Die mittlere Höhe des arteriellen Blutdruckes (AP) ist von zentraler Bedeutung für das kardiovaskuläre Risiko Hochdruckkranker. Zusätzlich zeigen neuere Untersuchungen, daß Änderungen der Blutdruckdynamik eine wichtige Rolle in der Entwicklung hypertonieassoziierten Endorganschäden zukommt. Die Blutdruckvariabilität scheint in diesem Zusammenhang sogar einen eigenständigen Risikofaktor zu bilden. Der Einfluß kurzfristiger Blutdruckschwankungen auf zentrale Mechanismen der Langzeitblutdruckregulation, wie beispielsweise die renale Elimination von Natrium und Wasser, ist weitgehend unbekannt. Unsere Untersuchungen zeigen, daß schnelle Blutdruckschwankungen (BPO) kaum von der renalen Autoregulation der Durchblutung (RBF) unterdrückt werden können und zu Oszillation im Harnzeitvolumen führen. Es ist daher wahrscheinlich, daß BPO intrarenale System der Blutdruckregulation (wie beispielsweise das Renin-Angiotensin-System oder die schubspannungsabhängige Freisetzung von Stickoxid) modulieren können. Um diese Hypothese zu testen wurde der Einfluß von 0,1Hz BPO auf die Entwicklung eines renovaskulären Hypertonus untersucht. BPO um 85mmHg senkten signifikant die Plasmareninaktivität, erhöhten die tägliche Ausscheidung von Wasser, Natrium und Kalium und induzierten einen transienten Anstieg der Nitratspiegel im Urin wobei eine deutliche Senkung des arteriellen Blutdruckes beobachtet wurde. / The average level of arterial blood pressure (AP) is a major determinant of future cardiovascular complications in hypertension. In addition, recent investigations demonstrate that the dynamic properties of BP are of significant importance for the development of hypertension - related end organ damage in patients. Thus, hypertension - related changes in blood pressure dynamics seem to establish an independent risk factor for cardiovascular complications. Little is known regarding the influence of such short - term changes in AP on kidney function, a crucial control element for long - term AP regulation. Our investigations show that fast blood pressure oscillations (BPO) are not effectively buffered by renal blood flow autoregulation and induce oscillations in urine flow. It seems, therefore, likely that AP fluctuations can modulate intrarenally located systems involved in blood pressure regulation (e.g., renin release or shear stress dependent release of endothelium derived nitric oxide). To test this hypothesis we investigated the impact of induced BPO with a frequency of 0.1Hz on the onset of renovascular hypertension. BPO around 85mmHg significantly decreased plasma renin activity, enhanced 24h fluid, sodium and potassium excretion, and induced a transient increase in urinary nitrate excretion, thereby, attenuating renovascular hypertension.

Baroreflex sensitivity (BRS) is often reduced in elderly populations and patients with chronic cardiovascular diseases leading to a concomitant rise in blood pressure variability (BPV) that is associated with increased cardiovascular related morbidity and mortality. Thus, there is a need to better understand the mechanisms by which BPV causes cardiovascular end-organ damage. Animal studies using sinoaortic denervation (SAD) to increase BPV have demonstrated pathologic changes in the structure of the heart and blood vessels; however, there is a paucity of data investigating changes in functional measures of the heart and smaller, resistance type arteries. Furthermore, the pathogenic mechanisms involved in BPV-induced cardiovascular end-organ damage remain unknown. Baroreceptor denervation results in multiple cardiac stressors, many of which are associated with production of reactive oxygen species. Oxidative stress is known to promote cardiovascular end-organ damage but it is unclear if it plays a role in models of increased BPV. Thus, this study was designed to investigate the functional responses of smaller resistance type arteries and the heart to chronic exposure to enhanced BPV. In addition, the role of oxidative stress on these functional responses in a normotensive rat model of increased BPV was also investigated. Rats were subjected to either SAD surgery or a sham procedure and were observed for six weeks. To determine the role of oxidative stress, SAD rats were either treated with the superoxide dismutase mimetic tempol or left untreated. During the observation period, mean blood pressure remained normotensive, whereas baroreflex sensitivity was reduced and BPV increased two to three fold. Weekly in vivo assessment of vascular function of the long posterior ciliary artery (LPCA) demonstrated a significant reduction in endothelial-dependent dilation starting three weeks after SAD surgery compared to the sham group. Endothelial-independent dilation was not affected by SAD. Structural changes were not evident in the LPCA following SAD. However, structural (wall thickness, wall area, and wall area/lumen area ratio) and functional (strain and distensibility) changes were observed in the aorta. Cardiac structural (hypertrophy) and functional (diastolic dysfunction) effects were also evident following six weeks of increased BPV. Antioxidant treatment with tempol did not have any effect on the SAD-induced increase in BPV or decrease in BRS. Nevertheless, chronic tempol treatment prevented or reduced the cardiovascular end-organ damage (endothelial-dependent vascular dysfunction, decreased aortic distensibility, cardiac and vascular hypertrophy, and cardiac dysfunction) observed in the untreated SAD group. These findings suggest that the pathology observed following SAD is at least partly mediated by oxidative stress. Antioxidant treatment in patients with increased BPV (e.g., hypertension, diabetes, heart failure) may prevent or ameliorate cardiovascular end-organ damage and reduce the overall risk for cardiovascular disease events.

