lynx   »   [go: up one dir, main page]

Skip to main content

Prof Aideen Sullivan

Development of Novel Neuroprotective or Disease-modifying Therapies

Professor Aideen Sullivan 

Professor Aideen Sullivan is Director of UCC Futures : Future Ageing and Brain Science. She leads an active research group focused on Parkinson’s disease, which is the second most common neurodegenerative disorder worldwide, and for which there is currently no cure. There are currently over 10 million people living with Parkinson’s, and this incidence is projected to increase to 20 million by 2040.

 

Aideen’s particular research interest is the development of novel neuroprotective or disease-modifying therapies, which have potential to slow disease progression in Parkinson’s. Her research group uses preclinical models (both in vitro and in vivo laboratory models) to examine potential agents that might eventually be used clinically to help people with Parkinson’s. Her group has a strong track record in research on neurotrophic factors as disease-modifying therapies for Parkinson’s.

Current projects include: Gene therapy to deliver the dopaminergic neurotrophic factors GDF5 and GDNF as neurorestorative therapies for Parkinson’s; Use of human stem cell-derived dopamine neurons to investigate Parkinson's risk factors and novel therapies; Epigenetic enzymes HDAC5 and HDAC9 as novel therapeutic targets for Parkinson’s; Roles of the gut microbiome in Parkinson’s disease pathology and treatment; Small molecule regulators of BMP-Smad signalling as novel therapies for Parkinson’s disease.

 

Aideen also conducts patient-facing research, with a focus on the impacts of lifestyle and environmental factors on quality-of-life, and on motor and non-motor symptoms, in people with Parkinson’s. These projects have strong patient engagement and collaboration, and are often co-designed with people with Parkinson’s and patient advocates.

Current projects include: Pesticide exposure and risk of Parkinson’s; Exercise strategies for People with Parkinson’s; and Tracking symptoms and medications across the menstrual cycle in Women with Parkinson’s.

 

Aideen has supervised to completion 19 PhDs, 2 MDs, 22 MScs and 13 postdoctoral researchers, and she is currently supervising 7 PhDs and 1 MSc student.

 

Aideen welcome enquires from students interested in discussing MSc or PhD opportunities, from post-doctoral researchers wishing to join her research group, and from potential research collaborators. If you would like to discuss such possibilities, please contact her on a.sullivan@ucc.ie

 

 

Publications:

  1. Collins, M, Roberts, R, Crowley, E.K, Heaney, M, Lazic, S.E, Sullivan, A.M. (2024) Remote exercise classes are associated with better quality of life in people with Parkinson’s during the Covid-19 pandemic. F1000 Research. 13: 266.
  2. Morales-Prieto, N., Bevans, R. O’Mahony, A. Barron, A. Giles Doran, C. McCarthy, E., Concannon, R. Goulding, S.R., McCarthy, C.M., Collins, L.M.*, Sullivan, A.M.*, O'Keeffe, G.W.* (2024) Human a-synuclein overexpression upregulates SKOR1 in a rat model of simulated nigrostriatal ageing. Aging Cell. Mar 26:e14155. doi: 10.1111/acel.14155. PMID: 38529808  (*joint senior authors)
  1. Giles Doran, C., Wilson, F .Goulding, S.R., Mazzocchi, M., Collins, L.M., Sullivan, A.M.*, O'Keeffe, G.W.* (2023) Bioinformatics and immunohistochemical analyses support preserved expression of GDNF receptor RET in Parkinson’s. Movement Disorders 38(6):1115-1116. doi: 10.1002/mds.29443. PMID: 37475614 (*joint senior authors)
  2. Goulding,  S.R., Concannon, R.M., Morales-Prieto, N., Villalobos-Manriquez, F., Clarke,  G., Collins,  L.M., Lévesque, M., Wyatt,  S.L., Sullivan, A.M.*, O'Keeffe, G.W.* (2021) Growth differentiation factor 5 exerts neuroprotection in an α-synuclein rat model of Parkinson’s disease. Brain 144(2):e14. PMID: 33253375 (*joint senior authors)
  3. Mazzocchi M, Goulding SR, Morales-Prieto N, Foley T, Collins LM, Sullivan AM*, O'Keeffe GW* (2022) Peripheral administration of the Class-IIa HDAC inhibitor MC1568 partially protects against nigrostriatal neurodegeneration in the striatal 6-OHDA rat model of Parkinson's disease. Brain Behav Immun. 102:151-160. PMID: 35217173 (*joint senior authors)

 

Ph.D/Postgrad projects:

PhDs

  • Adam O’Mahony ‘Defining the potential of HDAC5 and HDAC9 as novel therapeutic targets for Parkinson’s disease’
  • Fionnuala Wilson ‘Neuroprotective and neurorestorative efficacy of AAV-hGDF5 and AAV-GDNF in the AAV-α-synuclein rat model of Parkinson’s disease’
  • Joan Omosefe Osayande ‘An investigation of the role of the gut microbiome in the maintenance of nigrostriatal and motor function in a rat model of Parkinson’s disease’
  • Rebekah Bevans ‘Characterising intracellular regulators of BMP-Smad signalling as novel therapeutics targets for Parkinson’s disease’
  • Jolie Morisho ‘Effects of AAV-hGDF5 and AAV-GDNF in α-synuclein-based in vitro models of Parkinson’s disease’
  • Rachel Roberts ‘Investigation of Parkinson's risk factors and novel therapies in human stem cell-derived dopamine neurons’
  • Lauren Barrett ‘SKOR1 inhibition as a therapeutic approach to prevent α-synuclein-induced degeneration in models of Parkinson’s disease’

Research MSc

  • Sarah Moore ‘Fluctuations in Parkinson's disease symptoms and effectiveness of medications over the menstrual cycle’

 

Aideen welcome enquires from students interested in discussing MSc or PhD opportunities, from post-doctoral researchers wishing to join her research group, and from potential research collaborators. If you would like to discuss such possibilities, please contact her on a.sullivan@ucc.ie

Department of Pharmacology and Therapeutics

Cógaseolaíocht agus Teiripic

Room 2.36B, 2nd floor floor, T12XF62

Top
Лучший частный хостинг