<p>The duodenal lumen is exposed to aggressive factors with a high potential to cause damage to the mucosa. Bicarbonate secretion by the duodenal mucosa is accepted as the primary important defense mechanism against the hydrochloric acid intermittently expelled from the stomach.</p><p>The present thesis concerns the influence of the central nervous system and the effects of the hormone melatonin on bicarbonate secretion in anesthetized rats in vivo. Effects of melatonin on intracellular calcium signaling by duodenal enterocyte in vitro were examined in tissues of both human and rat origin. The main findings were as follows:</p><p>Melatonin is a potent stimulant of duodenal mucosal bicarbonate secretion and also seems to be involved in the acid-induced stimulation of the secretion. Stimulation elicited in the central nervous system by the α1-adrenoceptor agonist phenylephrine induced release of melatonin from the intestinal mucosa and a four-fold increase in alkaline secretion. The melatonin antagonist luzindole abolished the duodenal secretory response to administered melatonin and to central nervous phenylephrine but did not influence the release of intestinal melatonin. Central nervous stimulation was also abolished by synchronous ligation of the vagal trunks and the sympathetic chains at the sub-laryngeal level. </p><p>Melatonin induced release of calcium from intracellular stores and also influx of extracellular calcium in isolated duodenal enterocytes. Enterocytes in clusters functioned as a syncytium.</p><p>Overnight fasting rapidly and profoundly down-regulated the responses to the duodenal secretagogues orexin-A and bethanechol but not those to melatonin or vasoactive intestinal polypeptide.</p><p>In conclusion, the results strongly suggest that intestinal melatonin plays an important role in central nervous elicited stimulation of duodenal mucosal bicarbonate secretion. Sensitivity of this alkaline secretion to some peripheral stimulators markedly depends on the feeding status.</p>

The duodenal lumen is exposed to aggressive factors with a high potential to cause damage to the mucosa. Bicarbonate secretion by the duodenal mucosa is accepted as the primary important defense mechanism against the hydrochloric acid intermittently expelled from the stomach. The present thesis concerns the influence of the central nervous system and the effects of the hormone melatonin on bicarbonate secretion in anesthetized rats in vivo. Effects of melatonin on intracellular calcium signaling by duodenal enterocyte in vitro were examined in tissues of both human and rat origin. The main findings were as follows: Melatonin is a potent stimulant of duodenal mucosal bicarbonate secretion and also seems to be involved in the acid-induced stimulation of the secretion. Stimulation elicited in the central nervous system by the α1-adrenoceptor agonist phenylephrine induced release of melatonin from the intestinal mucosa and a four-fold increase in alkaline secretion. The melatonin antagonist luzindole abolished the duodenal secretory response to administered melatonin and to central nervous phenylephrine but did not influence the release of intestinal melatonin. Central nervous stimulation was also abolished by synchronous ligation of the vagal trunks and the sympathetic chains at the sub-laryngeal level. Melatonin induced release of calcium from intracellular stores and also influx of extracellular calcium in isolated duodenal enterocytes. Enterocytes in clusters functioned as a syncytium. Overnight fasting rapidly and profoundly down-regulated the responses to the duodenal secretagogues orexin-A and bethanechol but not those to melatonin or vasoactive intestinal polypeptide. In conclusion, the results strongly suggest that intestinal melatonin plays an important role in central nervous elicited stimulation of duodenal mucosal bicarbonate secretion. Sensitivity of this alkaline secretion to some peripheral stimulators markedly depends on the feeding status.

