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dc.contributor.authorJonsson Eskelin, John
dc.date.accessioned2021-05-27T10:38:40Z
dc.date.available2021-05-27T10:38:40Z
dc.date.issued2021-05-27
dc.identifier.isbn978-91-8009-370-5 (PRINT)
dc.identifier.isbn978-91-8009-371-2 (PDF)
dc.identifier.urihttp://hdl.handle.net/2077/68073
dc.description.abstractThis thesis investigates a physiological phenomenon observed in the peripheral sympathetic nervous system in response to various stressors and tries to bring it closer to clinical research. Sudden surprising stimulation can evoke a transient inhibition of sympathetic nerve activity to blood vessels in the human body which is also predictive of the blood pressure response. The underlying medical hypothesis is that this may be important for long term blood pressure. In Paper I we investigate the possible genetic contribution to this response pattern in a group of monozygotic twins. Results show that genes do not play a significant role in this response and so the clinical interest is strengthened. In Paper II, correlates to sympathetic inhibition are described in pre-defined areas of the cerebral cortex with magnetoencephalography (MEG) and magnetic resonance imaging. We find strong correlations related to stimulus processing and cortical thickness as an index of long-term plastic changes. The anterior cingulate, a region known to be involved in threat evaluation and autonomic control is implicated. In Paper III another of these correlates, namely beta oscillations in the sensorimotor cortex, is used to evaluate the feasibility of using a routine clinical electro-encephalogram (EEG) for non-invasive characterization of the peripheral nerve reaction. The prospect of using EEG as a simple mode of classification is not well supported but MEG remains a promising candidate for developing a non-invasive method of gauging individual defense-related responses. Given the role of hypertension as the leading risk factor for global disease burden, a continued evaluation of underlying mechanisms is essential.sv
dc.language.isoengsv
dc.relation.haspart1. Lundblad, L. C., Eskelin, J. J., Karlsson, T., Wallin, B. G., & Elam, M. (2017). Sympathetic Nerve Activity in Monozygotic Twins: Identical at Rest but Not During Arousal. Hypertension, 69(5), 964-969. ::doi::10.1161/HYPERTENSIONAHA.117.09079sv
dc.relation.haspart2. Riaz, B., Eskelin, J. J., Lundblad, L. C., Wallin, B. G., Karlsson, T., Starck, G., Lundqvist, D., Ooostenveld, R., Schneiderman, J. F., & Elam, M. Brain structural and functional correlates to defense-related inhibition of muscle sympathetic nerve activity in man. Manuscriptsv
dc.relation.haspart3. Eskelin, J. J., Lundblad, L. C., Wallin, B. G., Karlsson, T., Riaz B., Lundqvist, D., Schneiderman, J. F., & Elam, M. Simultaneous recordings of EEG and MSNA during somatosensory stimulation – prospects of a non-invasive biomarker for defense-related sympathetic inhibition. Manuscriptsv
dc.subjectmicroneurographysv
dc.subjectMEGsv
dc.subjectEEGsv
dc.subjectMRIsv
dc.subjectblood pressuresv
dc.subjectdefence reactionsv
dc.subjectcortical autonomic networksv
dc.titleDefense-related inhibition of sympathetic nerve activity: Insights from neuroimaging and monozygotic twins on related cortical processes and clinical potentialsv
dc.typetexteng
dc.type.svepDoctoral thesiseng
dc.gup.mailjohn.jonsson.eskelin@gu.sesv
dc.type.degreeDoctor of Philosophy (Medicine)sv
dc.gup.adminAvhandlingen har en undertitel. Jag angav den som en del av huvudtiteln, men jag vet inte om den bör stå i fältet för 'alternativ titel'. Titeln har också ändrats efter att den registrerades första gången varför jag ersatte den som var ifylld.sv
dc.gup.originUniversity of Gothenburg. Sahlgrenska Academysv
dc.gup.departmentInstitute of Neuroscience and Physiology. Department of Clinical Neurosciencesv
dc.gup.defenceplaceFredagen den 18 juni 2021, kl. 13.00, sal 2119, Hus 2, Hälsovetarbacken, Arvid Wallgrens Backe, Göteborg. https://gu-se.zoom.us/j/63037687043?pwd=WHJaVDJrMTNEcWJta2RwbTIyWERvQT09sv
dc.gup.defencedate2021-06-18
dc.gup.dissdb-fakultetSA


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