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Name of the thesis Reactive oxygen species and their neurophysiological role Aim of the thesis Aim of the theoretical part is to provide overview of reactive oxygen species (ROS) and show their place in organism - posstive and necessary effects for the organism on the one hand and source of serious diseases on the other hand. Futhermore, the theoretical part deals with the restoration balance between the production of free radicals and antioxidants protection. Theoretical part also deals with substance FeTTPS. Aim of the experimental part is to determinate whether the application of FeTTPS affects cerebral blood flow during trancallosal stimulation with increasing frequency. Futhermore, to determinate whether the applicatication of this substance affects the slope of the curve and threshold of evoked potencials and number and duration of afterdischargers. Research method The research took place at the premises of Onstitue of Physiology, Academy of Sciences, Czech Republic. Experiments were carried out on laboratory albine Wistar rats. General anesthesia was performed to rats, stimulating and sensing electrodes were implated in epidural area of sensorimotoor cortex and Laser Doppler flow probe was implated into the contralateral hemisphere. In the first part of experiment included 11 animals. We...

Imagem por ressonância magnética tem sido um dos principais métodos para a aquisição de imagens para diagnósticos na medicina, em especial para a obtenção de medidas do cérebro. Apesar de se mostrar muito eficiente, o método atualmente utilizado para a realização da ressonância em hospitais e centros de diagnósticos, em alguns casos, necessita da aplicação de um contraste de gadolínio intravenoso. Essa injeção do contraste pode mostrar-se um tanto quanto invasivo, podendo em alguns casos resultar em algumas reações indesejadas nos pacientes. Em vista disso, um método que tem sido bastante estudado recentemente e muito promissor é o de Arterial Spin Labeling (ASL). Este método tem como sua principal vantagem o fato de não ser invasivo e de possibilitar a quantificação da perfusão sanguínea cerebral (CBF). No presente trabalho, foi feita uma otimização do contraste na aquisição das fases mais tardias da metodologia de ASL em múltiplas fases. Isso foi feito através de uma modulação do angulo de flip e é particularmente importante para a análise das imagens de pacientes com problemas neurovasculares, principalmente aqueles associados ao retardo nos tempos de trânsito do sangue arterial. Também, foi realizada toda a obtenção e processamento de dados para a avaliação da perfusão sanguínea cerebral utilizando o método proposto. / Magnetic resonance imaging has been one of the major methods to acquire images for medical diagnoses, specially, for obtaining brain images. Although the major method using magnetic resonance used today has high efficiency, in some cases it needs an injection of intravascular contrast agent, like gadolinium. This contrast agent application can be a lot invasive for the patient, in extremes cases resulting to allergic reactions the patient. Therefore, a method that has been studied recently and is very promising is the Arterial Spin Labeling (ASL). This method has the major advantage the feature that it is completely non invasive for the patient and it allows to quantify the perfusion value. In this work, it was implemented an optimization of the contrast in the late phases of ASL multiphase acquisition. It was made using a modulation of the flip angle and it is critical to analyze images from patients with some neurovascular disease, especially those associated with arterial blood transit time delay. Besides that, it was made all data acquisition and data processing for the brain perfusion evaluation using the proposed method.