La rigidité artérielle ayant une valeur prédictive forte et indépendante d'évènements cardiovasculaires, nous émettons l'hypothèse que l'accumulation de variations de contraintes hémodynamiques altère la fonction et la structure des gros troncs artériels, indépendamment du niveau de pression artérielle. Nous avons donc mesuré l'impact de la variabilité tensionnelle sur la rigidité et la structure artérielles dans différents modèles de variabilité tensionnelle chez le rat.Chez le rat barodénervé et le rat sympathectomisé par la guanéthidine, 2 modèles de variabilité tensionnelle à court terme, une augmentation de la rigidité artérielle est associée à des altérations tissulaires différentes. En effet chez les rats barodénervés, une hypertrophie aortique est couplée à une augmentation du collagène et des attachements cellule-matrice (fibronectine et intégrine α5). Au contraire, chez les rats sympathectomisés, une hypotrophie vasculaire est associée à une diminution de l'élastine et une augmentation des attachements via l'intégrine αv.Nous avons ensuite créé, caractérisé et validé un modèle de variabilité tensionnelle à long terme, le rat spontanément hypertendu traité de façon discontinue par un antihypertenseur. Le traitement discontinu réduit la pression artérielle systolique tout en augmentant isolément la variabilité tensionnelle à long terme. La rigidité artérielle, élevée sous traitement discontinu, est associée à une hypertrophie vasculaire avec augmentation des attachements (fibronectine et intégrine αv) et sans modification du rapport élastine/collagène.En conclusion, l'élevation de variabilité tensionnelle engendre de la rigidité artérielle, et ce à pression artérielle constante. Les altérations structurales dans les modèles de variabilité tensionnelle étudiés impliquent des mécanismes différents reposant sur des modifications des relations cellule-matrice, mettant en jeu la fibronectine et les intégrines α5 et αv. / Arterial stiffness is nowadays accepted as a strong and independent predictor of cardiovascular disease. We hypothesized that increased blood pressure variability (BPV) may lead to arterial damage, independently of the blood pressure level. We thus aimed investigating the relationship between BPV and arterial stiffness and composition of the aorta in different rat models of increased BPV.In a first study performed in two models of increased short term BPV, sinoaortic denervated and chemically sympathectomized rats, an increase in wall stiffness was associated with different modifications of cell-extracellular matrix adhesion. Indeed in sinoaortic denervated rats, increased media cross-sectional area was coupled with an increased collagen content and muscle cell attachments to its cell-extracellular matrix (fibronectin and its α5β1 integrin). In contrast, chemically sympathectomized rats were characterized by a reduced media cross-sectional area associated to a reduction of elastin content and upregulation of αvβ3 integrin.In a second study, we created, characterized and validated a new experimental model of long term BPV by discontinuously treating spontaneously hypertensive rats with valsartan. Discontinuous treatment reduced systolic blood pressure level but increased long term BPV. In addition, this treatment regimen failed to reduce arterial stiffness and induced a vascular hypertrophy without modification of elastin/collagen ratio. Discontinuous treatment also highly increased vascular fibronectin in parallel to αv integrin.In conclusion, a rise of both short- and long-term BPV leads to an increase in arterial stiffness, independently of blood pressure level. The structural changes at the origin of this increase in arterial rigidity involve different mechanisms, in which fibronectin and integrin α5 and αv play a key role.

