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The Global ETD Search service is a free service for researchers
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Showing 141 to 150 of 162 (0.021 seconds)Spelling suggestions: "subject:"gehirn"" "subject:"endhirn""
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Neuroendocrine effects of the endocrine disruptors Vinclozolin and Equol in the adult male rat / Neuroendokrine Effekte der endokrinen Disruptoren Vinclozolin und Equol in der erwachsenen männlichen RatteLoutchanwoot, Panida 19 November 2007 (has links)
No description available.
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Graph Metrics of Structural Brain Networks in Individuals with Schizophrenia and Healthy Controls: Group Differences, Relationships with Intelligence, and GeneticsYeo, Ronald A., Ryman, Sephira G., van den Heuvel, Martijn P., de Reus, Marcel A., Jung, Rex E., Pommy, Jessica, Mayer, Andrew R., Ehrlich, Stefan, Schulz, S. Charles, Morrow, Eric M., Manoach, Dara, Ho, Beng-Choon, Sponheim, Scott R., Calhoun, Vince D. 02 June 2020 (has links)
Objectives: One of the most prominent features of schizophrenia is relatively lower general cognitive ability (GCA). An emerging approach to understanding the roots of variation in GCA relies on network properties of the brain. In this multi-center study, we determined global characteristics of brain networks using graph theory and related these to GCA in healthy controls and individuals with schizophrenia.
Methods: Participants (N = 116 controls, 80 patients with schizophrenia) were recruited from four sites. GCA was represented by the first principal component of a large battery of neurocognitive tests. Graph metrics were derived from diffusion-weighted imaging.
Results: The global metrics of longer characteristic path length and reduced overall connectivity predicted lower GCA across groups, and group differences were noted for both variables. Measures of clustering, efficiency, and modularity did not differ across groups or predict GCA. Follow-up analyses investigated three topological types of connectivity—connections among high degree “rich club” nodes, “feeder” connections to these rich club nodes, and “local” connections not involving the rich club. Rich club and local connectivity predicted performance across groups. In a subsample (N = 101 controls, 56 patients), a genetic measure reflecting mutation load, based on rare copy number deletions, was associated with longer characteristic path length.
Conclusions: Results highlight the importance of characteristic path lengths and rich club connectivity for GCA and provide no evidence for group differences in the relationships between graph metrics and GCA.
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Identification and characterisation of novel zebrafish brain development mutants obtained by large-scale forward mutagenesis screeningKlisa, Christiane 09 January 2004 (has links)
Developmental biology adresses how cells are organised into functional structures and eventually into a whole organism. It is crucial to understand the molecular basis for processes in development, by studying the expression and function of relevant genes and their relationship to each other. A gene function can be studied be creating loss-of-function situations, in which the change in developmental processes is examined in the absense of a functional gene product, or in gain-of-function studies, where a gene product is either intrinsically overproduced or ectopically upregulated. One approach for a loss-of-function situation is the creation of specific mutants in single genes, and the zebrafish (Danio rerio) has proven to be an excellent model organism for this purpose. In this thesis, I report on two forward genetic screens performed to find new mutants affecting brain development, in particular mutants defective in development and function of the midbrain-hindbrain boundary (MHB), an organiser region that patterns the adjacent brain regions of the midbrain and the hindbrain. In the first screen, I could identify 10 specific mutants based on morphology and the analysis of the expression patterns of lim1 and fgf8, genes functioning as early neuronal markers and as a patterning gene, respectively. Three of these mutants lacked an MHB, and by complementation studies, I identified these mutants as being defective in the spg locus. The second screen produced 35 new mutants by screening morphologically and with antibodies against acetylated Tubulin, which marks all axonal scaffolds, and anti-Opsin, which is a marker for photoreceptors in the pineal gland. According to their phenotype, I distributed the mutant lines into 4 phenotypic subgroups, of which the brain morphology group with 18 mutant lines was studied most intensively. In the last part of my thesis, I characterise one of these brain morphology mutants, broken heart. This mutant is defective in axonal outgrowth and locomotion, and shows a striking reduction of serotonergic neurons in the epiphysis and in the raphe nuclei in the hindbrain, structures involved in serotonin and melatonin production. Studies in other model organisms suggested a role of factors from the floor plate and the MHB in induction of the serotonergic neurons in the hindbrain, and using broken heart, I show that Fgf molecules such as Fgf4 and Fgf8 can restore partially the loss of serotonergic neurons in the mutant. I conclude that forward genetic screens are an invaluable tool to generate a pool of mutations in specific genes, which can be used to dissect complex processes in development such as brain development.