Orientador: Fernando Gomes Romeiro / Resumo: Aminoácidos de cadeia ramificada aumentam a perfusão cerebral de pacientes com encefalopatia hepática (EH), mas o aminoácido responsável por esse aumento e os mecanismos envolvidos ainda não são conhecidos. Este estudo comparou a perfusão cerebral e a melhora clínica durante a suplementação de leucina ou isoleucina. Após a randomização, 27 indivíduos com cirrose e EH receberam suplementos de leucina ou isoleucina por um ano. Exames de tomografia computadorizada por emissão de fóton único (SPECT) e cintilografia cerebral dinâmica (DBS) foram realizados antes do estudo e após 1, 8 e 12 meses de suplementação. Apenas o grupo que recebeu isoleucina teve aumento da perfusão cerebral aos 8 meses de tratamento pelo exame de SPECT e pela cintilografia (p<0,001 e p = 0,05, respectivamente), também observado pelo SPECT aos 12 meses de suplementação (p < 0,05). O aumento do fluxo cerebral foi associado a melhora da EH aos 8 e 12 meses de suplementação (p=0,008 e 0,004, respectivamente), porém essa melhora não foi observada no grupo que recebeu leucina (p=0,313 e 0,055, respectivamente). A suplementação com isoleucina obteve melhor impacto na restauração da perfusão cerebral em pacientes com EH. / Abstract: Branched-chain amino acids increase the brain perfusion of patients with hepatic encephalopathy (HE), but the amino acid and the mechanisms involved are still unknown. This study compared brain perfusion and clinical improvement during leucine or isoleucine supplementation. After randomization, 27 subjects with cirrhosis and HE received leucine or isoleucine supplements for one year. Brain single photon emission computed tomography (SPECT) and dynamic brain scintigraphy (DBS) were performed pretreatment and at 1, 8 and 12 months of supplementation. Brain perfusion was increased only in the isoleucine group at 8 months of treatment by both SPECT and DBS (p<0.001 and p = 0.05, respectively) and by SPECT at the 12th month (p < 0.05). This was associated with hepatic encephalopathy improvement at 8 and 12 months (p=0.008 and 0.004, respectively), which was not observed in the leucine group (p=0.313 and 0.055, respectively). Isoleucine supplementation achieved a better impact on brain perfusion restoration in HE. / Doutor

New optical technologies were developed to continuously measure cerebral blood flow (CBF) and oxygen metabolism (CMRO2) non-invasively through the skull. Methods and devices were created to improve the performance of near-infrared spectroscopy (NIRS) and diffuse correlation spectroscopy (DCS) for use in experimental animals and humans. These were employed to investigate cerebral metabolism and cerebrovascular reactivity under different states of anesthesia and during models of pathological states. Burst suppression is a brain state arising naturally in pathological conditions or under deep general anesthesia, but its mechanism and consequences are not well understood. Electroencephalography (EEG) and cortical hemodynamics were simultaneously measured in rats to evaluate the coupling between cerebral oxygen metabolism and neuronal activity in the burst suppressed state. EEG bursts were used to deconvolve NIRS and DCS signals into the hemodynamic and metabolic response function for an individual burst. This response was found to be similar to the stereotypical functional hyperemia evoked by normal brain activation. Thus, spontaneous burst activity does not cause metabolic or hemodynamic dysfunction in the cortex. Furthermore, cortical metabolic activity was not associated with the initiation or termination of a burst. A novel technique, time-domain DCS (TD-DCS), was introduced to significantly increase the sensitivity of transcranial CBF measurements to the brain. A new time-correlated single photon counting (TCSPC) instrument with a custom high coherence pulsed laser source was engineered for the first-ever simultaneous measurement of photon time of flight and DCS autocorrelation decays. In this new approach, photon time tags are exploited to determine path-length-dependent autocorrelation functions. By correlating photons according to time of flight, CBF is distinguished from superficial blood flow. Experiments in phantoms and animals demonstrate TD-DCS has significantly greater sensitivity to the brain than existing transcranial techniques. Intracranial pressure (ICP) modulates both steady-state and pulsatile CBF, making CBF a potential marker for ICP. In particular, the critical closing pressure (CrCP) has been proposed as a surrogate measure of ICP. A new DCS device was developed to measure pulsatile CBF non-invasively. A novel method for estimating CrCP and ICP from DCS measurement of pulsatile microvascular blood flow in the cerebral cortex was demonstrated in rats. / 2018-03-08T00:00:00Z

