阳极损毁海马腹侧下托可减少成瘾大鼠的条件位置偏爱  被引量:1

Electrolytic lesions of ventral subiculum to reduce conditioned place preference in drug addicted rats

在线阅读下载全文

作  者:王建[1] 宋乐[1] 胡三觉[1] 

机构地区:[1]第四军医大学全军神经科学研究所,陕西西安710033

出  处:《第四军医大学学报》2006年第12期1083-1085,共3页Journal of the Fourth Military Medical University

基  金:国家自然科学基金重点项目30530260

摘  要:目的:研究损毁腹侧海马下托(VSUB)是否能够阻止成瘾大鼠的条件位置偏爱.方法:雌性SD大鼠,经过吗啡强化训练使其形成条件位置偏爱(CPP).CPP形成并稳定之后,将大鼠分成3组:损毁组20只,接受双侧VSUB的直流电损毁;假手术组10只,接受与手术组相同的手术操作,但不通电流;空白对照组10只,不作任何处理.经过5d的恢复,3组大鼠再次测定CPP时间,确定其药物渴求的程度.结果:行为学测试结束后,将样本灌注切片进行组织学评定,损毁组脑片组织缺损位置局限于VSUB区域.损毁组大鼠伴药箱停留时间明显减少[(93.1±26.0)s],相对于假手术组[(10.1±4.5)s]和空白对照组[(5.1±4.1)s]的大鼠在伴药侧停留的时间减少量有显著性差异(P<0.05).结论:VSUB在大鼠对药物的渴求中起着非常重要的作用,损毁该部位可以阻止成瘾大鼠的条件位置偏爱.AIM: To investigate whether the ventral subiculum (VSUB) lesions can release the drug craving from drug addicted rats. METHODS: Female SD rats were trained to acquire the morphine conditioned place preference (CPP), After the preference was established, the rats were divided to 3 groups, The lesion group ( n = 20) received the electrolytic lesions of VSUB, the sham lesion group ( n = 10) received the same operation to the lesion group but no current passed, and the control group ( n = 10) received no operation. After 5 d recovery, the 3 groups underwent the CPP testing again to observe the extent of drug craving, RESULTS: A histological test was performed on postlesion rats after a behavioral test, and the lesions were found confined to the VSUB. The time that the lesion group spent in the drug-paired side was significant decreased [ (93. 1 ± 26.0) s ] compared with both sham group [ ( 10. 1 ± 4. 5 ) s ] and control group [(5. 1 ±4.1) s]. (P〈0.05). CONCLUSION: The VSUB play an important role in drug addiction and lesions of the exact part can release the drug craving from drug addicted rats.

关 键 词:条件位置偏爱 海马 电解损毁 吗啡依赖 药物渴求 

分 类 号:Q189[生物学—神经生物学] Q55[生物学—普通生物学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象