Heart rate varies constantly as a consequence of activity in the sympathetic and parasympathetic autonomic nervous systems (SNS and PNS). In short-term recordings, heart rate variability (HRV) is mostly related to the inhibitory activity of the vagal nerves, which are part of the PNS. HRV is lower when under stress as well as in several illnesses and psychiatric conditions. Decreased HRV is also related to cardiac disease, which is the leading cause of death worldwide. Autonomic imbalance, measured as HRV, is suggested as a mediator between psychosocial distress and cardiovascular disease. The aim of the present thesis was to investigate the connection between HRV and psychosocial distress, including psychiatric problems (studies I and II), and lifestyle factors (study III). In study I, additional physiological measures sensitive to autonomic activity and results from a continuous attention test were investigated in parallel with HRV. In studies II and III the participants were adolescents. The results show that HRV is lower in women with stress-related fatigue and adolescent girls with a psychiatric diagnosis compared to healthy control groups. However, these groups did not exhibit an increase in physiological measures of SNS origin, which supports the assumption that the observed hyperarousal is related to decreased vagal activity rather than increased SNS activity. Women with stress-related fatigue made more impulsive errors and had a “risky” response style in the continuous attention test. There was a negative correlation between test performance and HRV. Decreased vagal activity is thus associated with deficient behavioural inhibition. In study III, HRV in a group of healthy adolescent boys and girls was positively associated with physical activity but not with other lifestyle measures. Even at young age HRV is a sensitive marker of autonomic imbalance resulting from psychosocial stress. Future longitudinal research will show whether HRV can be used for early identification of people at risk of cardiovascular disease and whether such interventions will lower the risk of cardiac morbidity.

No description available.

Vagus nerve stimulation (VNS) treats patients with drug-resistant epilepsy, depression and heart failure, but the mechanisms responsible are uncertain. The mild stimulus intensities used in chronic VNS suggest activation of myelinated primary visceral afferents projecting to the nucleus of the solitary tract (NTS). Here, we monitored the activity of second and higher order NTS neurons in response to peripheral vagal activation using therapeutic VNS criteria. A bipolar stimulating electrode activated the left cervical vagus nerve, and stereotaxically placed single tungsten electrodes recorded unit activity from the left caudomedial NTS of chloralose-anaesthetized rats. High-intensity single electrical stimuli established vagal afferent conduction velocity (myelinated A-type or unmyelinated C-type) as well as synaptic order (second vs. higher order using paired electrical stimuli) for inputs to single NTS neurons. Then, VNS treatment was applied. A mid-collicular knife cut (KC) divided the brainstem from all supramedullary regions to determine their contribution to NTS activity. Our chief findings indicate that the KC reduced basal spontaneous activity of second-order NTS neurons receiving myelinated vagal input by 85%. In these neurons, acute VNS increased activity similarly in Control and KC animals. Interestingly, the KC interrupted VNS activation of higher order NTS neurons and second-order NTS neurons receiving unmyelinated vagal input, indicating that supramedullary descending projections to NTS are needed to amplify the peripheral neuronal signal from VNS. The present study begins to define the pathways activated during VNS and will help to better identify the central nervous system contributions to the therapeutic benefits of VNS therapy. KEY POINTS: Vagus nerve stimulation is routinely used in the clinic to treat epilepsy and depression, despite our uncertainty about how this treatment works. For this study, the connections between the nucleus of the solitary tract (NTS) and the higher brain regions were severed to learn more about their contribution to activity of these neurons during stimulation. Severing these brain connections reduced baseline activity as well as reducing stimulation-induced activation for NTS neurons receiving myelinated vagal input. Higher brain regions play a significant role in maintaining both normal activity in NTS and indirect mechanisms of enhancing NTS neuronal activity during vagus nerve stimulation.

