Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/119472
Type: Thesis
Title: Determining if pre-existing inflammation affects facial motoneuronal survival
Author: Katharesan, Viythia
Issue Date: 2016
School/Discipline: Adelaide Medical School
Abstract: Motor Neuron Disease (MND) is a debilitating condition affecting ageing individuals that is characterised by the death of motoneurones. Changes in the neurotrophic support of motoneurones, altered glial and synaptic activity and levels of inflammation have been proposed as mechanisms underlying MND, but these have not been considered in the light of advancing age, which is the single biggest risk factor for MND. This thesis investigates the roles of age, neurotrophic factors, perineuronal responses through glial and synaptic activity, and levels of inflammation in experimental models of rat facial motoneuronal death and rescue. It pays particular attention to an isoform of IGF-1 derived from active muscle, known as Mechano Growth Factor (MGF) and its mechanism of action. It investigates if perineuronal responses can predict the fate of injured motoneurones. It also correlates age-related changes in levels of inflammatory mediators with motoneuronal survival after injury. It reports that: (i) MGF rescues mature motoneurones by a mechanism that is independent of the IGF-1 receptor and Protein Kinase C; (ii) perineuronal responses such as glial and synaptic activity may still predict the fate of injured motoneurones; (iii) the survival of avulsed facial motoneurones increases with age and that this is associated with an increase in levels of inflammation in the CNS but not in the blood; (iv) immune-priming does not affect the survival of mature motoneurones and (v) the immune response to challenge changes with age. Results are considered in the context of current ideas on the roles of ageing, perineuronal activity, neurotrophic factors and inflammation in neuronal death and survival. It is proposed that immature and mature motoneurones respond differently to motoneurone rescue factors and changes in levels of inflammation. This calls into question some commonly held views on the mechanisms underlying age-related neuronal degeneration such as MND.
Dissertation Note: Thesis (Ph.D.) (Research by Publication) -- University of Adelaide, Adelaide Medical School, 2017
Provenance: This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
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