Antipsychotics (dopamine antagonists)- reduce the action of dopamine in areas of the brain associated with symptoms of schizophrenia
Two types of antipsychotics
Typical
Atypical
Typical antipsychotics
Bind to dopamine receptors without stimulating them
Reduces positive symptoms
Kapur et al (2000)
estimated that 60-70% of receptors in the mesolimbic pathway must be blocked for typical antipsychotics to be effective
A similar number of receptors must be blocked in other areas of the brain
Leads to undesirable side-effects
Chlorpromazine is a common typical antipsychotic
Atypical antipsychotics
2nd generation- reduced side effects
Temporarily block receptors
Act on serotonin and glutamine receptors
Reduce both positive and negative symptoms
Strengths- supporting evidence
Thornley et al (2003)- Chlorpromazine reduced symptom severity more affectively than a placebo
Meltzer (2012)- Clozapine is effective in 30-50% of treatment-resistant cases where typical antipsychotics have failed
Weaknesses
Flaws: Healy (2012)
Serious side effects- dizzy, weight gain, sleepy and tardive dyskinesia. Most serious is neuroleptic malignant syndrome where dopamine action is blocked in the hypothalamus- causes high temp, coma and fatality
Healy (2012)
Drug trials were short term only
Some successful trials had their data published multiple times- overstating the amount of supporting evidence
Moral dilemma
Can help patients engage with other treatment more effectively
Antipsychotics are used to sedate patients and make staff's jobs easier
Drugs can be dehumanising as they reduce the person's control and consent