgenological images. CM: conus medullaris. (<b>c</b>) Scattered plots showing the extent of dispersion in the spinal cord of contrast medium on intrathecal administration at 40, 60, 80 or 100 μL. Values are mean ± SEM of seven animals.</p>
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<p>Illustrative examples of real-time and online recording of common phasic changes in mean arterial pressure (MAP), heart rate (HR), power density of the low-frequency component in systolic blood pressure spectrum (BLF), baroreflex sensitivity (BRS) or baroreflex effectiveness index (BEI), simultaneous with carotid blood flow (CBF) in Group 2 animals (<b>a</b>); or concurrent with tissue perfusion (Tissue Flow), tissue oxygen tension (PO<sub>2</sub>) or tissue temperature in the cerebral cortex in Group 3 animals (<b>b</b>) on intrathecal administration of 80 μL of bupivacaine (at arrow).</p>
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<p>Common response patterns of MAP, HR, BLF, BRS and CBF or tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex to intrathecal administration of 80 μL of bupivacaine. Note that values for MAP, HR, BLF and BRS are mean ± SEM of 33 animals (17 from Group 2 plus 16 from Group 3); values for CBF are mean ± SEM of 17 animals from Group 2; and values for tissue perfusion PO<sub>2</sub> or temperature in the cerebral cortex are mean ± SEM of 16 animals from Group 3. * <span class="html-italic">p</span> &lt; 0.05 versus data obtained under basal conditions in the post hoc Dunnett multiple-range analysis; <sup>+</sup> <span class="html-italic">p</span> &lt; 0.05 versus data obtained during Phase I in the post hoc Tukey multiple-range analysis.</p>
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<p>Common (<b>a</b>) and anomalous (<b>b</b>) response patterns of BEI to intrathecal administration of 80 μL of bupivacaine. Values for (<b>a</b>) are mean ± SEM from 33 animals (17 from Group 2 plus 16 from Group 3); and values for (<b>b</b>) are mean ± SEM of 15 animals (7 from Group 2 plus 8 from Group 3). * <span class="html-italic">p</span> &lt; 0.05 versus data obtained under basal conditions in the post hoc Dunnett multiple-range analysis. (<b>c</b>) Insignificant changes of BEI under isoflurane alone without spinal anesthesia. Values are mean ± SEM of 14 animals from Group 4. No significance among all groups (<span class="html-italic">p</span> &gt; 0.05).</p>
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<p>Zoomed-in view of 40 min of real-time recording from <a href="#biology-10-00617-f002" class="html-fig">Figure 2</a>a of Phase I changes in MAP, BLF and CBF on intrathecal administration of 80 μL of bupivacaine (at arrow). Note that the red and green dotted lines denote time points at which reduction of BLF power and MAP or CBF commenced.</p>
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<p>Illustrative examples of real-time and online recording of anomalous phasic changes in MAP, HR, BLF, BRS or BEI, simultaneous with CBF in Group 2 animals (<b>a</b>); or concurrent with tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex in Group 3 animals (<b>b</b>) with intrathecal administration of 80 μL of bupivacaine (at arrow).</p>
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<p>Anomalous response patterns of MAP, HR, BLF, BRS and CBF or tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex to intrathecal administration of 80 μL of bupivacaine. Note that values for MAP, HR, BLF and BRS are mean ± SEM of 15 animals (7 from Group 2 plus 8 from Group 3); values for CBF are mean ± SEM of 7 animals from Group 2; and values for tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex are mean ± SEM of 8 animals from Group 3. * <span class="html-italic">p</span> &lt; 0.05 versus data obtained under basal conditions in the post hoc Dunnett multiple-range analysis; + <span class="html-italic">p</span> &lt; 0.05 versus data obtained during Phase I in the post hoc Tukey multiple-range analysis.</p>
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<p>Insignificant changes of MAP, HR, BLF, BRS and CBF or tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex under 1.5% isoflurane anesthesia alone. Note values for MAP, HR, BLF and BRS are mean ± SEM of 14 animals (7 from Group 4 CBF experiments plus 7 from Group 4 tissue perfusion experiments); values for CBF are mean ± SEM of 7 animals; and values for tissue perfusion, PO<sub>2</sub> or temperature in the cerebral cortex are mean ± SEM of 7 animals. No significance among all groups (<span class="html-italic">p</span> &gt; 0.05).</p>
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14 pages, 629 KiB  
Article
Influence of Heart Rate Variability on Abstinence-Related Changes in Brain State in Everyday Drinkers
by Hope Peterson, Rhiannon E. Mayhugh, Mohsen Bahrami, Walter Jack Rejeski, Sean L. Simpson, Keri Heilman, Stephen W. Porges and Paul J. Laurienti
Brain Sci. 2021, 11(6), 817; https://doi.org/10.3390/brainsci11060817 - 20 Jun 2021
Cited by 5 | Viewed by 3391 | Correction
Abstract
Alcohol consumption is now common practice worldwide, and functional brain networks are beginning to reveal the complex interactions observed with alcohol consumption and abstinence. The autonomic nervous system (ANS) has a well-documented relationship with alcohol use, and a growing body of research is [...] Read more.
