By Prof. Hanan Hagar Pharmacology unit Medical College.
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Transcript of By Prof. Hanan Hagar Pharmacology unit Medical College.
![Page 1: By Prof. Hanan Hagar Pharmacology unit Medical College.](https://reader036.fdocuments.net/reader036/viewer/2022081508/56649f335503460f94c4fbe9/html5/thumbnails/1.jpg)
By Prof. Hanan HagarPharmacology unit
Medical College
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ILOs:
At the end of this lecture you will be able to:-
• Recognize the symptoms and pathophysiology of parkinsonism
• Understand the pharmacology of drugs used for treatment of
parkinsonism.
• Define pharmacokinetics, pharmacodynamics and side effects of
different drugs used for the treatment of parkinsonism.
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A progressive neurological disorder that occurs mainly in the elderly and can lead to disability unless effective treatment is provided.
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Characters of Parkinson's disease:
• Tremors at rest
• Bradykinesia (slowness in initiating and carrying out voluntary movements) or Akinesia
• Muscle rigidity
• Postural and gait abnormalities
• Anxiety or depression
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occurs mainly due to reduction of dopamine
content in substantia nigra & corpus striatum
that are involved in motor control.
Pathphysiology of Parkinson’s disease
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Causes Parkinson’s disease is an idiopathic disease but some causes may be: Genetic. Toxins (MPTP= methyl phenyl tetrahydropyridine) Head trauma. Cerebral anoxia . Oxidative stress Drug-induced Parkinson's disease
e.g. antipsychotics like haloperidol. Dopamine antagonists as metoclopramide
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Parkinson’s disease
• Deficiency of dopamine
• Predominance of Ach
Parkinson’s disease
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main approachDrugs to increase dopaminergic activity
Or Drugs to block cholinergic activity
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1) Drugs that increase dopaminergic activities:
Dopamine precursor:
L-dopa + carbidopa
Dopamine agonists Ergot derivatives: bromocriptine Non ergot derivatives: pramipexole
Dopamine releaser: amantadine
COMT inhibitors: entacapone
MAO-B inhibitors: selegiline
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2) Drugs that decrease cholinergic activity
Muscarinic antagonists e.g. benzatropine
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Levodopa (L-dopa)
Is a precursor of dopamine (converted into dopamine centrally and peripherally).
98-99% is decarboxylated in gut and liver
1-2% crosses BBB and dopamine is formed
given combined with carbidopa (peripheral dopa decarboxylase inhibitor).
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Carbidopa: • Is a peripheral dopa decarboxylase inhibitor
• Inhibits peripheral conversion of L-dopa to
dopamine
L-dopa dopamine dopa decarboxylase
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Why carbidopa is combined with L-dopa?
• diminsh peripheral metabolism of L-dopa in GIT and other peripheral tissues (thus increasing t1/2 ).
• increase availability of levodopa to CNS.
• reduce dose of levodopa and side effects.
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Levodopa (L-dopa) Given orally (should be taken on empty
stomach).
absorbed from the small intestine and taken up to CNS by active transport system.
High protein meal interferes with its absorption and transport into CNS
Short duration of action (t½ =2 h)
(fluctuation of plasma concentration).
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Uses The most efficacious therapy
The best results of levodopa are obtained in the first few years of treatment.
L-dopa ameliorates all signs of parkinsonism particularly bradykinesia & rigidity but does not cure the disease.
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Adverse drug effectsPeripheral effects:
Anorexia, nausea, vomiting (due to stimulation of emetic center).
Cardiac arrhythmias. Mydriasis, orthostatic hypotension
CNS effects:
(Psychological disorders) mainly depression
delusions, hallucinations, confusion, sleep
Disturbances.
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Dyskinesia and response fluctuations
Dyskinesia (involuntary movements occurs in 40 to 90% of patients) due to fluctuating plasma levels of levodopa.
Wearing-off effect (duration of “on” states becomes shorter).
On-off phenomenon (On= improved mobility & Off=Akinesia or hypomobility).
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Drug Interactions:-
High proteins meals.
Pyridoxine (Vitamin B6).
Nonselective MAO inhibitors (phenelzine) due to peripheral accumulation of norepinephrine.
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Psychotic patient.
Glaucoma (due to mydriatic effect).