The aim of this dissertation was to address several gaps in the existing literature focused on the association between levels and variability in blood pressure (BP) and cognitive functioning. Using Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), Chapter 1 synthesizes and critically analyzes the outcomes of research reporting the association between BP variability (BPV) and cognition. Fifty-five studies met eligibility criteria, including reports measuring short-term, mid-term, and long-term BPV. Despite substantial between-study heterogeneity in study characteristics, the majority of studies reported that higher systolic BPV is associated with adverse cognitive outcomes. Further, Chapter 1 identified several gaps in the existing literature. For instance, no research has investigated the association between BPV and short-term fluctuations in cognitive functioning, or the association between mid-term BPV and concurrent cognitive functioning. Building on Chapter 1, Chapter 2 used an intensive measurement design to investigate the extent to which mid-term variability in BP, recorded using home-based BP monitoring, is associated with levels and variability in cognitive functioning in a sample of community-living older adults (N=64; Mage=70.58, SD=3.5; 77% female) assessed twice daily over a two-week period. Partial correlation coefficients estimated the association between BPV and variability in several ambulatory cognitive assessments, accounting for the learning effect during the study protocol, while multi-level models (MLMs) estimated the association between BPV and concurrent cognitive functioning. In addition, MLMs examined the extent to which BP and cognitive functioning fluctuate within and between days at the intraindividual and interindividual levels. Findings suggest that more BPV may be associated with slower or more variable reaction time, while higher BP may be associated with worse performance on accuracy tasks. / Graduate / 2022-08-30

Purpose: Evidence has accumulated to show that blood pressure variability (BPV) has a striking relationship with cardiovascular (CV) risk. Despite the mounting evidence implicating BPV as a CV risk factor, scant attention has been paid to: (1) the mechanisms by which high BPV confers greater CV risk; and (2) the efficacy of non-pharmacologic treatment modalities in the attenuation of BPV. In order to address these two unresolved questions, the purpose of this dissertation was twofold. The purpose of study #1 was to investigate the association between measures of short-term BPV (24-hour BPV) and long-term BPV (visit-to-visit BPV) with markers of endothelial health in a cohort of African Americans in order to determine if increased BPV may confer greater CV risk by eliciting injury to the endothelium. The purpose of study #2 was to investigate the effects of a 6-month aerobic exercise training (AEXT) intervention on visit-to-visit BPV and 24-hour BPV in the same cohort of African Americans in order to provide the first available data on the efficacy of a non-pharmacologic treatment modality in the lowering of BPV. Methods: We recruited 72 African Americans who were sedentary, non-diabetic, non-smoking, and free of CV and renal disease. Before and after a 6-month AEXT intervention, office blood pressure (BP) was measured at 3 separate visits and 24-hour ambulatory BP monitoring (ABPM) was conducted to measure visit-to-visit BPV and 24-hour BPV, respectively. Right brachial artery diameter was assessed at rest, during flow-mediated dilation (FMD), and after nitroglycerin-mediated dilation (NMD). Peak and area under the curve (AUC) were calculated as measures of FMD and NMD, and the FMD/NMD ratio was calculated as a measure of endothelial function normalized by smooth muscle function. Fasted blood samples were obtained and were analyzed for circulating EMPs expressed as CD31+CD42- and CD62E+ EMPs. Results: In study #1, participants with higher 24-hour diastolic BPV (DBPV) had significantly lower CD31+CD42- EMPs compared to participants with lower 24-hour DBPV. When categorized according to visit-to-visit DBPV, participants with higher visit-to-visit DBPV had a significantly lower FMD/NMD ratio, and significantly higher %NMDpeak and NMDAUCs compared to participants with lower visit-to-visit DBPV. When analyzed as continuous variables, 24-hour mean arterial pressure variability (MAPV) was inversely associated with CD31+CD42- EMPs visit-to-visit DBPV was inversely