Sections
History and Discovery | Structure–Activity Relations | Pharmacological Profile | Pharmacokinetics and Disposition | Mechanism of Action | Indications and Efficacy | Side Effects and Toxicology | Drug–Drug Interactions | Conclusion | References | Suggested Reading
Excerpt
Prior to the introduction of classic antipsychotic medications
in the 1950s, treatment for psychotic disorders primarily consisted
of humane containment and supportive care. A variety of remedies
without empirical support were popular in different cultures for
brief periods of time but went out of vogue because they were ineffective.
One approach to the treatment of psychosis that survived through
the ages was the use of reserpine as a folk medicine in India. In
the Ayurveda (the traditional Indian medical system originating
5,000 years ago), Sarpagundha (Rauwolfia serpentina, or
Indian snakeroot, from which reserpine is derived) was recommended
as the treatment for "unmada" (psychosis). In
the early 1950s, reserpine was found to improve psychosis and reduce
violent behavior in clinical trials among aggressive mentally ill
patients in state hospitals in New York and California, and this
led to its introduction as an antipsychotic in 1954 (2 years after
chlorpromazine). However, reserpine's popularity declined
after 1957 because of its high level of side effects and low safety
index. Although the use of reserpine has been completely discontinued
in some countries (e.g., the United Kingdom) because of its significant
drug interactions and adverse effects, it is available in the United States,
where it is still used, albeit very infrequently, as an alternative
or augmentation treatment in patients with schizophrenia refractory
to other antipsychotic treatment.