Dopamine Receptor Agonists Health Article

Definition

Dopamine receptor agonists are a class of drugs with similar actions to dopamine, a neurotransmitter that occurs naturally in the brain. A neurotransmitter is a chemical that allows the movement of information from one nerve cell (neuron) across the gap between the adjacent neuron. Dopaminergic receptors are protein complexes on the surface of certain neurons of the sympathetic autonomic nervous system that bind to dopamine.

Purpose

Dopamine stimulates the heart, increases the blood flow to the liver, spleen, kidneys, and other visceral organs, and controls muscle movements and motor coordination through an inhibitory action over stimuli response. Abnormal low levels of dopamine are associated with tremors, muscular rigidity, low blood pressure, and low cardiac input. Therefore, dopamine and dopaminergic agonist drugs are administered to treat shock and congestive heart failure and to improve motor functions in patients with Parkinson's disease and other movement disorders. The balance between two neurotransmitter levels, acetylcholine and dopamine, is essential for motor and fine movement coordination. The balance is frequently found altered in movement disorders, due to a dopamine deficiency that results in excessive stimulation of skeletal muscles. In Parkinson's disease, either dopamine levels or the number of dopamine receptors are progressively decreased, resulting in tremors, slowness of movements, muscle rigidity, and poor posture and gait (manner of walking). Symptoms of Parkinson's disease are treated with anticholinergic drugs and/or dopamine receptor agonists. Dopaminergic agonist drugs such as levodopa (L-dopa) along with carbidopa, bromocriptine mesylate, cabergoline, pergolide mesylate, pramipexole, and ropini-role hydrochloride are prescribed to treat the symptoms of Parkinson's disease, either alone or in combinations.

Description

L-dopa (levodopa) is a precursor of dopamine, i.e., is converted into dopamine by the body. Levodopa thus increases dopamine levels in the motor areas of the central nervous system (CNS), especially in the initial stages of the disease. However, as the disease progresses, the drug loses its efficacy (effectiveness). When administered with carbidopa, levodopa's effects are enhanced because carbidopa increases L-dopa transport to the brain and decreases its gastrointestinal metabolism. Therefore, two beneficial effects are achieved: better results with lower doses of levodopa (4–5 times lower doses than in L-dopa therapy alone); and reduction or prevention of levodopa side effects, such as nausea, anorexia, vomiting, rapid heart rate, low blood pressure, mood changes, anxiety, and depression.

Bromocriptine mesylate is a derivative of ergotamine that inhibits the production of prolactin hormone by the pituitary gland. It is used in association with levodopa, in order to allow lower doses of the latter, especially in long-term therapy. Bromocriptine is also used to treat some menstrual disorders and infertility. This drug shows poor results in patients who do not respond to levodopa.

Pergolide mesylate has an action similar to that of bromocriptine, also inhibiting prolactin secretion. Also used in Parkinson's in association with L-dopa and carbidopa, pergolide is eliminated from the body through the kidneys. Cabergoline also inhibits prolactin secretion and is used to decrease abnormally high levels of this hormone, whether due to endocrine dysfunction or due to an existing pituitary tumor. The drug is also prescribed to regulate the menstrual cycle in cases of polycystic ovaries, and to control symptoms in Parkinson's disease.

Pramipexole and ropinirole are dopaminergic agonists that show good results in controlling Parkinson's symptoms in patients still in the initial stages of the disease and not yet treated with L-dopa, thus postponing the need of levodopa administration to a later phase. They work as well in those patients with advanced Parkinson's symptoms already taking levodopa.