Search Results - "Tomoko Horisawa"
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The effects of selective antagonists of serotonin 5-HT7 and 5-HT1A receptors on MK-801-induced impairment of learning and memory in the passive avoidance and Morris water maze tests in rats: Mechanistic implications for the beneficial effects of the novel atypical antipsychotic lurasidone
Published in Behavioural brain research (20-06-2011)“…We have previously reported that lurasidone, a novel atypical antipsychotic with potent serotonin 5-HT(7) antagonist and 5-HT(1A) partial agonist activities,…”
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Blonanserin extensively occupies rat dopamine D3 receptors at antipsychotic dose range
Published in Journal of pharmacological sciences (01-03-2015)“…Antagonism of the dopamine D3 receptor has been hypothesized to be beneficial for schizophrenia cognitive deficits, negative symptoms and extrapyramidal…”
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The role of 5-HT7 receptor antagonism in the amelioration of MK-801-induced learning and memory deficits by the novel atypical antipsychotic drug lurasidone
Published in Behavioural brain research (01-05-2013)“…► MK-801 induced cognitive deficits in passive avoidance responses in rats. ► Lurasidone, an antipsychotic with 5-HT7 antagonism, reversed the effect of…”
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Binding of lurasidone, a novel antipsychotic, to rat 5-HT7 receptor: Analysis by [3H]SB-269970 autoradiography
Published in Progress in neuro-psychopharmacology & biological psychiatry (10-01-2013)“…Lurasidone is a novel antipsychotic agent with high affinity for dopamine D2 and serotonin 5-HT7, 5-HT2A, and 5-HT1A receptors. We previously reported that in…”
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Evaluation of dopamine D2/D3 and serotonin 5-HT2A receptor occupancy for a novel antipsychotic, lurasidone, in conscious common marmosets using small-animal positron emission tomography
Published in Psychopharmacology (2013)“…Rationale Lurasidone is a novel antipsychotic drug with potent binding affinity for dopamine D 2 and serotonin (5-hydroxytryptamine, 5-HT) 2A , 5-HT 7 , and…”
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Pharmacological profile of lurasidone, a novel antipsychotic agent with potent 5-hydroxytryptamine 7 (5-HT7) and 5-HT1A receptor activity
Published in The Journal of pharmacology and experimental therapeutics (01-07-2010)“…Lurasidone [(3aR,4S,7R,7aS)-2-[(1R,2R)-2-[4-(1,2-benzisothiazol-3-yl)piperazin-1-ylmethyl]cyclohexylmethyl]hexahydro-4,7-methano-2H-isoindole-1,3-dione…”
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2P434 5-HT1A receptor-mediated [35S]GTP 7 S binding in Chinese Hamster Ovary (CHO) cells expressing human 5-HT1A receptors and native rat brain membranes: Effects of clozapine and perospirone
Published in Journal of Pharmacological Sciences (2003)“…Clozapine is a prototype of atypical antipsychotics, which elicit superior efficacy for negative or cognitive symptoms of schizophrenia to conventional…”
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8
5-HT1A receptor-mediated [35S]GTPγS binding in Chinese Hamster Ovary (CHO) cells expressing human 5-HT1A receptors and native rat brain membranes: Effects of clozapine and perospirone
Published in Journal of Pharmacological Sciences (2003)“…Clozapine is a prototype of atypical antipsychotics, which elicit superior efficacy for negative or cognitive symptoms of schizophrenia to conventional…”
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9
Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT1A weak partial agonistic activity showing the antidepressant-like effect
Published in Bioorganic & medicinal chemistry (01-01-2017)“…[Display omitted] We report the discovery of a novel benzylpiperidine derivative with serotonin transporter (SERT) inhibitory activity and 5-HT1A receptor weak…”
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10
Structural insight into receptor-selectivity for lurasidone
Published in Neurochemistry international (01-12-2012)“…► Structural models of lurasidone–GPCRs were constructed by in silico study. ► We elucidated structural features that gave lurasidone high receptor…”
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11
Evaluation of dopamine D sub(2)/D sub(3) and serotonin 5-HT sub(2A) receptor occupancy for a novel antipsychotic, lurasidone, in conscious common marmosets using small-animal positron emission tomography
Published in Psychopharmacology (01-01-2013)“…Rationale: Lurasidone is a novel antipsychotic drug with potent binding affinity for dopamine D sub(2) and serotonin (5-hydroxytryptamine, 5-HT) sub(2A), 5-HT…”
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12
Evaluation of dopamine D.sub.2/D.sub.3 and serotonin 5-HT.sub.2A receptor occupancy for a novel antipsychotic, lurasidone, in conscious common marmosets using small-animal positron emission tomography
Published in Psychopharmacology (01-01-2013)“…Rationale Lurasidone is a novel antipsychotic drug with potent binding affinity for dopamine D.sub.2 and serotonin (5-hydroxytryptamine, 5-HT).sub.2A,…”
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13
The effects of selective antagonists of serotonin 5-HT 7 and 5-HT 1A receptors on MK-801-induced impairment of learning and memory in the passive avoidance and Morris water maze tests in rats: Mechanistic implications for the beneficial effects of the novel atypical antipsychotic lurasidone
Published in Behavioural brain research (2011)“…► MK-801 impaired passive avoidance (PA) and Morris water maze (MWM) learning in rats. ► The 5-HT 7 antagonist SB-269970 reversed the PA and MWM learning…”
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14
Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT 1A weak partial agonistic activity showing the antidepressant-like effect
Published in Bioorganic & medicinal chemistry (01-01-2017)“…We report the discovery of a novel benzylpiperidine derivative with serotonin transporter (SERT) inhibitory activity and 5-HT receptor weak partial agonistic…”
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15
Effects of SM-13496, an atypical antipsychotic agent, on MK-801-induced learning deficit in rats
Published in Journal of Pharmacological Sciences (2004)“…It is generally assumed that schizophrenia patients show cognitive impairment as well as positive symptoms and negative symptoms and that typical…”
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Potential role of 5-HT2 and D2 receptor interaction in the atypical antipsychotic action of the novel succimide derivative, perospirone
Published in Polish journal of pharmacology (01-08-1997)“…The pharmacological profile of the novel serotonin-dopamine antagonists (SDA)-type antipsychotic, perospirone, was compared with other SDA and typical…”
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