Blog#10
The 2 main groups are:
- Drugs that increase dopaminergic activities
- Drugs that decrease cholinergic activities
- This drug is a Metaffinoid potentiater of Dopamine. (Increases Dopamine release), it increases Dopamine synthesis and blocks the reuptake of Dopamine.
- It is a NMDA antagonist.
- Amantadine is an Adenosine alpha-2 antagonist. It works as an anti-viral drug that inhibits the D2 receptor function.
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Drug that work indirectly, increase the Dopamine concentration and do not require enzymatic conversion to an active metabolite.They have any potentially toxic active metabolites.they do not work directly n the post sinaps.
The ergot derivatives are:
Ergot derivatives:
- Pramipexole
- Pergolide
- Bromocriptine
Non-ergot derivatives:
- Ropinirole
- Rotigotine
Dopamine 3 = Pramipexole
Dopamine 2 = Ropinirole
Dopamine 1,2 and 3 = Rotigotine
Dopamine 2 = Bromocriptine
Dopamine 1 and 2 = Pergolide
MAO-B inhibitors such as Rasagiline and Selegiline are classified as neuro protective drugs. This means that the Dopamine concentration levels in the central nervous system are increased and not decreased.
These drugs work with drugs such as Levodopa. MAO-B inhibitors prolong the duration of the effects of Levodopa.
COMT inhibitors metabolize L-dopa to 3-O-methyl dopa (30MD), the increased levels of 3OMD leads to a weak therapeutic response with L-dopa. 30MD competes with L-dopa for active transport processes. These drugs increase the duration of L-dopa thus, decreasing peripheral metabolism and improving bioavailability of the drug.
This drug inhibits Dopamine 2 functioning by antagonising adenosine activity preventing the inhibition of dopamine functions. It is an additional therapy to L-dopa or cardidopa therapy that experiences on-off episodes.
Safinamide, increases Dopamine activity, this results in the potent reversible inhibition of MAO-B and results in the inhibition of Dopamine reuptake. This drug also results in the decrease of glutamate release.