Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/5135
Title: Effects of Asenapine and Paliperidone on Depression, Anxiety and Analgesy in Mice: Alterations in Brain Neurotrophic Factors, Neurogenesis, and Blood Enzyme Levels
Authors: Gumuslu, Esen
Mutlu, Oguz
Kokturk, Sibel
Ulak, Guner
Eraldemir, Fatma Ceyla
Tatar, Ozan Can
Yasar, Alisan Burak
Tanyeri, Pelin
Akar, Furuzan
Erden, Faruk
Ordu Üniversitesi
0000-0001-5636-3300
0000-0001-5636-3300
0000-0002-2987-5834
0000-0003-0952-0742
0000-0002-9046-7362
0000-0001-9410-8554
0000-0002-6778-3009
Keywords: antipsychotics, behaviour, neurodegeneration, neurotrophic factors
ELEVATED PLUS-MAZE, SIGNALING PATHWAY, ANTIDEPRESSANTS, HALOPERIDOL, RISPERIDONE, SCHIZOPHRENIA, EXPRESSION, OLANZAPINE, CLOZAPINE, IMPAIRMENT
Issue Date: 2018
Publisher: WOLTERS KLUWER MEDKNOW PUBLICATIONS-MUMBAI
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. Chin. J. Physiol., 61(5), 280-292. https://doi.org/10.4077/CJP.2018.BAH626
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.
Description: WoS Categories: Physiology
Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED)
Research Areas: Physiology
URI: http://dx.doi.org/10.4077/CJP.2018.BAH626
https://www.webofscience.com/wos/woscc/full-record/WOS:000454048700003
http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/5135
ISSN: 0304-4920
2666-0059
Appears in Collections:Temel Tıp Bilimleri

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