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Wednesday, September 15, 2021

09-15-2021-0437 - Dopamine (DA, a contraction of 3,4-dihydroxyphenethylamine)

Dopamine (DA, a contraction of 3,4-dihydroxyphenethylamine) is a neurotransmitter that plays several important roles in the brain and body. It is an organic chemical of the catecholamine and phenethylamine families. Dopamine constitutes about 80% of the catecholamine content in the brain. It is an aminesynthesized by removing a carboxyl group from a molecule of its precursor chemicalL-DOPA, which is synthesized in the brain and kidneys. Dopamine is also synthesized in plants and most animals. In the brain, dopamine functions as a neurotransmitter—a chemical released by neurons (nerve cells) to send signals to other nerve cells. Neurotransmitters are synthesized in specific regions of the brain, but affect many regions systemically. The brain includes several distinct dopamine pathways, one of which plays a major role in the motivational component of reward-motivated behavior. The anticipation of most types of rewards increases the level of dopamine in the brain,[3] and many addictive drugs increase dopamine release or block its reuptakeinto neurons following release. Other brain dopamine pathways are involved in motor control and in controlling the release of various hormones. These pathways and cell groups form a dopamine system which is neuromodulatory.[citation needed]

In popular culture and media, dopamine is usually seen as the main chemical of pleasure, but the current opinion in pharmacology is that dopamine instead confers motivational salience;[4][5][6] in other words, dopamine signals the perceived motivational prominence (i.e., the desirability or aversiveness) of an outcome, which in turn propels the organism's behavior toward or away from achieving that outcome.[6][7]

Outside the central nervous system, dopamine functions primarily as a local paracrinemessenger. In blood vessels, it inhibits norepinephrine release and acts as a vasodilator (at normal concentrations); in the kidneys, it increases sodium excretion and urine output; in the pancreas, it reduces insulin production; in the digestive system, it reduces gastrointestinal motility and protects intestinal mucosa; and in the immune system, it reduces the activity of lymphocytes. With the exception of the blood vessels, dopamine in each of these peripheral systems is synthesized locally and exerts its effects near the cells that release it.

Several important diseases of the nervous system are associated with dysfunctions of the dopamine system, and some of the key medications used to treat them work by altering the effects of dopamine. Parkinson's disease, a degenerative condition causing tremor and motor impairment, is caused by a loss of dopamine-secreting neurons in an area of the midbrain called the substantia nigra. Its metabolic precursor L-DOPA can be manufactured; Levodopa, a pure form of L-DOPA, is the most widely used treatment for Parkinson's. There is evidence that schizophrenia involves altered levels of dopamine activity, and most antipsychotic drugs used to treat this are dopamine antagonists which reduce dopamine activity.[8] Similar dopamine antagonist drugs are also some of the most effective anti-nausea agents. Restless legs syndromeand attention deficit hyperactivity disorder (ADHD) are associated with decreased dopamine activity.[9]  Dopaminergic stimulants can be addictive in high doses, but some are used at lower doses to treat ADHD.  Dopamine itself is available as a manufactured medication for intravenous injection: although it cannot reach the brain from the bloodstream, its peripheral effects make it useful in the treatment of heart failure or shock, especially in newborn babies.

Dopamine structure
Skeletal formula of dopamine
Clinical data
Other names
  • DA,
  • 2-(3,4-Dihydroxyphenyl)ethylamine,
  • 3,4-Dihydroxyphenethylamine,
  • 3-Hydroxytyramine,
  • Oxytyramine,
  • Prolactin inhibiting factor,
  • Prolactin inhibiting hormone,
  • Intropin,
  • Revivan

 https://en.wikipedia.org/wiki/Dopamine



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