Fond : Le substrat de fibrillation auriculaire (FA) vagale et celui secondaire à remodelage par tachycardie auriculaire (RTA) partagent beaucoup des caractéristiques : période réfractaire efficace (PRE) réduite, hétérogénéité accrue de PRE et quelques mécanismes moléculaires communs. Cette étude a comparé les 2 substrats à une abréviation comparable de PRE. Méthodes : Chez chacun de 6 chiens de groupe de stimulation vagal (SV), les paramètres de stimulation cervicale bilatérale de nerves vagaux ont été ajustés pour produire la même PRE moyenne (calculé à 8 sites des oreillettes gauche et droite) avec 6 chiens de groupe de RTA assorti à sexe et poids. Des paramètres électrophysiologiques, la durée moyenne de la fibrillation auriculaire (DAF) et les fréquences dominantes (FD) locales ont étés calculés. Résultats : En dépit des PREs assorties (SV: 80±12msec contre RTA: 79±12msec) la DAF était plus longue (*), l’hétérogénéité de conduction était plus élevée (*), la FD était plus rapide (*) et la variabilité de FD plus grande (*) chez les chiens SV. Les zones de maximum FD qui reflètent les zones d’origine de FA étaient à côté de ganglions autonomes chez les chiens SV. Conclusions : Pour un PRE atriale comparable, la FA secondaire à SV est plus rapide et plus persistante que la FA avec un substrat de RTA. Ces résultats sont consistants avec des modèles de travail suggérant que l'hyperpolarisation SV-induite contribue de façon important à la stabilisation et à l'accélération des rotors qui maintiennent la FA. La similitude de la distribution de FD du groupe vagal avec la distribution des lésions d’ablation après cartographie des électrogrammes atriales fragmentés suggère des nouvelles techniques d’ablation. La distribution des FD entre le SV et le RTA fournit de nouvelles idées au sujet de possible rémodelage neuroreceptorial et indique des différences importantes entre ces substrats de FA superficiellement semblables. / Background: Vagal nerve stimulation (VS) and atrial tachycardia remodeled (ATR) atrial fibrillation (AF) substrates share many features: reduced effective refractory period (ERP), increased ERP heterogeneity and some common molecular mechanisms. This study compared VS and ATR substrates at comparable ERP abbreviation. Methods: In each of 6 VS dogs, bilateral cervical VS parameters were adjusted to produce the same mean ERP as a sex and weight matched ATR dog. Electrophysiological parameters, mean duration of AF (DAF) and local dominant frequencies (DF) were determined (before (CTL) and after VS in VS dogs). Results: Despite matched ERPs (VG: 80±12msec vs ATR: 79±12msec) DAF was greater (*), conduction heterogeneity was greater (*), DF was faster (*) and DF variability greater (*) in VS dogs. AF drivers reflected by maximum DF zones were adjacent to autonomic ganglia in VS dogs; there was a tendency (p<0.07) to faster driver zones in the left atrium comparing to the right in ATR dogs. Conclusions: For a comparable atrial ERP, VS AF is faster and more persistent than AF with an ATR substrate. These results are consistent with modeling work suggesting that VS-induced hyperpolarization is an important contributor to AF-maintaining rotor stabilization and acceleration. Similarities in DF distribution in VS dogs with distribution of ablation lesions performed after Complex Fractionated Atrial Electrograms mapping suggests new curative ablation methods. DF distribution differences between VS and ATR provides new ideas about possible neuroreceptorial remodeling and indicates important differences between these superficially similar AF substrates.

