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Noradrenergic and dopaminergic interrelation in schizophrenia
F Brambilla1, S Marini, A Saito
1Center of Psychoneuroendocrinology, Ospedale Psichiatrico Pini, Milano, Italy.
Psychiatry Research
|September 1, 1994
Summary
Growth hormone (GH) and prolactin (PRL) levels in schizophrenic patients showed varied responses to clonidine and apomorphine. Some patients exhibited blunted GH responses, correlating with illness chronicity and specific symptoms.
Area of Science:
- Neuroendocrinology
- Psychiatry
- Pharmacology
Background:
- Schizophrenia is a complex psychiatric disorder.
- Growth hormone (GH) and prolactin (PRL) are pituitary hormones.
- Dysregulation of neuroendocrine pathways may be implicated in schizophrenia.
Purpose of the Study:
- To investigate GH and PRL responses to clonidine and apomorphine in schizophrenic patients.
- To compare hormonal responses between patients and healthy controls.
- To explore correlations between hormonal responses and clinical symptoms of schizophrenia.
Main Methods:
- 20 drug-free schizophrenic patients (subchronic and chronic) and 9 controls participated.
- Acute administration of clonidine (150 µg) and apomorphine (0.5 mg).
- Parallel measurement of GH and PRL levels before and after drug administration.
Main Results:
- No significant differences in basal GH/PRL or mean responses between groups.
- Blunted GH response to clonidine in 8 patients and apomorphine in 7 patients.
- Blunted GH response to apomorphine correlated with illness chronicity.
- Exaggerated GH response to clonidine in paranoid patients.
- Correlations found between negative symptoms and GH/PRL responses, and positive symptoms and PRL responses.
Conclusions:
- While mean hormonal responses to clonidine and apomorphine do not differ between schizophrenic patients and controls, individual variations exist.
- Blunted GH responses and their correlation with chronicity suggest neuroendocrine alterations in schizophrenia.
- Specific symptom clusters in schizophrenia are associated with distinct GH and PRL response patterns.