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Effects of Asenapine and Paliperidone on Depression, Anxiety and Analgesy in Mice: Alterations in Brain Neurotrophic Factors, Neurogenesis, and Blood Enzyme Levels

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dc.contributor.authors Gumuslu, E; Mutlu, O; Kokturk, S; Ulak, G; Eraldemir, FC; Tatar, OC; Yasar, AB; Tanyeri, P; Akar, F; Erden, F;
dc.date.accessioned 2020-02-27T08:27:42Z
dc.date.available 2020-02-27T08:27:42Z
dc.date.issued 2018
dc.identifier.citation Gumuslu, E; Mutlu, O; Kokturk, S; Ulak, G; Eraldemir, FC; Tatar, OC; Yasar, AB; Tanyeri, P; Akar, F; Erden, F; (2018). Effects of Asenapine and Paliperidone on Depression, Anxiety and Analgesy in Mice: Alterations in Brain Neurotrophic Factors, Neurogenesis, and Blood Enzyme Levels. CHINESE JOURNAL OF PHYSIOLOGY, 61, 292-280
dc.identifier.issn 0304-4920
dc.identifier.uri https://doi.org/10.4077/CJP.2018.BAH626
dc.identifier.uri https://hdl.handle.net/20.500.12619/65993
dc.description.abstract Schizophrenia, an important brain neurodevelopmental disorder, is observed in 1% of the global population. New-generation antipsychotics have been developed as alternatives to typical antipsychotics for more effective and safe therapy. Chronic administration of asenapine and paliperidone compared to haloperidol on depression, anxiety and analgesy in the forced swimming test (FST), elevated plus maze (EPM) and hot plate tests were examined in mice. Moreover effects of drugs, on expression levels of brain neurotrophic factors [brain-derived neurotrophic factor (BDNF), cAMP response element binding protein (CREB),nerve growth factor (NGF), synapsin and fibroblast growth factor 2 (FGF2)] in the hippocampus of mice, neurogenesis and neurodegeneration, and blood enzyme levels were also investigated. In FST, haloperidol (0.25 mg/kg) significantly increased immobility time while both asenapine (0.075 mg/kg) and paliperidone (0.25 and 0.50 mg/kg) significantly diminished this parameter. In EPM test, haloperidol significantly increased both %, time spent in open arms and % open arm entries. Asenapine (0.075 mg/kg) and paliperidone (0.50 mg/kg) significantly increased % time spent in the open arms. They also increased % open arm entries, but this parameter failed to reach a statistically significant value. In hot plate test, haloperidol (0.125 and 0.25 mg/kg) and paliperidone (0.25 and 0.50 mg/kg) significantly increased the latency to lick the hind paws but asenapine had no effect. Asenapine and paliperidone upregulated more neurotrophic factors in the brain and caused less neurodegeneration compared to haloperidol. Investigated drugs had no effect on liver enzymes and plasma glucose levels. Asenapine and paliperidone may be preferred over classical antipsychotics since they have antidepressant-like effect, upregulate more neurotrophic factors and cause less neurodegeneration in naive mice without having diabetogenic and liver damaging effects. Paliperidone seems to possess superior effects compared to asenapine since it also exerts analgesic-like effect.
dc.language English
dc.publisher WOLTERS KLUWER MEDKNOW PUBLICATIONS
dc.subject Physiology
dc.title Effects of Asenapine and Paliperidone on Depression, Anxiety and Analgesy in Mice: Alterations in Brain Neurotrophic Factors, Neurogenesis, and Blood Enzyme Levels
dc.type Article
dc.identifier.volume 61
dc.identifier.startpage 280
dc.identifier.endpage 292
dc.contributor.department Sakarya Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü
dc.contributor.saüauthor Tanyeri, Pelin
dc.contributor.saüauthor Tanyeri, Pelin
dc.contributor.saüauthor Tanyeri, Pelin
dc.relation.journal CHINESE JOURNAL OF PHYSIOLOGY
dc.identifier.wos WOS:000454048700003
dc.identifier.doi 10.4077/CJP.2018.BAH626
dc.identifier.eissn 2666-0059
dc.contributor.author Esen Gumuslu
dc.contributor.author Oguz Mutlu
dc.contributor.author Sibel Kokturk
dc.contributor.author Guner Ulak
dc.contributor.author Fatma Ceyla Eraldemir
dc.contributor.author Ozan Can Tatar
dc.contributor.author Alisan Burak Yasar
dc.contributor.author Tanyeri, Pelin
dc.contributor.author Tanyeri, Pelin
dc.contributor.author Tanyeri, Pelin
dc.contributor.author Furuzan Akar
dc.contributor.author Faruk Erden


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