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  Vol. 36 No. 3, March 1979 TABLE OF CONTENTS
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Improvement of Schizophrenic Patients Treated With Des-Tyr1]-{gamma}-endorphin (DT{gamma}E)

Wim M. A. Verhoeven, MD; Herman M. van Praag, MD; Jan M. van Ree, MD; David de Wied, MD

Arch Gen Psychiatry. 1979;36(3):294-298.


Abstract

• It was postulated from animal experiments that {gamma}-endorphin and, in particular, the nonopiate-like peptide [des-Tyr1]-{gamma}-endorphin (DT{gamma}E, β-lipotropin [β-LPH]62-77) have neuroleptic-like activity. To test this, 14 patients with long-lasting, relapsing schizophrenic or schizoaffective psychosis resistant to conventional neuroleptics were treated with DT{gamma}E. An open design was used first for six patients (study 1) and a double-blind, crossover design for the other eight (study 2). In study 1, all neuroleptic medication was discontinued and 1 mg of DT{gamma}E zinc phosphate was given daily intramuscularly for about seven days. In study 2, six patients were maintained with neuroleptic therapy and two patients were drug free; all eight received daily intramuscular injections of 1 mg of nonlasting DT{gamma}E in saline solution for eight days. There was transient or semipermanent improvement in both studies in which the psychotic symptoms diminished or even disappeared. In study 2, there was a slight but significant improvement with the first treatment. Improvement continued and by day 4, the psychotic symptoms had almost disappeared. No toxic side effects were noted. These effects of DT{gamma}E may be a consequence of the normalization of β-endorphin homeostasis in the brain.



Author Affiliations

From the Department of Psychiatry (Drs Verhoeven and Praag), and the Rudolf Magnus Institute for Pharmacology (Drs van Ree and de Wied), State University, Utrecht, The Netherlands.


Footnotes

Accepted for publication Nov 21, 1978.

Reprint requests to the Department of Psychiatry, State University, Nicolaas Beetsstraat 24, Utrecht, The Netherlands (Dr Verhoeven).



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