associated with the FMD/NMD ratio and positively associated with %NMDpeak and NMDAUC; and 24-hour DBPV was positively associated with NMDAUC. All associations were independent of age, gender, BMI, mean BP, and pulse pressure. In study #2 investigating the effects of AEXT in 33 participants who completed the study, 24-hour DBPV and 24-hour MAPV were significantly increased after AEXT. The increase in 24-hour DBPV was independent of changes in BMI, mean BP, and self-reported sleep time. Heart rate variability (HRV) derived from ABPM was associated with the changes in 24-hour DBPV and 24-hour MAPV. There were no significant changes in visit-to-visit BPV after AEXT. Conclusions: The results from study #1 provide evidence that BPV is associated with vascular health as endothelial function was decreased in participants with high visit-to-visit DBPV, while smooth muscle function was increased in participants with higher visit-to-visit and 24-hour DBPV. The findings from study #2 show that 6-months of AEXT do not elicit beneficial changes in BPV. The finding of an association between changes in 24-hour BPV with HRV could indicate, however, that changes in activity levels during ABPM, in part, contributed to the observed changes in 24-hour BPV. / Kinesiology

Ce travail avait pour but de déterminer, chez le rat vigil, le rôle de l’innervation sympathique dans le contrôle de l’hémodynamique cérébrale 1/ au cours d’une période d’activité normale d’environ 4 heures, et 2/ lors d’une augmentation aiguë de la pression artérielle (PA) induite par un stress émotionnel (jet d’air). Les débits sanguins dans les artères carotides internes (DSCa) ont été mesurés grâce à des sondes Doppler chroniquement implantées, chez des rats intacts ou ayant subi l’exérèse unilatérale du ganglion cervical supérieur. Le stress induit une élévation brusque et importante de la PA qui s’accompagne d’une hyperémie et d’une vasodilatation beaucoup plus marquées du côté dénervé que du côté innervé. Dans les conditions de base, l’analyse spectrale révèle une augmentation de la variabilité du DSCa du côté dénervé. La cohérence entre les deux DSCa, qui fournit un index de corrélation linéaire dans le domaine fréquentiel, a été calculée avant (cohérence ordinaire) et après élimination mathématique de l’influence de la PA (cohérence partielle). Les cohérences ordinaire et partielle sont diminuées par la sympathectomie unilatérale dans une bande de fréquences comprises entre 0,01 et 0,1 Hz. Ceci suggère un rôle modulateur important de l’innervation sympathique vis-à-vis de ces fluctuations lentes des DSCa. Ces résultats montrent que chez le rat vigil, l’innervation sympathique exerce un rôle protecteur de la circulation cérébrale face aux augmentations de PA au cours du stress émotionnel. Par ailleurs, cette innervation module des fluctuations spontanées lentes du débit sanguin cérébral qui ne sont pas directement reliées aux fluctuations de la PA. / The goal of the present work was to determine, in conscious rats, the role of the sympathetic innervation in the control of cerebral hemodynamics 1/ during a baseline period lasting ~4 h, and 2/ during an acute increase in blood pressure (BP) evoked by an emotional stressor (jet of air). Blood flows in internal carotid arteries (CaBF) were recorded with Doppler flow probes chronically implanted in intact rats and in rats that underwent unilateral excision of the superior cervical ganglion. Stress induced a large and brisk increase in BP which was accompanied by hyperemia and vasodilatation that were much stronger on the denervated than on the intact side. Spectral analysis demonstrated an overall enhancement of CaBF variability on the denervated side. Coherence between the two CaBFs, which provides an index of linear correlation in the frequency domain, was computed before (ordinary coherence) and after (partial coherence) mathematically eliminating the influence of BP. Both ordinary and partial coherences were lowered by unilateral sympathectomy in the 0.01-0.1 Hz frequency range, which suggests an important modulatory role for sympathetic innervation with respect to these slow CaBF fluctuations. These results indicate that in the conscious rat, sympathetic innervation plays a protective role of the cerebral circulation in the face of stress-induced increases in BP. On the other hand, this innervation modulates slow, spontaneous fluctuations of cerebral blood flow which are not directly related to BP fluctuations.

