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dc.contributor.authorPrestipino, Louise
dc.date.accessioned2020-08-04
dc.date.available2020-08-04
dc.date.issued2020en_AU
dc.identifier.urihttps://hdl.handle.net/2123/23005
dc.description.abstractThere is accumulating evidence that hypertension is a symptom of underlying autonomic dysfunction, including aberrant stress responses. Before autonomic activity is examined in models of hypertension, the underlying connectivity that drives stress responses under physiological conditions must be further elucidated. In Chapter 3, we examined the afferent connectivity of the dorsomedial hypothalamus (DMH) by combining retrograde tracing and Fos immunohistochemistry following air jet stress. Stress-activated, DMH-projecting neurons were located predominantly in forebrain nuclei. Total numbers of these cells were modest, suggesting that their role may involve contextual modulation of the DMH output. In chapter 4, we demonstrated that gestational dofetilide programs hypertensive offspring with impaired stress habituation. Spectral analysis provided evidence of increased sympathetic vasomotor tone. Dofetilide shares its mechanism of action with several other drugs, thus, the results emphasise the need for further research into gestational drug use and potential programming effects. In chapter 5, we present the first evidence in rodents that advanced maternal age (AMA) programs offspring with lower blood pressure. Despite the proclivity for metabolic dysfunction, AMA offspring display reduced indices of sympathetic vasomotor tone and improved baroreflex. We hypothesise that the positive influence of maternal attentiveness programs improved blood pressure regulation. In chapter 6, we present preliminary data that show the DMH is influenced by reactive oxygen species. DMH microinjection of the O2 scavenger Tempol appeared to attenuate the sympathoexcitatory effects of a GABA(A) antagonist. Data from models of programmed hypertension indicate that the hypertensive phenotype is preceded by elevated oxidative stress. If ROS stimulates excitation of the DMH, this may explain why antioxidant intervention has proven to be an effective treatment in programmed hypertension.en_AU
dc.language.isoenen_AU
dc.publisherUniversity of Sydneyen_AU
dc.subjectdevelopmental programmingen_AU
dc.subjectneuroanatomyen_AU
dc.subjecthypertensionen_AU
dc.subjectadvanced maternal ageen_AU
dc.subjectgestational drug useen_AU
dc.subjectHRV BPVen_AU
dc.titleDevelopmental Programming of Cardiovascular Control: How Maternal Factors Influence the Health of the Adult Offspringen_AU
dc.typeThesis
dc.type.thesisDoctor of Philosophyen_AU
dc.rights.otherThe author retains copyright of this thesis. It may only be used for the purposes of research and study. It must not be used for any other purposes and may not be transmitted or shared with others without prior permission.en_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::School of Medical Sciencesen_AU
usyd.departmentDiscipline of Physiologyen_AU
usyd.departmentCardiovascular Neuroscience Laboratoryen_AU
usyd.degreeDoctor of Philosophy Ph.D.en_AU
usyd.awardinginstThe University of Sydneyen_AU
usyd.advisorPolson, Jaimie


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