Fond : Le substrat de fibrillation auriculaire (FA) vagale et celui secondaire à remodelage par tachycardie auriculaire (RTA) partagent beaucoup des caractéristiques : période réfractaire efficace (PRE) réduite, hétérogénéité accrue de PRE et quelques mécanismes moléculaires communs. Cette étude a comparé les 2 substrats à une abréviation comparable de PRE. Méthodes : Chez chacun de 6 chiens de groupe de stimulation vagal (SV), les paramètres de stimulation cervicale bilatérale de nerves vagaux ont été ajustés pour produire la même PRE moyenne (calculé à 8 sites des oreillettes gauche et droite) avec 6 chiens de groupe de RTA assorti à sexe et poids. Des paramètres électrophysiologiques, la durée moyenne de la fibrillation auriculaire (DAF) et les fréquences dominantes (FD) locales ont étés calculés. Résultats : En dépit des PREs assorties (SV: 80±12msec contre RTA: 79±12msec) la DAF était plus longue (*), l’hétérogénéité de conduction était plus élevée (*), la FD était plus rapide (*) et la variabilité de FD plus grande (*) chez les chiens SV. Les zones de maximum FD qui reflètent les zones d’origine de FA étaient à côté de ganglions autonomes chez les chiens SV. Conclusions : Pour un PRE atriale comparable, la FA secondaire à SV est plus rapide et plus persistante que la FA avec un substrat de RTA. Ces résultats sont consistants avec des modèles de travail suggérant que l'hyperpolarisation SV-induite contribue de façon important à la stabilisation et à l'accélération des rotors qui maintiennent la FA. La similitude de la distribution de FD du groupe vagal avec la distribution des lésions d’ablation après cartographie des électrogrammes atriales fragmentés suggère des nouvelles techniques d’ablation. La distribution des FD entre le SV et le RTA fournit de nouvelles idées au sujet de possible rémodelage neuroreceptorial et indique des différences importantes entre ces substrats de FA superficiellement semblables. / Background: Vagal nerve stimulation (VS) and atrial tachycardia remodeled (ATR) atrial fibrillation (AF) substrates share many features: reduced effective refractory period (ERP), increased ERP heterogeneity and some common molecular mechanisms. This study compared VS and ATR substrates at comparable ERP abbreviation. Methods: In each of 6 VS dogs, bilateral cervical VS parameters were adjusted to produce the same mean ERP as a sex and weight matched ATR dog. Electrophysiological parameters, mean duration of AF (DAF) and local dominant frequencies (DF) were determined (before (CTL) and after VS in VS dogs). Results: Despite matched ERPs (VG: 80±12msec vs ATR: 79±12msec) DAF was greater (*), conduction heterogeneity was greater (*), DF was faster (*) and DF variability greater (*) in VS dogs. AF drivers reflected by maximum DF zones were adjacent to autonomic ganglia in VS dogs; there was a tendency (p<0.07) to faster driver zones in the left atrium comparing to the right in ATR dogs. Conclusions: For a comparable atrial ERP, VS AF is faster and more persistent than AF with an ATR substrate. These results are consistent with modeling work suggesting that VS-induced hyperpolarization is an important contributor to AF-maintaining rotor stabilization and acceleration. Similarities in DF distribution in VS dogs with distribution of ablation lesions performed after Complex Fractionated Atrial Electrograms mapping suggests new curative ablation methods. DF distribution differences between VS and ATR provides new ideas about possible neuroreceptorial remodeling and indicates important differences between these superficially similar AF substrates.

Using Indigenous methodology and a story telling method this thesis is the result of research that looks at the benefits of traditional Indigenous ceremony and healing practices as a way to heal from traumatic experiences. A thematic analysis technique was employed to reveal four themes that emerged from the stories told by Indigenous Knowledge Keeper participants. The first theme is the importance of our connection to all living things including our own selves. Another is recognizing our greatest teachers nature and animals. Cleansing emerged at the center of all traditional healing strategies and the final theme encompasses all that we are as life on this planet spirit or energy. Trauma can be understood as any event that creates difficulty for the individual to cope whether the event that caused the experience was purposeful or accidental. While people do find amazing ways to cope with circumstances that are overwhelming, neurobiology tells us how trauma is processed and