tricyclic antidepressant drug

…in the 1950s the first tricyclic antidepressants were discovered. These agents, so called because they are composed chemically of three carbon rings, inhibit the active reuptake, to varying degrees, of norepinephrine, serotonin, and dopamine in the brain. The tricyclics include imipramine, amitriptyline, desipramine, nortriptyline, and a

…have fewer side effects than tricyclics or MAOIs. SSRIs include fluoxetine (Prozac), paroxetine (Paxil), and sertraline (Zoloft). SSRIs are also used in the treatment of anxiety, eating disorders, panic disorder, obsessive-compulsive disorder, and borderline personality disorder.

…and best-studied class is the tricyclic antidepressants, which are divided into tertiary amines and secondary amines. Most tricyclics have a sedating effect, cardiac toxicity, and varying degrees of anticholinergic side effects, which some individuals, especially the elderly, have difficulty tolerating. Anticholinergic effects, which result from the blockage of parasympathetic nerve…

tricyclic antidepressants, and antihistamines can also induce drowsiness, though this is not their primary function. Most over-the-counter sleeping aids use antihistamines as their active ingredient.

Tricyclic antidepressants interfere with the reuptake of norepinephrine, serotonin, and dopamine. The side effects of these drugs are mostly due to their interference with the function of the autonomic nervous system and may include dryness of the mouth, blurred vision, constipation, and difficulty urinating. Weight…

The first tricyclic (so called because of its three-ringed chemical structure) antidepressant drug, imipramine, was originally designed as an antipsychotic drug and was investigated by Swiss psychiatrist Roland Kuhn. He found it ineffective in treating symptoms of schizophrenia but observed its antidepressant effect, which he reported in…