Antiparkinsonian

Effects

The majority of antiparkinsonian drugs are directly or indirectly dopaminergic. Some are anticholinergic in action.

Indications

Parkinson’s disease, including drug-induced Parkinson’s disease in some cases.

Drug treatment

Overview of drug therapy:

1. dopaminergic agents

Levodopa is a precursor of dopamine and is considered the most important and effective pharmacotherapy for PD. Combining it with peripheral decarboxylase inhibitors prevents the formation of dopamine from levodopa in the periphery:

Dopamine agonists stimulate central dopamine receptors:

  • Apomorphine (solution for injection).
  • Bromocriptine (Parlodel)
  • Pergolide (Permax, out of commerce).
  • Pramipexole (Sifrol)
  • Ropinirole (Requip, Adatrel)
  • Rotigotine (Neupro)

COMT inhibitors inhibit peripheral metabolism of levodopa via catechol- methyltransferase (COMT):

  • Entacapone (Comtan, Stalevo).
  • Opicapone (Ongentys)
  • Tolcapone (Tasmar)

Monoamine oxidase inhibitors inhibit dopamine degradation by inhibiting monoamine oxidase MAO-B:

NMDA antagonists block strial NMDA receptors, reducing the disturbed balance between dopaminergic inhibition and glutaminergic stimulation of cholinergic neurons:

2. central anticholinergics

Anticholinergics inhibit central cholinergic (muscarinic) receptors and wind effective against rigor, tremor, and akinesia:

  • Biperiden (akinetone -/retard).
  • Procyclidine (kemadrin)

3. other active ingredients

Cholinesterase inhibitors (antidementia drugs) are used to treat Parkinson’s dementia:

  • Rivastigmine (Exelon)