Patients with history of melanoma Why?
Note: L-dopa is a precursor of melanin
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Dopamine receptor agonistsBromocriptine, pergolide, Pramipexole
Ergot derivatives: Bromocriptine, pergolide
Non ergot derivatives: Pramipexole
Have longer duration of action than L-dopa
(less likely to cause dyskinesias than levodopa)
Dopamine agonists are used as initial therapy
They are used in advanced Parkinson's disease
with fluctuation and dyskinesia due to L-dopa.
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Is an ergot derivative D2 agonist Is given orally Half life= 6-8 h
Used for the treatment of Parkinson’s disease
Hyperprolactinemia (galactorrhea).
Infertility in women.
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Adverse drug effects Nausea, vomiting, postural hypotension Cardiac arrythmias Confusion, hallucinations, delusions Dyskinesias (less prominent).
Contraindications Psychosis Peripheral vascular disease Recent myocardial infarction
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Non Ergot dopamine agonist
D3 agonist Is given orally Has the advantage of being free radicals
scavenger.
Used alone as initial therapy or in combination with L-dopa.
Side effects: similar to L-dopa, but less dyskinesias.
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Amantadine originally introduced as an
antiviral. Amantadine increases
dopamine release. acts as an antagonist at
muscarinic and NMDA (N-methyl-D-aspartate) receptors.
given orally with short half life most of the drug being excreted
unchanged in the urine
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Amantadine Less efficacious than L-dopa Its benefits last only for short period (few
weeks) and only used for L-dopa resistance.
Adverse effects Nausea, anxiety, insomnia, confusion,
hallucinations (dopamine like side effects). Dry mouth, urinary retention (anticholinergic
effects). Restlessness and hallucinations (NMDA
antagonist).
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Monoamine oxidase-B inhibitors
Selegiline is a selective irreversible inhibitor of MAO-B
at normal doses. It inhibits dopamine degradation by MAO-B in
CNS. It increases endogenous dopamine available for
its receptors.
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Selegiline
Selegiline may have neuroprotective effect.
It has antioxidant activity against toxic free radicals produced during dopamine metabolism.
Selegiline is metabolized to desmethylselegiline, Which is antiapoptotic.
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Uses of selegiline
Adjunctive to levodopa / carbidopa in later-stage parkinsonism to:
reduce the required dose of levodopa
delay the onset of dyskinesia and motor
fluctuations that usually accompany long-
term treatment with levodopa.
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Adverse drug effectsAt high doses, selegiline may inhibit MAO-A (hypertensive crises).May cause insomnia when taken later during the day.
ContraindicationsSelegiline should not be co-administered with tricyclic antidepressants, or selective serotonin reuptake inhibitors (may cause hyperpyrexia, agitation, delirium, coma).
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COMT Inhibitors(Catechol-O- methyl transferase) Inhibitors
Entacapone • Acts peripherally to inhibit COMT enzyme
required for L-dopa degradation
• Diminishes peripheral metabolism of L-dopa
• It is used: as adjuvant to L-dopa to:
– Decrease fluctuations
– Improve response
– Prolonged the ON-Time
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COMT Inhibitors(Catechol-O- methyl transferase) Inhibitors
Side effects:
• L-Dopa side effects.
• Orange discoloration of urine.
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Anticholinergic DrugsBenztropine, Trihexphenidyl
Central muscarinic antagonist.
Has modest anti- parkinsonian actions.
They improve tremor & rigidity but have little effect on bradykinesia.
Provide benefit in drug-induced parkinsonism (due to antipsychotics).
used during the early stages of the disease or as an adjunct to levodopa therapy.
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Adverse effects Cycloplegia, mydriasis, dry mouth, urinary
retention, constipation. Confusion, delirium, and hallucinations may
occur at higher doses.
Contraindications
• Prostatic hypertrophy
• Glaucoma
• Intestinal obstruction
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In mild cases, selegiline, amantadine or anticholinergics can be used.
Levodopa and carbidopa is the main treatment All other medications are adjuncts to levodopa
therapy Other useful drugs include bromocriptine
(dopamine agonist), selegiline (monoamine oxidase-B inhibitor), amantadine (enhances dopamine release) and benztropine (muscarinic receptor antagonist, that is used for parkinsonism caused by antipsychotic drugs.