Neuronal cholecystokinin and schizophrenia: pathogenic and therapeutic studies.

Abstract:

:Neuroleptic-free schizophrenic patients received caerulein, a potent analogue of cholecystokinin octapeptide, in a fixed- and rising-dose schedule. In addition, neuroleptic-treated patients received a single dose of the peptide with a 4-week follow-up. No significant change in mental status was observed after any of these administration schedules. Peak plasma levels of caerulein were noted at 20-30 min after IM administration; at this time no changes in cortical evoked potential were demonstrated. Furthermore, levels of cholecystokinin were not found to be reduced, but were in fact elevated in lumbar cerebrospinal fluid of schizophrenic patients. These data argue against the antipsychotic efficacy of systemic caerulein administration and, because evidence of CNS response to CCK is lacking, suggest that other pharmacologic strategies may be necessary to effectively modify central peptide systems with systemically administered drugs.

journal_title

Psychopharmacology

authors

Tamminga CA,Littman RL,Alphs LD,Chase TN,Thaker GK,Wagman AM

doi

10.1007/BF00180843

subject

Has Abstract

pub_date

1986-01-01 00:00:00

pages

387-91

issue

3

eissn

0033-3158

issn

1432-2072

journal_volume

88

pub_type

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