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Growth and design strategies of organic dendritic networksCiccone, Giuseppe, Cucchi, Matteo, Gao, Yanfei, Kumar, Ankush, Seifert, Lennart Maximilian, Weissbach, Anton, Tseng, Hsin, Kleemann, Hans, Alibart, Fabien, Leo, Karl 05 March 2024 (has links)
A new paradigm of electronic devices with bio-inspired features is aiming to mimic the brain’s fundamental mechanisms to achieve recognition of very complex patterns and more efficient computational tasks. Networks of electropolymerized dendritic fibers are attracting much interest because of their ability to achieve advanced learning capabilities, form neural networks, and emulate synaptic and plastic processes typical of human neurons. Despite their potential for braininspired computation, the roles of the single parameters associated with the growth of the fiber are still unclear, and the intrinsic randomness governing the growth of the dendrites prevents the development of devices with stable and reproducible properties. In this manuscript, we provide a systematic study on the physical parameters influencing the growth, defining cause-effect relationships for direction, symmetry, thickness, and branching of the fibers. We build an electrochemical model of the phenomenon and we validate it in silico using Montecarlo simulations. This work shows the possibility of designing dendritic polymer fibers with controllable physical properties, providing a tool to engineer polymeric networks with desired neuromorphic features.
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Die Isolierung und Charakterisierung der cDNA und des Gens Metr-1 der Maus, einem Vertreter der Bruno-like Genfamilie und Analysen zur Expression / The isolation and characterization of the cDNA und gene Metr-1 of the mouse, a member of the Bruno-like gene family, and expression analysisWilhelm, Christian 30 January 2002 (has links)
No description available.
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Interindividual Differences in Mid-Adolescents in Error Monitoring and Post-Error AdjustmentRodehacke, Sarah, Mennigen, Eva, Müller, Kathrin U., Ripke, Stephan, Jacob, Mark J., Hübner, Thomas, Schmidt, Dirk H. K., Goschke, Thomas, Smolka, Michael N. 14 July 2014 (has links) (PDF)
A number of studies have concluded that cognitive control is not fully established until late adolescence. The precise differences in brain function between adults and adolescents with respect to cognitive control, however, remain unclear. To address this issue, we conducted a study in which 185 adolescents (mean age (SD) 14.6 (0.3) years) and 28 adults (mean age (SD) 25.2 (6.3) years) performed a single task that included both a stimulus-response (S-R) interference component and a task-switching component. Behavioural responses (i.e. reaction time, RT; error rate, ER) and brain activity during correct, error and post-error trials, detected by functional magnetic resonance imaging (fMRI), were measured. Behaviourally, RT and ER were significantly higher in incongruent than in congruent trials and in switch than in repeat trials. The two groups did not differ in RT during correct trials, but adolescents had a significantly higher ER than adults. In line with similar RTs, brain responses during correct trials did not differ between groups, indicating that adolescents and adults engage the same cognitive control network to successfully overcome S-R interference or task switches. Interestingly, adolescents with stronger brain activation in the bilateral insulae during error trials and in fronto-parietal regions of the cognitive control network during post-error trials did have lower ERs. This indicates that those mid-adolescents who commit fewer errors are better at monitoring their performance, and after detecting errors are more capable of flexibly allocating further cognitive control resources. Although we did not detect a convincing neural correlate of the observed behavioural differences between adolescents and adults, the revealed interindividual differences in adolescents might at least in part be due to brain development.
