Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.790825
Title: Investigating the potential of therapeutically targeting the Insulin and Insulin-like Signalling cascade in neurodegeneration
Author: Paulin, J. J. W.
ISNI:       0000 0004 8499 6094
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2017
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Abstract:
Decreasing signalling through the Insulin and Insulin-like Signalling (IIS) cascade by genetic and pharmacological means can increase the lifespan and healthspan of many organisms. Crucially, when long-lived animals are crossed with animal models of neurodegenerative disorders, the onset of pathology is slowed. Pharmacological inhibitors of the IIS cascade have also shown neurodegeneration delaying and neuroprotective properties. Furthermore, IIS is changed in neurodegenerative disorders; with increased astrocyte IGF1, localised increased ERK1/2 phosphorylation (p-ERK), and brain insulin and IGF1 resistance observed. The IIS cascade therefore seems critically implicated in neurodegeneration, and crucially via pharmacological means could yield disease-modifying interventions. To investigate pharmacological IIS manipulation for therapeutic gain in neurodegeneration, I firstly characterised changes in IIS in human Alzheimer's Disease patient brain samples, and in brain samples of mice modelling rising amyloid beta and plaque levels, or rising hyperphosphorylated tau and tangle levels; finding increased IIS at early ages in these models. I subsequently designed a bilaminar neuron and astrocyte co-culture model of acute neurodegeneration, whereby I identified that increased astrocyte Igf1 expression following a noxious stimulus is dependent on the presence of neurons during stress. I then manipulated IIS during the noxious stimulus by either knocking down increased Igf1 expression, inhibiting p-ERK with the drug Trametinib, or both. I identified that increased astrocyte Igf1 expression contributes to neuronal cell death, and that Trametinib was protective against neuronal cell death, but the mechanism of Igf1 induced neuronal cell death was not due to increase p-ERK. This confirms IIS as a viable pharmacological target for intervening in neurodegeneration.
Supervisor: Edwards, F. A. ; Salih, D. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.790825  DOI: Not available
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