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Classes of antidepressants Tricyclic antidepressants were named after their characteristic chemical structure, although a number of the newer drugs in this group have a different chemical structure but still share similar pharmacological profiles. Tricyclic antidepressants inhibit the re-uptake of serotonin and noradrenaline into nerve endings. This leads to a build up of neurotransmitter at receptor sites in synapses. They also reduce the number of some receptors, which may contribute to the therapeutic action, but their complete mechanism of action is unknown. Examples of tricyclic antidepressants include imipramine and amitriptyline (for use of amitriptyline in neuropathic pain.
Atypical anti-psychotic drugs are recommended for newly diagnosed schizophrenics and those who cannot tolerate other drugs or who are not getting adequate control from other drugs. All are thought to improve negative as well as positive symptoms of schizophrenia in addition to causing fewer motor side effects and are less likely to affect prolactin secretion. Examples of atypical anti-psychotic drugs are clozapine, risperidone, olanzapine and quetiapine. Clozapine can cause agranulocytosis and should only be used if other drugs are not effective.
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The gland consists of the posterior pituitary and the anterior pituitary (adenohypophysis). The functions of the two are not related but both are controlled by the hypothalamus. The posterior pituitary gland secretes two hormones, antidiuretic hormone and oxytocin. They are both synthesized in the hypothalamus and reach the posterior pituitary via a neural connection. ADH is secreted in response to an increase in plasma sodium chloride concentration or a decrease in circulating blood volume.
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Authored by Dr. Raheel Bengali, MD