Low-dose prazosin in combination with 5-HT6 antagonist PRX-07034 has antipsychotic effects

被引:6
作者
Abraham, Renny [1 ,2 ]
Nirogi, Ramakrishna [1 ]
Shinde, Anil [1 ]
Irupannanavar, Shantaveer [1 ]
机构
[1] Suven Life Sci Ltd, Discovery Res, Serene Chambers, Hyderabad 500055, Andhra Pradesh, India
[2] Jawaharlal Nehru Technol Univ, Dept Pharmaceut Sci, Hyderabad 500085, Andhra Pradesh, India
关键词
schizophrenia; open field; prepulse inhibition; stereotypy assay; object recognition task; MEDIAL PREFRONTAL CORTEX; RECEPTOR ANTAGONIST; PREPULSE INHIBITION; SEROTONIN(1A) RECEPTORS; COGNITIVE IMPAIRMENT; RECOGNITION MEMORY; DOPAMINE RELEASE; SCHIZOPHRENIA; RISPERIDONE; CLOZAPINE;
D O I
10.1139/cjpp-2014-0254
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An extensive amount of research has focused on the development of new pharmacological agents to treat schizophrenia. Varying from person to person, schizophrenia is a heterogeneous disease with symptoms of positive, negative, and cognitive deficits. PRX-07034, a 5-hydroxytryptamine(6) (5-HT6) receptor antagonist has been evaluated for its potential in treating obesity and cognitive deficits. This study evaluated PRX-07034 (0.1, 0.3, and 1.0 mg/kg body mass, by intraperitoneal (i.p.) injection), in combination with a low dose of prazosin (0.3 mg/kg, i.p.), for its antipsychotic potential. The research utilized a stereotypy assay, an open field test, an object recognition task, and prepulse inhibition. Dizocilpine, a non-competitive N-methyl-D-aspartate (NMDA) antagonist, was also administered in the above-mentioned assays as a psychomimetic. The combination of PRX-07034 and prazosin alleviated stereotypy and hyperlocomotor activity while enhancing memory in an object recognition task, and reversed sensory-gating deficits induced by dizocilpine. Examination of the medial prefrontal cortex revealed that a combination of PRX-07034 and prazosin reduced the dizocilpine-mediated increase of 5-HT. These results suggest that the combination of a 5-HT6 antagonist with low doses of prazosin could have therapeutic potential in the treatment of schizophrenia.
引用
收藏
页码:13 / 21
页数:9
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