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GehirnforschungPalm, Kerstin 27 April 2017 (has links) (PDF)
Gehirnforschung ist ein naturwissenschaftlicher Forschungsbereich, der sich aus den Disziplinen Anatomie, Embryologie, Physiologie, Pharmakologie und Psychologie entwickelt hat. Gendertheoretisch informierte historische Studien zur Gehirnforschung fokussieren ideologiekritische und diskursanalytische Betrachtungen androzentrischer bzw. sexistischer Körpervorstellungen von der Antike bis zum 21. Jh., welche u. a. die bürgerliche Geschlechterordnung argumentativ gestützt und naturalisiert hatten.
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Simultane Erfassung cerebraler Aktivität mittels Dipol-Quellenlokalisation und funktioneller MRT am Beispiel einer somatosensorischen KategorisierungsaufgabeThees, Sebastian 10 November 2004 (has links)
Mit dieser Arbeit ist es erstmalig gelungen, funktionelle MRT und Dipol-Quellenlokalisation in einer Weise zu kombinieren, die es erlaubt, ein und dieselbe kortikale Aktivität simultan mit beiden Verfahren zu erfassen. Insbesondere wurde dies durch (a) Korrektur eines vom Tomographen induzierten Artefaks in den EKPs und (b) durch eine deutliche Verbesserung des experimentellen Designs, und damit einer wesentlich effektiveren Nutzung von EEG und fMRT-Messzeit erreicht. So wurde es dadurch möglich, mit beiden Methoden die kortikale Aktivität einer Einzelpulsstimulation noch aufzulösen. Eine wesentliche Voraussetzung für die simultane Kombination beider Verfahren: Aufgrund der sehr verschiedenen Latenzen von elektrophysiologischer (< 1ms) und vaskulärer (SII->ant. Inseln und medialeWand) in Übereinstimmung mit der Literatur (Forss et al., 1996; Mauguiere et al., 1997b) blieb. So ergab die Quellenlokalisation für die Wahlreaktionsaufgabe fünf Dipole innerhalb des Gehirns, welche mittels Koregistrierung den Aktivierungen des primären somatosensorschen Kortex (20 - 140ms), des sekundären somatosensorischen Kortex (50 - 150ms), der beiden anterioren Inseln (80 - 140ms) und des supplementär-motorischen Region (90 - 140ms, 220 - 270ms) aus der funktionellen MRT zugeordnet wurden. Durch einen Vergleich der Aktivierungsmuster von Wahl- und Einfachreaktionsaufgabe jeweils in der Dipol-Quellenanalyse und in der funktionellen MRT konnten weitere Belege dafür gefunden werden, daß, wie in der Literatur postuliert (Romo and Salinas, 2001), der kontralaterale sekundäre somatosensorische Kortex an der Kategorisierung somatosensorischer Stimulusattribute beteiligt ist. So ergab ein Vergleich der Dipolzeitverläufe für Wahl- und Einfachreaktionsaufgabe lediglich für den Dipol im kontralateral somatosensorischen Kortex im Intervall 57-62 ms nach Stimulusapplikation einen signifikant unterschiedlichen Aktivierungsverlauf (p < 0,001). Übereinstimmend zeigte die funktionelle MRT für die Wahlreaktionsaufgabe neben einer stärkeren Aktivierung der SMA eine hochsignifikant stärkere Aktivierung im Areal des kontralateralen sekundären somatosensorischen Kortex (p-cluster < 0,001). / In this study, we have shown that it is feasible to perform dipole source analysis and fMRI based on the same neuronal activity associated with somatosensory categorization. This was possible by reduction of scanner-induced baseline artifact interfering with the ERPs as well as an optimized experimental protocol for interleaved EEG and fMRI acquisition. We consider this study to be a further step toward imaging brain activity simultaneously at high spatial and temporal resolution. Since an event-related protocol with a single brief pulse stimulation paradigm was successfully employed, this approach seems to be suitable for the investigation of cognitive tasks. By further technical improvements also the exploration of brain activity in single subjects might become possible, opening the field of clinical applications. In particular for the characterization of irregular and nonreproducible events, a substantial contribution of combined EEG–fMRI studies toward a more detailed understanding of physiological processes underlying cerebral activations is expected.
