2016
DOI: 10.1002/ddr.21337
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Improving Current Treatments for Schizophrenia

Abstract: Preclinical Research After the identification of the schizophrenia as an illness over a century ago, treatment of affected individuals included unspecific, mostly very robust methods including deep insulin coma and lobectomy/leucotomy. The first relatively specific treatment of schizophrenia started about 60 years ago with the antipsychotic chlorpromazine. All currently approved antipsychotic drugs block dopamine receptors, indicating that manipulation of dopaminergic function is fundamental to a therapeutic r… Show more

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Cited by 58 publications
(25 citation statements)
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“…While the dopamine D2 receptors are being blocked, psychotic symptoms can be improved obviously. A major issue with TAPs is the limited ability to treat negative and cognitive domains of schizophrenia, alongside with the risk of extrapyramidal symptoms (EPS) 2…”
Section: Introductionmentioning
confidence: 99%
“…While the dopamine D2 receptors are being blocked, psychotic symptoms can be improved obviously. A major issue with TAPs is the limited ability to treat negative and cognitive domains of schizophrenia, alongside with the risk of extrapyramidal symptoms (EPS) 2…”
Section: Introductionmentioning
confidence: 99%
“…Till the first half of the 20 th century, a lot of trial and error treatments (many of which were painful, bizarre and unsuccessful) for schizophrenia were being applied [17]. These treatments, sometimes called 'biological therapies' include fever therapy (induction of fevers by injecting sulphur and oil, or causing abscesses), gas therapy, electroconvulsive therapy, frontal lobotomy, simple sedation, deep insulin coma, lobectomy/leucotomy, and so on [17,200]. Many of these 'treatments' are fanciful but ineffective, and dangerous by today's standard; but they were applied in an era when there was a lack of understanding of the neurochemical basis of the disorder.…”
Section: Pharmacotherapy Past Present and Futurementioning
confidence: 99%
“…chlorpromazine; high potency drugs e.g. pimozide, haloperidol, fluphenazine); second generation: dopamine-serotonin antagonists (risperidone, paliperidone) and multitargeted antipsychotics (clozapine, olanzapine, ziprasidone, quetiapine, asenapine, iloperidone); third generation: dopamine-functionally selective (aripirazole, brexpiprazole, cariprazine) [200]. These classifications also give some clues regarding the neurotransmitter receptors that the drugs interact with.…”
Section: Pharmacotherapy Past Present and Futurementioning
confidence: 99%
“…However, other studies of α7 nAChR agonists failed to show any benefit on either cognitive deficits or negative symptoms (Preskorn et al, ; Walling et al, ). PAMs with selectivity for α7 nAChRs have been proposed as an alternative therapeutic strategy to orthosteric activation of these receptors, which might avoid producing unwanted side effects (Dunlop and Brandon, ; Maric et al, ).…”
Section: Cholinergic Neurotransmissionmentioning
confidence: 99%