impacts the workings of the brain. Trauma in the nervous system can be understood as the result of a person or group or community’s inability to stay safe or to feel safe during the experiences. Indigenous people live with the ongoing effects of intergenerational trauma caused by colonization including the Indian Residential School experience, as well as ongoing systemic oppression. All traumas can activate the deeply held traumas that have been transmitted trans-generationally. In essence we carry intergenerational traumas. I believe that Indigenous people were practicing healing on a regular basis within their traditional ceremonies, dances and practices before contact and these practices may inform a model of health and wellness that could be useful in healing the effects of trauma that impacts Indigenous people today. Ceremonies and traditional teachings were shared communally before contact and are now being revived as we embrace the cultural practices of our ancestors across this land. Within our Indigenous ways of knowing we recognize that we are related to everything in creation we are connected and depend on one another. In 1884, under the Potlatch Law & section141 of the Indian Act our ceremonies, spiritual practices and traditional knowledges were made illegal; our people were imprisoned for practicing them (UBC First Nations Studies, 2009). Today we are in a state of desperation for healing strategies that work for who we are as a people. The Elders in this research shared how this can be done. / Graduate / 0452 / 0622 / 0347 / sheilanyman@shaw.ca

INTRODUÇÃO: A atuação do sistema nervoso parassimpático em células imunes é conhecida como \"Via Anti-inflamatória Colinérgica\". Trabalhos prévios demonstraram que a estimulação vagal reduz a inflamação e melhora a sobrevida em modelos experimentais com sepse. Neste estudo avaliamos se o uso do anticolinesterásico piridostigmina: altera o número de linfócitos T (CD4+ e CD8+) convencionais (CD25+Foxp3-) e reguladores (CD25+Foxp3+) no sangue periférico, no baço e no miocárdio; modifica a concentração de citocinas (interleucina 1, interleucina 6, TNFalfa) no miocárdio; e influencia a função ventricular após infarto agudo do miocárdio experimental (IAM) em ratos. MÉTODOS: Utilizamos ratos machos adultos da linhagem Wistar, com peso variando entre 200 e 250 g, divididos em 3 grupos de 20 animais cada: grupo controle (GC), grupo infartado sem tratamento (IC) e grupo infartado tratado com piridostigmina (IP). O infarto agudo do miocárdio (IAM) foi obtido com a técnica da ligadura da artéria coronária esquerda, e o grupo IP recebeu piridostigmina na dose de 40mg/kg/dia na água de beber, iniciada 4 dias antes do IAM. Todos os animais foram submetidos à canulação da artéria femoral no dia seguinte ao IAM para registro das curvas de pressão arterial, e posterior análise dos componentes da variabilidade da freqüência cardíaca (VFC), domínio do tempo (SDNN e RMSSD) e da freqüência (componentes LF e HF); o estudo ecocardiográfico foi realizado no segundo dia pós IAM. No terceiro dia pós IAM, os ratos foram divididos em subgrupos de 10 animais, e sacrificados de forma específica para coleta de materiais: 500 ul de sangue periférico e baço fresco para realização da técnica de citometria de fluxo; ventrículo esquerdo para dosagem de citocinas pela técnica de ELISA; e ventrículo esquerdo para realização de imunohistoquímica. Foram usadas as técnicas padronizadas e de uso corrente nos laboratórios. Os resultados foram avaliados por análise de variância (ANOVA) multifatorial, usando o programa GraphPad Prism com teste post hoc de Tukey. RESULTADOS: O grupo IC comparado ao grupo controle apresentou queda significativa da pressão arterial e aumento da freqüência cardíaca. O grupo IP, comparado ao grupo IC, apresentou maior atividade vagal, caracterizada pela significante redução da FC e aumento da VFC (SDNN, 9,2±1,5 vs 5,2±0,5 p < 0,05). Os parâmetros ecocardiográficos avaliados evidenciaram presença de área hipo/acinética e redução da fração de ejeção do ventrículo esquerdo nos grupos infartados, de