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Neurostimulations-KulturKalmbach-Özdem, Monika 12 1900 (has links)
Die Medizintechnik Tiefe-Hirnstimulation ist nicht nur als naturwissenschaftlich-technisches Produkt zu sehen, sondern vor allem auch als kultur-technische Leistung mit historischen Wurzeln. Dieserart Schnittstellenhandlungen nehmen einen festen Platz in der Medizingeschichte ein und sind nicht losgelöst von dieser zu bestimmen. Ein- und zugreifende Praktiken wie Trepanationen und Schädelkulte sind vielfältig verankert und offenbaren einen menschheitsalten Wunsch nach Einflussnahme und Bemächtigung. Hierüber lässt sich der Mensch als verknüpf-, einstell- und gestaltbare Entität im Rahmen 'eutoper' Welt- und Technikbilder sowie deterministischer Menschenbilder darstellen. Mit der Integration aktiver, technischer Elemente in den menschlichen Körper verschieben wir die Grenzverläufe zwischen biologischen und artifiziellen Entitäten. Sowohl die Hardware-Software-Relationen als auch die Körper-Geist-Relationen unterliegen dabei Verknüpfungs- und Gestaltungsprozessen. Aus der Interaktion zwischen menschlichen und nicht-menschlichen Handlungsteilnehmern resultieren neuartige Wechselbeziehungen, welche unter Zuhilfenahme der Embodiment- und Embedded-Theorie nachgezeichnet werden. Den schwerwiegenden Aus- und Nebenwirkungen dieser Interkation wird mit einem empirischen Fallbeispiel nahegekommen. Dass diese Entwicklung hin zu einer konfigurierenden Gestaltungskultur risikobehaftet ist, wird unter Zuhilfenahme des Terminus 'Experimentalsystem' dargelegt. Dabei ist festzuhalten, dass die Tiefe-Hirnstimulation nicht trotz sondern wegen experimenteller Faktoren erfolgreich und faszinierend ist. Neurostimulationen in erster Linie als Konzept zu begreifen bedeutet, den Fokus auf kulturelle Anschichten und Handlungen zu lenken. In welchem Ausmaß wir zu ein- und zugreifenden Gestaltungen unserer Selbst bereit sind, hängt in letzter Konsequenz an unserem menschlichen Selbstverständnis. / Medical technology deep brain stimulation is not only a scientific and technical product, but also a cultural and technical achievement with historical roots. This kind of interface actions occupy a firm place in medical history and cannot be determined separately from it. Interfering practices such as trepanations and cults of the skull are rooted in many different ways and reveal an ancient human desire for influence and empowerment. In this way, man can be represented as a connectable, adjustable and configurable entity within the framework of 'eutoper' world and technology images as well as deterministic human images. By integrating active technical elements into the human body, we are shifting the boundaries between biological and artificial entities. Both the hardware-software-relations as well as the body-spirit-relations are subject to connection and design processes. The interaction between human and non-human action participants results in novel interrelationships, which are traced with the aid of the Embodiment and Embedded Theory. The serious side effects of this interaction are approached with an empirical case study. The fact that this development towards a configuring design culture entails risk is explained with the help of the term 'experimental system'. It should be noted that deep brain stimulation is successful and fascinating not despite but because of experimental factors. Understanding neurostimulation primarily as a concept means focusing on cultural strata and actions. The extent to which we are prepared to embrace and intervene in shaping ourselves depends ultimately on our human self-conception.
