
- CB1 Allosteric Enhancers
- CB1 Allosteric Inhibitors
- GPR55 Antagonists
- A Novel Target for Diastolic Heart Failure
- Novel Fungal Diagnostics and Therapeutics
- CB1 Receptor PET Ligands
- Rheumatoid Arthritis
- Antifungal Agents: chitin synthase inhibitors
- A Novel Treatment for Hypertension
- PET Tracers for Alzheimer's Disease
- Insulin Gene Therapy
- HIV Entry Inhibitors
- A Novel Target for Prostate Cancer
- A Novel Anthelmintic Target
- Neuroprotective Agents
- Hypothalamic Receptors for Metabolic Health
- SBF: Delivery of drugs across the BBB using shark VNAR biotools
- 18F-FDR as a New Powerful Radiolabelling Agent for PET
- PET Tracers for Hypoxia
- Angiogenesis Tracers
- Development of PET Tracers for Membrane Transporters
- A Novel Retinoid Pathway
Neuroprotective Agents
We have identified a series of novel compounds which protect against neurodegeneration in model systems, and thus respresent an exciting new approach to the treatment of conditions such as Parkinson's disease
Parkinson's is a disease of the elderly and is more prevalent in the Western world; consequently with our ageing society, Scotland is particuarly hard hit both socially and economically by the disease. As a progressive disorder, the patient may require care for many years, either from relatives, who frequently need to give up work to provide the necessary care, or at great cost within the NHS. Existing therapies for Parkinson's disease have a palliative effect only; by increasing the amount of dopamine in the brain, they mask the effects of the death of dopamine-producing neurones that is one of the consequences of the disease.
We have discovered the importance of a particular signalling cascade in the neurodegenerative process and have developed a series of compounds able to block this cascade and actually prevent the loss of dopaminergic neurones and increase levels of dopamine. These compounds thus have the potential to actually halt the process of neurological damage and give stability to patients rather than simply masking disease progression.
Project Team: Dr Peter Teismann and Dr Iain Greig
Funding: Parkinson's Disease Society

University of Aberdeen
King's College
Aberdeen
AB24 3FX