<p>Ischemic neuronal injury continues to be a major delimiting factor in achieving successful clinical outcomesafter resuscitation from cardiac arrest. In this thesis, a pig model of cardiopulmonary resuscitation (CPR) wasused to address the effects of different interventions on cerebral blood flow and oxygenation during CPR and theinitial postresuscitation period. A novel technique is presented to quantify the reperfusion oxidative injury.</p><p>Maximization of cerebral blood flow during CPR by open-chest cardiac compression, continuous aortic balloon occlusion, and intra-aortic administration of hypertonic saline-dextran (HSD) did not ameliorate thepostresuscitation hypoperfusion or improve the cerebral oxygen extraction ratio or tissue pH. These findings disaffirm earlier studies suggesting that conserving brain viability after global ischemia is mostly a question ofmaintaining high perfusion pressure.</p><p>Despite an increased cerebral perfusion pressure during CPR, intra-aortic administered epinephrineabove the aortic balloon occlusion did not further improve cerebral blood flow and oxygenation. This findingmay indicate adverse effects of epinephrine on cerebral vascular beds, possibly induced by a relatively highconcentration of epinephrine when administered above the site for aortic balloon occlusion.</p><p>The IV administration of equipotent doses of epinephrine or vasopressin during CPR resulted incomparable hemodynamic changes. The peak increase in cerebral cortical blood flow, however, was reachedapproximately 30 sec later by vasopressin. Furthermore, the second bolus of vasopressin during CPR did notaugment cerebral perfusion, whereas epinephrine did. Consequently, reports suggesting that vasopressin issuperior to epinephrine with respect to its effects on central hemodynamics and vital organ blood flow may bebiased by the pharmacodynamic differences between the drugs, depending on the time point at which blood flowmeasurements are performed.</p><p>In comparison with IV vasopressin, vasopressin administered above the aortic balloon occlusion resulted in a significant increase in cerebral perfusion pressure during CPR, but not after restoration of spontaneous circulation (ROSC). Cerebral cortical blood flow was, however, not improved <i>during</i> CPR, whereas a significant increase was recorded <i>after</i> ROSC. Relatively higher concentrations of vasopressin above the sitefor intra-aortic balloon occlusion may, therefore, predominantly induce cerebral cortical vasoconstriction duringCPR but induce vasodilatation after ROSC.</p><p>Assessment of oxidative stress or inflammation have been extremely difficult to attain. In our pig model of resuscitation, an association wasobserved between the duration of cardiac arrest and jugular bulb levels of 8-iso-PGF_2α, a major isoprostane and a novel index of oxidative injury. 8-iso-PGF_2α, and the prostaglandin 15-K-DH-PGF_2α, increased within 5 min after ROSC and remained so up to 2 h, indicating the interval of time during which cerebral reperfusion oxidative injury and inflammatory response may occur and are potentially preventable.</p>

