Table of Contents
Tremors are rhythmic oscillatory movements around a joint. They include resting tremors, postural tremors, or intention tremors.
Unpredictable, irregular, and involuntary muscle jerks in different parts of the body that impair voluntary activities are known as chorea. Such violent abnormal movements occurring in proximal muscles of the limbs are known as ballismus.
Athetosis is a slow and writhing abnormal movement, while dystonias are sustained abnormal movements causing abnormal postures.
Tics are sudden, coordinated, repetitive abnormal movements. They are common in children and often involve the head and face.
Rigidity, bradykinesia, tremors at rest, and postural instability are the most important clinical features seen in parkinsonism. Other features are a cognitive decline, personality changes, affective disorders, autonomic abnormalities, sleep disorders, and sensory disturbances. Idiopathic parkinsonism is known as Parkinson’s disease or paralysis agitans.
Dopamine levels are found to be reduced in the basal ganglia of the brain in parkinsonism. In idiopathic parkinsonism, nigrostriatal dopaminergic neurons that inhibit striatal GABAergic neurons are lost.
Most of the drugs used in treatment of parkinsonism act by increasing dopaminergic activity or restore the balance between cholinergic and dopaminergic activities. Drugs that antagonize dopamine or that damage dopaminergic nigrostriatal neurons can cause parkinsonism.
D2 receptors are present presynaptically on axons in the substantia nigra and postsynaptically on striatal neurons. They are the most important subtype of dopaminergic receptors for the antiparkinsonian effect of drugs.
Drugs used in the treatment of parkinsonism can be broadly classified into dopamine precursor, dopamine agonists, MAO inhibitors, COMT inhibitors, and muscarinic antagonists.
Dopamine precursor – levodopa
Dopamine cannot cross the blood-brain barrier, and hence cannot be used in the treatment of parkinsonism.
Levodopa is a levo-isomer of dopa and a metabolic precursor of dopamine that can enter the brain via L-amino acid transporter and is then decarboxylated by dopa decarboxylase into dopamine. It is rapidly absorbed from the small intestine and its absorption is delayed by foods, hence it is best taken 30-60 minutes before meals.
Due to decarboxylation by peripheral dopa decarboxylase, only 1-3% of the ingested levodopa reaches the brain. Hence, it is administered along with carbidopa, a dopa decarboxylase inhibitor that does not enter the brain; therefore, it increases the half-life of levodopa by reducing its peripheral metabolism and reduces its dose by ~75%.
Dopamine improves most of the clinical features of parkinsonism, but it particularly improves bradykinesia. However, it does not prevent the progression of parkinsonism and the clinical response usually decreases with time due to the progression of the disease.
Fluctuations in clinical response occur in relation to the timing of consumption (end-of-dose akinesia or wearing-off reactions) or due to an on-off phenomenon (‘off-periods’ of akinesia alternating with ‘on-periods’ of improved mobility with dyskinesias).
Important side effects are gastrointestinal (anorexia, nausea, vomiting), postural hypotension, cardiac (tachycardia, asystole, arrhythmias such as ventricular extrasystoles or atrial fibrillation), dyskinesias, and behavioral disturbances (confusion, agitation, anxiety, depression, mood changes, personality changes, hallucinations, delusions, insomnia, somnolence, nightmares).
Other possible side effects are mydriasis (can precipitate acute glaucoma), hot flashes, gout, smell disturbances, taste disturbances, brownish discoloration of secretions, priapism, blood dyscrasia, and positive Coomb’s test.
Dyskinesias can occur in up to 80% of patients after 10 or more years of duration of treatment. The most common of them is choreoathetosis of the face and distal extremities, others being chorea, ballismus, tremors, tics, myoclonus, etc. Their incidence is low with continuous drug delivery systems such as intraduodenal or intrajejunal administration.
Gastrointestinal side effects of levodopa can be reduced by combining the drug with carbidopa, by taking it in divided doses, by taking it with or immediately after meals, by very slow uptitration of the dose, or by taking antacids 30-60 minutes before the dose.
Behavioral disturbances are more common with a levodopa-carbidopa combination than with levodopa alone and can be precipitated by surgery or concurrent illness. They can be treated by atypical antipsychotics such as risperidone, clozapine, olanzapine, and quetiapine.
With time, tolerance can develop to lead to emetic effects and postural hypotension.
Drug holidays (discontinuation of levodopa for 3-21 days) are not recommended due to increased risk of thromboembolism, aspiration pneumonia, and depression in patients with severe parkinsonism, although they may improve responsiveness to levodopa and reduce some side effects.
In absence of carbidopa, pyridoxine (vitamin B6) reduces the therapeutic effects of levodopa by enhancing its peripheral metabolism.
