Biological treatments for schizophrenia focus on addressing the underlying neurochemical imbalances and brain dysfunction associated with the disorder.
Primary biological treatments include:
Antipsychotic drugs (typical and atypical)
Emerging treatments (e.g., brain stimulation)
👉 Main aim: Reduce psychotic symptoms by altering dopamine and other neurotransmitter activity.
Developed in the 1950s.
Primarily target the dopamine hypothesis — excessive dopamine activity in the mesolimbic pathway.
Block dopamine D2 receptors in the brain to reduce dopamine transmission.
Examples:
Chlorpromazine
Haloperidol
Effects:
✅ Effective at reducing positive symptoms (hallucinations, delusions).
❌ Less effective for negative symptoms (avolition, social withdrawal).
❌ High risk of side effects:
Extrapyramidal symptoms (motor control issues, tremors)
Tardive dyskinesia (involuntary facial and body movements)
Sedation and weight gain
Developed in the 1990s.
Target dopamine and serotonin receptors (especially 5-HT2A).
Weaker dopamine antagonism → fewer motor side effects.
Examples:
Clozapine – most effective but can cause agranulocytosis (potentially fatal drop in white blood cells).
Risperidone – more balanced dopamine/serotonin activity; fewer side effects.
Olanzapine – effective for both positive and negative symptoms.
Effects:
✅ Reduce both positive and negative symptoms.
✅ Lower risk of motor side effects.
❌ Still cause weight gain, sedation, and metabolic issues.
❌ Clozapine requires regular blood monitoring.
Schizophrenia is linked to hyperactivity of dopamine in the mesolimbic pathway → causes positive symptoms.
Typical antipsychotics reduce dopamine activity by blocking D2 receptors.
Atypical antipsychotics block both dopamine and serotonin receptors.
Reduces dopamine in some brain regions → treats positive symptoms.
Increases dopamine in others → reduces negative and cognitive symptoms.
✔ Antipsychotics reduce positive symptoms for 70% of patients.
✔ Atypical antipsychotics improve both positive and negative symptoms.
✔ Allow many patients to live independently.
✖ Only effective for positive symptoms — negative and cognitive symptoms often persist.
✖ High relapse rates if medication is stopped (40% within a year).
✖ Side effects can reduce compliance (patients stop taking medication).
✖ Ethical issues – risk of over-sedation and chemical restraint.
Uses magnetic fields to stimulate brain areas linked to schizophrenia.
Mixed evidence — may help with negative symptoms.
Target glutamate activity (linked to cognitive symptoms).
Still in experimental stages — potential for future use.
Meta-analysis of 29 studies.
Relapse rates:
Placebo = 55%
Antipsychotics = 19%
👉 Antipsychotics are highly effective in preventing relapse.
Examined the effectiveness of treating 1st instance schizophrenia with 1st and 2nd generation medications -
Found antipsychotics are effective for at least a year, but that 2nds weren't any more effective than 1sts.
Meta-analysis of 65 studies.
Antipsychotics were significantly more effective than placebo in treating positive symptoms.
Atypical antipsychotics were slightly more effective than typical antipsychotics for negative symptoms.
.Thornley et al carried out a meta-analysis comparing the effects of Chlorpromazine to placebo conditions
Found Chlorpromazine to be associated with better overall functioning – Drug therapy is an effective treatment for SZ.
✔ Strong empirical support for antipsychotic effectiveness.
✔ Atypical drugs offer broader symptom relief and fewer motor side effects.
✔ Medications reduce relapse rates and improve functioning.
✖ Side effects → reduced compliance.
✖ Not a cure → symptoms may persist.
✖ Treats symptoms, not underlying cause.
✖ Ethical concerns – sedation and long-term dependency.