Alcohol consumption is now common practice worldwide, and functional brain networks are beginning to reveal the complex interactions observed with alcohol consumption and abstinence. The autonomic nervous system (ANS) has a well-documented relationship with alcohol use, and a growing body of research is finding links between the ANS and functional brain networks. This study recruited everyday drinkers in an effort to uncover the relationship between alcohol abstinence, ANS function, and whole brain functional brain networks. Participants (n = 29), 24–60 years-of-age, consumed moderate levels of alcohol regularly (males 2.4 (±0.26) drinks/day, females 2.3 (±0.96) drinks/day). ANS function, specifically cardiac vagal tone, was assessed using the Porges-Bohrer method for calculating respiratory sinus arrhythmia (PBRSA). Functional brain networks were generated from resting-state MRI scans obtained following 3-day periods of typical consumption and abstinence. A multi-task mixed-effects regression model determined the influences of HRV and drinking state on functional network connectivity. Results showed differences in the relationship between the strength of network connections and clustering coefficients across drinking states, moderated by PBRSA. Increases in connection strength between highly clustered nodes during abstinence as PBRSA increases demonstrates a greater possible range of topological configurations at high PBRSA values. This novel finding begins to shed light on the complex interactions between typical alcohol abstinence and physiological responses of the central and autonomic nervous system. Full article
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<p>The bars capture the slope of the relationship between clustering coefficient and connection strength, across drinking states and as PB<sub>RSA</sub> increases. Numbers above the bar are slope values, and numbers in parentheses are standard error. At lower RSA values, there is minimal difference in the relationship between drinking states, whereas at higher PB<sub>RSA</sub> values, there is a much larger change in the slope of the relationship between clustering and strength.</p>
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<p>(Trending only). The bars capture the slope of the relationship between global efficiency and connection strength, across drinking states and as PB<sub>RSA</sub> increases. Numbers above the bar are slope values, and numbers in parenthesis are standard error. At both the upper and lower bounds of PB<sub>RSA</sub>, the relationship between global efficiency and strength was steeper during normal drinking. At lower PB<sub>RSA</sub> values, the slope decreased minimally during abstinence, whereas at higher PB<sub>RSA</sub> values, the slope decreased to a more significant degree following abstinence.</p>
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12 pages, 580 KiB  
Article
Heart Rate Variability Responses to a Training Cycle in Female Youth Rowers
by Rohan Edmonds, Julian Egan-Shuttler and Stephen J. Ives
Int. J. Environ. Res. Public Health 2020, 17(22), 8391; https://doi.org/10.3390/ijerph17228391 - 13 Nov 2020
Cited by 4 | Viewed by 2803
Abstract
Heart rate variability (HRV) is a reputable estimate of cardiac autonomic function used across multiple athletic populations to document the cardiac autonomic responses to sport demands. However, there is a knowledge gap of HRV responses in female youth rowers. Thus, the purpose of [...] Read more.
Heart rate variability (HRV) is a reputable estimate of cardiac autonomic function used across multiple athletic populations to document the cardiac autonomic responses to sport demands. However, there is a knowledge gap of HRV responses in female youth rowers. Thus, the purpose of this study was to measure HRV weekly, over a 15-week training period, covering pre-season and up to competition in youth female rowers, in order to understand the physiological response to long-term training and discern how fluctuations in HRV may relate to performance in this population. Measures of heart rate and heart rate variability were recorded before training each Friday over the monitoring period in seven athletes. Analysis of heart rate variability focused on time domain indices, the standard deviation of all normal to normal R–R wave intervals, and the root mean square of successive differences as markers of cardiac parasympathetic modulation. Training load was quantified by multiplying the rating of perceived exertion of the weeks training and training duration. A decrease was identified in cardiac parasympathetic modulation as the season progressed (Effect Size (Cohen’s d) = −0.34 to −0.8, weeks 6 and 11–15), despite no significant relationship between training load and heart rate variability. Factors outside of training may further compound the reduction in heart rate variability, with further monitoring of external stressors (e.g., school) in adolescent athletes. Full article
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<p>Changes from baseline over the 15-week monitoring period for (<b>A</b>) training load, (<b>B</b>) mean heart rate, (<b>C</b>) root mean square of successive RR interval differences (RMSSD), and (<b>D</b>) the standard deviation of all normal to normal RR intervals (SDNN). Data are presented as means ± SD, with dashed lines representing the positive and negative percentage smallest worthwhile change (%SWC, 3%) from baseline [<a href="#B31-ijerph-17-08391" class="html-bibr">31</a>]. a indicates possibly lower compared to baseline. b indicates likely lower compared to baseline. c indicates likely higher compared to baseline. d indicates very likely lower compared to baseline. e indicates very likely higher compared to baseline. * indicates likely higher compared to week 12. # indicates very likely higher compared to week 12.</p>
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