igual magnitude. Com relação ao número de linfócitos T, verificamos que o grupo IC, comparado ao grupo controle, apresentou número significativamente menor de linfócitos reguladores (CD25+Foxp3+) no sangue periférico (CD4+: 63,5 ±1,4 vs 70,6 ±3,2%, e CD8+: 68,3 ±1,9 vs 76,1 ± 2,8%). O grupo IP, comparado ao grupo IC, apresentou significativa redução do número de linfócitos T convencionais no sangue periférico (respectivamente, CD4+: 1,5 ±0,2 vs 2,2 ± 0,2 %; CD8+: 1,1 ± 0,1 vs 1,8 ± 0,9%), e no baço houve redução somente do tipo CD4+ (respectivamente, 1,4 ± 0,2 vs 2,2 ± 0,2%), com aumento do tipo CD8+ (respectivamente, 1,2 ± 0,1 vs 0,7 ± 0,1 %). O grupo IP também apresentou significativo aumento de linfócitos reguladores (CD25+Foxp3+) no sangue periférico (respectivamente, CD4+: 76,5 ± 2,9 vs 63,5 ± 1,4 %; CD8+: 75,1 ± 1,0 vs 68,3 ± 1,9 %), e não apresentou diferenças significativas no número dessas células no baço. O grupo IC comparado ao grupo controle apresentou significativa marcação de anticorpos para CD4 e CD8 nas áreas infartada e peri-infarto por meio da análise de imunohistoquímica. O grupo IP comparado ao grupo IC, apresentou significativo aumento de CD4+ (respectivamente, 20,9 ± 6,5 vs 12,2 ± 2,5, p < 0,05) e de CD8+ (respectivamente, 17,9 ± 2,8 vs 5,8 ± 1,1%, p < 0,05) na área infartada; observamos redução significativa na marcação de CD4+ (respectivamente, 6,0 ±1,2 vs 12,5 ±4,8) na área peri-infarto, sem alterações significativas na marcação de CD8+. CONCLUSÃO: O tratamento com piridostigmina em ratos com IAM está associado a aumento da atividade vagal, aumento do número de linfócitos reguladores (CD25+Foxp3+) no sangue periférico e maior mobilização de células inflamatórias (CD4+ e CD8+) para a área infartada no miocárdio, com redução de CD4+ na área peri-infarto, no entanto sem mudança de CD8+ nesta região. A mudança do perfil inflamatório decorrente do aumento da atividade vagal na fase aguda do IAM, pode ser um possível mecanismo para explicar os benefícios detectados no remodelamento cardíaco após o IAM, em especial, na redução da área de lesão e na melhora da função ventricular, com uso de anticolinesterásicos / INTRODUTION: The role of the parasympathetic nervous system in immune cells is known as \"Cholinergic anti-inflammatory pathway\". In previous work has demonstrated that vagal stimulation reduces inflammation and improves survival in experimental sepsis models. The aim of the present study evalued the use of anticholinesterase pyridostigmine: change the number of T lymphocytes (CD4+ and CD8+) conventional (CD25+Foxp3-) and regulatory (CD25+Foxp3+) in peripheral blood, spleen, and myocardium: modifies the concentration of cytokines (interleukin-1, interleukin-6, TNFalfa) in the myocardium, and influences ventricular function after experimental myocardial infarction (MI) in rats. METHODS: Adult male rats of Wistar strain, weighing between 200 and 250 g were divided into 3 groups of 20 animals each: control group (GC); untreated group without treatment (IC) and infarcted group treated with pyridostigmine (IP). Acute myocardial infarction (AMI) was obtained with the technique of ligation of the left coronary artery, and the IP group received pyridostigmine dose of 40 mg/Kg/day in drinking water starting 4 days before the AMI. All animals underwent cannulation of the femoral artery on the day following AMI to record the blood pressure curves, and subsequent analysis of the components of heart rate variability (HRV), the time domain (SDNN and RMSSD) and frequency (components LF and HF), the echocardiografic study was performed on the second day after AMI. On the third day post-MI, mice were divided into subgroups of 10 animals, and were sacrificed in order to collet specific materials: 500 ul of fresh peripheral blood and spleen technique for performing flow cytometry left ventricle for measurement of cytokine ELISA, and the left ventricle to perform immunohistochemistry. Techniques used were standardized and commonly used in laboraties. The results were evaluated by analysis of variance (ANOVA) multifactorial, using