Zusammenfassung der Ressource
Parkinson's Disease
- Excitotoxicity
- Calcium OVERLOAD
- Neuronal Death: Associated with
Ca++ overload of cells and
membrane damage
- Glutamate activates: - NMDA.
- AMPA, - Metabotropic
receptors
- Epidemology
- More Males are affected
- Age of onset >50 years old
- Possible Trigger
Factors
- Toxins
- (MPTP) •Contaminant in heroin
substitute led to "frozen addict‟
syndrome •induces parkinsonism –
similar to some herbicides
- Infection
- Encephalitis lethargica
- Genetic
- Not usually familial
- Enviromental
- Dopamine oxidation
- MPTP
- Rotenone (herbicide)
- Dopamine (DA) pathways
- Due to: •Dopaminergic depletion in basal ganglia (nigro-striatal pathway)
•Leading to a relative excess of acetylcholine in striatum
- Nigrostraital – motor
- Lack of DA or inhibition of
dopaminergic neurones may
lead to parkinsonism
- Inhibits release of
acetylcholine (ACh) from
striatum
- Mesolimbic & mesocortical – thought
- Excessive DA or overactive
dopaminergic neurones may
lead to psychosis
- Tuberohypophyseal
– hypothalamus/pituitary
- Prolactin release from pituitary gland
- inhibited by dopamine
- Chemoreceptor trigger zone
- vomiting reflex
- Dopaminergic stimulation
leads to vomiting
- Metabolism of
dopamine
- Dopamine eventually metabolised to
Homovanillic acid
- Metabolic Pathways
- Catechol-o-methyltransferase
- Monoamine oxidase
- Aldehyde dehydrogenase
- Symptoms
- TREMOR
- Rigidity
- COGWHEEL
- Bradykinesia
- Akinesia
- 'Pill rolling'
- Gait & Posture
- Shuffling
- Stooping
- Speech
- Montone
- Early Stages: Levodopa,
Dopamine Agonists,
MAO-B-I
- Treatment
- Dopamine Precursors
- Levodopa
- Short Half-Life = 2 hours
- May enhance DA in Limbic System
- S.E. N+V, Cardiovascular - Hypotension
- Treat with Domperidone, does NOT cross BBB
- Psychological effects – delusions and hallucinations, but more commonly (20%)
confusion, disorientation, insomnia or nightmares. Daytime drowsiness
- Dyskinesia
- Within 2 years of taking L-Dopa
- Involuntary writhing movements
- Motor Fluctuations ('On-off' effect)
- Dopa-decarboxylase inhibitor can be added
- Increases: Life expectancy. Improves:
motor function, quality of life.
- Some symptoms not improved –
e.g. dysphagia, cognitive decline
- MOA: Precursor of DA
- Dopa Decarboxylase Inhibitors
- Benserazide
- Can be combined with L-Dopa
to make Co-beneldopa
(Madopar)
- Carbidopa
- Can be combined with L-Dopa to
make Co-Careldopa (Sinemet)
- Intestinal Gel - Duodopa, for late stage PD
- Directly into Duodenum
- Requires electronic pump device
- Dose
- The total morning dose is usually 5-10 ml,
corresponding to 100-200 mg levodopa. (should
not exceed 15 ml (300 mg levodopa)
- MOA: Inhibit the breakdown of
L-Dopa to DA
- Monoamine Oxidase B Inhibitors
- DRUGS
- Selegilene
- Better with Levodopa than alone
- Rasagilene
- Neuroprotective properties
- Protect DA from intraneuronal breakdown
- Catechol-O-Methyltransferase Inhibitors
- DRUGS
- Entacapone
- Combo: Levodopa, Carbidopa & Entacopone
- STALEVO
- Tolcapone
- MOA: Inhibits breakdown of peripheral
l-dopa by COMT to increase levodopa
level and enhance effect. May be
able to reduce levodopa dose by 10-30%
- Amantadine
- MOA: Increase DA release inhibit
amine uptake, direct action on DA
receptors
- Limited by SE &
worsening on
withdrawal
- Anti-viral drug
- Dopamine Receptor Agonists
- Ergot-Derived (Fibrotic Reactions)
- Drugs
- Bromocriptine
- Cabergoline
- Lisuride
- Pergolide
- Increase risk of pulmonary,
retroperitoneal and cardiac
fibrosis
- Non-Ergot Derived
- Pramipexole
- Ropinirole
- Apomorphine
- D1 & D2 Agonist
- SC or Infusion
- Initiation - Hospital
- Discharge: Monitor, adjust dose
- Side Effects
- Nausea, vomiting, drowsiness,
hallucinations, injection site nodules, <
commonly postural hypotension, breathing
difficulties, dyskinesias, anaemia
- Expensive
- Increase sleepiness
- Side Effects
- Nausea/vomiting
- Postural hypotension
- Hallucinations
- Confusion
- Dyskinesias
- Reckless Behaviour /Gambling
- Antimuscarinic Drugs
- DRUGS
- Procyclidine
- Orphenadrine
- Artane
- Benzatropine
- Ach: excitatory effect on striatal
neurones. Also exerts presynaptic
inhibitory effect on dopaminergic nerve
terminals
- Treat tremor effectively
- SIDE EFFECTS
- dry mouth, urinary retention, visual
disturbances, constipation -
euphoria, drowsiness, confusion,
hallucinations, cognitive impairment
- Later Stages: Dopamine
Agonists, COMT-I, MAO-B-I
- 2nd Choice: Amantadine,
Apomorphine
- All must be used as
adjunctive therapy