General pharmacology of clozapine.

Author: CowardD M

Paper Details 
Original Abstract of the Article :
Clozapine shows neuroleptic-like inhibition of locomotor activity and conditioned avoidance responding in rodents, although tolerance develops on repeated treatment. EEG-based studies show strong arousal-inhibiting activity of clozapine as well as neuroleptic-like effects on both caudate spindle dur...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/1358127

データ提供:米国国立医学図書館(NLM)

General Pharmacology of Clozapine

The study delves into the fascinating world of clozapine, a medication used to treat schizophrenia. This research explores the pharmacological properties of clozapine, including its effects on various neurotransmitter systems and receptors. The study aims to understand the mechanisms underlying clozapine's unique therapeutic properties and its limited side effects compared to other antipsychotics.

Unlocking the Secrets of Clozapine

The research reveals that clozapine interacts with a wide range of receptors, including dopamine D4, 5-HT1C, 5-HT2, alpha 1, muscarinic, and histamine H1 receptors. The study highlights clozapine's unique affinity for these receptors, which might explain its efficacy in treating schizophrenia and its limited extrapyramidal side effects.

A Hopeful Path for Treating Schizophrenia

This study provides valuable insights into the pharmacology of clozapine, a medication that has revolutionized the treatment of schizophrenia. Understanding the mechanisms underlying clozapine's therapeutic properties opens up new avenues for developing more effective and safer treatments for mental illness.

Dr.Camel's Conclusion

Imagine the brain as a vast desert, where a sandstorm of disrupted neurotransmitters rages. Clozapine, like a calming oasis, helps to restore balance and reduce the storm's intensity. The study helps us understand how clozapine works, offering hope for navigating the challenges of mental illness and finding solace in the desert of the mind.

Date :
  1. Date Completed 1992-12-02
  2. Date Revised 2013-11-21
Further Info :

Pubmed ID

1358127

DOI: Digital Object Identifier

1358127

Related Literature

SNS
PICO Info
in preparation
Languages

English

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