Effects of ziprasidone, SCH23390 and SB277011 on spatial memory in the Morris water maze test in naive and MK-801 treated mice
Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment. Improvements in cognitive function should be a characteristic of all newly developed drugs for the treatment of schizophrenia with dementia. Thus, we investigate...
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Published in | Pharmacology, biochemistry and behavior Vol. 138; pp. 142 - 147 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.11.2015
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Abstract | Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment. Improvements in cognitive function should be a characteristic of all newly developed drugs for the treatment of schizophrenia with dementia. Thus, we investigated the effects of the second-generation antipsychotic ziprasidone, dopamine D1 antagonist SCH-23390 and dopamine D3 antagonist SB-277011 on spatial learning and memory.
Male inbred mice were used. The effects of ziprasidone, SCH-23390 and SB-277011 were investigated using the Morris water maze test.
Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the time spent in the target quadrant in naive mice. MK-801 (0.1mg/kg) significantly decreased the time spent in the target quadrant. The time spent in the target quadrant was significantly prolonged by Ziprasidone (0.5 and 1mg/kg) and SCH-23390 (0.1mg/kg), but not with SB-277011 (20mg/kg) in MK-801-treated mice.
Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the mean distance to the platform in naive mice. MK-801 significantly increased the mean distance to the platform. Ziprasidone (1mg/kg) and SCH-23390 (0.1mg/kg) significantly decreased the mean distance to the platform in MK-801-treated mice, but SB-277011 (20mg/kg) didn't.
MK-801 significantly increased the total distance moved. Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the total distance moved in naive mice. Ziprasidone (1mg/kg) and SCH-23390 (0.1mg/kg) significantly decreased the total distance moved in MK-801-treated mice, but SB-277011 (20mg/kg) didn't.
The second-generation antipsychotic drug ziprasidone and D1 antagonist SCH23390, but not the D3 antagonist SB277011, might be clinically useful for the treatment of cognitive impairments in patients with schizophrenia.
•Ziprasidone significantly prolonged the time spent in the target quadrant in MK-801-treated mice.•The time spent in the target quadrant is significantly prolonged by SCH-23390 in MK-801-treated mice.•Ziprasidone significantly decreased the mean distance to the platform in MK-801-treated mice.•SCH-23390 significantly decreased the mean distance to the platform in MK-801-treated mice. |
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AbstractList | Introduction: Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment. Improvements in cognitive function should be a characteristic of all newly developed drugs for the treatment of schizophreniawith dementia. Thus,we investigated the effects of the second-generation antipsychotic ziprasidone, dopamine D1 antagonist SCH-23390 and dopamine D3 antagonist SB-277011 on spatial learning and memory. Materials and methods: Male inbred mice were used. The effects of ziprasidone, SCH-23390 and SB-277011 were investigated using the Morris water maze test. Results: Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1 mg/kg) and SB-277011 (10 and 20 mg/kg) had no effect on the time spent in the target quadrant in naive mice.MK-801 (0.1mg/kg) significantly decreased the time spent in the target quadrant. The time spent in the target quadrant was significantly prolonged by Ziprasidone (0.5 and 1 mg/kg) and SCH-23390 (0.1 mg/kg), but not with SB-277011 (20 mg/kg) in MK-801-treated mice. Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1 mg/kg) and SB-277011 (10 and 20 mg/kg) had no effect on themean distance to the platformin naivemice.MK-801 significantly increased themean distance to the platform. Ziprasidone (1 mg/kg) and SCH-23390 (0.1 mg/kg) significantly decreased the mean distance to the platform in MK-801-treated mice, but SB-277011 (20 mg/kg) didn't. MK-801 significantly increased the total distance moved. Ziprasidone (0.5 and 1 mg/kg), SCH-23390 (0.05 and 0.1 mg/kg) and SB-277011 (10 and 20 mg/kg) had no effect on the total distance moved in naive mice. Ziprasidone (1 mg/kg) and SCH-23390 (0.1 mg/kg) significantly decreased the total distance moved in MK-801-treated mice, but SB-277011 (20 mg/kg) didn't. Conclusions: The second-generation antipsychotic drug ziprasidone and D1 antagonist SCH23390, but not the D3 antagonist SB277011, might be clinically useful for the treatment of cognitive impairments in patients with schizophrenia. Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment. Improvements in cognitive function should be a characteristic of all newly developed drugs for the treatment of schizophrenia with dementia. Thus, we investigated the effects of the second-generation antipsychotic ziprasidone, dopamine D1 antagonist SCH-23390 and dopamine D3 antagonist SB-277011 on spatial learning and memory. Male inbred mice were used. The effects of ziprasidone, SCH-23390 and SB-277011 were investigated using the Morris water maze test. Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the time spent in the target quadrant in naive mice. MK-801 (0.1mg/kg) significantly decreased the time spent in the target quadrant. The time spent in the target quadrant was significantly prolonged by Ziprasidone (0.5 and 1mg/kg) and SCH-23390 (0.1mg/kg), but not with SB-277011 (20mg/kg) in MK-801-treated mice. Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the mean distance to the platform in naive mice. MK-801 significantly increased the mean distance to the platform. Ziprasidone (1mg/kg) and SCH-23390 (0.1mg/kg) significantly decreased the mean distance to the platform in MK-801-treated mice, but SB-277011 (20mg/kg) didn't. MK-801 significantly increased the total distance moved. Ziprasidone (0.5 and 1mg/kg), SCH-23390 (0.05 and 0.1mg/kg) and SB-277011 (10 and 20mg/kg) had no effect on the total distance moved in naive mice. Ziprasidone (1mg/kg) and SCH-23390 (0.1mg/kg) significantly decreased the total distance moved in MK-801-treated mice, but SB-277011 (20mg/kg) didn't. The second-generation antipsychotic drug ziprasidone and D1 antagonist SCH23390, but not the D3 antagonist SB277011, might be clinically useful for the treatment of cognitive impairments in patients with schizophrenia. •Ziprasidone significantly prolonged the time spent in the target quadrant in MK-801-treated mice.•The time spent in the target quadrant is significantly prolonged by SCH-23390 in MK-801-treated mice.•Ziprasidone significantly decreased the mean distance to the platform in MK-801-treated mice.•SCH-23390 significantly decreased the mean distance to the platform in MK-801-treated mice. |
Author | Akar, Füruzan Yildiz Ulak, Güner Celikyurt, Ipek Komsuoglu Erden, Bekir Faruk Mutlu, Oguz Buyukokuroglu, Mehmet Emin Tanyeri, Pelin |
Author_xml | – sequence: 1 givenname: Pelin surname: Tanyeri fullname: Tanyeri, Pelin email: pelintanyeri@yahoo.com organization: Sakarya University, Faculty of Medicine, Department of Pharmacology, 54100 Sakarya, Turkey – sequence: 2 givenname: Mehmet Emin surname: Buyukokuroglu fullname: Buyukokuroglu, Mehmet Emin email: mebuyukokuroglu@yahoo.com organization: Sakarya University, Faculty of Medicine, Department of Pharmacology, 54100 Sakarya, Turkey – sequence: 3 givenname: Oguz surname: Mutlu fullname: Mutlu, Oguz email: oguzmutlu80@hotmail.com organization: Kocaeli University, Faculty of Medicine, Department of Pharmacology, 41380 Kocaeli, Turkey – sequence: 4 givenname: Güner surname: Ulak fullname: Ulak, Güner email: gunerulak@yahoo.com organization: Kocaeli University, Faculty of Medicine, Department of Pharmacology, 41380 Kocaeli, Turkey – sequence: 5 givenname: Füruzan Yildiz surname: Akar fullname: Akar, Füruzan Yildiz email: firuzanakar@gmail.com organization: Kocaeli University, Faculty of Medicine, Department of Pharmacology, 41380 Kocaeli, Turkey – sequence: 6 givenname: Ipek Komsuoglu surname: Celikyurt fullname: Celikyurt, Ipek Komsuoglu email: ikcelikyurt@gmail.com organization: Kocaeli University, Faculty of Medicine, Department of Pharmacology, 41380 Kocaeli, Turkey – sequence: 7 givenname: Bekir Faruk surname: Erden fullname: Erden, Bekir Faruk email: faruk.erden@isbank.net.tr organization: Kocaeli University, Faculty of Medicine, Department of Pharmacology, 41380 Kocaeli, Turkey |
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Keywords | MK-801 SB277011 Morris water maze Ziprasidone SCH23390 Cognition Mice |
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SubjectTerms | Animals Antipsychotic Agents - pharmacology Benzazepines - pharmacology Cognition Dizocilpine Maleate - pharmacology Excitatory Amino Acid Antagonists - pharmacology Male Maze Learning - drug effects Mice Mice, Inbred BALB C MK-801 Morris water maze Motor Activity - drug effects Nitriles - pharmacology Piperazines - pharmacology Psychomotor Performance - drug effects SB277011 SCH23390 Spatial Memory - drug effects Tetrahydroisoquinolines - pharmacology Thiazoles - pharmacology Ziprasidone |
Title | Effects of ziprasidone, SCH23390 and SB277011 on spatial memory in the Morris water maze test in naive and MK-801 treated mice |
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