Ischemic neuronal injury continues to be a major delimiting factor in achieving successful clinical outcomesafter resuscitation from cardiac arrest. In this thesis, a pig model of cardiopulmonary resuscitation (CPR) wasused to address the effects of different interventions on cerebral blood flow and oxygenation during CPR and theinitial postresuscitation period. A novel technique is presented to quantify the reperfusion oxidative injury. Maximization of cerebral blood flow during CPR by open-chest cardiac compression, continuous aortic balloon occlusion, and intra-aortic administration of hypertonic saline-dextran (HSD) did not ameliorate thepostresuscitation hypoperfusion or improve the cerebral oxygen extraction ratio or tissue pH. These findings disaffirm earlier studies suggesting that conserving brain viability after global ischemia is mostly a question ofmaintaining high perfusion pressure. Despite an increased cerebral perfusion pressure during CPR, intra-aortic administered epinephrineabove the aortic balloon occlusion did not further improve cerebral blood flow and oxygenation. This findingmay indicate adverse effects of epinephrine on cerebral vascular beds, possibly induced by a relatively highconcentration of epinephrine when administered above the site for aortic balloon occlusion. The IV administration of equipotent doses of epinephrine or vasopressin during CPR resulted incomparable hemodynamic changes. The peak increase in cerebral cortical blood flow, however, was reachedapproximately 30 sec later by vasopressin. Furthermore, the second bolus of vasopressin during CPR did notaugment cerebral perfusion, whereas epinephrine did. Consequently, reports suggesting that vasopressin issuperior to epinephrine with respect to its effects on central hemodynamics and vital organ blood flow may bebiased by the pharmacodynamic differences between the drugs, depending on the time point at which blood flowmeasurements are performed. In comparison with IV vasopressin, vasopressin administered above the aortic balloon occlusion resulted in a significant increase in cerebral perfusion pressure during CPR, but not after restoration of spontaneous circulation (ROSC). Cerebral cortical blood flow was, however, not improved during CPR, whereas a significant increase was recorded after ROSC. Relatively higher concentrations of vasopressin above the sitefor intra-aortic balloon occlusion may, therefore, predominantly induce cerebral cortical vasoconstriction duringCPR but induce vasodilatation after ROSC. Assessment of oxidative stress or inflammation have been extremely difficult to attain. In our pig model of resuscitation, an association wasobserved between the duration of cardiac arrest and jugular bulb levels of 8-iso-PGF2α, a major isoprostane and a novel index of oxidative injury. 8-iso-PGF2α, and the prostaglandin 15-K-DH-PGF2α, increased within 5 min after ROSC and remained so up to 2 h, indicating the interval of time during which cerebral reperfusion oxidative injury and inflammatory response may occur and are potentially preventable.

Chronic muscle pain is a significant medical and social problem and better understanding of the pathophysiological mechanisms involved is an important requirement for further development of diagnostics, treatment and rehabilitation methods. Experimental imaging studies have investigated functional neuroanatomy of different pain components. However, several aspects of brain mechanisms underlying brain processing of muscle pain remain unclear. The general goal of the present thesis was to study functional brain anatomy of systems underlying perception of muscle pain, processing of proprioceptive information and maintenance of fatiguing muscle contractions with an emphasize on their possible interrelations. Four series of experiment were carried out. Using an injection of hypertonic saline (HS) into the m. triceps to induce pain comparable with clinical muscle pain a significant activation of insula and putamen as well as decrease of activity in the temporal and occipital cortex in comparison with control stimulation were revealed. An advanced model of prolonged muscle pain were provided by the infusion of the HS during 20 minutes into m. erector spinae A complex dynamics of brain activity during the habituation to nociceptive stimulation was shown: initial activation of insula changed to decrease of activity in this and several other cortical areas. A conjunction analysis identified activations jointly significant in both experiments (despite localization of HS nociceptive stimulation) in the right insula, occipital and left parietal cortical areas. The study of brain activity in response to different modalities of prorioceptive inputs – passive movements, kinesthetic illusions and muscle vibration showed corresponding different patterns of activation in motor and somatosenory areas and temporal areas. Finally, the study of sustained isometric muscle contractions of various force levels and durations revealed that muscle fatigue is associated with contralateral activation of the motor and somatosensory areas and temporal areas and bilateral activation in the supplementary motor areas and cingular cortex, indicating that increased efforts needed to maintain required force and its eventual breakdown with fatigue might induce activation of additional cortical areas. Analysis of data obtained in all experimental series revealed that insula, secondary somatosensory and auditory areas are activated during both perception of muscle pain and processing of somatosensory afferentation. In conclusion, this thesis has elucidated brain processing of muscle pain showing distributed, bilateral patterns comprised of activated structures predominantly attributed to the medial pain system and deactivated structures. Furthermore, initial and late phases of tonic muscle pain are associated with different brain reactions, namely initial activation of the insula followed by a significant bilateral decrease of activity at the late stage. Area of brain cortex located near lateral sulcus and comprised of secondary somatosensory cortex, posterior part of the insula and adjacent auditory cortex is engaged in the perception of muscle pain and processing of somatosensory afferentation as well as maintenance of fatiguing muscle contractions.

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