the GraphPad Prism with Tukey post hoc test RESULTS: The HF group compared to the control group showed a significant drop in blood pressure and increased heart rate. The IP group compared to the IC group showed higher vagal activity, characterized by a significant reduction in HR and increase HVR (SDNN, 9.2 ± 1.5 vs 5.2 ± 0.5, p < 0.05). The echocardiography parameters evaluated showed presence of area hypo/acinetic and reduced ejection fraction of the left ventricle in infracted groups of equal magnitude. Regarding the number of T lymphocytes, we found that the IC group compared with the control group showed significantly fewer lymphocytes regulators (CD25+Foxp3+) in peripheral blood (CD4+:63.5 ± 1.4 vs 70.6 ± 3.2% and CD8+ cells: 68.3 ± 1.9 vs 76.1 ± 2.8%). The IP group compared to the IC group showed a significant reduction in the number of conventional T lymphocytes in peripheral blood (CD4+:1.5 ± 0.2 vs 2.2 ± 0.2%; CD8+: 1.1 ± 0.1 vs 1.8 ± 0.9%) and was reduced only in the spleen of the type CD4+(1.4 ± 0.2 vs 2.2 ± 0,2%) with increased CD8+(1.2 ± 0.1 vs 0.7 ± 0.1%). The IP group also showed a significant increase of lymphocytes regulators (CD25+Foxp3+) in peripheral blood (CD4+: 76.5 ± 2.9 vs 63.5 ± 1.4%; CD8+:75.1 ± 1.0 vs 68.3 ± 1.9%), and no significant differences in the number of these cells in the spleen. The IC group compared to the control group showed significant labeling antibodies to CD4 and CD8 areas infarcted and peri-infarction by immunohistochemical analysis. The IP group compared to the IC group showed a significant increase in CD4 (20.9 ± 6.5 vs 12.2 ± 2.5, p < 0.05) and CD8 (17.9 ± 2.8 vs 5.8 ± 1.1%, p < 0.05) in the infarcted area, and we observed a significant reduction in the labeling of CD4 (6.0 ± 1.2 vs 12.5± 4.8) in the peri-infraction without significant changes in the marking of CD8. CONCLUSION: The treatment with pyridostigmine in rats with acute myocardial infarction is associated with increased vagal activity, increased number of regulatory lymphocytes (CD25+Foxp3+) in peripheral blood and increased mobilization of inflammatory cells (CD4 and CD8) to the infarcted myocardium, with reduction of these cells in the peri-infarction. The change of the inflammatory profile due to increased vagal activity may be a possible mechanism to explain the benefits in the evolution of myocardial infarction, especially in the improvement of cardiac remodeling and maintenance of ventricular function with anticholinesterase drugs

Hintergrund: Vegetative Übererregbarkeit ist ein zentrales Symptom der posttraumatischen Belastungsstörung (PTBS), welche durch eine präfrontale Disinhibition des limbischen Systems mit hieraus folgenden maladaptiven peripheren Stressreaktionen erklärt wird. Lange Zeit hat die Forschung den starken Einfluss des Parasympathikus auf die Stressregulation vernachlässigt und durch Erfassung zu weniger Parameter der Komplexität der autonomen Stressregulation nicht ausreichend Rechnung getragen. In dieser Studie sollen die Auswirkungen der sympathovagalen Dysbalance auf alltägliche Stressreaktionen und das Entspannungsvermögen von Frauen mit PTBS im Vergleich zu gesunden Frauen untersucht und Erkenntnisse über verschiedene autonome Regulationsmechanismen gewonnen werden. Hierbei sollen auch medikamentöse Einflüsse berücksichtigt und das subjektive Stressempfinden mit den physiologischen Messwerten korreliert werden. Methoden: 52 Patientinnen (P) und 39 gematchte, gesunde Frauen (K) wurden mit Hilfe eines hämodynamischen Monitorsystems während zweier 5-­minütiger Stresstests (Rechentest: RT, Babyschreien: BS) und in Ruhe untersucht. Mittels EKG-­, Impedanz-­ und Blutdruckmessungen wurden für jeden Herzschlag die folgenden Parameter erhoben: Herzrate (HR), Herzindex (CI), Präejektionszeit (PEP), peripherer Gefäßwiderstandsindex (TPRI), systolischer Blutdruck (sBP), hoch-­ und niederfrequente Herzratenvariabilität (HF-­ und LF-­HRV), Standardabweichung der regulären RR-­‐Intervalle (SDNN) und Barorezeptorsensitivät (BRS). Neben dem globalen Gruppenvergleich wurde auch ein Subgruppenvergleich durchgeführt, bei