Barorezeptorsensitivität, Herzfrequenzvariabilität und Blutdruckvariabilität bei Patienten mit einem mild-moderaten Schlafapnoe Syndrom und bei gesunden Probanden Die Behandlung von Patienten mit einem mild-moderaten obstruktiven Schlafapnoe Syndrom (OSAS) wird von der klinischen Symptomatik und dem Herzkreislaufrisiko bestimmt. Wir konnten nachweisen, dass bei einem mild-moderaten OSAS unter der Beatmungstherapie neben der Beseitigung der nächtlichen Atmungsstörung auch eine Änderung der Mikrostruktur des Schlafes (Arousal) und der Müdigkeit am Tage zu verzeichnen ist. Das Herzkreislaufrisiko untersuchten wir anhand noninvasiver Parameter der sympathovagalen Balance. Dazu wurden die Herzfrequenzvariabilität (HRV), die Blutdruckvariabilität (BDV) und die Barorezeptorsensitivität (BRS) im Zeit- und Frequenzbereich bestimmt und diese Größen bei Patienten mit einem mild-moderaten OSAS im Vergleich zu gesunden Probanden als auch der Effekt einer CPAP-Therapie - im Schlaf als auch am Tage - analysiert. Bei gesunden Probanden fanden wir eine HRV- und BRS-Abnahme sowie eine BDV-Zunahme im REM- gegenüber dem NREM-Schlaf. OSAS Patienten haben im Vergleich zu Gesunden eine niedrigere BRS im NREM und eine erhöhte BDV sowohl im REM- als auch NREM-Schlaf. CPAP führt beim OSAS zu einer Abnahme der Herzfrequenz und Zunahme der BRS, vornehmlich im NREM Schlaf und bei zusätzlich bekannter Hypertonie. Die HRV nimmt ab und die BDV zu, jeweils unabhängig vom Schlafstadium bzw. einer bestehenden Hypertonie. Am Tage zeigt sich nur ein Kurzzeiteffekt hinsichtlich Zunahme der BRS und HRV. Dieser Effekt ist vom Ausmaß des OSAS und dem Vorhandensein einer Hypertonie abhängig und nach 4 Wochen Therapie nicht mehr nachweisbar. Untersucht man den Effekt der Beatmungstherapie auf HRV, BDV und BRS bei gesunden Probanden im Akutversuch, dann findet man eine Erhöhung des Blutdruckes bei Abnahme der Herzfrequenz und Zunahme der BRS. HRV, BDV und BRS als Parameter für das kardiovaskuläre Risiko zeigen nachweisbare Veränderungen bei Schlafapnoe Patienten, auch wenn nur ein mild-moderates OSAS vorliegt. Ein Therapieeffekt lässt sich anhand dieser Parameter auch nachweisen, wobei ein vorhandener Akuteffekt von Überdruckbeatmung auf HRV, BDV und BRS unabhängig von einem OSAS zu berücksichtigen ist. / Baroreceptor sensitivity, heart-rate variability, and blood-pressure variability in patients with mild to moderate sleep apnoea syndrome, and in healthy controls The treatment of patients with mild to moderate obstructive sleep apnoea syndrome, OSAS, is determined by the clinical symptom complex and by the cardiovascular risk. In patients with mild to moderate OSAS who received therapy in the form of assisted ventilation, we succeeded in evidencing that it is possible to influence the microstructure of sleep (i.e., of arousal) as well as fatigue experienced during the day, in addition to eliminating nocturnal respiratory disturbance. We investigated the cardiovascular risk by examining non-invasive parameters for sympathovagal balance. Therefore we analyzed heart-rate variability (HRV), blood-pressure variability (BPV), and baroreceptor sensitivity (BRS) over time and frequency ranges in patients with mild to moderate OSAS, in comparison to healthy controls. We likewise assessed the effects of CPAP therapy on these parameters, both during sleeping as well as non-sleeping hours. Among healthy test subjects, we determined decreases in HRV and BRS, as well as increase in BPV, during REM sleep, in comparison to NREM sleep. In comparison to healthy controls, OSAS patients have lower BRS during NREM and increased BPV in both REM and NREM sleep. In OSAS patients, CPAP leads to a decrease in heart rate and increase in BRS, especially in NREM sleep and in patients for whom hypertension is also known. HRV diminishes and BPV increases, in both cases regardless of the sleep stage or presence or absence of hypertension. During the day, only a short-term effect becomes apparent with respect to increases in BRS and HRV. This effect depends on the extent of OSAS and on the existence of hypertension; after four weeks of therapy, the effect is no longer in evidence. Acute testing of the effect of assisted ventilation on HRV, BPV, and BRS among healthy controls discloses increase in blood pressure, accompanied by decrease in heart rate and increase in BRS. HRV, BPV, and BRS as parameters for cardiovascular risk reveal evidence of alterations in sleep-apnoea patients, even for those suffering only from mild to moderate OSAS. Therapeutic effects are also in evidence on the basis of these parameters, whereby an existing acute effect of positive-pressure ventilation on HRV, BPV, and BRS regardless of OSAS must also be taken into account.

