TCA

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Tricyclic Antidepressants (TCA)

Tricyclic antidepressants (TCAs) are a class of medications that are primarily used to treat depression. They were first discovered in the early 1950s and were among the first antidepressants to be developed. TCAs are named for their chemical structure, which contains three rings of atoms.

Mechanism of Action[edit | edit source]

TCAs work by inhibiting the reuptake of neurotransmitters serotonin and norepinephrine in the brain, increasing their levels and prolonging their activity. This helps to improve mood and alleviate symptoms of depression. TCAs also affect other neurotransmitters, which can lead to a range of side effects.

Common TCAs[edit | edit source]

Some commonly prescribed TCAs include:

Uses[edit | edit source]

While primarily used to treat major depressive disorder, TCAs are also prescribed for other conditions, including:

Side Effects[edit | edit source]

TCAs can cause a variety of side effects due to their broad mechanism of action. Common side effects include:

More serious side effects can include cardiac arrhythmias, especially in overdose situations, which can be life-threatening.

Contraindications[edit | edit source]

TCAs are contraindicated in patients with certain conditions, such as:

Interactions[edit | edit source]

TCAs can interact with a variety of other medications, including:

History[edit | edit source]

The first TCA, imipramine, was discovered in the early 1950s by researchers at the Swiss pharmaceutical company Ciba-Geigy. It was initially developed as an antipsychotic but was found to have significant antidepressant effects. This discovery led to the development of other TCAs and the establishment of a new class of antidepressant medications.

Related Pages[edit | edit source]

Categories[edit | edit source]

Template:Psychopharmacology


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Contributors: Prab R. Tumpati, MD