약물 자가 투여 중독모델에서 TRPV1 수용체 조절을 통한 Methamphetamine 보상 기전 연구

项目来源

韩国国家研究基金(NRF)

项目主持人

장춘곤

项目受资助机构

성균관대학교

项目编号

2009-013-E00056

立项年度

2009

立项时间

未公开

项目级别

国家级

研究期限

未知 / 未知

受资助金额

未知

学科

의약학

学科代码

未公开

基金类别

人文社科-SD-Research

关键词

자가투여법 ; 보상 ; 약물의존 ; 필로폰 ; 약물남용 ; 약물자가투여 ; 약물중독 ; 재발 ; drug dependence ; methamphetamine ; reward ; self-administration ; drug abuse ; TRPV1

参与者

장춘곤

参与机构

未公开

项目标书摘要:Research Summary:The purpose of this study is to understand the reward mechanism of methamphetamine modulated by TRPV1 receptors and to learn the self-administration test which is the newest research skills and core skills in drug abuse.Methamphetamine self-administration established by conductiing FR,PR,and reinstatement schedules.TRPV1 antagonists,capsazepine and SB366791 inhibited reinstatement of methamphetamine-self administaration.During early withdrawal period from methamphetamine,rat showed depressive-like behavior,and after 2 weeks withdrawal from methamphetamine,the rats showed anxiogenic behavior.Also,new dopamine agonist,PKF-205,152 inhibited the methamphetamine self-administration in PR schedule.Taken together.these results suggest that TRPV1 receptors may be developed as a novel target for treatment of drug dependence.

Application Abstract: Research Summary:The purpose of this study is to understand the reward mechanism of methamphetamine modulated by TRPV1 receptors and to learn the self-administration test which is the newest research skills and core skills in drug abuse.Methamphetamine self-administration established by conductiing FR,PR,and reinstatement schedules.TRPV1 antagonists,capsazepine and SB366791 inhibited reinstatement of methamphetamine-self administaration.During early withdrawal period from methamphetamine,rat showed depressive-like behavior,and after 2 weeks withdrawal from methamphetamine,the rats showed anxiogenic behavior.Also,new dopamine agonist,PKF-205,152 inhibited the methamphetamine self-administration in PR schedule.Taken together.these results suggest that TRPV1 receptors may be developed as a novel target for treatment of drug dependence.

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