In this thesis, we included results from two studies. The first one considered the effects of the blood volume changes, during blood donation, on the heart rate variability (HRV) measured, non-invasively, form electrocardiographic (ECG) and photoplethysmographic (PPG) signals. Our results showed that, during blood donation, there were no significant changes in the pulsatile area of PPG signal, while heart rate increased. No significant changes were noticed in HRV extracted from both signals. Error analysis between the HRV extracted from ECG and peak interval variability (PIV) suggested that the error during blood donation was increased which means that the use of PIV extracted from PPG signal, used as a replacement diagnostic tool in clinical applications, needs further investigations and should be carefully studied in non-stationary cardiovascular situations such as blood donation. The imbalance between the two branches of the autonomic nervous system, sympathetic and parasympathetic, vagal, may result in a harmful activation of myocardial tissues which cause arrhythmias and sudden cardiac death. Although the study of the sympathovagal balance have been attracting many researchers, further studies are needed to elucidate the effects of many kinds of drugs on the autonomic modulation of the cardiac muscle, specifically, the cells of sinoatrial (SA) node. The aim of the second part of this thesis was to assess the effects of calcium channel blocker (Verapamil), calcium channel sensitizer (Levosimendan), calcium chloride (CaCl2), the combinations of verapamil/ CaCl2, levosimendan/ CaCl2, and noradrenaline infusion on beat-to-beat cardiovascular variability represented, in this research, by systolic blood pressure variability (SBPV), and stroke volume variability (SVV) signals. We used Fat Fourier Transform (FFT) to evaluate the power spectral density of the fluctuations in both signals to evaluate the effects of short-term treatments with those drugs on the sympathovagal balance in normal rats. Then, we compared the spectra obtained from SBPV and SVV to decide which of these fluctuations along with corresponding spectrum was more able to provide a clear feedback about the autonomic nervous system. Our data suggests that there were a significant correlations between low- (LF), mid- (MF), and high-frequency (HF) spectra obtained from SBPV and SVV except between the HF spectra estimated from after the infusion of levosimendan where a poor correlation (r = 0.530, p = 0.281) was noticed. This that both HF components obtained provide different information regarding the autonomic nervous system modulation of the SA node cells, while the results obtained from the rest of experiments showed that both signals provide same information about the modulation of sympathetic and parasympathetic tone due to all stages of different drugs infusion studied in this thesis. Besides that, we found that both spectra may be used to track the fluctuations in the cardiac output as a result of the drugs infusion.

In this thesis, we included results from two studies. The first one considered the effects of the blood volume changes, during blood donation, on the heart rate variability (HRV) measured, non-invasively, form electrocardiographic (ECG) and photoplethysmographic (PPG) signals. Our results showed that, during blood donation, there were no significant changes in the pulsatile area of PPG signal, while heart rate increased. No significant changes were noticed in HRV extracted from both signals. Error analysis between the HRV extracted from ECG and peak interval variability (PIV) suggested that the error during blood donation was increased which means that the use of PIV extracted from PPG signal, used as a replacement diagnostic tool in clinical applications, needs further investigations and should be carefully studied in non-stationary cardiovascular situations such as blood donation. The imbalance between the two branches of the autonomic nervous system, sympathetic and parasympathetic, vagal, may result in a harmful activation of myocardial tissues which cause arrhythmias and sudden cardiac death. Although the study of the sympathovagal balance have been attracting many researchers, further studies are needed to elucidate the effects of many kinds of drugs on the autonomic modulation of the cardiac muscle, specifically, the cells of sinoatrial (SA) node. The aim of the second part of this thesis was to assess the effects of calcium channel blocker (Verapamil), calcium channel sensitizer (Levosimendan), calcium chloride (CaCl2), the combinations of verapamil/ CaCl2, levosimendan/ CaCl2, and noradrenaline infusion on beat-to-beat cardiovascular variability represented, in this research, by systolic blood pressure variability (SBPV), and stroke volume variability (SVV) signals. We used Fat Fourier Transform (FFT) to evaluate the power spectral density of the fluctuations in both signals to evaluate the effects of short-term treatments with those drugs on the sympathovagal balance in normal rats. Then, we compared the spectra obtained from SBPV and SVV to decide which of these fluctuations along with corresponding spectrum was more able to provide a clear feedback about the autonomic nervous system. Our data suggests that there were a significant correlations between low- (LF), mid- (MF), and high-frequency (HF) spectra obtained from SBPV and SVV except between the HF spectra estimated from after the infusion of levosimendan where a poor correlation (r = 0.530, p = 0.281) was noticed. This that both HF components obtained provide different information regarding the autonomic nervous system modulation of the SA node cells, while the results obtained from the rest of experiments showed that both signals provide same information about the modulation of sympathetic and parasympathetic tone due to all stages of different drugs infusion studied in this thesis. Besides that, we found that both spectra may be used to track the fluctuations in the cardiac output as a result of the drugs infusion.

