D-serine treatment reduces cocaine-primed reinstatement in rats following extended access to cocaine self-administration.
D-serine treatment reduces cocaine-primed reinstatement in rats following extended access to cocaine self-administration.
复制标题
DOI:
10.1016/j.neuroscience.2010.06.006
复制
发表时间:
2010-09-01
期刊:
影响因子:
3.3
通讯作者:
Wagner, J. J.
中科院分区:
文献类型:
--
作者:
Kelamangalath, L.;Wagner, J. J.
The most intractable feature of drug addiction is the high rate of relapse, even following extended periods of abstinence from drug-taking. Evidence suggests that allowing rats extended access to cocaine self-administration leads to behavioral characteristics in these animals that are consistent with the development of addiction in humans. In the current study, rats were allowed to self-administer cocaine over a total of 22 daily sessions, the final 7 of which were long-access (LgA) sessions of 6 hours duration. Assessments of reinstatement of drug-seeking behavior were made following reintroduction to the drug-taking environment and noncontingent priming with either CS or cocaine in both extinguished and abstinent subject groups. Three separate groups of rats were treated with either saline or D-serine (100mg/kg i.p.) administered 2 hrs prior to, or immediately following, each extinction training session. Saline-treated LgA rats were resistant to the effects of extinction training to reduce noncontingent priming of reinstatement of drug-seeking behavior with either CS or cocaine. In contrast, treatment with D-serine either before or immediately following the sessions resulted in a significant enhancement in the ability of extinction training to reduce cocaine-primed reinstatement of drug-seeking behavior. These results suggest that D-serine can act to enhance the consolidation of extinction learning in LgA rats, and is therefore a promising adjunctive agent along with behavioral therapy for the treatment of cocaine addiction.
登录
查看更多内容
DOI:
10.1124/jpet.107.122861
发表时间:
2007-09-01
影响因子:
3.5
作者:
Knackstedt, Lori A.;Kalivas, Peter W.
通讯作者:
Kalivas, Peter W.
影响因子:
7.6
作者:
Duffy, Steven;Labrie, Viviane;Roder, John C.
通讯作者:
Roder, John C.
影响因子:
2.7
作者:
Karasawa, Jun-Ichi;Hashimoto, Kenji;Chaki, Shigeyuki
通讯作者:
Chaki, Shigeyuki
影响因子:
3.4
作者:
JAFFE, JH;CASCELLA, NG;SHERER, MA
通讯作者:
SHERER, MA
影响因子:
3.4
作者:
Mantsch, JR;Yuferov, V;Kreek, MJ
通讯作者:
Kreek, MJ