Psychosis and angle-closure glaucoma are contraindications for levodopa, while it should be used cautiously in patients with cardiac disease, active peptic ulcer, history of melanoma or suspicious undiagnosed skin lesions.
A combination of levodopa and monoamine A inhibitors can precipitate hypertensive crisis, hence it should not be given to patients taking a MAO inhibitor or within 2 weeks of its discontinuation.
These act directly on dopamine receptors in the brain and may be additionally beneficial over levodopa.
Response fluctuations and dyskinesias are less with dopamine agonists, hence they can be used as first-line therapy for parkinsonism or with low dose levodopa/carbidopa. In severe cases, they help to reduce the dose of levodopa.
Their role is important when patients taking levodopa experience end-of-dose akinesia, on-off phenomena, or are developing resistance to levodopa. General contraindications to dopamine agonists are psychosis, recent myocardial infarction, and active peptic ulcer.
Bromocriptine and pergolide are ergot derivatives that are rarely used in the treatment of parkinsonism at present.
Bromocriptine is a partial agonist at D2 receptors and is associated with side effects like anorexia, nausea, vomiting, dyskinesias, postural hypotension, behavioral disturbances, headache, nasal congestion, peripheral edema, erythromelalgia, pulmonary infiltrates, pleural fibrosis, retroperitoneal fibrosis, etc. Behavioral disturbances are more common with bromocriptine than with newer dopamine agonists.
Bromocriptine should be used cautiously in patients with peripheral vascular disease or history of myocardial infarction.
Pergolide is a D1 and D2 agonist and is associated with the development of valvular heart disease.
Ergot derivatives can also cause painless digital vasospasm after long-term use.
This is a non-ergot derivative with high affinity for D3 receptors which can be used as monotherapy in mild disease and with levodopa in advanced disease.
Its important side effects are anorexia, nausea, vomiting, postural hypotension, dyskinesias, behavioral disturbances (delusions, hallucinations, confusion, impulsivity, etc., more than those with levodopa), narcolepsy.
It is contraindicated in active peptic ulcer, psychosis, and recent myocardial infarction. Dose reduction is necessary for renal insufficiency as it is excreted mainly in the urine.
Pramipexole has a possible neuroprotective effect due to hydrogen peroxide scavenging action.
Ropinirole is a non-ergot derivative and a pure D2 agonist. It can be used as monotherapy in mild disease and with levodopa in advanced disease to smooth out response fluctuations.
It is metabolized by CYP1A2, hence caffeine and warfarin can reduce its clearance. Adverse effects and contraindications are similar to those of pramipexole, including narcolepsy.
This is a potent dopamine receptor agonist which is available in injectable form. Its subcutaneous administration is rapid, though temporarily, effective in treatment of “off-period” akinesia.
Severe nausea is an important side effect and can be prevented by pretreatment with antiemetics trimethobenzamide for 3 days. Other side effects are hypotension, drowsiness, chest pain, perspiration, dyskinesias, etc.
Rotigotine is available as a transdermal patch which delivers even drug levels over 24 hours and is effective in early parkinsonism.
Advantages and adverse effects are similar to those of other dopamine agonists; it can also cause reactions at the application site.
Monoamine Oxidase (MAO) Inhibitors
In the brain, norepinephrine, serotonin, and dopamine are metabolized by MAO-A, while MAO-B selectively metabolizes dopamine. MAO inhibitors reduce the metabolism of dopamine, thus enhance the effects of levodopa.
They should not be taken by patients taking tramadol, meperidine, propoxyphene, dextromethorphan, cyclobenzaprine, or John’s wort. Patients taking tricyclic antidepressants or serotonin reuptake inhibitors can develop serotonin syndrome like acute reactions if they also consume these drugs.
This drug selectively irreversibly inhibits MAO-B (also inhibits MAO-A at high doses). It is used as adjunctive therapy in parkinsonism to reduce on-off or wearing-off phenomena associated with levodopa.
An important side effect is insomnia, when taken later in the day.
Rasagiline is a more potent MAO-B inhibitor than selegiline that can be used in the early treatment of symptoms of parkinsonism. It is also used as adjunctive therapy in parkinsonism with levodopa.
Catechol-O-Methyltransferase (COMT) Inhibitors
COMT, present in both central nervous system and peripheral tissues, is an enzyme that metabolizes levodopa to 3-O-methyldopa (3-OMD), which then competes with levodopa for transport across intestine and BBB, thus reducing the therapeutic effect of levodopa. COMT inhibitors reduce the peripheral metabolism of levodopa and prolong its action by increasing its bioavailability.
COMT inhibitors are used as adjuncts in patients taking levodopa with having response fluctuations as they reduce fluctuations, prolong the ‘on-times,’ and reduce the total dose of levodopa.