Made available in DSpace on 2016-06-02T20:19:25Z (GMT). No. of bitstreams: 1 6555.pdf: 1289563 bytes, checksum: 019c580e1b818068847725c1d7aeadfa (MD5) Previous issue date: 2015-02-05 / Universidade Federal de Minas Gerais / Frailty is related to a decrease in the physiological reserves that causes a difficult to maintain homeostasis. The analysis of heart period (HP) and blood pressure (BP) variabilities can contribute to the understanding of cardiovascular homeostasis in the frailty syndrome. Objective: To compare HP and BP variabilities in frail, prefrail and nonfrail, un supine and orthostatic positions, by univariate and bivariate analysis. Methods: 39 elderly were evaluated and distributed in frail, prefrail and nonfrail groups, accordingly to frailty phenotype. The RR interval (RRi) and the systolic BP (SBP) series were registered for 15 minutes in the supine position and 15 minutes in orthostatic position. Univariate analysis (RRi: mean, variance, LFnu, HFabs and LF/HF and the SBP: mean, variance and LFabs) and bivariate analysis (phase, gain (α) and coherence (K2)) were performed. A two-way repeated measures ANOVA test was used for the statistical analysis; a 5% significance level was considered, along with group, position and interaction effects. Results: Univariate analysis do not detected changes in frailty syndrome. However, in the bivariate analysis frail presented lower K² than nonfrail in orthostatic position. Prefrail and frail reported a significant decrease in K² values in orthostatic position in comparison to the supine. Conclusion: Univariate analysis of HP and BP variabilities do not change when frailty syndrome is present. However, bivariate analysis indicated decoupling between HP and BP in frailty presence. Thus, a reduced K2 might be a marker of frailty process. / A fragilidade está associada à redução das reservas fisiológicas que leva à dificuldade na manutenção da homeostase. A análise da variabilidade da frequência cardíaca (FC) e da pressão arterial (PA) pode contribuir para a compreensão da homeostase cardiovascular na síndrome da fragilidade. Objetivo: Comparar a variabilidade da frequência cardíaca (VFC) e a variabilidade da pressão arterial sistólica (VPA) de indivíduos frágeis, pré-frágeis e robustos, nas posturas supina e ortostática, utilizando-se de análises univariada e bivariada. Métodos: Foram avaliados 39 idosos, alocados em 3 grupos de acordo com o fenótipo da fragilidade. As séries de intervalos RR (iRR) e de PA sistólica (PAS) foram registradas por 15 minutos em repouso na posição supina, e 15 minutos na posição ortostática. Foram realizadas as análises univariada (iRR: média, variância, baixa frequência em unidades normalizadas (BFun), alta frequência em unidades absolutas (AFabs) e razão entre a baixa e alta frequência (BF/AF) e PAS: média, variância e BFabs) e bivariada (fase, ganho (α) e coerência (K2)). Para análise estatística foi utilizado o teste Anova two way de medidas repetidas, com efeitos de grupo, posição e interação entre estes, considerando um nível de significância de 5%. Resultados: A análise univariada não detectou alterações na síndrome da fragilidade. Entretanto, na análise bivariada os frágeis apresentaram menores valores de K2 em comparação aos robustos na posição ortostática. Préfrágeis e frágeis apresentaram redução significativa nos valores de K2 na posição ortostática em comparação à supina. Conclusão: A variabilidade da FC e da PA, avaliada pela análise univariada, não se altera quando a fragilidade está presente. Por sua vez, a análise bivariada indicou um maior desacoplamento entre FC e PA na presença da síndrome da fragilidade. Desta forma, a K2 reduzida pode ser um marcador do processo de fragilização.