welchem die Reaktionen der Patientinnen ohne kardial wirksame Medikamente (P0, n=21) jeweils mit denen der Patientinnen mit kardial wirksamer Medikation (P1, n=27) und denen der Kontrollgruppe verglichen wurde. Zu Beginn der Untersuchung, nach jeder Stressphase und nach der abschließenden Entspannungsmusik wurde zudem das subjektive Stressempfinden auf einer SUD-­Skala von 0-­10 erfragt. Ergebnisse: Die HF-­HRV und die BRS von K fielen während des RT ab, während es zu einer Aktivierung der β-­adrenergen Parameter kam (CI↑, HR↑, PEP↓). Das BS verursachte bei K hingegen einen Anstieg von HF-­HRV und BRS, ohne dass hier starke sympathischen Reaktionen beobachtet werden konnten. P lag mit der HF-­HRV während aller Messphasen signifikant unter den Werten von K (p=0,0003). Signifikante Wechselwirkungen konnten für HR (p<0,0001), PEP (p=0,0032), BRS (p=0,0002) und CI (p=0,0106) nachgewiesen werden: während des RT stiegen die HR (p<0,0001) und der CI (p=0,041) von P signifikant schwächer an als bei K, während die PEP entsprechend weniger abfiel (p=0,006). Der Anstieg der BRS während des BS war bei P ebenfalls signifikant geringer ausgeprägt (p=0,009), zu vermehrten sympathischen Reaktionen kam es bei P dennoch ebenfalls nicht. Insgesamt zeigten sich auch keine signifikanten Unterschiede für den sBD. Dafür war das subjektive Stressempfinden von P über alle Messphasen und insbesondere während des BS signifikant höher (p=0,01). Eine geringe Korrelation war hier vor allem mit der HF-­HRV und der HR zu finden, für die meisten Parameter zeigte sich allerdings kein korrelativer Zusammenhang. Im Vergleich zwischen P0 und P1 fanden sich nur für CI, TPRI und SDNN signifikante Gruppenunterschiede (P1: CI↓, TPRI↑, SDNN↓) und für keinen der Parameter konnten im Subgruppenvergleich eine signifikante Wechselwirkung nachgewiesen werden. Insbesondere die HF-­HRV war auch bei P0 signifikant niedriger als bei K (p=0,0432). Das subjektive Stressempfinden beider Subgruppen unterschied sich nicht signifikant. Interpretation: Die gesunden Frauen reagierten während des Rechentests wie erwartet mit einer vagalen Disinhibition und der simultanen Aktivierung β-­adrenerger Aktivitätsparameter. Dies kann als eine aktive Stressbewältigung interpretiert werden. Während des Babyschreiens wurde jedoch offensichtlich eine andere autonome Reaktion ausgelöst, welche sich hauptsächlich in einer gesteigerten Vagusaktivität ausdrückte und kaum Veränderungen der sympathischen Parameter verursachte. Diese Studie zeigt somit als erste unterschiedliche vagale Reagibilitätsmuster auf externe Stimuli bei gesunden Frauen und verdeutlicht so den starken Einfluss der vagalen Modulation auf die verschiedenen Stressreaktionen. Bei den Patientinnen war hingegen bereits in Ruhe ein erniedrigter Vagotonus zu beobachten, welcher unter Stress eine reduzierte Reaktionsfähigkeit zeigte. Insbesondere während des Babyschreiens stiegen die vagalen Parameter bei ihnen nicht vergleichbar stark an. Darüber hinaus war bei den Patientinnen während des Rechnens eine geringere Aktivierung der β-­adrenergen Parameter und zu finden und auch während des Babyschreiens kam es trotz eines stärkeren subjektiven Stressempfindens nicht zu einer verstärkten sympathischen Reaktion. Diese Ergebnisse sprechen somit für eine vorwiegend vagale Dysfunktion bei PTBS im Sinne einer vagalen Hyporeagibilität bei insgesamt reduziertem Vagotonus. Auch wenn die Korrelation niedriger vagaler Werte mit einem erhöhten subjektiven Stressempfinden bei den Patientinnen nur schwach ist, ist sie mit den anderen Ergebnissen dieser Studie gut vereinbar. Stress scheint also möglicherweise auch durch den ausbleibenden Anstieg des Vagotonus zu entstehen und nicht nur durch eine Aktivierung des Sympathikus. Insgesamt muss jedoch eine Diskrepanz zwischen dem starken subjektiven Stresserleben und den nur gering reagierenden physiologischen Parametern hervorgehoben werden. Die kardialen Nebenwirkungen der Medikamente führten bei den Patientinnen lediglich zu einem Shift einiger Werte, nicht zu einem grundsätzlich veränderten Reaktionsmuster.