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Sauerstofftoxizität im unreifen GehirnMahler, Lieselotte 28 July 2005 (has links)
Die rasanten Fortschritte in der neonatalen Intensivmedizin haben zwar die Ueberlebenschancen von Fruehgeborenen enorm verbessert, aber auch viele Probleme und Fragen aufgeworfen. In dieser Arbeit wurde untersucht, ob Hyperoxie Einfluss nimmt auf die Expression von apoptotischen Genen, Wachstumsfaktoren und Zytokinen und so ueber verschiedene Mechanismen und Signalwege zu einem Ungleichgewicht der ueber das neuronale Ueberleben entscheidenden Faktoren fuehrt. 6-Tage alte Ratten wurden fuer bestimme Zeitabschnitte (2, 6, 12, 24, 48, 72 Stunden) einer 80%igen Sauerstoffkonzentration ausgesetzt. In dieser Arbeit konnte am unreifen Rattengehirn nachgewiesen werden, dass eine 80%ige Sauerstoffkonzentration in der Atemluft maximal nach 12 bis 24 Stunden zu einer ausgepraegten, diffusen apoptotischen Neurodegeneration im Gehirn fuehrt. Die Exposition mit hoher Sauerstoffkonzentration fuehrte im unreifen Gehirn zu einer deutlich verminderten Expression der Neurotrophinen, wie deren Signalproteine ERK 1/2 und Akt. Als spezifischer Nachweis fuer eine apoptotische Neurodegeneration wurden neben dem histologischen Verfahren auf molekularer Ebene apoptotische Gene untersucht. Unter Hyperoxie kam es zu einer erhoehten Expression des Todesrezeptors Fas und einer gesteigerten Aktivitaet von Caspase-3.Des Weiteren fand sich infolge der Hyperoxieexposition ein drastischer Anstieg der inflammatorischen Zytokine IL-1beta und IL-18. Es zeigt sich also, dass hohe Sauerstoffkonzentrationen in einer sehr vulnerablen Phase der Hirnentwicklung (Phase des rapiden Hirnwachstums) zu massiven Veraenderungen fuehren, welche den bisher ungeklaerten diffusen Neuronenuntergang bei Fruehgeborenen erklaeren koennten. Die vorliegenden Ergebnisse implizieren aeu§erste Vorsicht bei der therapeutischen Anwendung von Sauerstoff bei Fruehgeborenen, fuer die die postnatalen Konditionen, verglichen mit den intrauterinen Bedingungen, immer hyperoxisch sind und die noch ueber ein unreifes Antioxidationssystem verfuegen. / Infants born prematurely may develop neurocognitive deficits without an obvious cause. Oxygen, which is widely used in neonatal medicine, constitutes one possible contributing neurotoxic factor, because it can trigger neuronal apoptosis in the developing brain of rodents. Premature infants are exposed to partial oxygen pressures that are fourfold higher compared to intrauterine conditions, even if no supplemental oxygen is administered. Here is reported that short exposures to nonphysiologic oxygen levels can trigger apoptotic neurodegeneration in the developing brain. Vulnerability to oxygen neurotoxicity is confined to the first 2 weeks of life, a period characterized by rapid growth, which in humans expands from the sixth month of pregnancy to the third year of life. Hyperoxia caused decreased expression of neurotrophins, and inactivation of survival signalling proteins extracellular signal-regulated kinase (ERK1/2), and protein kinase B (Akt). In addition we hypothesized that two caspase-1-processed cytokines, interleukin (IL)-1beta and IL-18, are involved in oxygen-induced neuronal cell death. Six-day-old Wistar rats were exposed to 80% oxygen for various time periods (2, 6, 12, 24, 48, 72 hours). Neuronal cell death in the brain, as assessed by silver staining, peaked at 12 to 24 hours and was preceded by a marked increase in mRNA of IL-1beta, IL-18 and FAS and a decrease in mRNA and protein levels of neurotrophins and ERK1/2 and Akt Our findings reveal mechanisms that could potentially damage the developing brain of human premature neonates.
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