Literature DB >> 3097570

Neuropeptide therapies in chronic schizophrenia: TRH and vasopressin administration.

F Brambilla, E Aguglia, R Massironi, M Maggioni, W Grillo, R Castiglioni, M Catalano, F Drago.   

Abstract

Twenty-three chronic undifferentiated schizophrenics, 13 women and 10 men, aged 37-64 years with 15-to 40-year histories of the disease were given either thyrotropin-releasing hormone (TRH) (10 subjects) or DDAVP (13 subjects) with the aim to improve the negative symptoms of the disease and memory. TRH (600 micrograms i.v.) and DDAVP (4 micrograms i.m.) were administered every other day for 30 days. Negative symptoms were monitored by the Andreasen rating scale and by the Honingfeld NOSIE rating scale, memory by the Folstein 'Mini mental State' rating scale and by the Luria-Nebraska rating scale before therapy and then at days 15, 16, 30 and 31 of treatment. Both therapies significantly improved negative symptoms. Memory was significantly improved in all the patients treated with TRH and in 9 of the 13 patients treated with DDAVP, who presented less severe cognitive impairments. A peripheral mechanism of action of DDAVP was excluded by the observation that plasma electrolytes and osmolality, blood pressure, ECG patterns, 24-hour urine volume and specific gravity, basal plasma cortisol and growth hormone levels and weight of the patients were unchanged during therapy. TRH treatment induced a transient borderline hyperthyroidism at day 15 and a progressive decrease of the thyrotropin response to TRH stimulation. A common mechanism of action of the two peptides on the central noradrenergic system is suggested.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3097570     DOI: 10.1159/000118253

Source DB:  PubMed          Journal:  Neuropsychobiology        ISSN: 0302-282X            Impact factor:   2.328


  5 in total

1.  Acute effects of high-dose thyrotropin releasing hormone infusions in Alzheimer's disease.

Authors:  A M Mellow; T Sunderland; R M Cohen; B A Lawlor; J L Hill; P A Newhouse; M R Cohen; D L Murphy
Journal:  Psychopharmacology (Berl)       Date:  1989       Impact factor: 4.530

2.  Common Polymorphisms Within QPCT Gene Are Associated with the Susceptibility of Schizophrenia in a Han Chinese Population.

Authors:  Qiao-Quan Zhang; Teng Jiang; Li-Ze Gu; Xi-Chen Zhu; Hong-Dong Zhao; Qing Gao; Hai-Qing Zhu; Jun-Shan Zhou; Ying-Dong Zhang
Journal:  Mol Neurobiol       Date:  2015-11-16       Impact factor: 5.590

3.  Neuropeptides involved in the pathophysiology of schizophrenia and major depression.

Authors:  David De Wied; Hein O. Sigling
Journal:  Neurotox Res       Date:  2002 Aug-Sep       Impact factor: 3.911

Review 4.  Negative symptoms in schizophrenia: considerations for clinical trials. Working group on negative symptoms in schizophrenia.

Authors:  H J Möller; H M van Praag; B Aufdembrinke; P Bailey; T R Barnes; J Beck; H Bentsen; F X Eich; L Farrow; W W Fleischhacker
Journal:  Psychopharmacology (Berl)       Date:  1994-06       Impact factor: 4.530

5.  Electroencephalographic and early communicative abnormalities in Brattleboro rats.

Authors:  Robert E Lin; Lauren Ambler; Eddie N Billingslea; Jimmy Suh; Shweta Batheja; Valerie Tatard-Leitman; Robert E Featherstone; Steven J Siegel
Journal:  Physiol Rep       Date:  2013-10-20
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.