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 inPharmacology, biochemistry and behavior Vol. 138; pp. 142 - 147
Main Authors Tanyeri, Pelin, Buyukokuroglu, Mehmet Emin, Mutlu, Oguz, Ulak, Güner, Akar, Füruzan Yildiz, Celikyurt, Ipek Komsuoglu, Erden, Bekir Faruk
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LanguageEnglish
Published United States 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.
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
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Keywords MK-801
SB277011
Morris water maze
Ziprasidone
SCH23390
Cognition
Mice
Language English
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  issue: 7
  year: 2013
  ident: 10.1016/j.pbb.2015.09.014_bb0025
  article-title: Phencyclidine decreases tickling-induced 50-kHz ultrasound vocalizations in juvenile rats: a putative model of the negative symptoms of schizophrenia?
  publication-title: Behav. Pharmacol.
  doi: 10.1097/FBP.0b013e3283654044
  contributor:
    fullname: Boulay
– volume: 50
  start-page: 240
  issue: 2
  year: 1988
  ident: 10.1016/j.pbb.2015.09.014_bb0090
  article-title: Scopolamine interactions with D1 and D2 antagonists on radial-arm maze performance in rats
  publication-title: Behav. Neural Biol.
  doi: 10.1016/S0163-1047(88)90911-9
  contributor:
    fullname: Levin
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Snippet Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment. Improvements in...
Introduction: Patients with schizophrenia have cognitive dysfunctions; positive psychotic symptoms are the primary purposes for schizophrenia treatment....
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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
URI https://dx.doi.org/10.1016/j.pbb.2015.09.014
https://www.ncbi.nlm.nih.gov/pubmed/26394282
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https://search.proquest.com/docview/1732826043
Volume 138
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