Tolcapone and entacapone are COMT inhibitors. Tolcapone has both central and peripheral effects, while entacapone has only peripheral actions. As compared to entacapone, tolcapone is more potent and has a longer duration of action.
Important adverse effects are nausea, dyskinesias, and confusion (due to increased bioavailability of levodopa; reduced by lowering dose of levodopa within 48 hours of initiation), orthostatic hypotension, diarrhea, abdominal pain, sleep disturbances, and orange discoloration of urine.
Hepatotoxicity (increased liver enzymes and acute liver failure) is an important side effect of tolcapone and is not seen with entacapone.
This is an antiviral agent which is effective in parkinsonism by unknown mechanisms, possibly by potentiating the dopaminergic function by its effects on synthesis, release, or reuptake of dopamine. Other possible mechanisms are antagonism at adenosine A2A receptors (which inhibit D2 receptors), antimuscarinic effects, and inhibition of NMDA type glutamate receptors.
It improves bradykinesia, rigidity, and tremor, however, the effect lasts for a few weeks and it is less effective than levodopa. It also reduces iatrogenic dyskinesias seen in patients with advanced disease.
Important side effects are behavioral disturbances (insomnia, irritability, excitement, confusion, hallucinations, agitation, restlessness, acute toxic psychosis), livedo reticularis and other dermatologic reactions, peripheral edema (responds to diuretics), anorexia, nausea, dry mouth, constipation, postural hypotension, urinary retention, headache, rarely heart failure and seizures. It is used cautiously in persons with a history of heart failure or seizures.
These decrease excitatory effects of cholinergic neurons on striatal neurons and help to improve the dopamine/acetylcholine ratio in the brain. They improve tremor and rigidity, but not bradykinesia and have only an adjuvant role.
Common drugs are benztropine, trihexyphenidyl, biperiden, orphenadrine, and procyclidine.
Important side effects are behavioral effects (mood changes, hallucinations, delusions, confusion, inattention, drowsiness), dry mouth, constipation, and blurring of vision. They reduce some extrapyramidal symptoms induced by antipsychotics drugs but exacerbate tardive dyskinesias caused by them.
They are contraindicated in patients with prostatic hyperplasia, glaucoma, and pyloric stenosis.
|Drugs used to treat parkinsonism||Drugs used to treat other movement disorders|
Other Movement Disorders
Propranolol (β-adrenergic blocker) is used in the treatment of physiologic postural tremor and essential tremor. It should be cautiously used in patients with asthma, heart failure, heart block, and hypoglycemia.
Metoprolol (selective β1-blocker) can be used in the treatment of essential tremors when propranolol is contraindicated.
Other drugs that are used in the treatment of essential tremor are gabapentin, topiramate, primidone, alprazolam, and botulinum toxin.
This is a genetic disorder resulting from reduced GABAergic and cholinergic functions and enhanced dopaminergic functions in the brain presenting with progressive chorea and dementia.
Reserpine depletes cerebral dopamine and reduces abnormal movements. Common side effects are sedation, depression, hypotension, nasal congestion, and diarrhea. Tetrabenazine has similar action but has less side effects.
Antipsychotics (haloperidol, perphenazine, olanzapine) and antiepileptics (gabapentin, primidone, topiramate) may also be useful.
Gilles de la Tourette’s syndrome
Haloperidol and pimozide, D2 receptor antagonists, are commonly used in treatment.
Other less effective drugs are carbamazepine, clonazepam, clonidine, guanfacine, fluphenazine, risperidone, and aripiprazole.
Restless legs syndrome
This condition is characterized by unpleasant discomfort in the legs, especially at rest at night. The exact cause is unknown, but it is more common in pregnant women and patients with diabetes mellitus or uremia.
The dopamine agonists pramipexole and ropinirole are approved for its treatment. Other drugs that can be used are carbamazepine, benzodiazepines, gabapentin, and opioid analgesics.
This is a genetic disorder characterized by the deposition of copper salts in hepatic and brain tissues. Penicillamine, a chelating agent, is a mainstay of its treatment.
Butyrophenone and phenothiazine groups of antipsychotic drugs cause parkinsonism by D2 antagonism, which can be treated by reducing the dose, changing the drug, or by adding an antimuscarinic agent.
Reserpine and tetrabenazine cause parkinsonism by depleting brain dopamine, while MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) causes destruction of dopaminergic neurons in the nigrostriatal tract producing irreversible parkinsonism.
Parenteral benztropine or diphenhydramine can be used in the treatment of acute dystonias caused by antipsychotics. No specific drug is available for the treatment of tardive dyskinesias, although clonazepam, clozapine, risperidone have been used with limited success.