parkinsons disease pharmacology Flashcards
what is dopamine
catecholamine neurotransmitter - synthesised from tyrosine and metabolised by MAOB in the synaptic terminal
what are the two types of dopamine receptors
D1 like - act via G alpha S - increase cAMP (excitatory)
D2 like - act via G alpha I - decrease cAMP (inhibitory)
what are the D1 like receptors
D1 – most abundant, nigrostriatal, mesolimbic and mesocortical pathways
D5 – limbic system
what are the D2 like receptors
D2- nigrostriatal, mesolimbic and Tuberhypophyseal pathways and CTZ
D3
D4
what pathways are dopamine involved in
nigrostriatal - movement
mesolimbic - behavioural reward pathways
mesocortical - cognition and thought
Tuberhypophyseal - control of secretion
what is the pathophysiology of PD
loss of dopaminergic containing cells in the nigrostriatal pathway - between the substantia nigra and striatum
what are the 2 dopamine pathways in the nigrostriatal pathway
direct pathway - enables movement D1R
indirect pathway - inhibits movement (inhibited by the presence of dopamine) D2R
what is the effect of dopamine on ACh
- Dopamine usually inhibits ACh in the striatum – lack of dopamine leaves ACh unopposed – contributes to tremor in PD
what are lewy bodies
Intracellular aggregations of alpha-synuclein found in neuronal cells – normally involved in exocytosis of vesicles - associated with early onset
what role does mitochondrial damage play in PD
- Parkin/PINK1 mutations lead to PD through mitochondrial turnover
-Mitochondrial damage leads to cell death of dopaminergic neurons
what is levodopa and how does it work
dopamine precursor - crosses BBB
once in CNS, levodopa will be metabolised to dopamine
what medications can be co-administered with levodopa to reduce its metabolism
DOPA decarboxylase inhibitor – carbidopa or benderizine - Reduces dopamine in periphery – does not cross BBB- less s/e
Metabolism of dopamine in the CNS can be inhibited by inhibiting MAO-B
o Selegiline and rasagiline
what are dopamine agonists and how do they work in the treatment of PD
- Agonises D1/2 receptors in the place of dopamine
- More D2 selective
o Pramipexole, ropinirole, Rotigotine
what is amantadine
NMDAR agonist